SCHEMBL20911332

SCHEMBL20911332

CCCCCc1cc(O)c2c(c1)OC(C)(C)C1=C2C(O)C(C)(O)CC1

nearest known ligand 0.77

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ CNR2 P34972 12/20 0.77
▸ CNR1 P21554 10/20 0.77
▸ OPRM1 P35372 4/20 0.50
▸ TRPV1 Q8NER1 3/20 0.50
▸ TRPA1 O75762 1/20 0.50
▸ CYP1A1 P04798 1/20 0.50
▸ CYP1A2 P05177 1/20 0.50
▸ CYP2A6 P11509 1/20 0.50
▸ CYP2B6 P20813 1/20 0.50
▸ SLC6A2 P23975 1/20 0.50
▸ HTR2A P28223 1/20 0.50
▸ SLC6A4 P31645 1/20 0.50
▸ CYP2J2 P51589 1/20 0.50
▸ CYP1B1 Q16678 1/20 0.50
▸ TRPV3 Q8NET8 1/20 0.50
▸ TRPV4 Q9HBA0 1/20 0.50
▸ TRPV2 Q9Y5S1 1/20 0.50

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL29353562 1.00 CNR2 (0.77) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL22916046 1.00 CNR2 (0.77) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL13214138 1.00 CNR2 (0.77) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL13214146 1.00 CNR2 (0.77) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL13214147 1.00 CNR2 (0.77) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL16124350 0.97 CNR2 (0.72) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL13214144 0.93 CNR2 (0.66) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL23076632 0.86 CNR2 (0.66) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL29400773 0.86 CNR2 (0.66) CNR2CNR1OPRM1TRPV1TRPA1
SCHEMBL13214145 0.86 CNR2 (0.66) CNR2CNR1OPRM1TRPV1TRPA1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240199505-A1 SOIL AMENDMENT FOR SOLUBILIZING SILICATE IN SOIL MORGANICS CORP. (CA) 2024-06-20 — — US disclosed
US-11707444-B2 Antiviral composition for SARS-CoV-2 containing cannabinoids as active ingredient RESEARCH COOPERATION FOUNDATION OF YEUNGNAM UNIVERSITY (KR) 2023-07-25 — — US disclosed
US-11707444-B2 Antiviral composition for SARS-CoV-2 containing cannabinoids as active ingredient RESEARCH COOPERATION FOUNDATION OF YEUNGNAM UNIVERSITY (KR) 2023-07-25 — — US disclosed
US-20230002340-A1 SEPARATION OF CANNABINOIDS FROM MIXTURES THEREOF BY DISTILLATION CANOPY GROWTH CORPORATION (CA) 2023-01-05 — — US disclosed
US-20220332693-A1 SEPARATION OF CANNABINOIDS FROM MIXTURES THEREOF BY EXTRACTION AND DISTILLATION CANOPY GROWTH CORPORATION (CA) 2022-10-20 — — US disclosed
US-20220289703-A1 METHODS FOR CONVERTING TETRAHYDROCANNABINOLIC ACID INTO CANNABINOLIC ACID CANOPY GROWTH CORPORATION (CA) 2022-09-15 — — US disclosed
US-20220218653-A1 CARTRIDGE FOR VAPOR-PHASE CANNABINOID REACTIONS WITHIN A DEVICE CANOPY GROWTH CORPORATION (CA) 2022-07-14 — — US disclosed
US-20220202710-A1 WATER-SOLUBLE FORMULATIONS, METHODS OF MAKING AND USE CANOPY GROWTH CORPORATION (CA) 2022-06-30 — — US disclosed
US-20220177442-A1 METHODS FOR CONVERTING THC-RICH CANNABINOID MIXTURES INTO CBN-RICH CANNABINOID MIXTURES JGB COLLATERAL LLC 2022-06-09 — — US disclosed
WO-2021127788-A1 METHODS OF SYNTHESIZING HIGH-PURITY CANNABICYCLOL AND ARTIFICIAL RESINS COMPRISING CANNABICYCLOL CANOPY GROWTH CORPORATION (CA) 2021-07-01 — — WO disclosed
WO-2021016716-A1 SEPARATION OF CANNABINOIDS FROM CANNABINOID MIXTURES BY DERIVATIZATION CANOPY GROWTH CORPORATION (CA) 2021-02-04 — — WO disclosed
WO-2021016717-A1 SEPARATION OF CANNABINOIDS FROM MIXTURES THEREOF BY EXTRACTION AND DISTILLATION CANOPY GROWTH CORPORATION (CA) 2021-02-04 — — WO disclosed
WO-2020248056-A1 CARTRIDGE FOR VAPOR-PHASE CANNABINOID REACTIONS WITHIN A DEVICE CANOPY GROWTH CORPORATION (CA) 2020-12-17 — — WO disclosed
WO-2020248062-A1 IMPROVED METHODS FOR CANNABINOID ISOMERIZATION CANOPY GROWTH CORPORATION (CA) 2020-12-17 — — WO disclosed
WO-2020248059-A1 METHODS FOR PREPARING CANNABINOIDS BY BASE-PROMOTED DOUBLE-BOND MIGRATION CANOPY GROWTH CORPORATION (CA) 2020-12-17 — — WO disclosed
WO-2020248057-A1 METHODS FOR PREPARING CANNABINOIDS BY HETEROGENEOUS-ACID-PROMOTED DOUBLE-BOND MIGRATION CANOPY GROWTH CORPORATION (CA) 2020-12-17 — — WO disclosed
WO-2020107119-A1 COMPOSITIONS COMPRISING A CANNABINOID OR A CANNABIS-DERIVED COMPOUND, METHODS OF MAKING AND USE CANOPY GROWTH CORPORATION (CA) 2020-06-04 — — WO disclosed
WO-2020107114-A1 WATER-SOLUBLE FORMULATIONS OF CANNABINOIDS OR CANNABIS-DERIVED COMPOUNDS, METHODS OF MAKING AND USE CANOPY GROWTH CORPORATION (CA) 2020-06-04 — — WO disclosed
US-20200170950-A1 COMPOSITIONS COMPRISING A CANNABINOID OR A CANNABIS-DERIVED COMPOUND, METHODS OF MAKING AND USE WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT 2020-06-04 — — US disclosed
WO-2019071302-A1 METHODS AND COMPOSITIONS FOR TREATING OR PREVENTING SEIZURES THE UNIVERSITY OF SYDNEY (AU) 2019-04-18 — — WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20230002340-A1 SEPARATION OF CANNABINOIDS FROM MIXTURES THEREOF BY DISTILLATION CNR2, CNR1, PLEC CNR2 1/4885CNR1 2/4885OPRM1 244/4885
US-20220177442-A1 METHODS FOR CONVERTING THC-RICH CANNABINOID MIXTURES INTO CBN-RICH CANNABINOID MIXTURES CNR1, CNR2, FAAH CNR2 2/4885CNR1 1/4885OPRM1 152/4885
US-20220202710-A1 WATER-SOLUBLE FORMULATIONS, METHODS OF MAKING AND USE CNR1, CNR2, FAAH CNR2 2/4885CNR1 1/4885OPRM1 104/4885
US-20220289703-A1 METHODS FOR CONVERTING TETRAHYDROCANNABINOLIC ACID INTO CANNABINOLIC ACID CNR2, CNR1, FAAH CNR2 1/4885CNR1 2/4885OPRM1 687/4885
US-20200170950-A1 COMPOSITIONS COMPRISING A CANNABINOID OR A CANNABIS-DERIVED COMPOUND, METHODS OF MAKING AND USE CNR1, CNR2, CSGALNACT1 CNR2 2/4885CNR1 1/4885OPRM1 16/4885
US-20220218653-A1 CARTRIDGE FOR VAPOR-PHASE CANNABINOID REACTIONS WITHIN A DEVICE CNR1, CNR2, FAAH CNR2 2/4885CNR1 1/4885OPRM1 77/4885
US-20220332693-A1 SEPARATION OF CANNABINOIDS FROM MIXTURES THEREOF BY EXTRACTION AND DISTILLATION CNR2, CNR1, FAAH CNR2 1/4885CNR1 2/4885OPRM1 79/4885
US-11707444-B2 Antiviral composition for SARS-CoV-2 containing cannabinoids as active ingredient TMPRSS2, ACE2, CNR2 CNR2 3/4885CNR1 4/4885OPRM1 37/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

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