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N-glycosylpyrrolopyrimidine that is tubercidin in which the hydrogen at position 5 of the pyrrolopyrimidine moiety has been replaced by a cyano group.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:
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
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.
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
VengicideChemIDplus
SiromycinChemIDplus
Antibiotic A-399-Y4ChemIDplus
7-deaza-7-cyanoadenosineChemIDplus
Antibiotic 1037ChemIDplus
cyanotubericidinChemIDplus
Registry NumbersSources
Reaxys:48454Reaxys
CAS:606-58-6ChemIDplus
Citations