CHEBI:17575 - S-(5-deoxy-D-ribos-5-yl)-L-homocysteine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name S-(5-deoxy-D-ribos-5-yl)-L-homocysteine
ChEBI ID CHEBI:17575
ChEBI ASCII Name S-(5-deoxy-D-ribos-5-yl)-L-homocysteine
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12750, CHEBI:22071, CHEBI:8968
Supplier Information ChemicalBook:CB3364529, ChemicalBook:CB34796861, eMolecules:29538748, eMolecules:490388, Selleckchem:Chloramphenicol(Chloromycetin), ZINC000000113382
Download Molfile XML SDF
Formula C9H17NO6S
Net Charge 0
Average Mass 267.30042
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-BLELIYKESA-N
SMILES N[C@@H](CCSC[C@H]1OC(O)[C@H](O)[C@@H]1O)C(O)=O
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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing S-(5-deoxy-D-ribos-5-yl)-L-homocysteine (CHEBI:17575) has functional parent D-ribofuranose (CHEBI:47013)
S-(5-deoxy-D-ribos-5-yl)-L-homocysteine (CHEBI:17575) is a homocysteines (CHEBI:24610)
S-(5-deoxy-D-ribos-5-yl)-L-homocysteine (CHEBI:17575) is tautomer of S-(5-deoxy-D-ribos-5-yl)-L-homocysteine zwitterion (CHEBI:58195)
Incoming 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)
S-(5-deoxy-D-ribos-5-yl)-L-homocysteine zwitterion (CHEBI:58195) is tautomer of S-(5-deoxy-D-ribos-5-yl)-L-homocysteine (CHEBI:17575)
IUPAC Name
S-(5-deoxy-D-ribofuranos-5-yl)-L-homocysteine
Synonym Source
Ribose-5-S-homocysteine KEGG COMPOUND
Last Modified
23 June 2016