SCHEMBL10909436

SCHEMBL10909436

Cc1ccc(CC(=O)CC(C)(C)CC(=O)O)c(C)c1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RXRA P19793 2/20 0.44
RXRB P28702 2/20 0.44
SRC P12931 1/20 0.43
POLB P06746 1/20 0.42
NPC1 O15118 1/20 0.40
RAB9A P51151 1/20 0.40
RXRG P48443 1/20 0.40
NR1H4 Q96RI1 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
PSMB8 P28062 1/20 0.38
PSMB5 P28074 1/20 0.38
SLC13A5 Q86YT5 1/20 0.37
MEN1 O00255 3/20 0.37
KMT2A Q03164 3/20 0.37
MAPT P10636 2/20 0.37
CYP2C9 P11712 1/20 0.37
ALOX15 P16050 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
KDM4E B2RXH2 1/20 0.37
ALDH1A1 P00352 1/20 0.37

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
SCHEMBL10909003 0.88 SLC22A12 (0.43) SRCPOLBNPC1RAB9ASLC13A5
SCHEMBL8096852 0.84 NPC1 (0.38) RXRARXRBSRCNPC1RAB9A
SCHEMBL14729157 0.81 NPC1 (0.46) RXRARXRBSRCNPC1RAB9A
SCHEMBL1257788 0.79 SRC (0.62) RXRARXRBSRCNPC1RAB9A
SCHEMBL11217315 0.79 NPSR1 (0.52) RXRARXRBSRCPOLBNPC1
Hydrochloric Acid SCHEMBL2530248 0.78 SRC (0.61) RXRARXRBSRCNPC1RAB9A
SCHEMBL13091046 0.76 NPC1 (0.43) SRCNPC1RAB9ANPSR1PSMB8
SCHEMBL10912282 0.76 TSHR (0.50) RXRARXRBSRCPOLBNPC1
SCHEMBL30300608 0.75 NPC1 (0.42) RXRARXRBSRCNPC1RAB9A
SCHEMBL3015011 0.75 SMN1; SMN2 (0.49) SRCNPC1RAB9ANPSR1PSMB8

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
US-4613617-A Synergistic insecticidal compositions containing dione esters UNION CARBIDE CORPORATION (US) 1986-09-23 US disclosed
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-4256657-A CYCLIZATION, ACID CATALYST UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4256658-A CYCLIZATION, BASIC 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
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