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: CC(C)C[C@H]1C(=O)N2CCC[C@H]2[C@]2(O)O[C@](NC(=O)[C@@H]3C=C4c5cccc6[nH]c(Br)c(c56)C[C@H]4N(C)C3)(C(C)C)C(=O)N12. 


Answer: The molecule is an indole alkaloid. It has a role as an antiparkinson drug, a hormone antagonist, a dopamine agonist and an antidyskinesia agent. It derives from a hydride of an ergotaman.
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]1O[C@@H](OC[C@H]2O[C@@H](Oc3cc(O)c4c(c3)O[C@H](c3ccc(O)cc3)CC4=O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O. 


Answer: The molecule is a disaccharide derivative that is (S)-naringenin substituted by a 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. It has a role as an anti-inflammatory agent, an antioxidant and a metabolite. It is a disaccharide derivative, a dihydroxyflavanone, a member of 4'-hydroxyflavanones, a (2S)-flavan-4-one and a rutinoside. It derives from a (S)-naringenin.
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@H]1O[C@H]1C[C@@H](/C=C/C=C\C/C=C\CCCC(=O)O)OO. 


Answer: The molecule is a hydroperoxy fatty acid that is (14S,15R)-epoxy-(5Z,8Z,10E)-icosatrienoic acid in which the hydroperoxy group is located at position 12S. It has a role as a human xenobiotic metabolite and a mouse metabolite. It is a conjugate acid of a (12S)-hydroperoxy-(14S,15R)-epoxy-(5Z,8Z,10E)-icosatrienoate.
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](O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[C@@H]4O[C@H](CO)[C@H](O)[C@H](O)[C@H]4NC(C)=O)[C@H]3O)[C@H](O)[C@H]2O)[C@@H](CO)O[C@H]1O. 


Answer: The molecule is a linear amino tetrasaccharide composed of N-acetyl-beta-D-galactosamine, alpha-D-galactose, beta-D-galactose and N-acetyl-beta-D-galactosamine units joined by sequential (1->3)-, (1->4)- and (1->4)-linkages. It has a role as an epitope.
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@H]1OC(=O)c2coc3c2[C@@]1(C)C1=C(C3=O)[C@@H]2CCC(=O)[C@@]2(C)C[C@H]1OC(C)=O. 


Answer: The molecule is an organic heteropentacyclic compound, a delta-lactone, an acetate ester and a cyclic ketone. It has a role as an EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor and an anticoronaviral agent.
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(=C\c2ccc(Cl)cc2)C1(O)Cn1cncn1. 


Answer: The molecule is a member of the class of cyclopentanols carrying 1,2,4-triazol-1-ylmethyl and 4-chlorobenzylidene and geminal dimethyl substituents at positions 1, 2 and 5 respectively. It is a member of triazoles, a member of monochlorobenzenes, a member of cyclopentanols, a tertiary alcohol and an olefinic compound.
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: CCCCCCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCCOP(=O)([O-])O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O. 


Answer: The molecule is an anionic phospholipid that is the conjugate base of beta-D-mannosyl C32-phosphomycoketide obtained by deprotonation of the phosphate OH group; major species at pH 7.3. It derives from a phosphomycoketide C32(2-). It is a conjugate base of a beta-D-mannosyl C32-phosphomycoketide.
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)c1c(O[C@@H]2O[C@@H](C)[C@H](OC)[C@@H](OC)[C@H]2OC)cc2cc3c(c(O)c2c1C)C(=O)[C@]1(OC)C(=O)C=C(OC)[C@@H](O)[C@]1(O)C3=O. 


Answer: The molecule is a member of the class of tetracenomycins that is 8-demethyltetracenomycin C in which the hydroxyl hydrogens at position 8 and 10 a are replaced by a 2,3,4-tri-O-methyl-alpha-L-rhamnosyl and methyl groups respectively. It has a role as a bacterial metabolite and an antimicrobial agent. It is an alpha-L-rhamnoside, a carboxylic ester, an enol ether, an enone, a monosaccharide derivative, a member of phenols, a tetracenomycin, a methyl ester and a tertiary alpha-hydroxy ketone. It derives from a tetracenomycin C.
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: N[C@H]1C(=O)N[C@H]2Cc3ccc(c(Cl)c3)Oc3cc4cc(c3O)Oc3ccc(cc3Cl)[C@@H](O)[C@@H]3NC(=O)[C@H](NC(=O)[C@@H]4NC(=O)[C@@H](NC2=O)c2cc(O)cc(c2)Oc2cc1ccc2OS(=O)(=O)O)c1cc(Cl)c(O)c(c1)-c1c(O)cc(O)cc1[C@H](C(=O)O)NC3=O. 


Answer: The molecule is a cyclic peptide antibiotic produced by a strain of Streptomyces toyocaensis. It has a role as a fungal metabolite. It is a heterodetic cyclic peptide, a cyclic ether, an organochlorine compound, a polyphenol, a peptide antibiotic and an aryl sulfate. It is a conjugate acid of an A47934(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: CC1(S(=O)(=O)[O-])CC(=O)c2ccccc2C1=O. 


Answer: The molecule is an organosulfonate oxoanion that is the conjugate base of menadione sulfonic acid, arising from deprotonation of the sulfo group; major species at pH 7.3. It is a conjugate base of a menadione sulfonic 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: [25Mg]. 


Answer: The molecule is the stable isotope of magnesium with relative atomic mass 24.985837, 10.0 atom percent natural abundance and nuclear spin 5/2.
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: CCCCCC(=O)N[C@@H](O)C(=O)[O-]. 


Answer: The molecule is an N-acyl-(2S)-hydroxyglycinate resulting from the deprotonation of the carboxy group of N-hexanoyl-(2S)-hydroxyglycine. The major species at pH 7.3. It is a conjugate base of a N-hexanoyl-(2S)-hydroxyglycine.
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]1CC[C@H]2C(C(=O)O)=C[C@@H]3[C@@H](O)C(C)(C)C[C@@]132. 


Answer: The molecule is a tricyclic sesquiterpenoid that is pentalenene in which the 13-methyl group is oxidsed to the carboxylic acid and position 1 is substituted by a hydroxy group. It has a role as a metabolite. It is a sesquiterpenoid, a 5-hydroxy monocarboxylic acid and a carbotricyclic compound. It derives from a pentalenene. It is a conjugate acid of a pentalenate.
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](COP(=O)([O-])O[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1OC1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O)[C@H](O)CCCCCCCCCCCCCCCCC. 


Answer: The molecule is a mannosylinositol phosphorylceramide(1-) having a hexacosanoyl group amide-linked to a C20 sphinganine base, with no hydroxylation at C-4 of the long-chain base or on the C26 very-long-chain fatty acid. It is a conjugate base of a Man-1-2-Ins-1-P-Cer(d20:0/26:0).
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=P(O)(O)OC1[C@@H](OP(=O)(O)O)[C@H](OP(=O)(O)OP(=O)(O)O)C(O)[C@H](OP(=O)(O)OP(=O)(O)O)[C@H]1OP(=O)(O)O. 


Answer: The molecule is a myo-inositol bis(diphosphate) trisphosphate having the three phospho groups located at positions 4, 5 and 6 and the two diphospho groups at positions 1 and 3. It derives from a myo-inositol.
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: CCOP(=S)(OCC)Oc1ccc(S(C)=O)cc1. 


Answer: The molecule is an organic thiophosphate, a sulfoxide and an organothiophosphate insecticide. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an agrochemical, an avicide and a nematicide. It derives from a 4-(methylsulfinyl)phenol.
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: CNc1cc2c(cc1C)nc1c(=O)nc([O-])nc-1n2C[C@H](O)[C@H](O)[C@H](O)CO. 


Answer: The molecule is an organic anion that is the conjugate base of 8-demethyl-8-(methylamino)riboflavin, obtained by removal of the imide proton at position 3. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.). It is a conjugate base of an 8-demethyl-8-(methylamino)riboflavin.
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: [NH3+][C@@H](CS)C(=O)NCC(=O)[O-]. 


Answer: The molecule is the zwitterion of L-cysteinylglycine resulting from the transfer of a proton from the hydroxy group of glycine to the amino group of cysteine. Major microspecies at pH 7.3. It has a role as an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite and a human metabolite. It is a tautomer of a L-cysteinylglycine.
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@]1(CCO[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)CC[C@H]2C(=CC[C@@H]3[C@]2(C)CCC[C@]3(C)C(=O)O)C1. 


Answer: The molecule is a diterpene glycoside that is isopimar-7-en-19-oic acid attached to a alpha-D-mannopyranosyloxy residue at position 16. It has been isolated from the fungus, Xylaria species. It has a role as a fungal metabolite. It is a diterpenoid, a monosaccharide derivative, a monocarboxylic acid and a diterpene glycoside. It derives from an alpha-D-mannose. It derives from a hydride of an isopimarane.
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)=CCC/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/Cc1cc(C(=O)O)ccc1O. 


Answer: The molecule is a monohydroxybenzoic acid that is 4-hydroxybenzoic acid substituted at position 3 by a nonaprenyl group. It is a monohydroxybenzoic acid and an olefinic compound. It is a conjugate acid of a 4-hydroxy-3-all-trans-nonaprenylbenzoate.
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: Nc1cnn(C(=O)/C(O)=C/C=C/C(=O)O)c(=O)c1Cl. 


Answer: The molecule is an organochlorine compound and a pyridazinone. It derives from a muconic acid. It is a conjugate acid of a 5-amino-4-chloro-2-(2-oxidomuconoyl)pyridazin-3(2H)-one(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(=O)N(O)CCCN. 


Answer: The molecule is a member of the class of acetohydroxamic acids that is trimethylenediamine bearing N-hydroxy and N-acetyl substituents. It has a role as a metabolite. It derives from a trimethylenediamine.
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)(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@@H]1Cc2cc3ccc(=O)oc3cc2O1. 


Answer: The molecule is a member of the class of psoralens that is (-)-marmesin in which the hydroxy hydrogen is replaced by a beta-D-glucosyl residue. It has a role as a plant metabolite, a P450 inhibitor and an antioxidant. It is a beta-D-glucoside, a member of psoralens and a monosaccharide derivative. It derives from a nodakenetin.
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(NC(=O)CCC([NH3+])C(=O)[O-])C(=O)[O-]. 


Answer: The molecule is a peptide anion that is the conjugate base of gamma-Glu-Abu, obtained by removal of protons from the two carboxy groups as well as protonation of the amino group; major species at pH 7.3. It is a conjugate base of a gamma-Glu-Abu.
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: [Sm+3]. 


Answer: The molecule is a metal cation comprising samarium in the +3 oxidation state. It is a metal cation and a samarium molecular entity.
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](NC(=O)[C@H](C)NC(=O)CN)C(=O)O. 


Answer: The molecule is a tripeptide composed of glycine, L-alanine and L-alanine residues joined in sequence by peptide linkages. It derives from a L-alanine and a glycine.
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)(COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1OP(=O)(O)O)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)CC(=O)CCCCCCC(=O)O. 


Answer: The molecule is an acyl-CoA resulting from the formal condensation of the thiol group of coenzyme A with the 1-carboxy group of 3-oxodecanedioic acid. It is a conjugate acid of a 3-oxodecanedioyl-CoA(5-).
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)CNC(=O)c1ccccc1. 


Answer: The molecule is an N-acylglycine in which the acyl group is specified as benzoyl. It has a role as a uremic toxin and a human blood serum metabolite. It is a conjugate acid of a N-benzoylglycinate.
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)c1cnc(CSc2cnc(NC(=O)C3CCOCC3)s2)o1. 


Answer: The molecule is a secondary carboxamide resulting from the formal condensation of the carboxy group of tetrahydro-2H-pyran-4-carboxylic acid with the amino group of 5-{[(5-tert-butyl-1,3-oxazol-2-yl)methyl]sulfanyl}-1,3-thiazol-2-amine. It is a CDK18 kinase inhibitor. It has a role as an EC 2.7.11.22 (cyclin-dependent kinase) inhibitor. It is a member of 1,3-oxazoles, a member of 1,3-thiazoles, an organic sulfide, a secondary carboxamide and a member of oxanes.
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: Cc1ccc(N(CC2=NCCN2)c2cccc(O)c2)cc1. 


Answer: The molecule is a substituted aniline that is 3-aminophenol in which the hydrogens of the amino group are replaced by 4-methylphenyl and 4,5-dihydro-1H-imidazol-2-ylmethyl groups respectively. An alpha-adrenergic antagonist, it is used for the treatment of hypertension. It has a role as an alpha-adrenergic antagonist and a vasodilator agent. It is a member of imidazoles, a member of phenols, a tertiary amino compound and a substituted aniline.
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: COc1ccc(CCNCCCC(C#N)(c2ccc(OC)c(OC)c2)C(C)C)cc1OC. 


Answer: The molecule is a secondary amino compound that is 3,4-dimethoxyphenylethylamine in which one of the hydrogens attached to the nitrogen has been replaced by a 4-cyano-4-(3,4-dimethoxyphenyl)-5-methylhexyl group. It is an aromatic ether, a nitrile, a polyether and a secondary amino compound.
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: CCCCC1C(=O)N(c2ccccc2)N(c2ccc(O)cc2)C1=O.O. 


Answer: The molecule is a hydrate obtained by combining oxyphenbutazone with one molar equivalent of water. Commonly used to treat pain, swelling and stiffness associated with arthritis and gout, it was withdrawn from the market 1984 following association with blood dyscrasis and Stevens-Johnson syndrome. It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic, a gout suppressant, an antipyretic, an antimicrobial agent and an antineoplastic agent. It contains an oxyphenbutazone.
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: N[C@@H](CCP(=O)(O)O)C(=O)O. 


Answer: The molecule is a non-proteinogenc L-alpha-amino acid that is L-alpha-aminobutyric acid in which one of the hydrogens of the terminal methyl group has been replaced by a dihydroxy(oxido)-lambda(5)-phosphanyl group. It is a potent and selective agonist for the group III metabotropic glutamate receptors (mGluR4/6/7/8). It has a role as a metabotropic glutamate receptor agonist. It is a non-proteinogenic L-alpha-amino acid and a member of phosphonic acids.
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](OC[C@H](N)C(=O)O)O[C@H](CO[C@]2(C(=O)O)C[C@H](O)[C@@H](NC(C)=O)[C@H]([C@H](O)[C@H](O)CO)O2)[C@H](O)[C@@H]1O. 


Answer: The molecule is the L-alpha-amino acid that is N-acetyl-alpha-neuraminyl-(2->6)-N-acetyl-alpha-D-galactosamine linked via an alpha glycosidic bond to the O at position 3 of L-serine. It is a L-serine derivative and a non-proteinogenic L-alpha-amino acid.