SCHEMBL895629

SCHEMBL895629

Cc1cccc(C)c1SSc1c(C)cccc1C

nearest known ligand 0.47

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 2/20 0.47
CYP1A2 P05177 1/20 0.47
ACHE P22303 3/20 0.47
TSHR P16473 1/20 0.47
ALDH1A1 P00352 4/20 0.45
CA1 P00915 2/20 0.45
CA2 P00918 2/20 0.45
CA7 P43166 2/20 0.45
CA9 Q16790 2/20 0.45
SCN4A P35499 4/20 0.41
TRPA1 O75762 2/20 0.39
CD44 P16070 1/20 0.39
ATM Q13315 1/20 0.39
TDP1 Q9NUW8 2/20 0.36
CYP3A4 P08684 1/20 0.35

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
SCHEMBL9195424 0.84 ACHE (0.41) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL9190117 0.84 ACHE (0.50) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL9193601 0.84 HPGD (0.57) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL9805918 0.81 ACHE (0.52) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL9264116 0.81 ALDH1A1 (0.39) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL9193727 0.81 GABRA1 (0.43) ALDH1A1SCN4ATDP1CYP3A4
SCHEMBL1783489 0.80 CYP2A6 (0.47) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL1740911 0.79 CYP2A6 (0.41) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL9192081 0.79 ACHE (0.39) CYP2A6CYP1A2ACHETSHRALDH1A1
SCHEMBL30571175 0.79 TXN (0.36) CYP2A6CYP1A2ACHETSHRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5153305-A From diaryl disulfide; mild conditions using organometallic catalyst RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1992-10-06 US claimed
CN-122060162-A Method for preparing polyarylene sulfide by photo-induced diaryl disulfide oxidative polymerization without catalyst 南京工业大学 2026-05-19 CN disclosed
CN-118894883-A Organic thiophosphine compound and synthesis method thereof 中科纯萃科技(北京)有限公司 2024-11-05 CN disclosed
WO-2024128145-A1 SUBSTITUTED POLYPHENYLENE SULFIDE RESIN 株式会社ダイセル 2024-06-20 WO disclosed
EP-4361200-A1 METHOD FOR MANUFACTURING SULFUR-CONTAINING POLYMER Nippon Shokubai Co., Ltd. (JP) 2024-05-01 EP disclosed
WO-2022270533-A1 METHOD FOR MANUFACTURING SULFUR-CONTAINING POLYMER 株式会社日本触媒 2022-12-29 WO disclosed
EP-2323975-B1 MULTI-RING ANTIOXIDANTS WITH ANTIWEAR PROPERTIES SI GROUP INC (US) 2019-04-24 EP disclosed
US-9796939-B2 Multi-ring antioxidants with antiwear properties SI GROUP, INC. (US) 2017-10-24 US disclosed
US-9365471-B2 Substituted phenylsulfur trifluoride and other like fluorinating agents UBE INDUSTRIES, LTD. (JP) 2016-06-14 US disclosed
US-9365471-B2 Substituted phenylsulfur trifluoride and other like fluorinating agents UBE INDUSTRIES, LTD. (JP) 2016-06-14 US disclosed
US-7265247-B1 E.g., 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride and 4-chlorophenylsulfur trifluoride; especially for fluorinating target compounds that have one or more oxygen or oxygen-containing groups that are replaced by the introduction of one or more fluorine atoms. IM&T RESEARCH, INC. (US) 2007-09-04 US disclosed
US-7265247-B1 E.g., 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride and 4-chlorophenylsulfur trifluoride; especially for fluorinating target compounds that have one or more oxygen or oxygen-containing groups that are replaced by the introduction of one or more fluorine atoms. IM&T RESEARCH, INC. (US) 2007-09-04 US disclosed
US-7265247-B1 E.g., 2,6-dimethyl-4-tert-butylphenylsulfur trifluoride and 4-chlorophenylsulfur trifluoride; especially for fluorinating target compounds that have one or more oxygen or oxygen-containing groups that are replaced by the introduction of one or more fluorine atoms. IM&T RESEARCH, INC. (US) 2007-09-04 US disclosed
EP-0402481-B1 PRODUCTION OF POLYARYLENE THIOETHER PROD DEV RES INST (JP) 1995-10-25 EP disclosed
US-5290911-A Forming polymers by catalytic oxidative coupling RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1994-03-01 US disclosed
US-5153305-A From diaryl disulfide; mild conditions using organometallic catalyst RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1992-10-06 US disclosed
US-4983720-A Process for preparing a polyarylene thioether IDEMITSU PETROCHEMICAL CO., LTD. (JP) 1991-01-08 US disclosed
EP-0402481-A1 PRODUCTION OF POLYARYLENE THIOETHER RESEARCH INSTITUTE FOR PRODUCTION DEVELOPMENT (JP) 1990-12-19 EP disclosed
US-4931542-A Process for preparing a polyarylene thioether IDEMITSU PETROCHEMICAL COMPANY, LIMITED (JP) 1990-06-05 US disclosed
EP-0281036-A2 A process for preparing a polyarylene thioether IDEMITSU PETROCHEMICAL CO. LTD. (JP) 1988-09-07 EP disclosed