CHEBI:43040 - hadacidin

ChEBI IDCHEBI:43040
ChEBI Namehadacidin
Stars
DefinitionA monocarboxylic acid that is N-hydroxyglycine in which the hydrogen attached to the nitrogen is replaced by a formyl group. It was originally isolated from cultures of Penicillium frequentans.
Last Modified8 January 2015
DownloadsMolfile
FormulaC3H5NO4
Net Charge0
Average Mass119.076
Monoisotopic Mass119.02186
SMILESO=CN(O)CC(=O)O
InChIInChI=1S/C3H5NO4/c5-2-4(8)1-3(6)7/h2,8H,1H2,(H,6,7)
InChIKeyURJHVPKUWOUENU-UHFFFAOYSA-N
Roles Classification
Chemical Roles:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
Penicillium metabolite  Any fungal metabolite produced during a metabolic reaction in Penicillium.
teratogenic agent  A role played by a chemical compound in biological systems with adverse consequences in embryo developments, leading to birth defects, embryo death or altered development, growth retardation and functional defect.
antimicrobial agent  A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
hadacidin (CHEBI:43040) has role Penicillium metabolite (CHEBI:76964)
hadacidin (CHEBI:43040) has role antimicrobial agent (CHEBI:33281)
hadacidin (CHEBI:43040) has role antineoplastic agent (CHEBI:35610)
hadacidin (CHEBI:43040) has role teratogenic agent (CHEBI:50905)
hadacidin (CHEBI:43040) is a N-hydroxy-α-amino-acid (CHEBI:50760)
hadacidin (CHEBI:43040) is a aldehyde (CHEBI:17478)
hadacidin (CHEBI:43040) is a monocarboxylic acid (CHEBI:25384)
IUPAC Name 
N-formyl-N-hydroxyglycine
Synonyms  Source
HADACIDINPDBeChem
N-hydroxyformamidoacetic acidChEBI
N-formyl-N- hydroxyaminoacetic acidChEBI
N-formyl hydroxyaminoacetic acidChemIDplus
[formyl(hydroxy)amino]acetic acidIUPAC
Manual XrefsDatabases
HDAPDBeChem
US3154578Patent
DB02109DrugBank
Registry NumbersSources
Reaxys:1927168Reaxys
CAS:689-13-4ChemIDplus
Citations