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

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name S-(5-deoxy-β-D-ribos-5-yl)-L-homocysteine
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
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
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)
(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
View more database links
Registry Number Type Source
9571171 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
24967680 PubMed citation Europe PMC
25849497 PubMed citation Europe PMC
Last Modified
23 June 2016