Nabilone

Nabilone

SCHEMBL2762240

CCCCCCC(C)(C)c1cc(O)c2c(c1)OC(C)(C)[C@H]1CCC(=O)C[C@H]21

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 SCHEMBL17223864 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL11268571 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL33339 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
SCHEMBL11615666 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL29475614 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL29448222 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL15520922 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL13759779 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL563809 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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4075230-A Preparation of optically active trans-hexahydrodibenzopyranones ELI LILLY AND COMPANY (US) 1978-02-21 — — US claimed
WO-2024145493-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING NABILONE FOR THE TREATMENT OF OPHTHALMIC CONDITIONS ADTECH PHARMA, INC. (US) 2024-07-04 — — WO disclosed
US-20230210786-A1 METHOD FOR SOLUBILIZING NATURAL, ENDOGENOUS AND SYNTHETIC CANNABINOIDS ATHENION AG (CH) 2023-07-06 — — US disclosed
US-11670410-B1 Systems and methods to automatically administer a psychoactive substance to an airway of a user based on a detected event or condition Green Sky Creations LLC (US) 2023-06-06 — — US disclosed
US-11670410-B1 Systems and methods to automatically administer a psychoactive substance to an airway of a user based on a detected event or condition Green Sky Creations LLC (US) 2023-06-06 — — US disclosed
EP-4157215-A1 METHOD FOR SOLUBILIZING NATURAL, ENDOGENOUS AND SYNTHETIC CANNABINOIDS Athenion AG (CH) 2023-04-05 — — EP disclosed
US-11464758-B2 Cannabinoid co-drug compounds KOTZKER CONSULTING LLC (US) 2022-10-11 — — US disclosed
US-20220151981-A1 USE OF CANNABINOIDS AND TERPENES FOR TREATMENT OF ORGANOPHOSPHATE AND CARBAMATE TOXICITY KOTZKER CONSULTING LLC (US) 2022-05-19 — — US disclosed
US-11266623-B2 Use of cannabinoids and terpenes for treatment of organophosphate and carbamate toxicity KOTZKER CONSULTING LLC (US) 2022-03-08 — — US disclosed
US-20210393575-A1 N-ACYLATED FATTY AMINO ACIDS TO REDUCE ABSORPTION VARIABILITY IN CANNABINOID BASED COMPOSITIONS RECEPTOR HOLDINGS, INC. (US) 2021-12-23 — — US disclosed
US-20100298579-A1 Process for preparing synthetic cannabinoids THC PHARM GMBH (DE) 2010-11-25 — — US disclosed
US-20100168086-A1 7,8,10,10A-TETRAHYDRO-6H-BENZO[C]CHROMEN-9(6AH)-ONE MODULATORS OF CANNABINOID RECEPTORS AUSPEX PHARMACEUTICALS, INC. (US) 2010-07-01 — — US disclosed
US-20060074101-A1 Method of treating post operative nausea and vomiting HELSINN HEALTHCARE SA (CH) 2006-04-06 — — US disclosed
US-4208351-A Stereoselective preparation of hexahydro dibenzopyranones and intermediates therefor ELI LILLY AND COMPANY (US) 1980-06-17 — — US disclosed
US-4195025-A 9-Amino-dibenzopyrans ELI LILLY AND COMPANY (US) 1980-03-25 — — US disclosed
US-4176233-A Stereoselective preparation of hexahydro dibenzopyranones and intermediates therefor ELI LILLY AND COMPANY (US) 1979-11-27 — — US disclosed
EP-0003883-A1 Amino-dibenzopyrans, their preparation, formulations containing them and their use as pharmaceuticals ELI LILLY AND COMPANY (US) 1979-09-05 — — EP disclosed
US-4152450-A 9-Amino-dibenzopyrans ELI LILLY AND COMPANY (US) 1979-05-01 — — US disclosed
US-4102902-A Stereoselective preparation of hexahydro dibenzopyranones and intermediates therefor ELI LILLY AND COMPANY (US) 1978-07-25 — — US disclosed
US-4075230-A Preparation of optically active trans-hexahydrodibenzopyranones ELI LILLY AND COMPANY (US) 1978-02-21 — — 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 (7 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-20100168086-A1 7,8,10,10A-TETRAHYDRO-6H-BENZO[C]CHROMEN-9(6AH)-ONE MODULATORS OF CANNABINOID RECEPTORS CNR1, CNR2, GPR18 CNR1 1/4885CNR2 2/4885NR1I2 264/4885
US-11464758-B2 Cannabinoid co-drug compounds ACHE, CNR2, CNR1 CNR1 3/4885CNR2 2/4885NR1I2 808/4885
US-20060074101-A1 Method of treating post operative nausea and vomiting HTR3A, HTR3C, HTR5A CNR1 102/4885CNR2 77/4885NR1I2 2396/4885
US-20210393575-A1 N-ACYLATED FATTY AMINO ACIDS TO REDUCE ABSORPTION VARIABILITY IN CANNABINOID BASED COMPOSITIONS FAAH, CNR2, FABP2 CNR1 5/4885CNR2 2/4885NR1I2 1840/4885
US-20100298579-A1 Process for preparing synthetic cannabinoids CNR2, CNR1, FAAH CNR1 2/4885CNR2 1/4885NR1I2 2185/4885
US-20220151981-A1 USE OF CANNABINOIDS AND TERPENES FOR TREATMENT OF ORGANOPHOSPHATE AND CARBAMATE TOXICITY ACHE, BCHE, CNR2 CNR1 4/4885CNR2 3/4885NR1I2 756/4885
US-11266623-B2 Use of cannabinoids and terpenes for treatment of organophosphate and carbamate toxicity ACHE, BCHE, CNR1 CNR1 3/4885CNR2 4/4885NR1I2 858/4885

“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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