SCHEMBL6683028

SCHEMBL6683028

CC(C)(Cl)c1ccccc1Cl

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNN4 O15554 3/20 0.46
TSHR P16473 6/20 0.45
LMNA P02545 2/20 0.45
HTR2A P28223 2/20 0.38
HTR2C P28335 2/20 0.38
OPRK1 P41145 2/20 0.38
KCNH2 Q12809 2/20 0.38
ADRA1A P35348 1/20 0.38
TDP1 Q9NUW8 3/20 0.37
ALDH1A1 P00352 2/20 0.37
CYP3A4 P08684 2/20 0.36
MAPK1 P28482 2/20 0.36
KCNA3 P22001 2/20 0.35
HSD11B1 P28845 2/20 0.34
CYP19A1 P11511 3/20 0.34
CYP1A2 P05177 3/20 0.34
CA2 P00918 2/20 0.34
ADRB2 P07550 2/20 0.34
ADRB1 P08588 2/20 0.34
MEN1 O00255 1/20 0.34

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
SCHEMBL28826593 0.84 KCNN4 (0.46) KCNN4TSHRLMNAHTR2AHTR2C
SCHEMBL29913900 0.83 TSHR (0.43) KCNN4TSHRLMNATDP1ALDH1A1
SCHEMBL672576 0.83 TSHR (0.43) KCNN4TSHRLMNATDP1ALDH1A1
SCHEMBL78489 0.81 TSHR (0.50) KCNN4TSHRLMNAHTR2AHTR2C
SCHEMBL7571745 0.81 KCNN4 (0.48) KCNN4TSHRLMNAHTR2AHTR2C
SCHEMBL29617470 0.80 TSHR (0.53) KCNN4TSHRLMNAHTR2AHTR2C
SCHEMBL197704 0.80 TSHR (0.53) KCNN4TSHRLMNAHTR2AHTR2C
SCHEMBL27641406 0.80 KCNN4 (0.43) KCNN4TSHRLMNAHTR2AHTR2C
SCHEMBL6683582 0.79 KCNN4 (0.46) KCNN4TSHRLMNAHTR2AHTR2C
Benzene SCHEMBL28296949 0.79 KCNN4 (0.52) KCNN4TSHRLMNAHTR2AHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109761757-A A kind of synthetic method of chlorophenesic acid 山东润博生物科技有限公司 2019-05-17 CN disclosed
CN-104529789-B Synthetic process of 3,5-dichloro-alpha,alpha-dimethyl benzylamine 苏州市玮琪生物科技有限公司 2017-02-22 CN disclosed
EP-0985649-B1 Method for producing an aromatic compound having an alkyl group with at least three carbon atoms TORAY INDUSTRIES (JP) 2004-11-24 EP disclosed
US-6462248-B1 THROUGH CONVERSION, ISOMERIZATION AND/OR ADSORPTIVE SEPARATION OF AROMATIC COMPOUNDS TORAY INDUSTRIES, INC. (JP) 2002-10-08 US disclosed
EP-0985649-A2 Method for producing an aromatic compound having an alkyl group with at least three carbon atoms TORAY INDUSTRIES, INC. (JP) 2000-03-15 EP disclosed
EP-0360829-A1 DEHYDROBROMINATION OF SUBSTITUTED ALPHA-HALOCUMENE. DOW CHEMICAL CO (US) 1990-04-04 EP disclosed
WO-1988009319-A1 DEHYDROBROMINATION OF SUBSTITUTED alpha-HALOCUMENE THE DOW CHEMICAL COMPANY (US) 1988-12-01 WO disclosed