FMT

FORMIC ACID

Created: 1999-07-08
Last modified:  2024-09-27

Find related ligands:

Chemical Details

Formal Charge0
Atom Count5
Chiral Atom Count0
Bond Count4
Aromatic Bond Count0
2D diagram of FMT

Chemical Component Summary

NameFORMIC ACID
Systematic Name (OpenEye OEToolkits)methanoic acid
FormulaC H2 O2
Molecular Weight46.025
TypeNON-POLYMER

Chemical Descriptors

TypeProgram Version Descriptor
SMILESACDLabs11.02O=CO
SMILESCACTVS3.352OC=O
SMILESOpenEye OEToolkits1.7.0C(=O)O
Canonical SMILESCACTVS3.352 OC=O
Canonical SMILESOpenEye OEToolkits1.7.0 C(=O)O
InChIInChI1.03 InChI=1S/CH2O2/c2-1-3/h1H,(H,2,3)
InChIKeyInChI1.03 BDAGIHXWWSANSR-UHFFFAOYSA-N

Drug Info: DrugBank

DrugBank IDDB01942 
NameFormic acid
Groups
  • experimental
  • investigational
DescriptionFormic acid (systematically called methanoic acid) is the simplest carboxylic acid. It is an important intermediate in chemical synthesis and occurs naturally, most famously in the venom of bee and ant stings. It is commonly used as a preservative and antibacterial agent in livestock feed.
Synonyms
  • Acide formique
  • Formic acid
  • Bilorin
  • Aminic acid
  • Methanoic acid
Brand Names
  • Prenate Essential
  • NESTABS Prenatal Multi-vitamin/Mineral Supplement
  • Nutri-Tab OB plus DHA
  • Pre-Tabs DHA Prenatal Multi-vitamin/Mineral Supplement with DHA/EPA
  • Prenate DHA
Categories
  • Acids, Acyclic
  • Blood Coagulation Factors
  • Hemostatics
CAS number64-18-6

Drug Targets

NameTarget SequencePharmacological ActionActions
Putative hydroxypyruvate isomerase YgbMMPRFAANLSMMFTEVPFIERFAAARKAGFDAVEFLFPYNYSTLQIQKQLE...unknown
Delta-aminolevulinic acid dehydrataseMSFTPANRAYPYTRLRRNRRDDFSRRLVRENVLTVDDLILPVFVLDGVNQ...unknown
Heme oxygenase 1MERPQPDSMPQDLSEALKEATKEVHTQAENAEFMRNFQKGQVTRDGFKLV...unknown
Ribonuclease pancreaticMALEKSLVRLLLLVLILLVLGWVQPSLGKESRAKKFQRQHMDSDSSPSSS...unknown
3-phosphoshikimate 1-carboxyvinyltransferaseMESLTLQPIARVDGTINLPGSKSVSNRALLLAALAHGKTVLTNLLDSDDV...unknown
View More
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS. Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682

Related Resource References

Resource NameReference
PubChem 18971002, 284
ChEMBL CHEMBL116736
ChEBI CHEBI:30751
CCDC/CSD FORMAC01, ACEROR, HMTOFA01, IWUYUW, HMTOFA03, BIRDOV, HMTOFA08, HMTOFA02, HMTOFA04, COTTIQ, KARGIW, JOHJUN, HMTOFA05, HEYJUR, HMTOFA06, ALERIT, GOKCEQ, KARGIW01, INIJEW, BEPKAI, ABIMON, GUVKAL, EHALAA, KARGES01, FOACAM, KARGAO01, HEYJAX, BEPJOV01, KARGAO, BIJGIN, KARGES, IYOWUQ, HMTOFA07, JUZCEP
COD 4117094