SCHEMBL429785

SCHEMBL429785

O=S(=O)(O)c1ccc2c(S(=O)(=O)O)cccc2c1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CASP6 P55212 4/20 0.58
ALDH1A1 P00352 6/20 0.51
HSD17B10 Q99714 4/20 0.51
CYP2C9 P11712 4/20 0.51
CYP2C19 P33261 3/20 0.51
HIF1A Q16665 4/20 0.50
CYP1A2 P05177 4/20 0.50
TSHR P16473 2/20 0.49
PTPRA P18433 1/20 0.49
PTPRB P23467 1/20 0.49
RAPGEF4 Q8WZA2 1/20 0.49
RHOA P61586 1/20 0.48
TTR P02766 1/20 0.47
TDP1 Q9NUW8 3/20 0.47
MEN1 O00255 2/20 0.47
KMT2A Q03164 2/20 0.47
THRB P10828 1/20 0.47
ATIC P31939 2/20 0.47
DUSP5 Q16690 1/20 0.46
NSD2 O96028 3/20 0.45

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
SCHEMBL31255683 1.00 CASP6 (0.58) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL5346617 0.98 CASP6 (0.56) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL10864839 0.98 CASP6 (0.56) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
Hydrochloric Acid SCHEMBL11155537 0.98 CASP6 (0.56) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL2290226 0.98 CASP6 (0.56) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
Guanidine SCHEMBL29508909 0.92 CASP6 (0.51) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL31401976 0.88 CYP1A2 (0.53) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL1902549 0.88 CYP1A2 (0.53) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL29370096 0.87 ALDH1A1 (0.54) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL479266 0.87 ALDH1A1 (0.54) CASP6ALDH1A1HSD17B10CYP2C9CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116004485-B Pseudomonas, microbial inoculum and method and device for treating dye wastewater by using same 江苏聚庚科技股份有限公司 2023-05-30 CN claimed
CN-116004485-A Pseudomonas, microbial inoculum and method and device for treating dye wastewater by using same 江苏聚庚科技股份有限公司 2023-04-25 CN claimed
CN-107615069-B Heme protein preserving fluid and method for stabilizing heme protein 荣研化学株式会社 2021-04-20 CN claimed
CN-108088917-B Method for detecting naphthalene disulfonic acid isomer 北京工业大学 2021-01-01 CN claimed
CN-109220316-B Multifunctional plant planting equipment 新昌县天姥园艺发展有限公司 2020-10-16 CN claimed
US-10780404-B2 Polyaniline membranes, uses, and methods thereto THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2020-09-22 US claimed
US-20190217254-A1 POLYANILINE MEMBRANES, USES, AND METHODS THERETO THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2019-07-18 US claimed
US-10265662-B2 Polyaniline membranes, uses, and methods thereto THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-04-23 US claimed
CN-104884490-B Polyaniline film, its purposes and its method 加州大学评议会 2018-11-23 CN claimed
CN-106928100-B A kind of continuous nitrification method of naphthalene sulfonic acids class compound 沈阳化工研究院有限公司 2018-11-13 CN claimed
US-5427677-A Using a naphthalenesulfonic acid LEARONAL, INC. (US) 1995-06-27 US claimed
CN-1103533-A Biologically active ureido derivatives useful as anti-metastatic agents ERBA CARLO SPA (IT) 1995-06-07 CN claimed
EP-0639073-A1 BIOLOGICALLY ACTIVE UREIDO DERIVATIVES USEFUL AS ANTIMETASTATIC AGENTS PHARMACIA & UPJOHN S.p.A. (IT) 1995-02-22 EP claimed
WO-1994020095-A1 BIOLOGICALLY ACTIVE UREIDO DERIVATIVES USEFUL AS ANTIMETASTATIC AGENTS FARMITALIA CARLO ERBA S.R.L. (IT) 1994-09-15 WO claimed
EP-0427785-A4 HIGH SERVICE TEMPERATURE CONDUCTIVE POLYMERS AND METHOD OF PRODUCING SAME 1992-01-02 EP claimed
EP-0427785-A1 HIGH SERVICE TEMPERATURE CONDUCTIVE POLYMERS AND METHOD OF PRODUCING SAME LOCKHEED CORPORATION (US) 1991-05-22 EP claimed
US-4935163-A High service temperature conductive polymers and method of producing same LOCKHEED CORPORATION (US) 1990-06-19 US claimed
WO-1990001775-A1 HIGH SERVICE TEMPERATURE CONDUCTIVE POLYMERS AND METHOD OF PRODUCING SAME LOCKHEED CORPORATION (US) 1990-02-22 WO claimed
US-4324742-A SELECTIVE SEPARATION OF ISOMERS BY CRYSTALLIZATION SUGAI CHEMICAL INDUSTRY CO., LTD. (JP) 1982-04-13 US claimed
US-4171459-A Manufacture of α-naphthol BASF AKTIENGESELLSCHAFT (DE) 1979-10-16 US claimed