# Therapeutic potential of acidic cannabinoids: an update

**Authors:** Santosh Kumar Singh, Coralie Antoine, Calvin Tse, Lawrence Ji, Miranda Reed, Wayne Grant Carter, Viviana Trezza, Hemant Kumar Bid

PMC · DOI: 10.1186/s42238-026-00387-y · 2026-01-16

## TL;DR

This paper reviews the potential of acidic cannabinoids, like THCA and CBDA, as non-intoxicating therapeutic compounds with unique effects on inflammation, seizures, and cell growth.

## Contribution

The paper systematically reviews the pharmacology and therapeutic potential of acidic cannabinoids, highlighting their distinct biological activities and underexplored clinical value.

## Key findings

- Acidic cannabinoids show neuroprotective, anti-inflammatory, and anticonvulsant effects through targets like 5-HT1A and COX-2.
- They are non-intoxicating and suitable for children and the elderly, unlike THC.
- Low bioavailability and lack of human trials hinder their clinical use despite promising properties.

## Abstract

Cannabis sativa yields a wide range of bioactive compounds, including terpenes, flavonoids, and cannabinoids. Tetrahydrocannabinolic acid (THCA), cannabidiolic acid (CBDA), cannabigerolic acid (CBGA), and cannabichromenic acid (CBCA) are the acidic biosynthetic precursors of the neutral cannabinoids Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD), which have been the subject of much research. This review examines the biosynthesis, decarboxylation, molecular pharmacology, and therapeutic significance of acidic cannabinoids, intending to address a significant knowledge gap. Peer-reviewed literature from major scientific databases was used in a systematic narrative review with an emphasis on investigations of acidic cannabinoid chemistry, pharmacology, pharmacokinetics, and disease-specific applications. According to the reviewed data, acidic cannabinoids exhibit unique biological activities that distinguish them from their neutral counterparts. These include neuroprotective, anti-inflammatory, anticonvulsant, and anti-proliferative actions, which are mediated by molecular targets such as serotonin 5-HT1A receptors, cyclooxygenase-2 (COX-2), transient receptor potential (TRP) channels, and peroxisome proliferator-activated receptor-γ (PPARγ). Acidic cannabinoids are more appealing for therapeutic usage in children and the elderly, considering that they are not intoxicating like THC; however, this distinction applies primarily to non‑heated consumption. Chemical instability, low bioavailability, and a dearth of controlled human trials impede clinical translation despite their potential. According to the findings, acidic cannabinoids are an underutilized yet potentially valuable class of precision medicines. In this study, we outline existing understanding on acidic cannabinoids, discuss their production and transformation, and identify research needs that could influence cannabis science research.

## Linked entities

- **Proteins:** HTR1A (5-hydroxytryptamine receptor 1A), COX2 (cytochrome c oxidase subunit II), TYRP1 (tyrosinase related protein 1), PPARG (peroxisome proliferator activated receptor gamma)
- **Chemicals:** THCA (PubChem CID 6155526), CBDA (PubChem CID 160570), CBGA (PubChem CID 6449999), CBCA (PubChem CID 3084339), THC (PubChem CID 16078), CBD (PubChem CID 644019)
- **Species:** Cannabis sativa (taxon 3483)

## Full-text entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468] {aka CIMT1, FPLD3, GLM1, NR1C3, PPARG1, PPARG2}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}
- **Diseases:** inflammatory (MESH:D007249)
- **Chemicals:** CBGA (MESH:C100679), Delta9-tetrahydrocannabinol (MESH:D013759), cannabinoid (MESH:D002186), CBD (MESH:D002185), CBCA (-), CBDA (MESH:C006884), terpenes (MESH:D013729), flavonoids (MESH:D005419)
- **Species:** Cannabis sativa (species) [taxon 3483], Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12895846/full.md

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Source: https://tomesphere.com/paper/PMC12895846