SCHEMBL1713075

SCHEMBL1713075

CSc1cc(Cl)cc(Cl)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.50
CYP3A4 P08684 3/20 0.38
TP53 P04637 1/20 0.38
SOD1 P00441 1/20 0.34
MEN1 O00255 2/20 0.33
CYP1A2 P05177 2/20 0.33
CYP2C9 P11712 2/20 0.33
CYP2C19 P33261 2/20 0.33
KMT2A Q03164 2/20 0.33
ALDH1A1 P00352 2/20 0.33
RECQL P46063 2/20 0.33
RAB9A P51151 1/20 0.33
CYP2D6 P10635 1/20 0.32
MAPT P10636 1/20 0.32
TPMT P51580 1/20 0.32
SLC6A2 P23975 1/20 0.31
SLC6A4 P31645 1/20 0.31
SLC6A3 Q01959 1/20 0.31
HSD17B10 Q99714 1/20 0.30
TRPM8 Q7Z2W7 1/20 0.30

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
SCHEMBL3784461 0.94 TSHR (0.41) TSHRCYP3A4TP53SOD1MEN1
SCHEMBL8487167 0.87 TSHR (0.38) TSHRCYP3A4TP53
SCHEMBL9910728 0.84 RAPGEF4 (0.34) TSHRRAPGEF4
SCHEMBL30253256 0.82 TSHR (0.32) TSHR
SCHEMBL11257348 0.82 TSHR (0.32) TSHR
SCHEMBL3786358 0.82 CYP3A4 (0.55) TSHRCYP3A4TP53ALDH1A1
SCHEMBL16951388 0.82 TSHR (0.32) TSHR
SCHEMBL15279054 0.82 RAPGEF4 (0.36) TSHRRAPGEF4
SCHEMBL16562812 0.78 CYP1A1 (0.43) CYP1A2ALDH1A1MAPT
SCHEMBL11909347 0.78 MEN1 (0.37) CYP3A4TP53MEN1CYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119352051-A Method for preparing sulfoxide by electrocatalytic oxidation of thioether with heterogeneous catalyst with high Faraday efficiency 齐鲁工业大学(山东省科学院) 2025-01-24 CN disclosed
EP-4455126-A1 LIGHT-MEDIATED AEROBIC OXIDATION METHOD Ecosynth (BE) 2024-10-30 EP disclosed
US-20240272108-A1 NANOPARTICLES FOR CHEMIRESISTOR SENSORS NANOSCENT LTD. (IL) 2024-08-15 US disclosed
WO-2024165619-A1 LIGHT-MEDIATED AEROBIC OXIDATION METHOD HG HOLDING B.V. (NL) 2024-08-15 WO disclosed
WO-2024044493-A2 TREATMENT OF REPEAT EXPANSION DISEASE THE JOHNS HOPKINS UNIVERSITY (US) 2024-02-29 WO disclosed
CN-117486662-A Method for synthesizing sulfoxide compound by heterogeneous catalysis 成都理工大学 2024-02-02 CN disclosed
WO-2023156402-A1 PESTICIDALLY ACTIVE THIOSEMICARBAZONE COMPOUNDS BASF SE (DE) 2023-08-24 WO disclosed
US-20230212119-A1 N,N-DIMETHYLTRYPTAMINE AND RELATED PSYCHEDELICS AND USES THEREOF TERRAN BIOSCIENCES INC. 2023-07-06 US disclosed
WO-2023058028-A1 NANOPARTICLES FOR CHEMIRESISTOR SENSORS NANOSCENT LTD. (IL) 2023-04-13 WO disclosed
CN-113651734-B Method for catalytically oxidizing thioether into sulfone 成都理工大学 2023-02-14 CN disclosed
WO-2010031047-A2 DETECTION OF VAPOR PHASE COMPOUNDS BY CHANGES IN PHYSICAL PROPERTIES OF A LIQUID CRYSTAL PLATYPUS TECHNOLOGIES, LLC (US) 2010-03-18 WO disclosed
US-6646165-B2 Reacting halothiophenol compound with an alkali metal hydroxide to obtain an alkali metal halothiophenolate compound; oxidizing in the presence of a mineral acid to produce bishalophenyl disulfide SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 2003-11-11 US disclosed
US-20030060665-A1 Process for producing bishalophenyl disulfide SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 2003-03-27 US disclosed
EP-1277731-A1 PROCESS FOR PRODUCING BISHALOPHENYL DISULFIDE SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 2003-01-22 EP disclosed
EP-0742201-A1 PROCESS FOR PRODUCING AROMATIC OR HETEROAROMATIC SULFUR COMPOUNDS SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 1996-11-13 EP disclosed
EP-0034924-B1 PROCESS FOR PREPARING 3-IODOMETHYL CEPHALOSPORINS ELI LILLY AND COMPANY (US) 1984-07-04 EP disclosed
US-4337341-A 4a-Aryl-octahydro-1H-2-pyrindines ELI LILLY AND COMPANY (US) 1982-06-29 US disclosed
EP-0034924-A2 Process for preparing 3-iodomethyl cephalosporins ELI LILLY AND COMPANY (US) 1981-09-02 EP disclosed
US-4266049-A Process for 3-iodomethyl cephalosporins ELI LILLY AND COMPANY (US) 1981-05-05 US disclosed
EP-0002937-A1 Novel pyrindines and their preparation, formulations and use ELI LILLY AND COMPANY (US) 1979-07-11 EP 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 (2 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-20230212119-A1 N,N-DIMETHYLTRYPTAMINE AND RELATED PSYCHEDELICS AND USES THEREOF PNMT, HTR5A, HNMT TSHR 3083/4885CYP3A4 1244/4885TP53 4713/4885
US-20030060665-A1 Process for producing bishalophenyl disulfide MPST, TST, GRHPR TSHR 1496/4885CYP3A4 83/4885TP53 2507/4885

“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.