Reported cannabinoid research / identity review ongoing
(-)-7R-cannabicoumarononic acid A: reported identity research
This research-index record shows how (-)-7R-cannabicoumarononic acid A has been described in cited chemical-identity research. It is a source map, not an independent chemistry verification and not a page about health effects.
Publication status
Research index published; compound identity not independently verified
A human approved publication of this source-linked record on July 24, 2026. That editorial decision allows the cited identity report and its locator to be indexed. It does not verify the chemical identity, approve a health claim, establish safety, or convert AI-assisted extraction into a scientific conclusion.
Reported in research
The page names the source, evidence role, and precise location used by the candidate registry.
Identity review
The compound remains in the registry-gated lane until a distinct human identity-verification decision is recorded.
Effects and safety
This identity record does not make a clinical, therapeutic, dosing, product, or personal-safety claim.
What the registry records
Source-linked identity summary
Our candidate registry summarizes the cited identity record this way: The 7R carboxylic-acid derivative of cannabicoumaronone was isolated from high-potency Cannabis and assigned using high-resolution mass spectrometry, GC-MS, NMR, ROESY, circular dichroism, and optical rotation.
This wording is deliberately limited to identity and occurrence. “Reported,” “isolated,” “detected,” or “characterized” describes what the cited paper says it did; those words do not mean Cannabinoid Encyclopedia independently repeated the laboratory work. The original source and locator below are the controlling evidence trail.
Candidate identity snapshot
Names and classification recorded for (-)-7R-cannabicoumarononic acid A
| Field | Candidate registry value |
|---|---|
| Reported name | (-)-7R-cannabicoumarononic acid A |
| Molecular formula | C22H28O5 |
| Registry family | Cannabicoumaronone Type |
| Reported occurrence | Isolated From Cannabis |
| Registry subtype | Phytocannabinoid Acid |
| Recorded aliases | 7R-cannabicoumarononic acid A, cannabicoumarononic acid A, (-)-7R-cannabicoumarononic acid A |
These fields help readers find the cited record and distinguish similarly named compounds. They remain candidate metadata while identity review is ongoing. A molecular formula or familiar abbreviation alone is not proof that two records describe the same material, stereochemistry, preparation, or natural occurrence.
Identity evidence trail
1 identity record from 1 peer-reviewed source
Each entry states why a source was connected to this candidate and where its support should be checked. Readers should inspect the cited paper when exact analytical methods, spectra, comparison standards, stereochemistry, or sample provenance matter.
Identity record 1
Isolation And Structure Elucidation
Biologically Active Cannabinoids from High-Potency Cannabis sativa
Radwan MM, ElSohly MA, Slade D, Ahmed SA, Khan IA, Ross SA / 2009-04-03
Support locator: Abstract; Results and Discussion for compound 4; Figures 1-2; Table 1; and the compound 4 Isolates entry: C22H28O5 assignment by HRESIMS and GC-MS, carboxyl placement, and converging ROESY, CD, rotation, and comparative NMR support for 7R.
Extraction: Ai Assisted; publication approved as a research-index record, not identity verification.
Candidate evidence was checked against the primary article's full text; stereochemical numbering remains a human-review item and no approval was applied.
Candidate identifiers
External identifiers are recorded with limits
| System | Value | Source note |
|---|---|---|
| PubChem CID | 44139614 | PubChem compound record titled (-)-7R-cannabicoumarononic acid A with the matching C22H28O5 formula and explicit stereochemistry; human review must confirm numbering equivalence. |
An identifier can help locate a database record. It does not by itself establish that a compound was naturally present in a sample, that a published structure assignment is final, or that a commercial product contains the reported compound.
Mandatory editorial note
What must stay attached to this record
The source assigns the 7R absolute configuration from converging ROESY, circular-dichroism, optical-rotation, and comparative NMR evidence. A human chemistry reviewer must confirm that the PubChem stereochemical record and historical cannabinoid numbering represent the same entity.
The source extraction was prepared for human review and the page publication was approved as a research-index record. A later identity decision may verify, revise, merge, exclude, or supersede this candidate. Corrections should preserve the prior evidence trail rather than silently overwriting it.
What this page cannot answer
Identity research is not an effects guide
- This page does not establish that (-)-7R-cannabicoumarononic acid A has a health benefit or treats a condition.
- It does not establish human safety, intoxication risk, interactions, dosing, or suitability for any person.
- It does not verify a retail product, label, certificate of analysis, extract, or formulation.
- It does not transfer findings from THC, CBD, another cannabinoid, an animal model, or a laboratory assay to this candidate.
- It does not replace the original analytical paper or a qualified chemical review of that paper.
Continue the identity index
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These links are navigation through the candidate registry, not evidence that the compounds are interchangeable.
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Help us improve the source trail
If a structure assignment has been corrected, a source has been retracted, an identifier is mismatched, or a stronger identity record exists, send the DOI or PMID and a precise locator. The editorial team can review the evidence and preserve the decision history.