SCHEMBL2237751

SCHEMBL2237751

CCC(CCl)c1ccccc1

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.48
CCR5 P51681 1/20 0.44
TAAR1 Q96RJ0 5/20 0.40
TSHR P16473 1/20 0.40
CYP2D6 P10635 1/20 0.40
MIF P14174 1/20 0.39
HKDC1 Q2TB90 1/20 0.38
TRPA1 O75762 1/20 0.38
HTR2A P28223 2/20 0.38
HRH1 P35367 1/20 0.38
AOC3 Q16853 1/20 0.37
NOS3 P29474 1/20 0.37
NOS2 P35228 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
ESR1 P03372 1/20 0.36
ESR2 Q92731 1/20 0.36

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
SCHEMBL5598365 0.85 TSHR (0.48) LMNATAAR1TSHRCYP2D6HTR2A
SCHEMBL169508 0.85 LMNA (0.56) LMNACCR5TAAR1CYP2D6MIF
Hypochlorous Acid SCHEMBL11415854 0.83 LMNA (0.56) LMNACCR5TAAR1TSHRCYP2D6
Ammonia Solution, Strong SCHEMBL1640901 0.82 LMNA (0.54) LMNACCR5TAAR1CYP2D6MIF
SCHEMBL6175656 0.82 LMNA (0.45) LMNACCR5TAAR1TSHRCYP2D6
SCHEMBL6686932 0.82 AOC3 (0.43) LMNACCR5TAAR1TSHRHTR2A
SCHEMBL11745184 0.82 LMNA (0.45) LMNACCR5TAAR1TSHRCYP2D6
SCHEMBL6173744 0.82 LMNA (0.45) LMNACCR5TAAR1TSHRCYP2D6
Methylamine SCHEMBL27931105 0.80 LMNA (0.52) LMNACCR5TAAR1CYP2D6HTR2A
SCHEMBL9397889 0.79 ALDH1A1 (0.44) LMNACYP2D6TDP1ESR1ESR2

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 92 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-60067486-A None JP disclosed
EP-4508101-B1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2026-03-25 EP disclosed
EP-4709518-A1 PROCESS FOR THE PREPARATION OF POLYISOBUTENE FROM OLEFINS FROM ISOBUTANOL OBTAINED FROM MIXED GUERBET REACTION OF ETHANOL AND METHANOL BASF SE (DE) 2026-03-18 EP disclosed
EP-4667447-A1 PROCESS FOR THE PREPARATION OF POLYISOBUTENE FROM BIO-BASED OLEFINS FROM PRIMARY ALCOHOL BASF SE (DE) 2025-12-24 EP disclosed
US-20250250403-A1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2025-08-07 US disclosed
US-20250250382-A1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2025-08-07 US disclosed
US-20250179224-A1 MEDIUM MOLECULAR POLYISOBUTENE WITH A CERTAIN DISTRIBUTION OF DOUBLE BOND ISOMERS BASF SE (DE) 2025-06-05 US disclosed
US-20250145742-A1 MEDIUM MOLECULAR POLYISOBUTENE WITH A HIGH CONTENT OF CERTAIN DOUBLE BOND ISOMERS BASF SE (DE) 2025-05-08 US disclosed
WO-2025082909-A1 PROCESS FOR IMPROVING THE STABILITY OF POLYISOBUTENES BASF SE (DE) 2025-04-24 WO disclosed
EP-4508100-A1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2025-02-19 EP disclosed
US-20110201772-A1 PROCESS FOR PREPARING HIGH-REACTIVITY ISOBUTENE HOMO- OR COPOLYMERS BASF SE (DE) 2011-08-18 US disclosed
CN-101378757-A Thiadiazole derivatives for the treatment of neuro degenerative diseases REMYND NV (BE) 2009-03-04 CN disclosed
CN-100405220-C Acid-decomposable resin composition containing ketone-aldehyde copolymer NIPPON SODA CO (JP) 2008-07-23 CN disclosed
CN-1630835-A Acid-decomposable resin composition containing ketone-aldehyde copolymer NIPPON SODA CO (JP) 2005-06-22 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-1053990-A2 A method of producing an aromatic ketone and an aromatic ketone composition containing it TORAY INDUSTRIES, INC. (JP) 2000-11-22 EP 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
JP-S6067486-A OPTICALLY ACTIVE ORGANOTIN COMPOUND CONTAINING ASYMMETRIC GROUP OSAKA SODA CO LTD 1985-04-17 JP disclosed
US-4046819-A Alkylation of alkyl, cycloalkyl and aralkyl halides UOP INC. (US) 1977-09-06 US disclosed