SCHEMBL4815560

SCHEMBL4815560

Cc1ccc(S(=O)(=O)OCCCCCCOS(=O)(=O)c2ccc(C)cc2)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2C9 P11712 1/20 0.48
CYP2C19 P33261 1/20 0.48
GAA P10253 2/20 0.46
CA12 O43570 2/20 0.46
CA1 P00915 2/20 0.46
CA9 Q16790 2/20 0.46
PSMD10 O75832 1/20 0.44
STAT3 P40763 1/20 0.44
G6PD P11413 1/20 0.44
CYP24A1 Q07973 2/20 0.43
CA2 P00918 1/20 0.43
CA3 P07451 1/20 0.43
CA6 P23280 1/20 0.43
CA5A P35218 1/20 0.43
CA7 P43166 1/20 0.43
CA5B Q9Y2D0 1/20 0.43
VDR P11473 1/20 0.42
TLR9 Q9NR96 1/20 0.42

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
SCHEMBL8484861 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL3545668 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL8483813 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL4812770 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL11050599 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL4951882 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL4954181 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL890725 0.98 ALDH1A1 (0.50) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL483847 0.94 ALDH1A1 (0.50) ALDH1A1CYP3A4CYP2C9CYP2C19GAA
SCHEMBL4193998 0.93 RECQL (0.50) ALDH1A1CYP3A4CYP2C9CYP2C19CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115785144-B Thiazole orange organosilicon quaternary ammonium salt compound, and preparation method and application thereof 苏州百灵威超精细材料有限公司 2025-06-10 CN disclosed
CN-115724890-B Thiazole orange organosilicon quaternary ammonium quaternary phosphonium salt compound, and preparation method and application thereof 苏州百灵威超精细材料有限公司 2024-12-27 CN disclosed
WO-2024185588-A1 POLYETHER RESIN, METHOD FOR PRODUCING SAME, AND USE OF SAME 大阪ガスケミカル株式会社 2024-09-12 WO disclosed
CN-117321115-A Polyether resin, process for producing the same, and use thereof 大阪燃气化学有限公司 2023-12-29 CN disclosed
WO-2023243651-A1 POLYETHER-BASED RESIN, METHOD FOR PRODUCING SAME, AND APPLICATION THEREOF 大阪ガスケミカル株式会社 2023-12-21 WO disclosed
CN-115785144-A Thiazole orange organosilicon quaternary ammonium salt compound and preparation method and application thereof 苏州百灵威超精细材料有限公司 2023-03-14 CN disclosed
CN-115724890-A Thiazole orange organosilicon quaternary ammonium phosphonium salt compound and preparation method and application thereof 苏州百灵威超精细材料有限公司 2023-03-03 CN disclosed
WO-2022244451-A1 POLYETHER-BASED RESIN, AND PRODUCTION METHOD AND APPLICATION THEREFOR 大阪ガスケミカル株式会社 2022-11-24 WO disclosed
US-9240614-B2 Nonaqueous electrolyte solution and electrochemical element using same UBE INDUSTRIES, LTD. (JP) 2016-01-19 US disclosed
EP-2579377-B1 NONAQUEOUS ELECTROLYTE SOLUTION AND ELECTROCHEMICAL ELEMENT USING SAME UBE INDUSTRIES (JP) 2014-09-03 EP disclosed
US-7411096-B2 Process for producing optically active phosphorus heterocyclic dimer NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2008-08-12 US disclosed
US-20060211888-A1 2,2'-bis-(1-alkylphosphetanes); a primary alkyl or cycloalkyl phosphine is reacted with 1,3-dichloropropane, in the presence of n-butyllithium, and then reacted with boron trihydride, oxygen, or sulfur, dimerizing, removing the boron trihydride, oxygen, or sulfur; assymetric hydrogenation catalysts NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2006-09-21 US disclosed
EP-1650216-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE DIMER OF PHOSPHORUS HETEROCYCLE NIPPON CHEMICAL INDUSTRIAL COMPANY LIMITED (JP) 2006-04-26 EP disclosed
EP-1086063-A4 NOVEL POTASSIUM CHANNEL DRUGS AND THEIR USES ADVANCED MEDICINE INC (US) 2001-03-28 EP disclosed
EP-1086063-A1 NOVEL POTASSIUM CHANNEL DRUGS AND THEIR USES Advanced Medicine, Inc. (US) 2001-03-28 EP disclosed
WO-1999064050-A9 NOVEL POTASSIUM CHANNEL DRUGS AND THEIR USES ADVANCED MEDICINE INC (US) 2000-04-20 WO disclosed
WO-1999064050-A1 NOVEL POTASSIUM CHANNEL DRUGS AND THEIR USES ADVANCED MEDICINE, INC. (US) 1999-12-16 WO disclosed
EP-0608132-B1 Coating varnish composition and antifouling coating composition HITACHI CHEMICAL CO LTD (JP) 1998-05-20 EP disclosed
US-5439511-A Composition containing polymer obtained by polymerizing unsaturated acid anhydride and another unsaturated compound, specified additive HITACHI CHEMICAL COMPANY, LTD. (JP) 1995-08-08 US disclosed
EP-0608132-A1 Coating varnish composition and antifouling coating composition HITACHI CHEMICAL CO., LTD. (JP) 1994-07-27 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 (1 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-20060211888-A1 2,2'-bis-(1-alkylphosphetanes); a primary alkyl or cycloalkyl phosphine is reacted with 1,3-dichloropropane, in the presence of n-butyllithium, and then reacted with boron trihydride, oxygen, or sulfur, dimerizing, removing the boron trihydride, oxygen, or sulfur; assymetric hydrogenation catalysts OSBP2, OXSR1, OCIAD2 ALDH1A1 3674/4885CYP3A4 3353/4885CYP2C9 3111/4885

“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.