SCHEMBL11226652

SCHEMBL11226652

Cc1ccccc1C1C(=O)CC2(CCCCC2)CC1=O

nearest known ligand 0.53

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.53
GSK3B P49841 2/20 0.40
GSK3A P49840 1/20 0.40
DDB1 Q16531 1/20 0.39
CRBN Q96SW2 1/20 0.39
HTR1A P08908 1/20 0.39
ADRA1B P35368 1/20 0.39
ALDH1A1 P00352 5/20 0.36
GAA P10253 1/20 0.36
MAPT P10636 1/20 0.36
KDM4E B2RXH2 1/20 0.36
HSD17B10 Q99714 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
HTR2A P28223 1/20 0.35
HTR2C P28335 1/20 0.35
HTR2B P41595 1/20 0.35

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
SCHEMBL11222787 0.81 HTR1A (0.41) SMN1; SMN2HTR1AADRA1BALDH1A1KDM4E
SCHEMBL11227840 0.81 HTR1A (0.48) SMN1; SMN2GSK3BGSK3AHTR1AADRA1B
SCHEMBL11046467 0.80 ALDH1A1 (0.54) SMN1; SMN2GSK3BDDB1CRBNALDH1A1
SCHEMBL11215167 0.75 DDB1 (0.47) GSK3BDDB1CRBNALDH1A1GAA
SCHEMBL1049215 0.72 MAPT (0.68) ALDH1A1GAAMAPTKDM4EHTR2A
SCHEMBL8718210 0.69 HTR2C (0.46) SMN1; SMN2DDB1CRBNHTR2C
SCHEMBL11219061 0.69 HTR1A (0.42) HTR1AADRA1BALDH1A1GAAMAPT
SCHEMBL10740394 0.68 ALDH1A1 (0.49) SMN1; SMN2GSK3BGSK3ADDB1CRBN
SCHEMBL10736527 0.67 SMN1; SMN2 (0.34) SMN1; SMN2
SCHEMBL8718213 0.67 HTR2C (0.47) SMN1; SMN2DDB1CRBNKDM4EHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0007243-B1 2-ARYL-1,3-CYCLOHEXANEDIONE COMPOUNDS AND ALKALI METAL SALTS, AMMONIUM SALTS AND ENOL ESTERS THEREOF, COMPOSITION AND METHOD OF CONTROLLING ACARINA ECTOPARASITES ON WARMBLOODED ANIMALS UNION CARBIDE CORPORATION (US) 1982-11-17 EP disclosed
US-4257858-A REACTING A CYCLOHEXA-1,3-DIONE-2-DIAZIDE WITH AN ARYL COMPOUND UNION CARBIDE CORPORATION (US) 1981-03-24 US disclosed
US-4256658-A CYCLIZATION, BASIC CATALYST UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4256657-A CYCLIZATION, ACID CATALYST UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4256659-A Method of preparing 2-aryl-1,3-cyclohexanedione compounds UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4209532-A Biocidal 2-aryl-1,3-cyclohexane dione compounds and alkali metal and ammonium salts thereof UNION CARBIDE CORPORATION (US) 1980-06-24 US disclosed
EP-0007243-A1 2-Aryl-1,3-cyclohexanedione compounds and alkali metal salts, ammonium salts and enol esters thereof, composition and method of controlling acarina ectoparasites on warmblooded animals UNION CARBIDE CORPORATION (US) 1980-01-23 EP disclosed
US-4175135-A Method of controlling acarina ectoparasites on warmblooded animals by orally administering to the animal an ectoparasitically effective amount of a 2-aryl-1,3-cyclohexanedione compound, and alkali metal salts, ammonium salts and enol esters thereof UNION CARBIDE CORPORATION (US) 1979-11-20 US disclosed