SCHEMBL11222787

SCHEMBL11222787

Cc1ccc(C2C(=O)CC3(CCCCC3)CC2=O)c(C)c1

nearest known ligand 0.45

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 4/20 0.41
SMN1; SMN2 Q16637 1/20 0.40
ADRA1B P35368 3/20 0.38
ADRA1A P35348 2/20 0.38
KDM4E B2RXH2 2/20 0.38
HTT P42858 1/20 0.38
ATM Q13315 1/20 0.38
KMT2A Q03164 2/20 0.36
MEN1 O00255 1/20 0.36
ALDH1A1 P00352 1/20 0.36
HPGD P15428 1/20 0.36
ALOX15 P16050 1/20 0.36
ALOX12 P18054 1/20 0.36
BRCA1 P38398 1/20 0.36
HSD17B10 Q99714 1/20 0.36
NPC1 O15118 1/20 0.35
RAB9A P51151 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
SCHEMBL11216206 0.82 KDM4E (0.36) HTR1ASMN1; SMN2KDM4EHTTATM
SCHEMBL11226652 0.81 SMN1; SMN2 (0.53) HTR1ASMN1; SMN2ADRA1BKDM4EALDH1A1
SCHEMBL10729989 0.81 ALDH1A1 (0.44) SMN1; SMN2KDM4EHTTKMT2AMEN1
SCHEMBL11227870 0.80 SMN1; SMN2 (0.40) HTR1ASMN1; SMN2ADRA1BADRA1AKDM4E
SCHEMBL10735338 0.77 ALDH1A1 (0.41) KDM4EKMT2AMEN1ALDH1A1HPGD
SCHEMBL10900447 0.77 HSD17B10 (0.44) KMT2AMEN1ALDH1A1HPGDALOX15
SCHEMBL11248721 0.76 LMNA (0.37) HTR1AKDM4EKMT2AMEN1ALDH1A1
SCHEMBL8863053 0.74 KMT2A (0.42) KDM4EHTTATMKMT2AMEN1
SCHEMBL7769002 0.74 KMT2A (0.42) KDM4EHTTATMKMT2AMEN1
SCHEMBL11219061 0.73 HTR1A (0.42) HTR1AADRA1BADRA1AHTTALDH1A1

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