Olivetolic acid

Olivetolic acid
Names
Preferred IUPAC name
2,4-Dihydroxy-6-pentylbenzoic acid
Identifiers
CAS Number
  • 491-72-5 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:66955
ChEMBL
  • ChEMBL3134414
ChemSpider
  • 2104822
PubChem CID
  • 2826719
UNII
  • 3Y8J575L93 checkY
CompTox Dashboard (EPA)
  • DTXSID20197688 Edit this at Wikidata
InChI
  • InChI=1S/C12H16O4/c1-2-3-4-5-8-6-9(13)7-10(14)11(8)12(15)16/h6-7,13-14H,2-5H2,1H3,(H,15,16)
    Key: SXFKFRRXJUJGSS-UHFFFAOYSA-N
  • CCCCCC1=C(C(=CC(=C1)O)O)C(=O)O
Properties
Chemical formula
 C12H16O4
Molar mass 224.256 g·mol−1
Related compounds
Related compounds
 Cannabidiolic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Olivetolic acid is an organic compound that is an intermediate in the biosynthetic pathway of the cannabinoids in Cannabis sativa.[1]

The ester dimer of olivetolic acid, anziaic acid, is found in lichen.[2]

References

  1. ^ Fellermeier, Monika; Zenk, Meinhart H (May 1998). "Prenylation of olivetolate by a hemp transferase yields cannabigerolic acid, the precursor of tetrahydrocannabinol". FEBS Letters. 427 (2): 283–285. doi:10.1016/S0014-5793(98)00450-5. PMID 9607329.
  2. ^ Cheng, Bokun; Cao, Shugeng; Vasquez, Victor; Annamalai, Thirunavukkarasu; Tamayo-Castillo, Giselle; Clardy, Jon; Tse-Dinh, Yuk-Ching (8 April 2013). "Identification of Anziaic Acid, a Lichen Depside from Hypotrachyna sp., as a New Topoisomerase Poison Inhibitor". PLOS ONE. 8 (4): e60770. Bibcode:2013PLoSO...860770C. doi:10.1371/journal.pone.0060770. PMC 3620467. PMID 23593306.
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