SCHEMBL9568926

SCHEMBL9568926

CC(=O)C1=CCCN(C)C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CHRM2 P08172 2/20 0.65
CHRM4 P08173 2/20 0.65
CHRM5 P08912 2/20 0.65
CHRM1 P11229 2/20 0.65
CHRM3 P20309 2/20 0.65
LMNA P02545 2/20 0.65
THRB P10828 1/20 0.65
CHRNB2 P17787 1/20 0.65
CHRNA4 P43681 1/20 0.65
BLM P54132 1/20 0.62
MCOLN3 Q8TDD5 1/20 0.62
CYP1A2 P05177 1/20 0.53
CYP2D6 P10635 1/20 0.53
NFKB1 P19838 1/20 0.53
THPO P40225 1/20 0.53
PMP22 Q01453 1/20 0.51

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
Bromide SCHEMBL10920212 0.98 BLM (0.66) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL5203140 0.83 CHRM2 (0.65) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL336164 0.83 CHRM2 (0.65) CHRM2CHRM4CHRM5CHRM1CHRM3
Hydrochloric Acid SCHEMBL11584066 0.82 CHRM2 (0.62) CHRM2CHRM4CHRM5CHRM1CHRM3
Bromide SCHEMBL9568894 0.82 BLM (0.66) CHRM2CHRM4CHRM5CHRM1CHRM3
Hydrochloric Acid SCHEMBL2197726 0.82 CHRM2 (0.62) CHRM2CHRM4CHRM5CHRM1CHRM3
Ammonia Solution, Strong SCHEMBL30785800 0.82 CHRM2 (0.62) CHRM2CHRM4CHRM5CHRM1CHRM3
Hydrochloric Acid SCHEMBL1897878 0.80 CHRM2 (0.61) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL12798275 0.79 CHRM2 (0.59) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL15600774 0.79 CHRM2 (0.64) CHRM2CHRM4CHRM5CHRM1CHRM3

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0288394-A2 1,2,5,6-Tetrahydropyridines, process for their preparation, their use as medicines and compositions containing them ROUSSEL-UCLAF (FR) 1988-10-26 EP claimed
US-4710508-A ANALGESICS WARNER-LAMBERT COMPANY (US) 1987-12-01 US claimed
EP-0091565-B1 PROCESS FOR THE MANUFACTURE OF ISOQUINOLINE DIONES F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1986-04-23 EP claimed
US-4495354-A Process for bicyclic diketones HOFFMANN-LA ROCHE INC. (US) 1985-01-22 US claimed
EP-0091565-A1 Process for the manufacture of isoquinoline diones F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1983-10-19 EP claimed
CN-110505884-B Anti-cancer combination therapy 勃林格殷格翰国际有限公司 2022-08-12 CN disclosed
US-7160900-B2 Tetrahydropyridino or piperidino heterocyclic derivatives TAISHO PHARMACEUTICAL CO., LTD. (JP) 2007-01-09 US disclosed
EP-0537993-A1 Nicotinic activity of a series of arecolones and isoarecolones ELI LILLY AND COMPANY (US) 1993-04-21 EP disclosed
US-4710508-A ANALGESICS WARNER-LAMBERT COMPANY (US) 1987-12-01 US disclosed
EP-0091565-B1 PROCESS FOR THE MANUFACTURE OF ISOQUINOLINE DIONES F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1986-04-23 EP disclosed
US-4495354-A Process for bicyclic diketones HOFFMANN-LA ROCHE INC. (US) 1985-01-22 US disclosed
EP-0091565-A1 Process for the manufacture of isoquinoline diones F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1983-10-19 EP disclosed