SCHEMBL3457995

SCHEMBL3457995

O=S(=O)(F)c1ccc(F)cc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MMP2 P08253 2/20 0.52
CA1 P00915 2/20 0.52
CA2 P00918 2/20 0.52
MMP1 P03956 1/20 0.52
MMP9 P14780 1/20 0.52
MMP8 P22894 1/20 0.52
MMP13 P45452 1/20 0.52
F2 P00734 3/20 0.48
TMPRSS4 Q9NRS4 2/20 0.48
TP53 P04637 1/20 0.48
CYP1A2 P05177 1/20 0.48
CYP2D6 P10635 1/20 0.48
TSHR P16473 1/20 0.48
SOS1 Q07889 1/20 0.46
PRSS1 P07477 1/20 0.46
PRSS2 P07478 1/20 0.46
PRSS3 P35030 1/20 0.46
PKM P14618 2/20 0.45
MEN1 O00255 1/20 0.45
ALDH1A1 P00352 1/20 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
SCHEMBL11574176 0.87 TSHR (0.56) MMP2CA1CA2MMP1MMP9
SCHEMBL27684445 0.81 CA1 (0.48) MMP2CA1CA2MMP1MMP9
SCHEMBL79787 0.79 HSD11B1 (0.55) MMP2CA1CA2MMP1MMP9
SCHEMBL2121770 0.79 HSD11B1 (0.55) MMP2CA1CA2MMP1MMP9
SCHEMBL30072318 0.79 HSD11B1 (0.55) MMP2CA1CA2MMP1MMP9
SCHEMBL548298 0.79 MMP2 (0.54) MMP2CA1CA2MMP1MMP9
SCHEMBL4328574 0.79 HSD11B1 (0.55) MMP2CA1CA2MMP1MMP9
SCHEMBL11573848 0.79 CA12 (0.52) MMP2CA1CA2F2TMPRSS4
SCHEMBL8696138 0.77 TSHR (0.48) MMP2CA1CA2MMP1MMP9
SCHEMBL1346329 0.77 MMP2 (0.52) MMP2CA1CA2MMP1MMP9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111370766-A Electrolyte containing-S-F group compound and electrochemical device thereof 青岛滨海学院 2020-07-03 CN claimed
CN-107935802-A A kind of method that biaryl compound is prepared using arylsulfonyl fluorine as raw material 遵义医学院 2018-04-20 CN claimed
US-12381257-B2 Nonaqueous electrolytic solution CENTRAL GLASS CO, LTD. (JP) 2025-08-05 US disclosed
WO-2025121400-A1 PRODUCTION METHOD FOR FLUORINATED THIO GROUP–CONTAINING ARYL COMPOUND AGC株式会社 2025-06-12 WO disclosed
CN-120005064-A Aryl ion polymer and preparation method and application thereof 佛山绿动氢能科技有限公司 2025-05-16 CN disclosed
US-20250105353-A1 Electrolyte Solution for Nonaqueous Electrolyte Batteries, and Nonaqueous Electrolyte Battery Using Same CENTRAL GLASS COOMPANY, LIMITED (JP) 2025-03-27 US disclosed
US-20250074942-A1 COMPOSITIONS AND METHODS FOR COVALENT PEPTIDE-BASED MODULATORS OF HLA-E CALICO LIFE SCIENCES LLC (US) 2025-03-06 US disclosed
US-12199241-B2 Electrolyte solution for nonaqueous electrolyte batteries, and nonaqueous electrolyte battery using same CENTRAL GLASS COMPANY, LIMITED (JP) 2025-01-14 US disclosed
CN-119264303-A Pendant group functionalized fluorine-containing polymer, preparation method of fluorine-containing polymer, ion exchange membrane and application 佛山绿动氢能科技有限公司 2025-01-07 CN disclosed
CN-119219809-A Fluorine-containing polymer, preparation method thereof and ion exchange membrane 佛山绿动氢能科技有限公司 2024-12-31 CN disclosed
CN-117954689-A Electrolyte for nonaqueous electrolyte battery and nonaqueous electrolyte battery using same 中央硝子株式会社 2024-04-30 CN disclosed
WO-2006038006-A2 5-SULFONYL-1-PIPERIDINYL SUBSTITUTED INDOLE DERIVATIVES AS 5-HT6 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF CNS DISORDERS GLAXO GROUP LIMITED (GB) 2006-04-13 WO disclosed
US-7022708-B2 4-piperazinyl benzenesulfonyl indoles and uses thereof ROCHE PALO ALTO LLC (US) 2006-04-04 US disclosed
US-20050261279-A1 Compounds GLAXO GROUP LIMITED (GB) 2005-11-24 US disclosed
EP-1556037-A1 4-PIPERAZINYL BENZENESULFONYL INDOLES WITH 5-HT6 RECEPTOR AFFINITY F. HOFFMANN-LA ROCHE AG (CH) 2005-07-27 EP disclosed
EP-1511727-A2 AROMATIC SULFONES AND THEIR MEDICAL USE GLAXO GROUP LIMITED (GB) 2005-03-09 EP disclosed
US-20040087593-A1 4-Piperazinyl benzenesulfonyl indoles and uses thereof ROCHE PALO ALTO LLC 2004-05-06 US disclosed
WO-2004035047-A1 4-PIPERAZINYL BENZENESULFONYL INDOLES WITH 5-HT6 RECEPTOR AFFINITY F. HOFFMANN-LA ROCHE AG (CH) 2004-04-29 WO disclosed
WO-2003099786-A2 AROMATIC SULFONES AND THEIR MEDICAL USE GLAXO GROUP LIMITED (GB) 2003-12-04 WO disclosed
US-4369145-A Preparation of fluorobenzenesulfonyl fluorides by exchange fluorination RHONE-POULENC INDUSTRIES (FR) 1983-01-18 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 (3 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-20050261279-A1 Compounds CBR1, CBR3, OXER1 MMP2 4112/4885CA1 187/4885CA2 513/4885
US-20250074942-A1 COMPOSITIONS AND METHODS FOR COVALENT PEPTIDE-BASED MODULATORS OF HLA-E MICA, CD74, HLA-DRB1 MMP2 3996/4885CA1 2450/4885CA2 3905/4885
US-20040087593-A1 4-Piperazinyl benzenesulfonyl indoles and uses thereof HTR6, HTR4, HTR5A MMP2 3593/4885CA1 4244/4885CA2 3132/4885

“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.