Nabilone

Nabilone

SCHEMBL11268571

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 SCHEMBL33339 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL17223864 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL29475614 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL2762240 1.00 CNR2 (1.00) CNR2CNR1NR1I2ADORA3SLC6A3
Nabilone SCHEMBL563809 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 37 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0004753-B1 PREPARATION OF TETRAHYDROBENZOXOCINS AND CIS-HEXAHYDRODIBENZOPYRANONES ELI LILLY AND COMPANY (US) 1982-05-26 EP 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-20210198223-A1 METHODS AND COMPOSITIONS RELATING TO ULTRAPURE 5-(1,1-DIMETHYLHEPTYL)-RESORCINOL CORBUS PHARMACEUTICALS, INC. 2021-07-01 US disclosed
US-8258322-B2 Synthesis of hexahydrodibenzopyranones WATSON LABORATORIES, INC. (US) 2012-09-04 US disclosed
US-8258322-B2 Synthesis of hexahydrodibenzopyranones WATSON LABORATORIES, INC. (US) 2012-09-04 US disclosed
US-20100056811-A1 Synthesis of Hexahydrodibenzopyranones WATSON LABORATORIES, INC. 2010-03-04 US disclosed
US-20100056811-A1 Synthesis of Hexahydrodibenzopyranones WATSON LABORATORIES, INC. 2010-03-04 US disclosed
WO-2010022520-A1 IMPROVED SYNTHESIS OF HEXAHYDRODIBENZOPYRANONES DALTON CHEMICAL LABORATORIES INC. (CA) 2010-03-04 WO disclosed
EP-0003883-B1 AMINO-DIBENZOPYRANS, THEIR PREPARATION, FORMULATIONS CONTAINING THEM AND THEIR USE AS PHARMACEUTICALS ELI LILLY AND COMPANY (US) 1982-10-06 EP disclosed
US-4087547-A Hexahydro-dibenzo[b,d]pyran-9-ones in treatment of glaucoma ELI LILLY AND COMPANY (US) 1978-05-02 US disclosed
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 disclosed
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 disclosed
US-4024275-A Method of reducing elevated blood pressure with dihydroxy-hexahydrodibenzo(b,d)pyrans ELI LILLY AND COMPANY (US) 1977-05-17 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 (2 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-20210198223-A1 METHODS AND COMPOSITIONS RELATING TO ULTRAPURE 5-(1,1-DIMETHYLHEPTYL)-RESORCINOL CNR1, DHCR24, CNR2 CNR1 1/4885CNR2 3/4885NR1I2 460/4885
US-20100056811-A1 Synthesis of Hexahydrodibenzopyranones GNE, GALE, UGDH CNR1 8/4885CNR2 6/4885NR1I2 2611/4885

“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.