blc-org/A-secret-data-repo huggingface dataset:
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)N[C@@H](CO[C@H]1O[C@H](CO)[C@H](OCc2ccc(F)cc2)[C@H](O)[C@H]1O)[C@H](O)[C@H](O)CCCCCCCCCCCCCC. 


Answer: The molecule is a glycophytoceramide having a 4-O-(4-fluorobenzyl)-alpha-D-galactosyl residue at the O-1 position and a hexacosanoyl group attached to the nitrogen. One of a series of an extensive set of 4"-O-alkylated alpha-GalCer analogues evaluated (PMID:30556652) as invariant natural killer T-cell (iNKT) antigens. It derives from an alpha-D-galactose.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCCCCCC)COP(=O)(O)OC1[C@H](O)[C@H](O)C(O)[C@H](O)[C@H]1O. 


Answer: The molecule is a 1-octadecanoyl-2-acyl-sn-glycero-3-phospho-1D-myo-inositol in which the 2-acyl group is specified as (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyl (arachidonoyl). It has a role as a mouse metabolite. It is a 1-octadecanoyl-2-acyl-sn-glycero-3-phospho-1D-myo-inositol and a phosphatidylinositol(18:0/20:4). It derives from an octadecanoic acid and an arachidonic acid. It is a conjugate acid of a 1-octadecanoyl-2-arachidonoyl-sn-glycero-3-phospho-D-myo-inositol(1-).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC1(C)CC[C@]2(C)CC[C@]3(C)C(=C[C@@H](O)[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1. 


Answer: The molecule is the pentacyclic triterpenoid that is the 11alpha-hydroxy derivative of beta-amyrin. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a beta-amyrin.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: Cc1cn([C@H]2C[C@H](O)[C@@H](COP(=O)([O-])OP(=O)([O-])O[C@@H]3C[C@H]([NH+](C)C)[C@H](O)[C@H](C)O3)O2)c(=O)[nH]c1=O. 


Answer: The molecule is a nucleotide-sugar oxoanion that is the conjugate base of dTDP-beta-L-rhodosamine, arising from deprotonation of the diphosphate group and protonation of the amino group; major species at pH 7.3. It is a conjugate base of a dTDP-beta-L-rhodosamine.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: C[C@H](CCC(=O)O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C. 


Answer: The molecule is a dihydroxy-5beta-cholanic acid that is (5beta)-cholan-24-oic acid substituted by beta-hydroxy groups at positions 3 and 7. It has a role as a human metabolite. It is a conjugate acid of an isoursodeoxycholate.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC1(C(=O)Nc2ccc(O)c(Cl)c2Cl)CCCCC1. 


Answer: The molecule is an aromatic amide resulting from the formal condensation of the carboxy group of 1-methylcyclohexanecarboxylic acid with the amino group of 4-amino-2,3-dichlorophenol. It has a role as an EC 1.14.13.72 (methylsterol monooxygenase) inhibitor, a sterol biosynthesis inhibitor and an antifungal agrochemical. It is a monocarboxylic acid amide, a member of phenols, an aromatic amide, a dichlorobenzene and an anilide fungicide.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCC(C)CCCCCCCCCCCCCCCCCCCCC(=O)O. 


Answer: The molecule is a methyl-branched fatty acid that is tetracosanoic acid (lignoceric acid) substituted by a methyl group at position 22. It is a branched-chain saturated fatty acid, a methyl-branched fatty acid and a very long-chain fatty acid. It derives from a tetracosanoic acid.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: O=C(O)C1CCCCN1. 


Answer: The molecule is a piperidinemonocarboxylic acid in which the carboxy group is located at position C-2. It is a conjugate acid of a pipecolate.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: O.O.O.O.O=S(=O)([O-])[O-].[Be+2]. 


Answer: The molecule is a hydrate of beryllium sulfate containing beryllium (in +2 oxidation state), sulfate and water moieties in the ratio 1:1:4. It contains a beryllium sulfate.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: Cc1nn(-c2cc(NS(C)(=O)=O)c(Cl)cc2Cl)c(=O)n1C(F)F. 


Answer: The molecule is a member of the class of triazoles that is 5-oxo-1,2,4-triazole which is substituted at positions 1, 3, and 4 by 2,4-dichloro-5-[(methylsulfonyl)amino]phenyl, methyl, and difluoromethyl groups, respectively. A protoporphyrinogen oxidase inhibitor, it is used as a herbicide to control broad-leaved weeds in soya and tobacco crops. Not approved for use within the European Union. It has a role as an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor, a herbicide and an agrochemical. It is a sulfonamide, a dichlorobenzene, an organofluorine compound and a member of triazoles.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: Nc1ccn([C@@H]2O[C@H](COP(=O)([O-])[O-])[C@@H](O)[C@H]2O)c(=O)n1.[Na+].[Na+]. 


Answer: The molecule is an organic sodium salt that is the disodium salt of CMP. It has a role as a human metabolite. It contains a cytidine 5'-monophosphate(2-).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CCCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O. 


Answer: The molecule is an unsaturated fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of (15Z,18Z,21Z,24Z,27Z)-triacontapentaenoic acid. It is an unsaturated fatty acyl-CoA and an ultra-long-chain fatty acyl-CoA. It is a conjugate acid of a (15Z,18Z,21Z,24Z,27Z)-triacontapentaenoyl-CoA(4-).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])[O-])OC(=O)CCCCCCCCCCCCCCC. 


Answer: The molecule is a 1-acyl-2-hexadecanoyl-sn-glycero-3-phosphate(2-) in which the 1-acyl group is also hexadecanoyl; major species at pH 7.3. It is a conjugate base of a 1,2-dihexadecanoyl-sn-glycerol-3-phosphate.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: O=c1[nH]c(=O)c2ncn([C@@H]3O[C@H](COP(=O)([O-])OP(=O)([O-])OP(=O)([O-])O)[C@@H](O)[C@H]3O)c2[nH]1. 


Answer: The molecule is trianion of xanthosine 5'-triphosphate arising from deprotonation of three of the four free triphosphate OH groups. It is a xanthosine 5'-phosphate and a ribonucleoside triphosphate oxoanion. It is a conjugate base of a XTP. It is a conjugate acid of a XTP(4-).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: C=C1CCOC1=O. 


Answer: The molecule is a butan-4-olide having a methylene group at the 3-position. It has a role as a gastrointestinal drug and an anti-ulcer drug.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: C[C@@H]1[C@H](O)[C@@H](C)/C=C/C=C/CC/C=C/C=C/C=C/C=C/C(O[C@H]2O[C@H](C)[C@@H](O)[C@H](N)[C@@H]2O)CC2O[C@](O)(CC(O)C(O)CCC(O)CC(O)CC(O)CC(=O)O[C@H]1C)CC(O)C2C(=O)O. 


Answer: The molecule is a polyene macrolide antibiotic; part of the nystatin complex produced by several Streptococcus species. It is a member of nystatins and a carboxylic acid.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: COC(C)(C)C(O)/C=C/C(C)=C/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(\C)CC/C=C(\C)CCC=C(C)C. 


Answer: The molecule is a carotenoid ether that is spheroidene substituted at position 2 by a hydroxy group. It is a carotenoid ether and a carotenol. It derives from a spheroidene.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC(C)CCCCCCCCCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(=O)([O-])OP(=O)([O-])OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)([O-])[O-]. 


Answer: The molecule is an acyl-CoA(4-) arising from deprotonation of the phosphate and diphosphate functions of isopalmitoyl-CoA. Major species at pH 7.3. It is a saturated fatty acyl-CoA(4-) and a long-chain fatty acyl-CoA(4-). It is a conjugate base of an isopalmitoyl-CoA.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCCCCCCCCCCCCC[C@@H](O)[C@H](O)[C@@H](N)CO. 


Answer: The molecule is a sphingoid having the structure of phytosphingosine but with R-configuration at C-3. It is a sphingoid, a triol and an amino alcohol.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC(=O)N[C@@H]1[C@@H](O)[C@H](O[C@@H]2O[C@H](CO[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3NC(C)=O)[C@H](O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@H]1O. 


Answer: The molecule is an amino trisaccharide consisting of N-acetyl-alpha-D-glucosamine, beta-D-galactose and N-acetyl-beta-D-glucosamine residues linked sequentially (1->6) and (1->4). It has a role as an epitope. It is an amino trisaccharide and a glucosamine oligosaccharide.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CN(C)c1ccc2[nH]c3c(C([NH3+])=O)cc(=O)c(=O)c=3oc2c1. 


Answer: The molecule is an organic cation that is 3,4-dihydroxyphenoxazin-5-ium carrying additional carbamoyl and dimethylamino groups at positions 1 and 7 respectively. The chloride salt is the histological dye 'Gallamin blue'. It has a role as a fluorochrome and a histological dye.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: COc1cc2oc(=O)cc(COC(=O)C=C(C)C)c2cc1OC. 


Answer: The molecule is a member of the class of coumarins that consists of coumarin substituted by a senecioyloxymethyl group at position 4 and methoxy groups at positions 6 and 7. Isolated from Crinum latifolium, it exhibits anti-angiogenic activity. It has a role as a metabolite and an angiogenesis modulating agent. It is a member of coumarins, an enoate ester and an aromatic ether. It derives from a 3-methylbut-2-enoic acid.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: NCCCC(O)(P(=O)(O)O)P(=O)(O)O. 


Answer: The molecule is a 1,1-bis(phosphonic acid) that is methanebis(phosphonic acid) in which the two methylene hydrogens are replaced by hydroxy and 3-aminopropyl groups. It has a role as an EC 2.5.1.1 (dimethylallyltranstransferase) inhibitor and a bone density conservation agent. It is a 1,1-bis(phosphonic acid) and a primary amino compound. It is a conjugate acid of an alendronate(1-).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: COC(=O)c1nc(C2CC2)nc(N)c1Cl. 


Answer: The molecule is a pyrimidinecarboxylate ester that is the methyl ester of aminocyclopyrachlor. It has a role as a herbicide and a synthetic auxin. It is a pyrimidinecarboxylate ester, a primary amino compound, an organochlorine pesticide and a methyl ester. It derives from an aminocyclopyrachlor.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CN[C@@H](C)C(=O)O. 


Answer: The molecule is a methyl-L-alanine in which one of the the amino hydrogen of L-alanine is replaced by a methyl group. It is a tautomer of a N-methyl-L-alanine zwitterion.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: COc1cc(/C=C/C(=O)OCCCCCCCCCCCCCCCC(=O)[O-])ccc1O. 


Answer: The molecule is a monocarboxylic acid anion that is the conjugate base of 16-feruloyloxypalmitic acid obtained by deprotonation of the carboxy group. It is a conjugate base of a 16-feruloyloxypalmitic acid.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: OC[C@H]1O[C@@H](O[C@@H]2[C@@H](O)[C@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](O)O[C@@H]3CO)O[C@H](CO)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O. 


Answer: The molecule is a glucotriose consisting of three beta-D-gluopyranose residues joined in sequence by (1->3) and (1->4) glycosidic bonds. It derives from a beta-cellobiose.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC(=O)N[C@H]1[C@@H](OP(=O)([O-])OP(=O)([O-])OC/C=C(/C)CC/C=C(/C)CC/C=C(/C)CC/C=C(/C)CC/C=C(/C)CC/C=C(/C)CC/C=C(/C)CC/C=C(/C)CC/C=C(\C)CC/C=C(\C)CCC=C(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]3O)[C@@H]2O)[C@@H]1O. 


Answer: The molecule is an organophosphate oxoanion obtained by deprotonation of both free diphosphate OH groups of alpha-D-mannosyl-(1->3)-alpha-D-mannosyl-(1->3)-alpha-D-mannosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-1-diphospho-ditrans,polycis-undecaprenol; major species at pH 7.3. It is a conjugate base of an alpha-D-mannosyl-(1->3)-alpha-D-mannosyl-(1->3)-alpha-D-mannosyl-(1->3)-N-acetyl-alpha-D-glucosaminyl-1-diphospho-ditrans,polycis-undecaprenol.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCCCCCCCCCCCCC[C@@H](O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O. 


Answer: The molecule is a 3-hydroxy fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of (3R,19Z,22Z,25Z,28Z)-3-hydroxytetratriacontatetraenoic acid. It is a (R)-3-hydroxyacyl-CoA, a 3-hydroxy fatty acyl-CoA, an unsaturated fatty acyl-CoA and an ultra-long-chain fatty acyl-CoA. It is a conjugate acid of a (3R,19Z,22Z,25Z,28Z)-3-hydroxytetratriacontatetraenoyl-CoA(4-).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC(C)c1cc(/C=C(\C#N)C(=O)NCCCc2ccccc2)cc(C(C)C)c1O. 


Answer: The molecule is a monocarboxylic acid amide obtained by formal condensation of the carboxy group of (2E)-2-cyano-3-[4-hydroxy-3,5-di(propan-2-yl)phenyl]prop-2-enoic acid with the amino group of 3-phenylpropylamine. It has a role as a vascular endothelial growth factor receptor antagonist. It is an enamide, a member of phenols, a nitrile, a monocarboxylic acid amide and a secondary carboxamide.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CCCCCCCc1[nH]c2ccccc2c(=O)c1O. 


Answer: The molecule is a quinolone consisting of quinolin-4(1H)-one carrying a heptyl substituent at position 2 and a hydroxy group at position 3. It has a role as a signalling molecule.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: CC1(C)CC[C@]2(C(=O)O)CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]2C1. 


Answer: The molecule is a pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by a beta-hydroxy group at position 3. It has a role as a plant metabolite. It is a pentacyclic triterpenoid and a hydroxy monocarboxylic acid. It is a conjugate acid of an oleanolate. It derives from a hydride of an oleanane.
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: C/C=C1/C[C@@H](C)[C@@](C)(O)C(=O)OCC2=CCN3CC[C@@H](OC1=O)[C@@H]23. 


Answer: The molecule is a pyrrolizidine alkaloid isolated from the plant species of the genus Senecio. It has a role as a plant metabolite. It is a lactone, a pyrrolizidine alkaloid and a tertiary alcohol. It derives from a senecionan. It is a conjugate base of a senecionine(1+).
Given the molecular SMILES, your task is to provide the detailed description of the molecule using your experienced chemical Molecular knowledge. 
 Input: Molecule SMILES string. Output: Molecular detailed description string.
Your final answer must be formatted as <answer> Description </answer>

Input molecular SMILES string: Nc1ccc2nc3ccc(N)cc3[n+](-c3ccccc3)c2c1.[Cl-]. 


Answer: The molecule is an organic chloride salt having 3,7-diamino-5-phenylphenazin-5-ium as the counterion. It is commonly used for staining Gram negative bacteria red in smears to contrast with the blue Gram positive organisms. It has a role as a fluorochrome, a histological dye and a photosensitizing agent. It contains a 3,7-diamino-5-phenylphenazin-5-ium.