ChemTEB Multilingual
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Multilingual Tasks in ChemTEB
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Diethylstilbestrol is an olefinic compound that is trans-hex-3-ene in which the hydrogens at positions 3 and 4 have been replaced by p-hydroxyphenyl groups. It has a role as an antineoplastic agent, a carcinogenic agent, a xenoestrogen, an EC 3.6.3.10 (H(+)/K(+)-exchanging ATPase) inhibitor, an antifungal agent, an endocrine disruptor, an EC 1.1.1.146 (11beta-hydroxysteroid dehydrogenase) inhibitor, an autophagy inducer and a calcium channel blocker. It is a polyphenol and an olefinic compound. | ãã¹ãã³ãªã³ïŒphosphocholineïŒã¯ãçµç¹å
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ãŸããCåå¿æ§èçœ (CRP) ã®çµåæšçã®äžã€ã§ããããããã£ãŠçŽ°èãæå·ãåããæãCRPã¯ãã¹ãã³ãªã³ã«çµåããèªèããã³é£äœçšå
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ãã¹ãã¡ããžã«ã³ãªã³ (PC) ã¯é¶åµïŒããã³ãã®ä»ã®å€ãã®åµïŒã®å€©ç¶æåã®äžã€ã§ãããEgg-PCã®åœ¢ã§ãã°ãã°çäœæš¡å£èã®ç 究ã«äœ¿çšãããŠãããæ§ã
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Flecainide is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of 2,5-bis(2,2,2-trifluoroethoxy)benzoic acid with the primary amino group of piperidin-2-ylmethylamine. An antiarrhythmic agent used (in the form of its acetate salt) to prevent and treat tachyarrhythmia (abnormal fast rhythm of the heart). It has a role as an anti-arrhythmia drug. It is a monocarboxylic acid amide, a member of piperidines, an organofluorine compound and an aromatic ether. It is a conjugate base of a flecainide(1+). | ã¯ãã©ã ãã§ãã³ãŒã« (Chloramphenicol) ã¯ããã¯ããªã¢ Streptomyces venezuelae ç±æ¥ã®æçç©è³ªã§ãããçŸåšã¯ååŠåæã«ãã£ãŠäœãããŠãããååç©å㯠2,2-ãžã¯ãã-N-(1R,2R)-2-ããããã·-1-ããããã·ã¡ãã«-2-ïŒ4-ããããã§ãã«ïŒãšãã«ïŒœã¢ã»ãã¢ããã§ããã | 0 |
4-Aminobenzoic acid (also known as para-aminobenzoic acid or PABA because the two functional groups are attached to the benzene ring across from one another in the para position) is an organic compound with the formula H2NC6H4CO2H. PABA is a white crystalline solid, although commercial samples can appear gray. It is slightly soluble in water. It consists of a benzene ring substituted with amino and carboxyl groups. The compound occurs extensively in the natural world. | ãã«ããŸãã (Bortezomibãæ²»éšã³ãŒãïŒPS-341ïŒã¯ãååæšçæ²»çè¬ã®äžã€ãåååã¯ãã«ã±ã€ãïŒVelcadeïŒã§ãæŠç°è¬åå·¥æ¥ã®åäŒç€Ÿã§ããç±³åœã®ãã¬ãã¢ã 補è¬ç€Ÿãéçºããã | 0 |
Malvidin 3-O-beta-D-glucoside is an anthocyanin cation consisting of malvidin having a beta-D-glucosyl residue attached at the 3-hydroxy position. It has a role as a metabolite. It is a beta-D-glucoside, an anthocyanin cation and an aromatic ether. It is functionally related to a malvidin. It is a conjugate acid of a malvidin 3-O-beta-D-glucoside betaine. | 鶎岡é£æºæ ç¹ããã¡ã¿ãããã¯ã¹ç 究ææå±ã®äžå±±æµäºç 究å¡ããçèå¢åŒ·ãšèèªæžå°ã§å©çšãããŠããæ¢åè¬ã®ã¢ãã¬ãã¹ããã³ã«ãã転移ãæå¶ããå¹æããŒãã©ãã£ãã·ã¥ãå©çšããŠç¢ºèªããããš2019幎11æ21æ¥ã«çºè¡šãããåå
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Atenolol is an ethanolamine compound having a (4-carbamoylmethylphenoxy)methyl group at the 1-position and an N-isopropyl substituent. It has a role as a beta-adrenergic antagonist, an anti-arrhythmia drug, an antihypertensive agent, a sympatholytic agent, a xenobiotic and an environmental contaminant. It is a member of ethanolamines, a monocarboxylic acid amide and a propanolamine. | ãã«ã¿ã¶ãã³ïŒMirtazapineïŒã¯ããªã©ã³ãã®ãªã«ã¬ãã³ç€ŸïŒåã·ã§ãªã³ã°ã»ãã©ãŠç€ŸãçŸã¡ã«ã¯ç€ŸïŒãåµè£œããåç°ç³»æãã€è¬ããã«ã¢ãã¬ããªã³äœåæ§ã»ç¹ç°çã»ãããã³äœåæ§æãã€è¬ (NaSSA) ãšããã«ããŽãªã«åé¡ããããSSRIãSNRIãšã¯ç°ãªãäœçšæ©åºã§ãããçæéã§å¹æãçºçŸããå¹æã¯æç¶çã§ããã
2009幎3æçŸåšã93ã«åœã§æ¿èªãããæ¥æ¬ã«ãããŠã¯ã2009幎7æã«ãå»è¬åå»çæ©åšç·åæ©æ§ãã補é 販売ãæ¿èªãããMSD(æ§ã·ã§ãªã³ã°ã»ãã©ãŠ)ããã¬ã¡ãã³ãMeiji Seika ãã¡ã«ããããªãã¬ãã¯ã¹ãšããåååã§è²©å£²ãããŠããã | 0 |
Muscimol (also known as agarin or pantherine) is one of the principal psychoactive constituents of Amanita muscaria and related species of mushroom. Muscimol is a potent and selective orthosteric agonist for the GABAA receptor and displays sedative-hypnotic, depressant and hallucinogenic psychoactivity. This colorless or white solid is classified as an isoxazole.
Muscimol went under clinical trial phase I for epilepsy, but the trial was discontinued.
Muscimol, an agonist for the GABAA receptor, was able to significantly alleviate pain in its peak effect, recent studies from 2023 show. It has since been federally banned in Australia and is pending FDA review in the United States, but scientists believe it may relieve pain as well as some opioids without much of the risk of addiction associated with opioids. | ã¢ã»ãã«ã³ãªã³ïŒè±èª: Acetylcholine, AChïŒã¯ãå¯äº€æç¥çµãéåç¥çµã®æ«ç«¯ããæŸåºãããç¥çµåºæ¿ãäŒããç¥çµäŒéç©è³ªã§ãããã³ãªã³ã®é
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Dauricine is a plant metabolite, chemically classified as a phenol, an aromatic ether, and an isoquinoline alkaloid. It has been isolated from the Asian vine Menispermum dauricum, commonly known as Asian moonseed, and the North American vine Menispermum canadense, commonly known as Canadian moonseed. Scientists Tetsuji Kametani and Keiichiro Fukumoto of Japan are credited with being the first to synthesize dauricine in 1964, using both the Arndt-Eistert reaction and Bischler-Napieralski reaction to do so. Dauricine has been studied in vitro for its potential to inhibit cancer cell growth and to block cardiac transmembrane Na+, K+, and Ca2+ ion currents. | ãã³ã¿ã¡ãã«ãã³ãŒã³ïŒè±: PentamethylbenzeneïŒã¯è³éŠæçåæ°ŽçŽ ã®äžçš®ã§ããã³ãŒã³ç°ã®æ°ŽçŽ åå6ã€äž5ã€ãã¡ãã«åºã«çœ®ãæãã£ãæ§é ãæã€ãåžžæž©ã§ã¯è³éŠã®ããåºäœã§ããããã·ã¬ã³ã®ã¡ãã«åã«ããåŸãããããã¥ã¬ã³åæ§ã«é»åãè±å¯ã§ãè³éŠææ±é»å眮æåå¿ã容æã«èµ·ãããäž»ã«ç 究çšã«çšããããç£æ¥çšéã§ã¯ããŸã䜿ãããªãã | 0 |
Titanium(III) oxide is a titanium oxide with formula Ti2O3. | é
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Tridecane is a straight chain alkane containing 13 carbon atoms. It forms a component of the essential oils isolated from plants such as Abelmoschus esculentus. It has a role as a plant metabolite and a volatile oil component. | ã³ãããã«ãã£ãªããŒã²ã³IïŒCoproporphyrinogen IïŒãšã¯ãæ¥æ§éæ¬ æ§ãã«ãã£ãªã³çã§äœå
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Fomepizole is a member of the class of pyrazoles that is 1H-pyrazole substituted by a methyl group at position 4. It has a role as an antidote, a protective agent and an EC 1.1.1.1 (alcohol dehydrogenase) inhibitor. It derives from a hydride of a 1H-pyrazole. | ããªã¢ããžã³ïŒBrimonidineïŒã¯ã¢ãã¬ããªã³Î±2å容äœäœåè¬ãåžžæž©ã§ã¯çœè²-埮é»è²ã®ç²æ«ãšãªãé
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Dimethylamine is a secondary aliphatic amine where both N-substituents are methyl. It has a role as a metabolite. It is a secondary aliphatic amine and a member of methylamines. It is a conjugate base of a dimethylaminium. | ãã¿ã«é
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Formaldehyde ( for-MAL-di-hide, US also fÉr-) (systematic name methanal) is an organic compound with the chemical formula CH2O and structure HâCHO, more precisely H2C=O. The compound is a pungent, colourless gas that polymerises spontaneously into paraformaldehyde. It is stored as aqueous solutions (formalin), which consists mainly of the hydrate CH2(OH)2. It is the simplest of the aldehydes (RâCHO). As a precursor to many other materials and chemical compounds, in 2006 the global production of formaldehyde was estimated at 12 million tons per year. It is mainly used in the production of industrial resins, e.g., for particle board and coatings. Small amounts also occur naturally.
Formaldehyde is classified as a carcinogen and can cause respiratory and skin irritation upon exposure. | ãã©ãªãã·å®æ¯éŠé
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žãšãã«ïŒãšãã«ãã©ãã³ãethyl 4-hydroxybenzoateïŒ
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žãããã«ïŒãããã«ãã©ãã³ãpropyl 4-hydroxybenzoateïŒ
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žãã³ãžã«ïŒãã³ãžã«ãã©ãã³ãbenzyl 4-hydroxybenzoateïŒ | 0 |
Chloramphenicol is an antibiotic useful for the treatment of a number of bacterial infections. This includes use as an eye ointment to treat conjunctivitis. By mouth or by injection into a vein, it is used to treat meningitis, plague, cholera, and typhoid fever. Its use by mouth or by injection is only recommended when safer antibiotics cannot be used. Monitoring both blood levels of the medication and blood cell levels every two days is recommended during treatment.
Common side effects include bone marrow suppression, nausea, and diarrhea. The bone marrow suppression may result in death. To reduce the risk of side effects treatment duration should be as short as possible. People with liver or kidney problems may need lower doses. In young infants, a condition known as gray baby syndrome may occur which results in a swollen stomach and low blood pressure. Its use near the end of pregnancy and during breastfeeding is typically not recommended. Chloramphenicol is a broad-spectrum antibiotic that typically stops bacterial growth by stopping the production of proteins.
Chloramphenicol was discovered after being isolated from Streptomyces venezuelae in 1947. Its chemical structure was identified and it was first synthesized in 1949. It is on the World Health Organization's List of Essential Medicines. It is available as a generic medication. | ã²ã ãã£ãããžã«ïŒGemfibrozilïŒã¯ãããã(Lopid)ãªã©ã®åååã§è²©å£²ãããŠãããç°åžžãªè¡äžè質ã¬ãã«ã®æ²»çã«çšããããå»è¬åã§ãããäžè¬çã«ã²ã ãã£ãããžã«ããã¹ã¿ãã³ãåªå
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Cacodylic acid is an organoarsenic compound with the formula (CH3)2AsO2H. With the formula R2As(O)OH, it is the simplest of the arsinic acids. It is a colorless solid that is soluble in water.
Neutralization of cacodylic acid with base gives cacodylate salts, e.g. sodium cacodylate. They are potent herbicides. Cacodylic acid/sodium cacodylate is a buffering agent in the preparation and fixation of biological samples for electron microscopy and in protein crystallography. | ã«ã³ãžã«é
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žïŒDimethylarsinic acidïŒã¯ååŠåŒ (CH3)2AsO2H ã§è¡šãããææ©ãçŽ ååç©ãäž¡æ§ã§ãããã«ã³ãžã«é
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Calcium nitrate are inorganic compounds with the formula Ca(NO3)2(H2O)x. The anhydrous compound, which is rarely encountered, absorbs moisture from the air to give the tetrahydrate. Both anhydrous and hydrated forms are colourless salts. Hydrated calcium nitrate, also called Norgessalpeter (Norwegian salpeter), is mainly used as a component in fertilizers, but it has other applications. Nitrocalcite is the name for a mineral which is a hydrated calcium nitrate that forms as an efflorescence where manure contacts concrete or limestone in a dry environment as in stables or caverns. A variety of related salts are known including calcium ammonium nitrate decahydrate and calcium potassium nitrate decahydrate. | ãã«ãªã¹ããã€ã·ã³ïŒè±ïŒFlurithromycinïŒã¯ç¬¬äºäžä»£ã®ãã¯ãã©ã€ãç³»æçç©è³ªã§ããããšãªã¹ããã€ã·ã³Aã®ããçŽ åèªå°äœã§ãã ããšãªã¹ããã€ã·ã³ãšåæ§ã®äœçšãæã€åºåã¹ãã¯ãã«æçç©è³ªã§ããããšãªã¹ããã€ã·ã³ãšç°ãªãããã«ãªã¹ããã€ã·ã³ã¯é
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Suberic acid is an alpha,omega-dicarboxylic acid that is the 1,6-dicarboxy derivative of hexane. It has a role as a human metabolite. It is an alpha,omega-dicarboxylic acid and a dicarboxylic fatty acid. It is a conjugate acid of a suberate(2-) and a suberate. | ã«ããºã¬ã³ (Chamazulene) ã¯ãã«ã¢ããŒã«ããã¬ãšã¢ã®ãã»ã€ãšãŠãã³ã®ãªãœãŠçã®æ€ç©ã«å«ãŸãããC14H16ã®åååŒãæã€è³éŠæååç©ã§ãããã«ããºã¬ã³ã¯ãã»ã¹ããã«ãã³ã§ãããããªã·ã³ããçåæãããé玫è²ã®ã¢ãºã¬ã³èªå°äœã§ãããã«ããºã¬ã³ã¯ãin vivoã§æççäœçšãæã€ã | 0 |
Betamethasone is a steroid medication. It is used for a number of diseases including rheumatic disorders such as rheumatoid arthritis and systemic lupus erythematosus, skin diseases such as dermatitis and psoriasis, allergic conditions such as asthma and angioedema, preterm labor to speed the development of the baby's lungs, Crohn's disease, cancers such as leukemia, and along with fludrocortisone for adrenocortical insufficiency, among others. It can be taken by mouth, injected into a muscle, or applied to the skin, typically in cream, lotion, or liquid forms.
Serious side effects include an increased risk of infection, muscle weakness, severe allergic reactions, and psychosis. Long-term use may cause adrenal insufficiency. Stopping the medication suddenly following long-term use may be dangerous. The cream commonly results in increased hair growth and skin irritation. Betamethasone belongs to the glucocorticoid class of medication. It is a stereoisomer of dexamethasone, the two compounds differing only in the spatial configuration of the methyl group at position 16 (see steroid nomenclature).
Betamethasone was patented in 1958, and approved for medical use in the United States in 1961. The cream and ointment are on the World Health Organization's List of Essential Medicines. It is available as a generic medication. In 2021, it was the 251st most commonly prescribed medication in the United States, with more than 1 million prescriptions. | å¡©åã¢ãªã«ïŒãããã¢ãªã«ãAllyl chlorideïŒã¯ãææ©ããã²ã³ååç©ã§ãããç¡è²ã®æ¶²äœã§ãæ°Žã«ã¯äžæº¶ã ããææ©æº¶åªã«ã¯æº¶ãããäžè¬ã«è£œè¬ã蟲è¬ã®ã¢ã«ãã«åå€ãšããŠäœ¿ãããŠããããŸããåææš¹èã®æ¶æ©å€åæãšããŠã䜿çšãããäžéšã®ç±ç¡¬åæ§æš¹èãæ§æããŠãããæ¯æ§ããããçããããç©è³ªã§ããã | 0 |
Pimelic acid is a natural product found in Phycomyces blakesleeanus, Arabidopsis thaliana, and other organisms with data available. | ãžã¡ãã«äºéïŒãžã¡ãã«ããããè±: dimethylzincïŒã¯ååŠåŒZn(CH3)2ã§è¡šãããææ©äºéååç©ã | 0 |
Propylamine, also known as n-propylamine, is an amine with the chemical formula CH3(CH2)2NH2. It is a colorless volatile liquid.
Propylamine is a weak base. Its Kb (base dissociation constant) is 4.7 à 10â4. | ãµã«ã³ã·ã³ïŒsarcosineïŒãŸãã¯N-ã¡ãã«ã°ãªã·ã³ïŒè±: N-methylglycine, NMGïŒã¯ãçèããã®ä»äœå
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Fosfomycin is a phosphonic acid having an (R,S)-1,2-epoxypropyl group attached to phosphorus. It has a role as an antimicrobial agent and an EC 2.5.1.7 (UDP-N-acetylglucosamine 1-carboxyvinyltransferase) inhibitor. It is an epoxide and a member of phosphonic acids. It is functionally related to a phosphonic acid. It is a conjugate acid of a (1R,2S)-epoxypropylphosphonate(1-). | ãžã¢ãã§ãã«ã¹ã«ãã³ïŒæ£ç¢ºã«ã¯ãžã¢ãããžãã§ãã«ã¹ã«ãã³ãdiaminodiphenyl sulfone; DDSïŒã¯ãè¬åŠçã«ã¯åææèå€ã»å
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Spiperone is an azaspiro compound that is 1,3,8-triazaspiro[4.5]decane which is substituted at positions 1, 4, and 8 by phenyl, oxo, and 4-(p-fluorophenyl)-4-oxobutyl groups, respectively. It has a role as a dopaminergic antagonist, a serotonergic antagonist, an alpha-adrenergic antagonist, an antipsychotic agent and a psychotropic drug. It is an organofluorine compound, an azaspiro compound, a member of piperidines, a tertiary amino compound and an aromatic ketone. | ã¢ã¹ã«ãªããŒã« (ascaridole) ã¯å€©ç¶ã«ååšããææ©ååç©ã®äžçš®ã§ãã¢ããã«ãã³ã«åé¡ããããã¢ã¹ã«ãªããŒã«ã®ããã«ãã«ãªãã·ãæ§é ãæã€å€©ç¶ç©ã¯å°ãªããã¢ã«ã¶å±ã®æ€ç©ãç¹ã«ã¢ãªã¿ãœãŠ (Chenopodium ambrosioides) ã®ç²Ÿæ²¹ã®äž»æåã§ããã | 0 |
Niridazole is a C-nitro compound and a member of 1,3-thiazoles. | ãµãã©ããŒã«(Safranal)ã¯ãã¯ããã«ã¹ã®è±ã®éãã矀ã§ãããµãã©ã³ããåé¢ãããææ©ååç©ã§ããããµãã©ã³ã®éŠãã®äž»æåã§ããã
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Benzothiazole is a natural product found in Camellia sinensis, Gymnodinium nagasakiense, and other organisms with data available. | 1995幎以åã¯è²Žéãªç³ã§ãããããã³ããã®æœåºãé£ãããäŸ¡æ Œã1kgããã3ïœ4äžåãšé«äŸ¡ã ã£ããã岡山çã®ãã€ãªäŒæ¥æ ªåŒäŒç€Ÿã»æåïŒçŸã»ãã¬ã»ãŽã£ãŒã¿ïŒãããã³ãã³ãããã¬ãããŒã¹ãçæããé
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Peroxynitric acid is a nitrogen oxoacid. It is a conjugate acid of a peroxynitrate. | ãã°ãªããŒã¹ïŒVogliboseïŒã¯ãç³å°¿ç
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Paraoxon is a natural product found in Apis cerana with data available. | ããªãã§ã³ (thiophene) ãšã¯ãææ©ååç©ã®äžçš®ã§ãç¡«é»ãå«ãè€çŽ ç°åŒååç©ãååŠåŒã¯ C4H4Sããã©ã³ã®é
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Anhydrous magnesium acetate has the chemical formula Mg(C2H3O2)2 and in its hydrated form, magnesium acetate tetrahydrate, it has the chemical formula Mg(CH3COO)2 ⢠4H2O. In this compound magnesium has an oxidation state of 2+. Magnesium acetate is the magnesium salt of acetic acid. It is deliquescent and upon heating, it decomposes to form magnesium oxide. Magnesium acetate is commonly used as a source of magnesium in biological reactions. | é
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Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH3)2CHCH2OH (sometimes represented as i-BuOH). This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters. Its isomers are 1-butanol, 2-butanol, and tert-butanol, all of which are important industrially. | ãããŸãŒã«ïŒè±èª: DanazolïŒã¯ãã¹ãã¹ããã³èªå°äœã§ããã婊人ç§é åã§äœãšã¹ããã²ã³ç¶æ
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Kinetin is a member of the class of 6-aminopurines that is adenine carrying a (furan-2-ylmethyl) substituent at the exocyclic amino group. It has a role as a geroprotector and a cytokinin. It is a member of furans and a member of 6-aminopurines. | ãªãã·ãããã³ïŒOxybutyninïŒã¯ããžãããã³ïŒDitropanïŒãªã©ã®åååã§è²©å£²ãããŠããé掻åèè±ã®æ²»çã«çšããããå»è¬åã§ããããã«ãããžã³ãšåæ§ã®å¹èœããããåäŸã®ããããã®æ²»çã«äœ¿çšãããããšãããããæçšæ§ãè£ä»ãã蚌æ ã¯ä¹ãããæäžæ³ã¯çµå£ãŸãã¯çµç®åžåã§ããã
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2-Naphthylamine or 2-aminonaphthalene is one of two isomeric aminonaphthalenes, compounds with the formula C10H7NH2. It is a colorless solid, but samples take on a reddish color in air because of oxidation. It was formerly used to make azo dyes, but it is a known carcinogen and has largely been replaced by less toxic compounds. | ãããã³ã»ãªã³ (è±èª: Blonanserin) ã¯ã倧æ¥æ¬äœå補è¬ãéçºããéå®åæ粟ç¥ç
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Famciclovir is 2-Amino-9H-purine in which the hydrogen at position 9 is substituted by a 4-acetoxy-3-(acetoxymethyl)but-1-yl group. A prodrug of the antiviral penciclovir, it is used for the treatment of acute herpes zoster (shingles), for the treatment or suppression of recurrent genital herpes in immunocompetent patients and for the treatment of recurrent mucocutaneous herpes simplex infections in HIV infected patients. It has a role as a prodrug and an antiviral drug. It is a member of 2-aminopurines and an acetate ester. | ããã¡ãã³ïŒNabumetoneïŒãšã¯ã2-(3-ãªããœããã«)-6-ã¡ããã·ããã¿ã¬ã³ã®ããšã§ãããã€ãŸããããã¿ã¬ã³ã®2äœãš6äœã«çœ®æåºãä»ããååç©ã§ãããéã¹ããã€ãæ§æççè¬ïŒNSAIDsïŒã«ã¯é
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Galactomannan is a heteroglycan consisting of a mannan backbone with galactose side groups. | ãšãã«ãã·ã³ïŒepirubicin, Epi-ADMïŒã¯ã1975幎ã«ã€ã¿ãªã¢ã®ãã¡ã«ãã¿ãªã¢ ã«ã«ããšã«ã瀟ïŒçŸ:ãã¡ã€ã¶ãŒæ ªåŒäŒç€ŸïŒã®F. Arcamoneãã«ãã£ãŠåæã»éçºãããã¢ã³ãã©ãµã€ã¯ãªã³ç³»ã®æè
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Diethylene glycol is a hydroxyether. | ãžãšãã¬ã³ã°ãªã³ãŒã« (diethylene glycol) ã¯ã°ãªã³ãŒã«ã®äžçš®ã§ããããžãšãã«ã°ãªã³ãŒã«ãšãåŒã°ããã2ååã®ãšãã¬ã³ã°ãªã³ãŒã«ãè±æ°Žçž®åããæ§é ãæã€ãIUPACå㧠2,2'-ãªãã·ãžãšã¿ããŒã«ãç²çš ãªç¡è²æ¶²äœã§ãæ°Žãªã©ã®æ¥µæ§æº¶åªã«æº¶ãããããäžå液çã«çšãããããæ¶é²æ³ã«å®ãã第4é¡å±éºç© 第3ç³æ²¹é¡ã«è©²åœããã | 1 |
Tolterodine, sold under the brand name Detrol among others, is a medication used to treat frequent urination, urinary incontinence, or urinary urgency. Effects are seen within an hour. It is taken by mouth.
Common side effects include headache, dry mouth, constipation, and dizziness. Serious side effects may include angioedema, urinary retention, and QT prolongation. Use in pregnancy and breastfeeding are of unclear safety. It works by blocking muscarinic receptors in the bladder thus decreasing bladder contractions.
Tolterodine was approved for medical use in 1998. It is available as a generic medication. In 2020, it was the 271st most commonly prescribed medication in the United States, with more than 1 million prescriptions. | ããããã·ã¯ãšã³é
žïŒããããã·ã¯ãšã³ãããhydroxycitric acidïŒã¯ãã¯ãšã³é
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A betaine () in chemistry is any neutral chemical compound with a positively charged cationic functional group that bears no hydrogen atom, such as a quaternary ammonium or phosphonium cation (generally: onium ions), and with a negatively charged functional group, such as a carboxylate group that may not be adjacent to the cationic site. Historically, the term was reserved for trimethylglycine (TMG), which is involved in methylation reactions and detoxification of homocysteine. This is a modified amino acid consisting of glycine with three methyl groups serving as methyl donor for various metabolic pathways. | é
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Sucrose octaacetate is a natural product found in Planchonella vitiensis with data available. | ãšããã·ãïŒEtoposideïŒãšã¯ãã¡ã®ç§ã®æ€ç©Podophyllum peltatum ãããã¯P.emodi ã®æ ¹èããæœåºããçµæ¶æ§æåã§ãããããã£ãããã·ã³ãåæãšãã1966幎ã«åæãããææªæ§è
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Meclizine, sold under the brand name Bonine, among others, is an antihistamine used to treat motion sickness and dizziness (vertigo). It is taken by mouth. Effects generally begin in an hour and last for up to a day.
Common side effects include sleepiness and dry mouth. Serious side effects may include allergic reactions. Use in pregnancy appears safe, but has not been well studied; use in breastfeeding is of unclear safety. It is believed to work in part by anticholinergic and antihistamine mechanisms.
Meclizine was patented in 1951 and came into medical use in 1953. It is available as a generic medication and often over the counter. In 2022, it was the 129th most commonly prescribed medication in the United States, with more than 4 million prescriptions. | ã¯ãªã¹ã¿ã«ãã€ãªã¬ããã©ã¯ãã³ã¯ã¯ãªã¹ã¿ã«ãã€ãªã¬ããã®ã©ã¯ãã³èªå°äœãéè²çºè²çšã®è²çŽ åé§äœïŒãã€ã³è²çŽ ïŒãšããŠçšããããã
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Diphenylmethane is a diarylmethane that is methane substituted by two phenyl groups. | ãã«ã²ãã³(Bergenin) ãŸãã¯ã¯ã¹ã¯ãã³(Cuscutin)ã¯ãããªããããã·å®æ¯éŠé
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Bergenia ciliata ãã«ã¬ããŠããã·ã¿ (Bergenia ligulata) çã®ããã©ã€ãŠããã·ã¿å± (Bergenia) ããŸãããã©ã€ãŠããã·ã¿ã®å°äžèããåé¢ãããããã®ä»ããªã¥ãŠããŠãžã¥ (Dryobalanops aromatica) ã®å¹¹ã®æš¹ç®ãã»ã€ãã³ãã³ãªã§ãŠ (Ardisia elliptica) ãã¢ã«ã¡ã¬ã·ã¯ (Mallotus japonicus) ã«ãèŠãããã | 0 |
Azosemide is a sulfonamide that is benzenesulfonamide which is substituted at positions 2, 4, and 5 by chlorine, (2-thienylmethyl)amino and 1H-tetrazol-5-yl groups, respectively. It is a diuretic that has been used in the management of oedema and hypertension. It has a role as a loop diuretic. It is a member of tetrazoles, a member of monochlorobenzenes, a sulfonamide and a member of thiophenes. | ããããªã³é
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Nifedipine is a dihydropyridine, a methyl ester and a C-nitro compound. It has a role as a calcium channel blocker, a vasodilator agent, a tocolytic agent and a human metabolite. | ãããµã¡ãã«ãã³ãŒã³ (hexamethylbenzene) ãšã¯ãææ©ååç©ã®ã²ãšã€ã§ããã³ãŒã³ã®6ã€ã®æ°ŽçŽ ååããã¹ãŠã¡ãã«åºã«å€ãã£ãæ§é ãæã€è³éŠæçåæ°ŽçŽ ãæ
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Nitroethane is a nitroalkane that is ethane substituted by a nitro group. It is a tautomer of an aci-nitroethane. | ã¢ã¹ã«ãªããŒã« (ascaridole) ã¯å€©ç¶ã«ååšããææ©ååç©ã®äžçš®ã§ãã¢ããã«ãã³ã«åé¡ããããã¢ã¹ã«ãªããŒã«ã®ããã«ãã«ãªãã·ãæ§é ãæã€å€©ç¶ç©ã¯å°ãªããã¢ã«ã¶å±ã®æ€ç©ãç¹ã«ã¢ãªã¿ãœãŠ (Chenopodium ambrosioides) ã®ç²Ÿæ²¹ã®äž»æåã§ããã | 0 |
Nitrofen is an organic molecular entity. It has a role as an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor and a herbicide. | ã¯ãããµã·ãªã³ïŒCloxacillinïŒãšã¯ãååæã®ããã·ãªã³ç³»ã®æèè¬ã®1çš®ã§ããã | 0 |
Oxytocin is a peptide hormone and neuropeptide normally produced in the hypothalamus and released by the posterior pituitary. Present in animals since early stages of evolution, in humans it plays roles in behavior that include social bonding, love, reproduction, childbirth, and the period after childbirth. Oxytocin is released into the bloodstream as a hormone in response to sexual activity and during childbirth. It is also available in pharmaceutical form. In either form, oxytocin stimulates uterine contractions to speed up the process of childbirth. In its natural form, it also plays a role in maternal bonding and milk production. Production and secretion of oxytocin is controlled by a positive feedback mechanism, where its initial release stimulates production and release of further oxytocin. For example, when oxytocin is released during a contraction of the uterus at the start of childbirth, this stimulates production and release of more oxytocin and an increase in the intensity and frequency of contractions. This process compounds in intensity and frequency and continues until the triggering activity ceases. A similar process takes place during lactation and during sexual activity.
Oxytocin is derived by enzymatic splitting from the peptide precursor encoded by the human OXT gene. The deduced structure of the active nonapeptide is:
Cys â Tyr â Ile â Gln â Asn â Cys â Pro â Leu â Gly â NH2, or CYIQNCPLG-NH2. | ã©ãã ã¹ãã³ïŒè±èª: Ranimustineãç¥ç§°:MCNUïŒ ã¯ãããããœãŠã¬ã¢ç³»ã®ã¢ã«ãã«åå€ã®äžã€ã§ãããã¹ãã¬ãããŸãã·ã³ãåºæ¬éªšæ ŒãšããŠãç°èŸºäžè±è£œè¬ã«ããåµè£œããããåååã¯æ³šå°çšãµã€ã¡ãªã³ã | 0 |
Ciclobendazole is an anthelmintic, that is a pharmaceutical drug against parasitic worms. It underwent a clinical trial in the 1970s, where it was found to be as effective as mebendazole in the treatment of hookworm infection and ascariasis, but significantly less effective in the treatment of trichuriasis.
It is not known to be marketed anywhere in the world. | ããã§ãžãã³ (Nifedipine) ã¯çå¿çãé«è¡å§ãã¬ã€ããŒçŸè±¡ãæ©ç£ã®éã«çšããããè¡ç®¡æ¡åŒµè¬ã®äžã€ã§ããããžãããããªãžã³ç³»ã®ã«ã«ã·ãŠã æ®æè¬ã«åé¡ããããããªã³ãã¡ã¿ã«çå¿çã®æ²»çã«æ¡çšããããéçåŠåš é«è¡å§ã®æ²»çã«ã䜿çšã§ãããæ©æé£çã«äœ¿çšãããšã¹ããã€ããããé·æé䜿çšã§ããå
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Mupirocin is an alpha,beta-unsaturated ester resulting from the formal condensation of the alcoholic hydroxy group of 9-hydroxynonanoic acid with the carboxy group of (2E)-4-[(2S)-tetrahydro-2H-pyran-2-yl]-3-methylbut-2-enoic acid in which the tetrahydropyranyl ring is substituted at positions 3 and 4 by hydroxy groups and at position 5 by a {(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl}methyl group. Originally isolated from the Gram-negative bacterium Pseudomonas fluorescens, it is used as a topical antibiotic for the treatment of Gram-positive bacterial infections. It has a role as a bacterial metabolite, an antibacterial drug and a protein synthesis inhibitor. It is a monocarboxylic acid, a member of oxanes, an epoxide, a secondary alcohol, a triol and an alpha,beta-unsaturated carboxylic ester. It is a conjugate acid of a mupirocin(1-). | ãªããã»ãã©ãã©ãŸã³ã¯ãβ-ã©ã¯ã¿ããŒãŒé»å®³å€ã§ããã¹ã«ãã¯ã¿ã ãšã®åå€ã補é ãããŠããã ã»ãã©ãã©ãŸã³ã¯ 现è㮠现èå£ åæãæå¶ããããšã§æ®ºèäœçšã瀺ããβ-ã©ã¯ã¿ããŒãŒé»å®³å€ã«ãããã»ãã©ãã©ãŸã³ã®å æ°Žå解ãæå¶ããæè掻æ§ãç¶æããããšãã§ããã | 0 |
Benzaldehyde is an arenecarbaldehyde that consists of benzene bearing a single formyl substituent; the simplest aromatic aldehyde and parent of the class of benzaldehydes. It has a role as a flavouring agent, a fragrance, an odorant receptor agonist, a plant metabolite, an EC 3.5.5.1 (nitrilase) inhibitor and an EC 3.1.1.3 (triacylglycerol lipase) inhibitor. | ã«ã¢ã¹ã¿ããïŒè±: Camostat,INN; éçºã³ãŒãFOY-305ïŒã¯ãã»ãªã³ãããã¢ãŒãŒé»å®³å€ã ã»ãªã³ãããã¢ãŒãŒïŒé
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3-hydroxyanthranilic acid is an aminobenzoic acid that is benzoic acid substituted at C-2 by an amine group and at C-3 by a hydroxy group. It is an intermediate in the metabolism of the amino acid tryptophan. It has a role as a human metabolite and a mouse metabolite. It is an aminobenzoic acid and a monohydroxybenzoic acid. It is functionally related to an anthranilic acid. It is a conjugate acid of a 3-hydroxyanthranilate. It is a tautomer of a 2,3-dihydro-3-oxoanthranilic acid. | ã«ã«ããªã«ïŒè±: Carbaryl, NACïŒã¯ãå¯éæ§ã³ãªã³ãšã¹ãã©ãŒãŒé»å®³å€ãã«ãŒãã¡ã€ã系殺è«å€ã®1çš®ã§ã蟲è¬ãåç©çšå»è¬åãšããŠçšããããã | 0 |
Amikacin is a natural product found in Stachybotrys chartarum, Streptomyces hygroscopicus, and Liquidambar formosana with data available. | ãããµãã«ã³ (hexadecane) ã¯çåæ°ŽçŽ ã®äžçš®ã§ãççŽ ã16é£ãªã£ãçŽéã¢ã«ã«ã³ãåååŒã¯ C16H34ã沞ç¹287âãèç¹18.2âãç°æ§äœã®æ°ã¯10359ã | 0 |
Pipemidic acid is a member of the pyridopyrimidine class of antibacterials, which display some overlap in mechanism of action with analogous pyridone-containing quinolones. It was introduced in 1979 and is active against gram negative and some gram positive bacteria. It was used for gastrointestinal, biliary, and urinary infections. The marketing authorization of pipemidic acid has been suspended throughout the EU. | ã¢ã¯ãªã«é
žïŒã¢ã¯ãªã«ãããè±: acrylic acidïŒã¯ãååŠåŒã CH2=CHCOOH ã§è¡šãããææ©ååç©ã§ãããæãåçŽãªäžé£œåã«ã«ãã³é
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žïŒ2-propenoic acidïŒãšè¡šãããã幎éã§100äžãã³ä»¥äžè£œé ãããŠããã
èç¹ 12 °Cãæ²žç¹ 141.6 °Cã®ç¡è²éæã®æ¶²äœã§ãç¹æã®åºæ¿èãæãããCASç»é²çªå·ã¯[79-10-7]ãé
žè§£é¢å®æ°(pKa)ã¯4.25ãç²åºŠã¯1.3 mPa sïŒ20 °CïŒã | 0 |
Captan is a general use pesticide (GUP) that belongs to the phthalimide class of fungicides. It is a white solid, although commercial samples appear yellow or brownish. | ãããŒã«ãããªã³ïŒè±: PyrrolnitrinïŒã¯ããããŒã«ç°ãæã€æçç©è³ªã»æçèè¬ã®äžçš®ãæ°Žè«è¬ãªã©ã«é
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Chloroxine is a monohydroxyquinoline that is quinolin-8-ol in which the hydrogens at positions 5 and 7 have been substituted by chlorine. A synthetic antibacterial prepared by chlorination of quinolin-8-ol, it is used for the treatment of dandruff and seborrhoeic dermatitis of the scalp. It has a role as an antibacterial agent, an antiseborrheic and an antifungal drug. It is a monohydroxyquinoline and an organochlorine compound. It is functionally related to a quinolin-8-ol. | ãã©ã³ïŒè±: furanïŒã¯ã4åã®ççŽ ååãš1åã®é
žçŽ ååããæ§æãããè€çŽ ç°åŒè³éŠæååç©ã§ãããåååŒ C4H4Oãååé 68.07 ã§ãCASç»é²çªå·ã¯[110-00-9]ããã©ã³ã¯IUPACåœåæ³ã«ããã蚱容æ
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Oxidopamine, also known as 6-hydroxydopamine (6-OHDA) or 2,4,5-trihydroxyphenethylamine, is a synthetic monoaminergic neurotoxin used by researchers to selectively destroy dopaminergic and noradrenergic neurons in the brain.
The main use for oxidopamine in scientific research is to induce Parkinsonism in laboratory animals by lesioning the dopaminergic neurons of the substantia nigra pars compacta, in order to develop and test new medicines and treatments for Parkinson's disease. | ç¡é
žã«ãããŠã ïŒãããããã«ãããŠã ãè± Cadmium nitrateïŒã¯ã«ãããŠã ã®ç¡é
žå¡©ã§ãååŠåŒCd(NO3)2ã§è¡šãããç¡æ©ååç©ãç¡æ°Žç©ãšæ°çš®é¡ã®æ°Žåç©ãããããäžè¬ã«ã¯åæ°Žåç©ãæµéããŠããã朮解æ§ã®ããçœè²ã®çµæ¶ã§ã人äœã«å¯Ÿãçºçæ§ããããæ¥æ¬ã®æ¯åæ³ã§ã¯åç©ã«åé¡ãããŠããã | 0 |
Vanillin is an organic compound with the molecular formula C8H8O3. It is a phenolic aldehyde. Its functional groups include aldehyde, hydroxyl, and ether. It is the primary component of the extract of the vanilla bean. Synthetic vanillin is now used more often than natural vanilla extract as a flavoring in foods, beverages, and pharmaceuticals.
Vanillin and ethylvanillin are used by the food industry; ethylvanillin is more expensive, but has a stronger note. It differs from vanillin by having an ethoxy group (âOâCH2CH3) instead of a methoxy group (âOâCH3).
Natural vanilla extract is a mixture of several hundred different compounds in addition to vanillin. Artificial vanilla flavoring is often a solution of pure vanillin, usually of synthetic origin. Because of the scarcity and expense of natural vanilla extract, synthetic preparation of its predominant component has long been of interest. The first commercial synthesis of vanillin began with the more readily available natural compound eugenol (4-allyl-2-methoxyphenol). Today, artificial vanillin is made either from guaiacol or lignin.
Lignin-based artificial vanilla flavoring is alleged to have a richer flavor profile than that from guaiacol-based artificial vanilla; the difference is due to the presence of acetovanillone, a minor component in the lignin-derived product that is not found in vanillin synthesized from guaiacol. | ãããªã³ïŒè¯å°Œæãè±: vanillinãäž: éŠèéïŒã¯ããããã€ãé¡ã«å±ãæãåçŽãªææ©ååç©ã§ãããããã©ã®éŠãã®äž»èŠãªæåãšãªã£ãŠããç©è³ªãã©ãã³èªèªã¿ã§ã¯ããªã³ãšåŒã°ããããšãããã | 1 |
Dimethazan is an oxopurine. | ã¹ãã©ãã(Spiramide)ã¯ã5-HT2Aå容äœã5-HT1Aå容äœåã³D2å容äœã®ã¢ã³ã¿ãŽãã¹ãã§ãããã5-HT2Cå容äœãžã®ã¢ãã£ããã£ãŒã¯ãªãã | 0 |
Diethyl sulfide (British English: diethyl sulphide) is an organosulfur compound with the chemical formula (CH3CH2)2S. It is a colorless, malodorous liquid. Although a common thioether, it has few applications. | ããã°ãªã¿ãŸã³ïŒTroglitazoneïŒã¯ããã€ãŠåžè²©ãããŠãããã¢ãŸãªãžã³ç³»ã®çµå£è¡ç³éäžè¬ãã€æççè¬ã§ããã第äžäžå
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Zingiberene is a natural product found in Humulus lupulus, Zanthoxylum simulans, and other organisms with data available. | ããã³ãã·ãªã³ïŒè±ïŒPivampicillinïŒã¯ã¢ã³ãã·ãªã³ã®ãããã€ã«ãªãã·ã¡ãã«ãšã¹ãã«ã§ããããããã©ãã°ã§ãã¢ã³ãã·ãªã³ã«æ¯ã¹ãŠèŠªæ²¹æ§ãé«ããããã¢ã³ãã·ãªã³ã®çµå£ãã€ãªã¢ãã€ã©ããªãã£ãé«ãããšèããããŠããã | 0 |
Fenchone is a carbobicyclic compound that is fenchane in which the hydrogens at position 2 are replaced by an oxo group. It is a component of essential oil from fennel (Foeniculum vulgare). It has a role as a plant metabolite. It is a fenchane monoterpenoid, a cyclic terpene ketone and a carbobicyclic compound. | ãã§ã³ã³ã³(Fenchone)ã¯ã倩ç¶ã«ååšããææ©ååç©ã§ãã¢ããã«ãã³åã³ã±ãã³ã«åé¡ããããæ²¹ç¶ã®éæãªæ¶²äœã§ãããæ§é ãåãã¯ãæšè³ã«äŒŒãã
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Evoxine is an organonitrogen heterocyclic compound, an oxacycle and an organic heterotricyclic compound. | ãšããã·ã³(Evoxine)ãŸãã¯ãããããªã³(haploperine)ã¯ãç¡ç è¬ããã³é®éè¬ã®äœçšãæã€ãããããªã³ã¢ã«ã«ãã€ãã§ãããEvodia xanthoxyloidesãTeclea gerrardiiçã®ããªãŒã¹ãã©ãªã¢ãã¢ããªã«ã®æ§ã
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Acetylcholine is actylcholine is an ester of acetic acid and choline, which acts as a neurotransmitter. It has a role as a vasodilator agent, a muscarinic agonist, a hormone, a human metabolite, a mouse metabolite and a neurotransmitter. It is an acetate ester and an acylcholine. | ããµã³ãã·ã³(Xanthosine)ã¯ãããµã³ãã³ãšãªããŒã¹ããçãããã¯ã¬ãªã·ãã§ããã | 0 |
Cytisine is an organic heterotricyclic compound that is the toxic principle in Laburnum seeds and is found in many members of the Fabaceae (legume, pea or bean) family. An acetylcholine agonist, it is widely used throughout Eastern Europe as an aid to giving up smoking. It has a role as a nicotinic acetylcholine receptor agonist, a phytotoxin and a plant metabolite. It is an alkaloid, an organic heterotricyclic compound, a secondary amino compound, a lactam and a bridged compound. | ã¡ãããµãã³ã¯ãα1ã¢ãã¬ããªã³äœåè¬ ã§ãããããµãã³ããžã¡ãã«ãªãã·ã¢ã³ãã§ã¿ãã³ãšæ§é ããã䌌ãŠããããã€ãŠã¯æè¡å®€ãªã©ã«ãããŠãè¡ç®¡åçž®è¬ãšããŠçšããããŠããããå¯äžã®è£œé å·¥å ŽãçŒå€±ããããã«2008幎12ææ«ã«è²©å£²çµäºãšãªã£ããåååã¯ãã¡ããµã³ã ãããŸã§ã¯èšåºã«ãããŠãéèå
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3,4-dimethoxyphenylethylamine is an aromatic ether that is the derivative of 2-phenylethylamine with methoxy substituents at the 3- and 4-positions. It is an alkaloid isolated from the Cactaceae family. It has a role as a plant metabolite and an allergen. It is a phenylethylamine, an aromatic ether and an alkaloid. It derives from a hydride of a 2-phenylethylamine. | ãšãªããªããŒã«(Erythritol)ãŸãã¯ãšãªã¹ãªããŒã«ãšã¯ãååç©ããã³ç³ã¢ã«ã³ãŒã«ã®äžçš®ã§ãããé£åæ·»å ç©ãç ç³ã®ä»£ããã«äœ¿ããããããŠã¢ãã³ã·ãåæã«ãé
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Choline is a natural product found in Amaranthus hybridus, Leonurus japonicus, and other organisms with data available. | ãããµã·ã¢ããé(III)é
žå¡©ïŒãããµã·ã¢ãããŠã€ããããããïŒã¯ã[Fe(CN)6]3âã€ãªã³åã³ãããå«ãå¡©ã§ãããæ
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Flumazenil is an organic heterotricyclic compound that is 5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine which is substituted at positions 3, 5, 6, and 8 by ethoxycarbonyl, methyl, oxo, and fluoro groups, respectively. It is used as an antidote to benzodiazepine overdose. It has a role as a GABA antagonist and an antidote to benzodiazepine poisoning. It is an ethyl ester, an organofluorine compound and an imidazobenzodiazepine. | 3,4-ãžããããã·ãã§ãã«é
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Salvinorin A is the main active psychotropic molecule in Salvia divinorum. Salvinorin A is considered a dissociative hallucinogen.
It is structurally distinct from other naturally occurring hallucinogens (such as DMT, psilocybin, and mescaline) because it contains no nitrogen atoms; hence, it is not an alkaloid (and cannot be rendered as a salt), but rather is a terpenoid. It also differs in subjective experience, compared to other hallucinogens, and has been described as dissociative.
Salvinorin A can produce psychoactive experiences in humans with a typical duration of action being several minutes to an hour or so, depending on the method of ingestion.
Salvinorin A is found with several other structurally related salvinorins. Salvinorin is a trans-neoclerodane diterpenoid. It acts as a kappa opioid receptor agonist and is the first known compound acting on this receptor that is not an alkaloid. | ã«ããã³(lupinine)ã¯ãã«ããã¹å±ã®æ€ç©ã«å«ãŸããèŠå³ãæã€ãããªãžãžã³ç³»ã®ã¢ã«ã«ãã€ãã§ãããåé¢ãåæã«ã€ããŠå€ãã®å ±åããããããŠãã¯ãã¡ã®ç¹åŸŽçãªèŠå³ã¯ãå«ãŸããã¢ã«ã«ãã€ãã«ãããã®ã§ãããé£çšã«é©ããªããã®ãšããŠãããããããããŠãã¯ãã¡ã¯ã¿ã³ãã¯è³ªå«éãé«ããæœåšçãªæ é€æºãšãªããããããã¢ã«ã«ãã€ãã®éãæžãããããçãåçš®ãéçºããããšãã£ãåªåãç¶ããããŠããã | 0 |
Taurocholic acid is a natural product found in Ursus thibetanus, Homo sapiens, and other organisms with data available. | ã¿ãŠãã³ãŒã«é
ž ïŒTaurocholic acidïŒã¯ãèèªãä¹³åããããšã®ã§ããè解æ§ã®éæãªé»è²ã®èæ±é
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Ethyl decanoate, also known as ethyl caprate, is a fatty acid ester formed from capric acid and ethanol. This ester is a frequent product of fermentation during winemaking, especially at temperatures above 15 °C. | ãªã³é
žããªãšãã«(Triethyl phosphate)ã¯ã(C2H5)3PO4ã®ååŠåŒãæã€ææ©ååç©ã§ãããç¡è²ã®æ¶²äœã§ããããªã³é
žãšãšã¿ããŒã«ã®ãšã¹ãã«ã§ãããæ¶é²æ³ã«å®ãã第4é¡å±éºç© 第3ç³æ²¹é¡ã«è©²åœããã | 0 |
3-Carene is a bicyclic monoterpene consisting of fused cyclohexene and cyclopropane rings. It occurs as a constituent of turpentine, with a content as high as 42% depending on the source. Carene has a sweet and pungent odor, best described as a combination of fir needles, musky earth, and damp woodlands.
A colorless liquid, it is not soluble in water, but miscible with fats and oils. It is chiral, occurring naturally both as the racemate and enantio-enriched forms. | ã·ã¯ããã³ã¿ãžãšã³ (è±: cyclopentadiene) ã¯åååŒ C5H6 ã§è¡šãããã5å¡ç°æ§é ãæã€ç°åŒãžãšã³ãçåæ°ŽçŽ ã®ã²ãšã€ãIUPACå ã¯ã·ã¯ããã³ã¿-1,3-ãžãšã³ (è±: cyclopenta-1,3-diene)ã
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Clonazepam, sold under the brand name Klonopin among others, is a benzodiazepine medication used to prevent and treat anxiety disorders, seizures, bipolar mania, agitation associated with psychosis, obsessiveâcompulsive disorder (OCD), and akathisia. It is a long-acting tranquilizer of the benzodiazepine class. It possesses anxiolytic, anticonvulsant, sedative, hypnotic, and skeletal muscle relaxant properties. It is typically taken orally (swallowed by mouth) but is also used intravenously. Effects begin within one hour and last between eight and twelve hours in adults.
Common side effects may include sleepiness, weakness, poor coordination, difficulty concentrating, and agitation. Clonazepam may also decrease memory formation. Long-term use may result in tolerance, dependence, and life-threatening withdrawal symptoms if stopped abruptly. Dependence occurs in one-third of people who take benzodiazepines for longer than four weeks. The risk of suicide increases, particularly in people who are already depressed. Use during pregnancy may result in harm to the fetus. Clonazepam binds to GABAA receptors, thus increasing the effect of the chief inhibitory neurotransmitter γ-aminobutyric acid (GABA).
Clonazepam was patented in 1960 and went on sale in 1975 in the United States from Roche. It is available as a generic medication. In 2022, it was the 57th most commonly prescribed medication in the United States, with more than 11 million prescriptions. In many areas of the world, it is commonly used as a recreational drug. | ããããããªã« (malononitrile) ãšã¯ææ©ååç©ã®äžçš®ã§ãããã³é
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Hydroxytyrosol is a member of the class of catechols that is benzene-1,2-diol substituted by a 2-hydroxyethyl group at position 4. Isolated from Olea europaea, it exhibits antioxidant and antineoplastic activities. It has a role as a metabolite, an antioxidant and an antineoplastic agent. It is a member of catechols and a primary alcohol. It is functionally related to a 2-(4-hydroxyphenyl)ethanol. | ç¡æ©ååŠã«ãããŠãç¡é
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Flutamide is a monocarboxylic acid amide and a member of (trifluoromethyl)benzenes. It has a role as an androgen antagonist and an antineoplastic agent. | ãã«ã¿ããïŒFlutamideïŒã¯ãéã¹ããã€ãæ§æã¢ã³ããã²ã³è¬ïŒNSAAïŒã§ãäž»ã«åç«è
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Temazepam is a benzodiazepine. | ã¢ã«ãã¡ãã«ïŒartemetherïŒã¯è溶æ§ã®ã¢ã«ããã·ãã³èªå°äœã§ããããã©ãªã¢ã®æ²»çã«çšããããè¬å€ã§ããã é床ã®ãã©ãªã¢ã«ã¯ãããŒããã泚å°åã®ã¢ã«ãã¡ãã«ãçšãããããã¢ã«ãã¹ãã€ãã»ã©ã®å¹æã蚺ãããªãããšããããæäžæ³ã¯çè泚å°ã§ããããŸãã«ã¡ãã¡ã³ããªã³ãšçµã¿åããããã¢ã«ãã¡ãã«/ã«ã¡ãã¡ã³ããªã³ã§ç¥ãããçµå£è¬ããããæ¥æ¬ã§ã2017幎ããã«ã¡ãã¡ã³ããªã³é
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Staurosporine (antibiotic AM-2282 or STS) is a natural product originally isolated in 1977 from the bacterium Streptomyces staurosporeus.
It was the first of over 50 alkaloids that were discovered to share this type of bis-indole chemical structure. The chemical structure of staurosporine was elucidated by X-ray crystalography in 1994.
Staurosporine was discovered to have biological activities ranging from anti-fungal to anti-hypertensive.
The interest in these activities resulted in a large investigative effort in chemistry and biology and the discovery of the potential for anti-cancer treatment. | ã¡ããã«ãã³ïŒè±: MetforminïŒã¯ããã°ã¢ãã€ãç³»è¬å€ã«åé¡ãããçµå£ç³å°¿ç
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Formate is a monocarboxylic acid anion that is the conjugate base of formic acid. Induces severe metabolic acidosis and ocular injury in human subjects. It has a role as a human metabolite and a Saccharomyces cerevisiae metabolite. It is a conjugate base of a formic acid. | ã°ãªã»ãªã³é
žïŒã°ãªã»ãªã³ãããglyceric acidïŒã¯ã倩ç¶ã«ååšããäžççŽ ã®ç³é
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Amikacin is an antibiotic medication used for a number of bacterial infections. This includes joint infections, intra-abdominal infections, meningitis, pneumonia, sepsis, and urinary tract infections. It is also used for the treatment of multidrug-resistant tuberculosis. It is used by injection into a vein using an IV or into a muscle.
Amikacin, like other aminoglycoside antibiotics, can cause hearing loss, balance problems, and kidney problems. Other side effects include paralysis, resulting in the inability to breathe. If used during pregnancy it may cause permanent deafness in the baby. Amikacin works by blocking the function of the bacteria's 30S ribosomal subunit, making it unable to produce proteins.
Amikacin was patented in 1971, and came into commercial use in 1976. It is on the World Health Organization's List of Essential Medicines. It is derived from kanamycin. | ã¬ãµãºãªã³ (Resazurin) ã¯ããã§ãããµãžã³è²çŽ ã®äžçš®ã§ããã匱ãèå
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Ambroxol is a drug that breaks up phlegm, used in the treatment of respiratory diseases associated with viscid or excessive mucus. Ambroxol is often administered as an active ingredient in cough syrup.
It was patented in 1966 and came into medical use in 1979. | å€ç³ååå
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Estragole is a natural product found in Cymbopogon martinii, Perilla frutescens, and other organisms with data available. | 3-ãªã¯ã¿ãã³ïŒè±: 3-OctanoneïŒã¯ãèèªæã±ãã³ã®äžçš®ã§ãããç¡è²ãªããèãé»è²ã®æ¶²äœã§ãããŒãããã«ãŒãã®ãããªéŠæ°ãæã€ãæ¶é²æ³ã«ãã第4é¡å±éºç© 第2ç³æ²¹é¡ã«è©²åœãã | 0 |
Histidine (symbol His or H) is an essential amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated âNH3+ form under biological conditions), a carboxylic acid group (which is in the deprotonated âCOOâ form under biological conditions), and an imidazole side chain (which is partially protonated), classifying it as a positively charged amino acid at physiological pH. Initially thought essential only for infants, it has now been shown in longer-term studies to be essential for adults also. It is encoded by the codons CAU and CAC.
Histidine was first isolated by Albrecht Kossel and Sven Gustaf Hedin in 1896. The name stems from its discovery in tissue, from ጱÏÏÏÏ histós "tissue". It is also a precursor to histamine, a vital inflammatory agent in immune responses. The acyl radical is histidyl. | ãšãã©ã»ã¿ã (Etiracetam)ã¯ãã©ã»ã¿ã ç³»ã®ã¹ããŒããã©ãã°ã§ãããRäœãšSäœãæ··åããŠããã©ã»ãäœãæãå称ã§ãçç掻æ§ãæã€ãšãã³ããªããŒã¯Säœã§ã¬ããã©ã»ã¿ã ãšããã | 0 |
Chloroform is a natural product found in Basella alba, Manilkara zapota, and other organisms with data available. | ãµã«ã³ã·ã³ïŒsarcosineïŒãŸãã¯N-ã¡ãã«ã°ãªã·ã³ïŒè±: N-methylglycine, NMGïŒã¯ãçèããã®ä»äœå
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Dichloroacetic acid is an organochlorine compound comprising acetic acid carrying two chloro substituents at the 2-position. It occurs in nature in seaweed, Asparagopsis taxiformis. It has a role as an astringent and a marine metabolite. It is a monocarboxylic acid and an organochlorine compound. It is functionally related to an acetic acid. It is a conjugate acid of a dichloroacetate. | ãã«ã³ïŒè±èª: decaneïŒã¯ãååŠåŒã C10H22 ã¢ã«ã«ã³ã§ããããã«ã³ã«ã¯75çš®ã®æ§é ç°æ§äœãååšããããéåžžã¯ååŠåŒã CH3(CH2)8CH3 ã®ãã«ãã«ãã«ã³ïŒn-ãã«ã³ïŒãããããããã®ç°æ§äœãæ§è³ªãé¡äŒŒããŠãããããçµæã«ã€ããŠã¯æ³šç®ãããªãããã«ã³ã¯ã¬ãœãªã³ãç¯æ²¹ã«ãããã«ïŒ1%æªæºïŒå«ãŸããŠãããå¯çæ§ãæ®çºæ§ããããåžžæž©åžžå§ã§ç¡è²ã®æ¶²äœãä»ã®ã¢ã«ã«ã³ãšåæ§ã«é極æ§æº¶åªã§ãããæ°Žã«ã¯æº¶ããªããçæã®æåã§ã¯ããããä»ã®ã¢ã«ã«ã³ãšã¯ç°ãªããååŠåæãšããŠã®éèŠæ§ã¯äœãã | 0 |
Sodium tungstate is the inorganic compound with the formula Na2WO4. This white, water-soluble solid is the sodium salt of tungstic acid. It is useful as a source of tungsten for chemical synthesis. It is an intermediate in the conversion of tungsten ores to the metal. | ã©ã¯ãããªã³é
žïŒLactobionic acidïŒLacAïŒã¯ãã°ã«ã³ã³é
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žïŒ4-O-β-galactopyranosyl-D-gluconic acidïŒãšããããã©ã¯ãããªã³é
žã®ã¢ããªã³åã¯ã©ã¯ãããªããŒãïŒlactobionateïŒãšããŠç¥ãããã | 0 |
Narcotoline is an opiate alkaloid chemically related to noscapine. It binds to the same receptors in the brain as noscapine to act as an antitussive, and has also been used in tissue culture media. | ããããŒã«ïŒè±: nonanalïŒã¯ãååŠåŒC9H18Oã§è¡šãããææ©ååç©ãã¢ã«ãããã®äžçš®ã§ãããã«ã¢ã«ããããšãåŒã°ããã | 0 |
Gyrophoric acid is a tridepside that can be found in the lichen Cryptothecia rubrocincta and in Xanthoparmelia pokomyi. It is a double ester of the orsellinic acid. It can also be found in most of the species of the Actinogyra, Lasallia, and Umbilicaria genera. | ã«ã«ãã·ã³é
žïŒCarnosic acidïŒã¯ãããŒãºããªãŒãã»ãŒãžã«å«ãŸããŠãã倩ç¶ã®ãã³ãŒã³ãžãªãŒã«ã¢ããšã¿ã³ã®ãžãã«ãã³ã§ãããããŒãºããªãŒãã»ãŒãžã®ä¹Ÿç¥èã«ã¯ã1.5ïŒ2.5ïŒ
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žåé²æ¢å€ãšããŠäœ¿çšãããéé£å補åã«ã¯äŸãã°æ¯ç£šãç²ãããŠã¹ãŠã©ãã·ã¥ããã¥ãŒã€ã³ã¬ã ïŒå£èã®åå ãšãªã埮çç©ã«å¯Ÿããæèå¹æãæã€ïŒãŸãã¯ã¹ãã³ã±ã¢è£œåãšããŠäœ¿çšãããã | 0 |
Dodecyl gallate, or lauryl gallate, is the ester of dodecanol and gallic acid. As a food additive it is used under the E number E312 as an antioxidant and preservative. | ãžã¡ããšãŒã(Dimethoate)ã¯ã殺è«å€ãšããŠåºãçšãããããªã³é
žãšã¹ãã«ã§ããã1950幎代ã«American Cyanamid瀟ã«ãã£ãŠçºæãããç¹èš±ãåããããä»ã®ãªã³é
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Phenoxybenzamine (PBZ, marketed under the trade names Dibenzyline and Dibenyline) is a non-selective, irreversible alpha blocker. | ãã§ãã«ãšãã«ããã³ã¢ããïŒè±èª: phenylethylmalonamideãPEMAïŒã¯ãæãŠãããè¬ã®ããªããã³ã®æŽ»æ§ä»£è¬ç©ã§ããããå¥ã®æŽ»æ§ä»£è¬ç©ã§ãããã§ããã«ãã¿ãŒã«ããã¯ããã«äœæ¿åºŠã§çæããã | 0 |
Carmofur is an organohalogen compound and a member of pyrimidines. | ãŠãããªããŒã²ã³(Urobilinogen)ã¯ããã ã®å解ã«ãã£ãŠçæããããªã«ãã³ã®éå
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Uvaricin is a polyketide. | ããããŸãŒã«ïŒTinidazoleïŒã¯ãåè«ææçã«äœ¿çšããããããã€ãããŸãŒã«ç³»æå¯çè«è¬ã§ãããå«æ°æ§ã¢ã¡ãŒãããã³çŽ°èææã®æ§ã
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Voacangine (12-methoxyibogamine-18-carboxylic acid methyl ester) is an alkaloid found predominantly in the root bark of the Voacanga africana tree, as well as in other plants such as Tabernanthe iboga, Tabernaemontana africana, Trachelospermum jasminoides, Tabernaemontana divaricata and Ervatamia yunnanensis. It is an iboga alkaloid which commonly serves as a precursor for the semi-synthesis of ibogaine. It has been demonstrated in animals to have similar anti-addictive properties to ibogaine itself. It also potentiates the effects of barbiturates. Under UV-A and UV-B light its crystals fluoresce blue-green, and it is soluble in ethanol. | ã¢ã»ããããªã«ïŒè±: acetonitrileïŒã¯ææ©æº¶åªã®äžçš®ã§ãæãåçŽãªãããªã«ã§ãããIUPAC系統åãšããŠãšã¿ã³ãããªã« (ethanenitrile)ãã·ã¢ã³åã¡ãã« (methyl cyanide) ã·ã¢ãã¡ã¿ã³ (cyanomethane) ãšè¡šèšã§ãããæ¶é²æ³ã«å®ãã第4é¡å±éºç© 第1ç³æ²¹é¡ã«è©²åœããã | 0 |
Camphor is a cyclic monoterpene ketone that is bornane bearing an oxo substituent at position 2. A naturally occurring monoterpenoid. It has a role as a plant metabolite. It is a bornane monoterpenoid and a cyclic monoterpene ketone. | ãã¡ãªã³é
žïŒãã¡ãªã³ãããè±: Pimelic acidïŒã¯ãççŽ æ°7ã®çŽé飜åèèªæãžã«ã«ãã³é
žãååŠåŒã¯HO2C(CH2)5CO2Hã§è¡šãããããã¡ãªã³é
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Uracil () (symbol U or Ura) is one of the four nucleotide bases in the nucleic acid RNA. The others are adenine (A), cytosine (C), and guanine (G). In RNA, uracil binds to adenine via two hydrogen bonds. In DNA, the uracil nucleobase is replaced by thymine (T). Uracil is a demethylated form of thymine.
Uracil is a common and naturally occurring pyrimidine derivative. The name "uracil" was coined in 1885 by the German chemist Robert Behrend, who was attempting to synthesize derivatives of uric acid. Originally discovered in 1900 by Alberto Ascoli, it was isolated by hydrolysis of yeast nuclein; it was also found in bovine thymus and spleen, herring sperm, and wheat germ. It is a planar, unsaturated compound that has the ability to absorb light.
Uracil that was formed extraterrestrially has been detected in the Murchison meteorite, in a near-Earth asteroid, and possibly on the surface of the moon Titan. It has been synthesized under cold laboratory conditions similar to outer space, from pyrimidine embedded in water ice and exposed to ultraviolet light. | ãªã¯ãããã³ïŒOctopamine, β,4-dihydroxyphenethylamineïŒãšã¯ãã¢ãã¬ããªã³ãšå¯æ¥ã«é¢é£ããå
å æ§ã®çäœã¢ãã³ã§ãããã¢ãã¬ããªã³äœåæ§ã·ã¹ãã ãšããŒããã³äœåæ§ã·ã¹ãã ã«åœ±é¿ãäžãããããã¯ãŸãããã¿ãŒãªã¬ã³ãžãå«ãå€ãã®æ€ç©ã§èŠã€ãã£ãŠãã | 0 |
Palmatine is a berberine alkaloid and an organic heterotetracyclic compound. It has a role as a plant metabolite. | L-ããããã·ãããªã³ïŒè±èª: L-hydroxyprolineïŒãŸãã¯ã(2S,4R)-4-ããããã·ãããªã³ïŒè±èª: (2S,4R)-4-HydroxyprolineïŒã¯ã倩ç¶ã«ååšããäºçŽç°ç¶ã¢ããé
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Phosphoramidate is a phosphoric acid derivative. It is a conjugate base of a phosphoramidic acid. | 2021幎1æãæ±åè¬åæ ªåŒäŒç€Ÿã¯ãè«žè¬ã®äºæ
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Orellanine is a natural product found in Cortinarius orellanus, Cortinarius speciosissimus, and Cortinarius rubellus with data available. | 1-ã¡ãã«ããã¿ã¬ã³ïŒ1-methylnaphthaleneïŒã¯ãè³éŠæçåæ°ŽçŽ ã®äžã€ãã»ã¿ã³äŸ¡ããŒãã§ããããã€ãŠã»ã¿ã³äŸ¡ã®äžéåºæºãšããŠäœ¿ããããçŸåšã§ã¯1-ã¡ãã«ããã¿ã¬ã³ã®é«äŸ¡ããæ±ãã®é£ããããã»ã¿ã³äŸ¡15ã®ã€ãœã»ã¿ã³ã«åã£ãŠä»£ããããŠãããæ¶é²æ³ã«å®ãã第4é¡å±éºç© 第3ç³æ²¹é¡ã«è©²åœããã | 0 |
Toxoflavin is a pyrimidotriazine that is 1,6-dimethyl-1,5,6,7-tetrahydropyrimido[5,4-e][1,2,4]triazine with oxo groups at positions 5 and 7. It has a role as an antineoplastic agent, a toxin, a Wnt signalling inhibitor, an apoptosis inducer, a bacterial metabolite, an antibacterial agent and a virulence factor. It is a pyrimidotriazine and a carbonyl compound. It is functionally related to a reumycin. | ãžãã«ãªãé
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Propranolol is a propanolamine that is propan-2-ol substituted by a propan-2-ylamino group at position 1 and a naphthalen-1-yloxy group at position 3. It has a role as a beta-adrenergic antagonist, an anxiolytic drug, an anti-arrhythmia drug, a vasodilator agent, an antihypertensive agent, a xenobiotic, an environmental contaminant and a human blood serum metabolite. It is a secondary amine, a propanolamine and a member of naphthalenes. It is functionally related to a 1-naphthol. | äºèçŽ é
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Bombykol is a pheromone released by the female silkworm moth to attract mates. It is also the sex pheromone in the wild silk moth (Bombyx mandarina). Discovered by Adolf Butenandt in 1959, it was the first pheromone to be characterized chemically.
Minute quantities of this pheromone can be used per acre of land to confuse male insects about the location of their female partners. It can thus serve as a lure in traps to remove insects effectively without spraying crops with large amounts of pesticides. Butenandt named the substance after the moth's Latin name Bombyx mori.
In vivo it appears that bombykol is the natural ligand for a pheromone binding protein, BmorPBP, which escorts the pheromone to the pheromone receptor. | ãã³ãã³ãŒã«ïŒè±: BombykolãååŠåŒ:C16H30OïŒã¯ã«ã€ã³ã¬ã®ã¡ã¹ãæŸåºãããã§ãã¢ã³ã§ããããã®ç©è³ªã¯1959幎ã«ãã€ãã®çååŠè
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ã§ã¯ããã§ãã¢ã³çµåã¿ã³ãã¯è³ªBmorPBPã®å€©ç¶ã®ãªã¬ã³ããšããŠäœçšããã | 1 |
Cadmium sulfide is a cadmium molecular entity. | ã¯ãã«ãŸããµãŸã³ïŒè±: chlorzoxazoneïŒã¯ããã³ãŸãªããµãŸãŒã«ç³»çåŒç·©å€ã®1çš®ã§ãããäžæ¢ç¥çµç³»ã«äœçšããããšã§çåŒç·©ãããããã | 0 |
Phthalic anhydride is the cyclic dicarboxylic anhydride that is the anhydride of phthalic acid. It has a role as an allergen. It is a cyclic dicarboxylic anhydride and a member of 2-benzofurans. | ã¹ãã¯ãããã€ã·ã³ïŒSpectinomycinïŒãšã¯çæ£çŽ°èã®Streptomyces spectabilis ã«ãã£ãŠç£çãããã¢ããã°ãªã³ã·ãç³»æçç©è³ªã§ãããæ·èææçã®æ²»çã«çšãããããå¡©é
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Amiodarone is a member of the class of 1-benzofurans that is 1-benzofuran substituted by a butyl group at position 2 and a 4-[2-(diethylamino)ethoxy]-3,5-diiodobenzoyl group at position 3. It is a cardiovascular drug used for the treatment of cardiac dysrhythmias. It has a role as a cardiovascular drug. It is a member of 1-benzofurans, an organoiodine compound, an aromatic ketone and a tertiary amino compound. | ããªã·ã¹ãã³(Baeocystin)ã¯ãããžãã¯ããã·ã¥ã«ãŒã ã«å«ãŸããã¢ã«ã«ãã€ãã§ãããã·ãã·ãã³ã®é¡çžäœãã·ãã·ãã³ãã·ãã·ã³ããã«ããªã·ã¹ãã³ãšå
±ã«ã»ãšãã©ã®ããžãã¯ããã·ã¥ã«ãŒã ã«å«ãŸããããŸãã·ãã·ãã³ããN-ãžã¡ãã«åããèªå°äœã§ããããŸãã4-HO-NMT (4-ããããã·-N-ã¡ãã«ããªãã¿ãã³)ã®ãªã³é
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Midazolam is an imidazobenzodiazepine that is 4H-imidazo[1,5-a][1,4]benzodiazepine which is substituted by a methyl, 2-fluorophenyl and chloro groups at positions 1, 6 and 8, respectively. It has a role as a GABAA receptor agonist, an anticonvulsant, an anxiolytic drug, an apoptosis inducer, an antineoplastic agent, a muscle relaxant, a sedative, a general anaesthetic and a central nervous system depressant. It is an organochlorine compound, an imidazobenzodiazepine and a member of monofluorobenzenes. | ã°ãŠã²ããã³ïŒè±ïŒGougerotinïŒã¯æ°Žæº¶æ§ã®ããªããžã³ç³»æçç©è³ªã§ãStreptomyces graminearusãšStreptomyces gougerotiiã«ãã£ãŠç£çããã ãã°ãŠã²ããã³ã¯ç®èç§å»Henri-EugÚne Gougerotã«ã¡ãªãã§åœåããã ãã°ãŠã²ããã³ã¯ã°ã©ã éœæ§èãšã°ã©ã é°æ§èã®ã¿ãªãããŠã€ã«ã¹ã«å¯ŸããŠæŽ»æ§ããã ã | 0 |
Rishitin is a polyol. | ã·ãã·ã³ããŸãã¯ãµã€ãã·ã³ (Psilocin)ãã¯ãäžéšã®ããã³ã«å«ãŸããã¢ã«ã«ãã€ãã§ãå¹»èŠäœçšãæã€ãã·ãã·ã³ã®ãªã³é
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Hygrine is a pyrrolidine alkaloid, found mainly in coca leaves (0.2%). It was first isolated by Carl Liebermann in 1889 (along with a related compound cuscohygrine) as an alkaloid accompanying cocaine in coca. Hygrine is extracted as a thick yellow oil, having a pungent taste and odor. | 'ã¹ã¯ããŒã¹ãªã¯ã¿ã¢ã»ã¿ãŒãïŒè±: sucrose octaacetateïŒã¯ãååŠåŒC28H38O19ãŸãã¯(C2H3O2)8(C12H14O3)ã§è¡šãããååŠç©è³ªã§ãããã¹ã¯ããŒã¹ãš8ã€ã®é
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This dataset is a multilingual extension of the PubChem & Wikipedia Paragraphs Pair Classification dataset. It includes pairs of paragraphs in English and Japanese (sent1 and sent2) with a binary labels column indicating whether the paragraphs describe the same entity (1) or different entities (0).