BEZ

BENZOIC ACID



Chemical Component Summary

NameBENZOIC ACID
Identifiersbenzoic acid
FormulaC7 H6 O2
Molecular Weight122.121
TypeNON-POLYMER
Isomeric SMILESc1ccc(cc1)C(=O)O
InChIInChI=1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
InChIKeyWPYMKLBDIGXBTP-UHFFFAOYSA-N

Chemical Details

Formal Charge0
Atom Count15
Chiral Atom Count0
Bond Count15
Aromatic Bond Count6

Drug Info: DrugBank

DrugBank IDDB03793 
NameBenzoic acid
Groups
  • approved
  • investigational
DescriptionA fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. As the sodium salt form, sodium benzoate is used as a treatment for urea cycle disorders due to its ability to bind amino acids. This leads to excretion of these amino acids and a decrease in ammonia levels. Recent research shows that sodium benzoate may be beneficial as an add-on therapy (1 gram/day) in schizophrenia. Total Positive and Negative Syndrome Scale scores dropped by 21% compared to placebo.
Synonyms
  • Sodium benzoate
  • Benzoic acid
  • Calcium benzoate
Brand Names
  • Seo Jeong Ho Hwang Chill Mist
  • S Panax Mist
  • Sodium Phenylacetate and sodium benzoate
  • S Panax All In One Mist
  • Glycothymoline
Categories
  • Acids, Carbocyclic
  • Alimentary Tract and Metabolism
  • Ammonium Ion Binding Activity
  • Anti-Infective Agents
  • Antifungal Agents
ATC-Code
  • A16AX30
  • A16AX11
  • V04CG30
CAS number65-85-0

Drug Targets

NameTarget SequencePharmacological ActionActions
Solute carrier family 15 member 1MGMSKSHSFFGYPLSIFFIVVNEFCERFSYYGMRAILILYFTNFISWDDN...unknown
Cocaine esteraseMVDGNYSVASNVMVPMRDGVRLAVDLYRPDADGPVPVLLVRNPYDKFDVF...unknownproduct of
D-amino-acid oxidaseMRVVVIGAGVIGLSTALCIHERYHSVLQPLDIKVYADRFTPLTTTDVAAG...unknown
Chlorocatechol 1,2-dioxygenaseMANTRVIELFDEFTDLIRDFIVRHEITTPEYETIMQYMISVGEAGEWPLW...unknownsubstrate
2-hydroxy-6-oxo-7-methylocta-2,4-dienoate hydrolaseMANLEIGKSILAAGVLTNYHDVGEGQPVILIHGSGPGVSAYANWRLTIPA...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
Pharos CHEMBL541
PubChem 243, 20144841
ChEMBL CHEMBL541
ChEBI CHEBI:30746
CCDC/CSD AFEREK, CUPCEY, AYUNUE, DUYWAV, EMOCUF, BUCCAG, BENZAC12, BUDWEC, CUCSEY10, CUSSOZ, DIKDOR, DAWKIX, BENZAC21, CILLEQ, CILMAN, DUPJEE, CICZUL, CILLOA, DOGBAF, CUCSEY01, EZOLOW, EXEYOW, EJOKAR, BENZAC20, COZXOF, COZXIZ, EJOKAR01, AWESUR, EJOKAR02, EZIFID, DUTSOB, COZXUL, EMOCOZ, EQOPUV, EBUZAG
COD 7200221, 7200222, 7200223, 7215557, 7215558, 7215559, 7210454, 2225365, 2225405