Cannabichromenic Acid (CBC-a) Research Dashboard
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Overview - Cannabichromenic Acid (CBC-a)
Description of Cannabichromenic Acid (CBC-a)
Cannabichromenic acid (CBCA) was isolated, and its structure was defined by a team of Japanese researchers (Y. Shoyama et al., 1968). CBCA is the precursor to CBC.
Other Names:
Cannabichromenic AcidCannabichromenic acid, (+)-Cannabichromenic acid and other supplier-based synonyms.
IUPAC Name: 5-hydroxy-2-methyl-2-(4-methylpent-3-enyl)-7-pentylchromene-6-carboxylic acid
Molecular Formula: C22H30O4
Source–PubChem
Cannabichromenic Acid (CBC-a) Properties and Effects
Only Members can view Properties and Effects information. See DEMO page.
Cannabichromenic Acid (CBC-a) Receptor Binding
Only Members can view Receptor Binding information. See DEMO page.
Disclaimer
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medical problem, promptly contact your health care provider.
Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.
