SCHEMBL1395645

SCHEMBL1395645

O=S(=O)(Cl)C(F)(F)C(F)(F)C(F)(F)F

nearest known ligand 0.40

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.40
CA1 P00915 2/20 0.39
MMP1 P03956 2/20 0.39
MMP2 P08253 2/20 0.39
MMP9 P14780 2/20 0.39
MMP8 P22894 2/20 0.39
MMP13 P45452 2/20 0.39
F2 P00734 2/20 0.34
PRSS1 P07477 2/20 0.34
PRSS2 P07478 2/20 0.34
PRSS3 P35030 2/20 0.34

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
SCHEMBL169112 0.91 CA2 (0.50) CA2CA1MMP1MMP2MMP9
SCHEMBL3685584 0.88 CA2 (0.54) CA2CA1MMP1MMP2MMP9
SCHEMBL1551243 0.88 CA2 (0.54) CA2CA1MMP1MMP2MMP9
SCHEMBL1146134 0.88 CA2 (0.54) CA2CA1MMP1MMP2MMP9
SCHEMBL2135574 0.88 CA2 (0.54) CA2CA1MMP1MMP2MMP9
SCHEMBL17185508 0.88 CA2 (0.54) CA2CA1MMP1MMP2MMP9
SCHEMBL22818194 0.88 CA2 (0.54) CA2CA1MMP1MMP2MMP9
SCHEMBL2493205 0.87 CA2 (0.32) CA2CA1MMP1MMP2MMP9
SCHEMBL1455645 0.87 CA2 (0.38) CA2CA1MMP1MMP2MMP9
SCHEMBL17185512 0.82 CA2 (0.32) CA2CA1MMP1MMP2MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106458903-B Method for producing heteroaromatic sulfonamide compound 宇部兴产株式会社 2021-02-05 CN claimed
EP-3156395-B1 METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND UBE INDUSTRIES (JP) 2019-01-09 EP claimed
US-20170121288-A1 METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND UBE INDUSTRIES, LTD. (JP) 2017-05-04 US claimed
EP-3156395-A1 METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND UBE Industries, Ltd. (JP) 2017-04-19 EP claimed
EP-3351548-B1 CROSSLINKED NUCLEIC ACID GUNA, METHOD FOR PRODUCING SAME, AND INTERMEDIATE COMPOUND MITSUBISHI TANABE PHARMA CORP (JP) 2025-08-20 EP disclosed
WO-2024106331-A1 METHOD FOR PRODUCING FLUORINE-CONTAINING SULFONYL CHLORIDE AND METHOD FOR PRODUCING FLUORINE-CONTAINING SULFONYL FLUORIDE AGC株式会社 2024-05-23 WO disclosed
CN-111051278-B Method for producing perfluoroalkyl sulfimide metal salt 中央硝子株式会社 2022-05-13 CN disclosed
CN-108137638-B Bridged nucleic acid GuNA, method for producing same, and intermediate compound 田边三菱制药株式会社 2022-05-03 CN disclosed
EP-3974436-A1 CROSSLINKED NUCLEIC ACID GUNA METHOD FOR PRODUCING SAME, AND INTERMEDIATE COMPOUND Mitsubishi Tanabe Pharma Corporation (JP) 2022-03-30 EP disclosed
US-10961269-B2 Bridged nucleic acid GuNA, method for producing same, and intermediate compound MITSUBISHI TANABE PHARMA CORPORATION (JP) 2021-03-30 US disclosed
CN-112424647-A Vehicle sensor including repellent surface, protective film, repellent coating composition, and method 3M创新有限公司 2021-02-26 CN disclosed
CN-111051278-A Method for producing perfluoroalkyl sulfimide metal salt 中央硝子株式会社 2020-04-21 CN disclosed
US-20150299132-A1 AROMATIC IMIDE COMPOUND AND METHOD FOR PRODUCING SAME AZ ELECTRONIC MATERIALS (LUXEMBOURG) S.A.R.L. (US) 2015-10-22 US disclosed
US-9073828-B2 Preparation method for perfluoroalkane sulfinate CENTRAL GLASS COMPANY, LIMITED (JP) 2015-07-07 US disclosed
US-20130137899-A1 PROCESS FOR PRODUCING FLUORINE-CONTAINING SULFONYLIMIDE COMPOUND MITSUBISHI MATERIALS ELECTRONIC CHEMICALS CO., LTD (JP) 2013-05-30 US disclosed
EP-2289875-B1 PROCESS FOR PRODUCING PERFLUOROALKANESULFINIC ACID SALT CENTRAL GLASS CO LTD (JP) 2013-04-10 EP disclosed
US-20130023695-A1 Preparation Method for Perfluoroalkane Sulfinate CENTRAL GLASS COMPANY, LIMITED (JP) 2013-01-24 US disclosed
EP-2543663-A1 PREPARATION METHOD FOR PERFLUOROALKANE SULFINATE Central Glass Company, Limited (JP) 2013-01-09 EP disclosed
EP-2289875-A1 PROCESS FOR PRODUCING PERFLUOROALKANESULFINIC ACID SALT Central Glass Company, Limited (JP) 2011-03-02 EP disclosed
US-RE29032-E ANTIINFLAMMATORY AGENTS RIKER LABORATORIES, INC. (US) 1976-11-09 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-20170121288-A1 METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND PFAS, SULT2A1, ARSA CA2 102/4885CA1 62/4885MMP1 3889/4885
US-10961269-B2 Bridged nucleic acid GuNA, method for producing same, and intermediate compound POLRMT, POLM, NSUN2 CA2 397/4885CA1 460/4885MMP1 3797/4885
US-20130023695-A1 Preparation Method for Perfluoroalkane Sulfinate PFAS, PFKFB1, PFKFB2 CA2 306/4885CA1 380/4885MMP1 2604/4885
US-20150299132-A1 AROMATIC IMIDE COMPOUND AND METHOD FOR PRODUCING SAME H1-0, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, HRH4 CA2 131/4885CA1 1693/4885MMP1 1703/4885

“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.