Cannabidiolic acid
Names
Preferred IUPAC name
(1′R ,2′R )-2,6-Dihydroxy-5′-methyl-4-pentyl-2′-(prop-1-en-2-yl)-1′,2′,3′,4′-tetrahydro[1,1′-biphenyl]-3-carboxylic acid
Identifiers
3DMet
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
InChI=1S/C22H30O4/c1-5-6-7-8-15-12-18(23)20(21(24)19(15)22(25)26)17-11-14(4)9-10-16(17)13(2)3/h11-12,16-17,23-24H,2,5-10H2,1,3-4H3,(H,25,26)/t16-,17+/m0/s1
Key: WVOLTBSCXRRQFR-DLBZAZTESA-N
CCCCCC1=CC(=C(C(=C1C(=O)O)O)[C@@H]2C=C(CC[C@H]2C(=C)C)C)O
Properties
C 22 H 30 O 4
Molar mass
358.478 g·mol−1
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Cannabidiolic acid (CBDA ), is a cannabinoid produced in cannabis plants.[ 1] It is most abundant in the glandular trichomes on the female seedless flowers or more accurately infructescence often colloquially referred to as buds or flowers.[ 2]
^ Takeda, Shuso (2013). "[Medicinal chemistry and pharmacology focused on cannabidiol, a major component of the fiber-type cannabis]" . Yakugaku Zasshi: Journal of the Pharmaceutical Society of Japan . 133 (10): 1093–1101. doi :10.1248/yakushi.13-00196 . ISSN 1347-5231 . PMID 24088353 .
^ Livingston, Samuel J.; Quilichini, Teagen D.; Booth, Judith K.; Wong, Darren C. J.; Rensing, Kim H.; Laflamme‐Yonkman, Jessica; Castellarin, Simone D.; Bohlmann, Joerg; Page, Jonathan E.; Samuels, A. Lacey (2020). "Cannabis glandular trichomes alter morphology and metabolite content during flower maturation" . The Plant Journal . 101 (1): 37–56. doi :10.1111/tpj.14516 . ISSN 1365-313X . PMID 31469934 .