SCHEMBL3786224

SCHEMBL3786224

FC(F)(F)c1cc(Cl)cc(C(F)(F)F)c1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAPGEF4 Q8WZA2 1/20 0.47
AHR P35869 1/20 0.46
CES2 O00748 1/20 0.46
TSHR P16473 2/20 0.43
ALDH1A1 P00352 1/20 0.43
CYP3A4 P08684 1/20 0.43
HPGD P15428 1/20 0.43
ALOX15 P16050 1/20 0.43
HIF1A Q16665 1/20 0.43
TXNRD1 Q16881 1/20 0.43
TXNRD3 Q86VQ6 1/20 0.43
TXNRD2 Q9NNW7 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
NOTUM Q6P988 1/20 0.43
IDO1 P14902 2/20 0.41
SLC13A3 Q8WWT9 1/20 0.41
P2RX1 P51575 4/20 0.39
P2RX4 Q99571 2/20 0.38
P2RX7 Q99572 2/20 0.38
TMPRSS4 Q9NRS4 2/20 0.38

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
SCHEMBL321756 0.94 AHR (0.52) RAPGEF4AHRCES2TSHRALDH1A1
Nitrogen SCHEMBL9592328 0.88 AHR (0.48) RAPGEF4AHRCES2TSHRALDH1A1
SCHEMBL16703924 0.87 RAPGEF4 (0.41) RAPGEF4AHRCES2TSHRALDH1A1
SCHEMBL13249067 0.87 RAPGEF4 (0.44) RAPGEF4AHRCES2TSHRALDH1A1
Nitrogen SCHEMBL28987389 0.86 AHR (0.47) RAPGEF4AHRCES2TSHRALDH1A1
SCHEMBL23045002 0.84 NOTUM (0.46) RAPGEF4AHRCES2TSHRALDH1A1
SCHEMBL7934061 0.84 RAPGEF4 (0.42) RAPGEF4AHRCES2TSHRALDH1A1
SCHEMBL440959 0.83 CES2 (0.58) RAPGEF4CES2TSHRALDH1A1CYP3A4
SCHEMBL15943174 0.82 RAPGEF4 (0.41) RAPGEF4AHRCES2TSHRALDH1A1
SCHEMBL6865601 0.82 AHR (0.48) RAPGEF4AHRCES2TSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116730879-B Method for selectively synthesizing 4-amino-N- (hetero) aryl sulfonamide compound SHAANXI NORMAL UNIVERSITY (CN) 2026-05-26 CN disclosed
CN-117185990-B Compound and organic electroluminescent device comprising same 烟台丰蓬液晶材料有限公司 2024-01-30 CN disclosed
CN-117185990-A Compound and organic electroluminescent device comprising same 烟台丰蓬液晶材料有限公司 2023-12-08 CN disclosed
CN-116730879-A Method for selectively synthesizing 4-amino-N- (hetero) aryl sulfonamide compound 陕西师范大学 2023-09-12 CN disclosed
CN-110730767-B Process for producing cycloalkyl (trifluoromethyl) benzene 东丽精细化工株式会社 2022-06-24 CN disclosed
US-11066422-B2 Method of producing cycloalkyl(trifluoromethyl)benzene TORAY FINE CHEMICALS CO., LTD. (JP) 2021-07-20 US disclosed
US-20210053992-A1 METHOD OF PRODUCING CYCLOALKYL(TRIFLUOROMETHYL)BENZENE TORAY FINE CHEMICALS CO., LTD. (JP) 2021-02-25 US disclosed
US-10899687-B2 Process for the preparation of organic halides TECHNION RESEARCH & DEVELOPMENT FOUNDATION LIMITED (IL) 2021-01-26 US disclosed
EP-3653594-A1 PRODUCTION METHOD FOR CYCLOALKYL(TRIFLUOROMETHYL)BENZENE Toray Fine Chemicals Co., Ltd. (JP) 2020-05-20 EP disclosed
US-20180282247-A1 PROCESS FOR THE PREPARATION OF ORGANIC HALIDES TECHNION RESEARCH & DEVELOPMENT FOUNDATION LIMITED (IL) 2018-10-04 US disclosed
EP-0968177-B1 METHOD FOR PRODUCING AROMATIC NITRILES BAYER AG (DE) 2002-01-23 EP disclosed
US-6268527-B1 REACTING TRIFLUOROMETHYL SUBSTITUTED AROMATIC COMPOUND WITH CARBON MONOXIDE AND HYDROXY COMPOUND IN PRESENCE OF METAL COMPOUND AND PHOSPHINE DERIVATIVE TO PRODUCE TRIFLUOROMETHYL SUBSTITUTED BENZOIC ACID DERIVATIVE CENTRAL GLASS COMPANY, LIMITED (JP) 2001-07-31 US disclosed
US-6162942-A Method for producing aromatic nitriles BAYER AKTIENGESELLSCHAFT (DE) 2000-12-19 US disclosed
JP-2000264853-A PRODUCTION OF NUCLEUS-CHLORINATED BIS(TRIHALOMETHYL) BENZENE ASAHI GLASS CO LTD 2000-09-26 JP disclosed
EP-0968177-A1 METHOD FOR PRODUCING AROMATIC NITRILES Bayer Aktiengesellschaft (DE) 2000-01-05 EP disclosed
WO-1998037058-A1 METHOD FOR PRODUCING AROMATIC NITRILES BAYER AKTIENGESELLSCHAFT (DE) 1998-08-27 WO disclosed
EP-0384392-A1 Cyanation of haloaromatics utilizing catalysts generated in situ starting with NiCl2 or NiCl2 6H2O OCCIDENTAL CHEMICAL CORPORATION (US) 1990-08-29 EP disclosed
US-4351975-A Process for preparing chlorinated compounds CIBA-GEIGY AG (CH) 1982-09-28 US disclosed
EP-0036840-A2 Process for the production of chlorinated compounds CIBA-GEIGY AG (CH) 1981-09-30 EP disclosed
US-4079090-A Preparation of trichloromethyl-trifluoro methyl-benzenes BAYER AKTIENGESELLSCHAFT (DT) 1978-03-14 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11066422-B2 Method of producing cycloalkyl(trifluoromethyl)benzene HCN4, MAP2K4, GRHPR RAPGEF4 3107/4885AHR 64/4885CES2 3206/4885
US-10899687-B2 Process for the preparation of organic halides HDHD5, CBR3, RCC2 RAPGEF4 3498/4885AHR 1828/4885CES2 188/4885
US-20180282247-A1 PROCESS FOR THE PREPARATION OF ORGANIC HALIDES HDHD5, CBR3, RCC2 RAPGEF4 3498/4885AHR 1828/4885CES2 188/4885
US-20210053992-A1 METHOD OF PRODUCING CYCLOALKYL(TRIFLUOROMETHYL)BENZENE HCN4, MAP2K4, GRHPR RAPGEF4 3107/4885AHR 64/4885CES2 3206/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.