SCHEMBL11219274

SCHEMBL11219274

O=C1CC2(CCCCC2)CC(=O)C1c1c(Cl)cccc1[N+](=O)[O-]

nearest known ligand 0.39

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 5/20 0.38
HPGD P15428 1/20 0.38
PDE7A Q13946 2/20 0.35
MAPK1 P28482 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
ALDH1A1 P00352 4/20 0.35
MEN1 O00255 3/20 0.34
KMT2A Q03164 3/20 0.34
PDE7B Q9NP56 1/20 0.34
MAPT P10636 1/20 0.34
ADRA1B P35368 2/20 0.33
CYP1A2 P05177 1/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
GAA P10253 1/20 0.33

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
SCHEMBL11230657 0.83 MAPT (0.45) HPGDMAPK1L3MBTL1ALDH1A1MEN1
SCHEMBL11226368 0.81 ALDH1A1 (0.41) HPGDALDH1A1MEN1KMT2AMAPT
SCHEMBL11219109 0.80 HTR1A (0.37) HTR1APDE7APDE7BADRA1B
SCHEMBL11225362 0.79 MAPT (0.40) HTR1APDE7AALDH1A1MAPTADRA1B
SCHEMBL11232894 0.79 HTR1A (0.36) HTR1APDE7APDE7BADRA1B
SCHEMBL11220871 0.77 ALDH1A1 (0.42) PDE7AALDH1A1MEN1KMT2AMAPT
SCHEMBL11227840 0.72 HTR1A (0.48) HTR1APDE7AADRA1B
SCHEMBL11232896 0.70 PDE7A (0.38) HTR1APDE7AADRA1B
SCHEMBL27168536 0.70 HPGD (0.45) HPGDMAPK1L3MBTL1ALDH1A1MEN1
SCHEMBL11219061 0.67 HTR1A (0.42) HTR1AALDH1A1MAPTADRA1BGAA

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