Nabilone

Nabilone

SCHEMBL563809

CCCCCCC(C)(C)c1cc(O)c2c(c1)OC(C)(C)C1CCC(=O)CC21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CNR1

The experimentally established mechanism targets of Nabilone. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
CNR1 known ✓ P21554 12/20 1.00
CNR2 P34972 14/20 1.00
NR1I2 O75469 1/20 1.00
ADORA3 P0DMS8 1/20 1.00
SLC6A3 Q01959 1/20 1.00

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
Nabilone SCHEMBL33339 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL17223864 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL29475614 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL11268571 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL2762240 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL13759779 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
SCHEMBL11615666 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL29448222 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL15520922 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
SCHEMBL11615083 0.99 CNR2 (0.98) CNR2CNR1NR1I2ADORA3SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021042001-A1 COMPOSITIONS AND METHODS RELATED TO DISSOLVED OXIDES Natural Extraction Systems, LLC (US) 2021-03-04 WO claimed
EP-3446681-B1 ABUSE RESISTANT CAPSULE SCHERER TECHNOLOGIES LLC R P (US) 2020-12-23 EP claimed
EP-2968129-B1 ABUSE RESISTANT CAPSULE SCHERER TECHNOLOGIES LLC R P (US) 2018-09-05 EP claimed
US-20120202891-A1 Cannabinoid-Containing Compositions and Methods for Their Use UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2012-08-09 US claimed
EP-0004753-B1 PREPARATION OF TETRAHYDROBENZOXOCINS AND CIS-HEXAHYDRODIBENZOPYRANONES ELI LILLY AND COMPANY (US) 1982-05-26 EP claimed
US-4278603-A SEDATIVES, ANTIDEPRESSANTS ELI LILLY AND COMPANY (US) 1981-07-14 US claimed
US-4148809-A Process for preparing dl-cis-1-hydroxy-3-substituted-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-ones ELI LILLY AND COMPANY (US) 1979-04-10 US claimed
US-4102902-A Stereoselective preparation of hexahydro dibenzopyranones and intermediates therefor ELI LILLY AND COMPANY (US) 1978-07-25 US claimed
US-4054582-A Process for converting cis-hexahydrodibenzo[b,d]pyran-9-ones to trans-hexahydrodibenzo[b,d]-pyran-9-ones ELI LILLY AND COMPANY (US) 1977-10-18 US claimed
US-4054581-A Preparation of cis-1-hydroxy-3-substituted-6,6-dimethyl-6,6a,7,8,10,10a-hexahydro-9H-dibenzo[b,d]pyran-9-ones and intermediates therefor ELI LILLY AND COMPANY (US) 1977-10-18 US claimed
US-3988439-A Dibenzo[b,d]pyranone dispersions ELI LILLY AND COMPANY (US) 1976-10-26 US claimed
US-20260083161-A1 CONTAINERS THAT CONTAIN ANIONIC CANNABINOIDS NATURAL EXTRACTION SYS LLC (US) 2026-03-26 US disclosed
EP-4667001-A2 FORMULATIONS OF CANNABINOIDS ADD Advanced Drug Delivery Technologies Ltd. (CH) 2025-12-24 EP disclosed
US-12484606-B2 Compositions and methods related to anionic cannabinoid molecules Natural Extraction Systems, LLC (US) 2025-12-02 US disclosed
EP-4074307-B1 FORMULATIONS OF CANNABINOIDS ADD ADVANCED DRUG DELIVERY TECH LTD (CH) 2025-11-12 EP disclosed
US-3988439-A Dibenzo[b,d]pyranone dispersions ELI LILLY AND COMPANY (US) 1976-10-26 US disclosed
US-3987188-A Hexahydro-dibenzo[b,d]pyran-9-ones as sedative drugs ELI LILLY AND COMPANY (US) 1976-10-19 US disclosed
US-3968125-A Dihydroxyhexahydrodibenzo[b,d]pyrans ELI LILLY AND COMPANY (US) 1976-07-06 US disclosed
US-3953603-A Hexahydro-dibenzo[b,d,]pyran-9-ones as psychotropic, particularly anti-depressant drugs ELI LILLY AND COMPANY (US) 1976-04-27 US disclosed
US-3944673-A Hexahydro-dibenzo[b,d]pyran-9-ones as analgesic drugs ELI LILLY AND COMPANY (US) 1976-03-16 US 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 (3 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-20260083161-A1 CONTAINERS THAT CONTAIN ANIONIC CANNABINOIDS CNR2, CNR1, OPRD1 CNR1 2/4885CNR2 1/4885NR1I2 3129/4885
US-12484606-B2 Compositions and methods related to anionic cannabinoid molecules CNR2, CNR1, PHOSPHO1 CNR1 2/4885CNR2 1/4885NR1I2 2621/4885
US-20120202891-A1 Cannabinoid-Containing Compositions and Methods for Their Use CNR2, CNR1, FAAH CNR1 2/4885CNR2 1/4885NR1I2 1144/4885

“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.