CHEBI:90364 - S-(5-deoxy-β-D-ribos-5-yl)-L-homocysteine

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ChEBI Name S-(5-deoxy-β-D-ribos-5-yl)-L-homocysteine ChEBI ID CHEBI:90364 ChEBI ASCII Name S-(5-deoxy-beta-D-ribos-5-yl)-L-homocysteine Definition An S-(5-deoxy-D-ribos-5-yl)-L-homocysteine in which the anomeric centre has β-configuration. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:45383 Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C9H17NO6S Net Charge 0 Average Mass 267.301 Monoisotopic Mass 267.07766 InChI InChI=1S/C9H17NO6S/c10-4(8(13)14)1-2-17-3-5-6(11)7(12)9(15)16-5/h4-7,9,11-12,15H,1-3,10H2,(H,13,14)/t4-,5+,6+,7+,9+/m0/s1 InChIKey IQFWYNFDWRYSRA-OEQWSMLSSA-N SMILES S(C[C@H]1O[C@@H](O)[C@@H]([C@@H]1O)O)CC[C@H](N)C(=O)O Metabolite of Species Details Mus musculus (NCBI:txid10090) See: MetaboLights Study Escherichia coli BL21 (NCBI:txid511693) of strain BL21 See: PubMed Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Biological Role(s): Escherichia coli metabolite Any bacterial metabolite produced during a metabolic reaction in Escherichia coli. View more via ChEBI Ontology ChEBI Ontology Outgoing S-(5-deoxy-β-D-ribos-5-yl)-L-homocysteine (CHEBI:90364) has functional parent L-homocysteine (CHEBI:17588) S-(5-deoxy-β-D-ribos-5-yl)-L-homocysteine (CHEBI:90364) has role Escherichia coli metabolite (CHEBI:76971) S-(5-deoxy-β-D-ribos-5-yl)-L-homocysteine (CHEBI:90364) is a S-(5-deoxy-D-ribos-5-yl)-L-homocysteine (CHEBI:17575) IUPAC Name (2S)-2-Amino-4-({[(2S,3S,4R,5R)-3,4,5-trihydroxytetrahydro-2-furanyl]methyl}sulfanyl)butanoic acid Synonyms Sources Ribose-5-S-homocysteine MetaCyc S-(5-Deoxy-D-ribos-5-yl)-L-homocysteine MetaCyc S-D-Ribosyl-L-homocysteine MetaCyc S-ribosyl-L-homocysteine ChEBI S-Ribosylhomocysteine MetaCyc Manual Xrefs Databases C00019629 KNApSAcK CPD-564 MetaCyc RHC PDBeChem View more database links Registry Number Type Source 9571171 Reaxys Registry Number Reaxys Citations Types Sources 24967680 PubMed citation Europe PMC 25849497 PubMed citation Europe PMC Last Modified 23 June 2016