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:
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.
Penicillium metabolite  Any fungal metabolite produced during a metabolic reaction in Penicillium.
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
N-formyl-N- hydroxyaminoacetic acidChEBI
N-formyl hydroxyaminoacetic acidChemIDplus
N-hydroxyformamidoacetic acidChEBI
[formyl(hydroxy)amino]acetic acidIUPAC
HADACIDINPDBeChem
Manual XrefsDatabases
DB02109DrugBank
HDAPDBeChem
US3154578Patent
Registry NumbersSources
Reaxys:1927168Reaxys
CAS:689-13-4ChemIDplus
Citations