CHEBI:134606 - toyocamycin

ChEBI IDCHEBI:134606
ChEBI Nametoyocamycin
Stars
DefinitionAn N-glycosylpyrrolopyrimidine that is tubercidin in which the hydrogen at position 5 of the pyrrolopyrimidine moiety has been replaced by a cyano group.
Last Modified17 February 2017
SubmitterGareth Owen
DownloadsMolfile
FormulaC12H13N5O4
Net Charge0
Average Mass291.267
Monoisotopic Mass291.09675
SMILESN#Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c2ncnc(N)c12
InChIInChI=1S/C12H13N5O4/c13-1-5-2-17(11-7(5)10(14)15-4-16-11)12-9(20)8(19)6(3-18)21-12/h2,4,6,8-9,12,18-20H,3H2,(H2,14,15,16)/t6-,8-,9-,12-/m1/s1
InChIKeyXOKJUSAYZUAMGJ-WOUKDFQISA-N
Species of MetaboliteComponentSourceComments
Streptomyces diastatochromogenes (ncbitaxon:1628) - PubMed (23775805)
Roles Classification
Biological Roles:
apoptosis inducer  Any substance that induces the process of apoptosis (programmed cell death) in multi-celled organisms.
antimetabolite  A substance which is structurally similar to a metabolite but which competes with it or replaces it, and so prevents or reduces its normal utilization.
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
toyocamycin (CHEBI:134606) has role antimetabolite (CHEBI:35221)
toyocamycin (CHEBI:134606) has role antineoplastic agent (CHEBI:35610)
toyocamycin (CHEBI:134606) has role apoptosis inducer (CHEBI:68495)
toyocamycin (CHEBI:134606) has role bacterial metabolite (CHEBI:76969)
toyocamycin (CHEBI:134606) is a N-glycosylpyrrolopyrimidine (CHEBI:48036)
toyocamycin (CHEBI:134606) is a antibiotic antifungal agent (CHEBI:86478)
toyocamycin (CHEBI:134606) is a nitrile (CHEBI:18379)
toyocamycin (CHEBI:134606) is a ribonucleoside (CHEBI:18254)
IUPAC Name 
4-amino-7-β-D-ribofuranosyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile
Synonyms  Source
4-amino-5-cyano-7-(D-ribofuranosyl)-7H-pyrrolo(2,3-d)pyrimidineChemIDplus
7-deaza-7-cyanoadenosineChemIDplus
A-399-Y4ChemIDplus
Ahygroscopin-BChemIDplus
Antibiotic 1037ChemIDplus
Antibiotic A-399-Y4ChemIDplus
Registry NumbersSources
Reaxys:48454Reaxys
CAS:606-58-6ChemIDplus
Citations