SCHEMBL1755142

SCHEMBL1755142

Nc1ccc2cc(S(=O)(=O)O)ccc2c1S(=O)(=O)O

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 5/20 0.65
ALDH1A1 P00352 4/20 0.65
CYP2C9 P11712 4/20 0.65
CASP6 P55212 3/20 0.65
CYP2C19 P33261 3/20 0.65
NT5E P21589 4/20 0.53
NSD2 O96028 2/20 0.49
DUSP3 P51452 1/20 0.49
PTPN5 P54829 1/20 0.49
PTPN11 Q06124 1/20 0.49
SENP2 Q9HC62 4/20 0.45
SUMO2 P61956 3/20 0.45
SUMO1 P63165 3/20 0.45
SENP7 Q9BQF6 3/20 0.45
SENP3 Q9H4L4 3/20 0.44
SENP1 Q9P0U3 3/20 0.44
TSHR P16473 3/20 0.42
CYP1A2 P05177 2/20 0.42
TDP1 Q9NUW8 1/20 0.42
SNCA P37840 2/20 0.41

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
SCHEMBL8497558 0.89 ALDH1A1 (0.51) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL1755144 0.88 ALDH1A1 (0.62) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL7528317 0.87 HSD17B10 (0.51) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL9340369 0.86 HSD17B10 (0.49) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
Sulfuric Acid SCHEMBL27948253 0.85 CASP6 (0.48) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL9354745 0.84 CASP6 (0.50) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL6051291 0.84 ALDH1A1 (0.67) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL3901952 0.84 ALDH1A1 (0.56) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL10390948 0.84 ALDH1A1 (0.47) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19
SCHEMBL10633425 0.84 ALDH1A1 (0.47) HSD17B10ALDH1A1CYP2C9CASP6CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0776947-B1 Fiber-reactive dyestuffs, their preparation and use CIBA SC HOLDING AG (CH) 2000-04-26 EP claimed
US-5837827-A Fibre-reactive dyes, their preparation and their use CIBA SPECIALTY CHEMICALS CORPORATION (US) 1998-11-17 US claimed
EP-0776947-A1 Fiber-reactive dyestuffs, their preparation and use Ciba SC Holding AG (CH) 1997-06-04 EP claimed
JP-6184454-A None JP disclosed
US-20250333472-A1 Binding Domain Mapping and Compounds, Compositions, Complexes, Methods, and Kits Related Thereto GEORGE MASON RES FOUNDATION INC (US) 2025-10-30 US disclosed
US-12331096-B2 Binding domain mapping and compounds, compositions, complexes, methods, and kits related thereto George Mason Research Foundation, Inc. (US) 2025-06-17 US disclosed
CN-102566269-B Coloured composition, colour filter and display element JSR株式会社 2016-06-15 CN disclosed
CN-104238267-A Coloring combination for color filter and color filter TOYO INK SC HOLDINGS CO LTD 2014-12-24 CN disclosed
CN-102549460-B Coloring composition and color filter TOYO INK SC HOLDINGS CO LTD 2014-09-24 CN disclosed
US-8834620-B2 Black disazo dyes, their preparation and use ILFORD IMAGING SWITZERLAND GMBH (CH) 2014-09-16 US disclosed
CN-101768369-B Weather-resistant perylene bisimide dye and preparation method and application thereof UNIV DALIAN TECH 2012-05-23 CN disclosed
EP-0133270-A1 Reactive dyes BASF Aktiengesellschaft (DE) 1985-02-20 EP disclosed
EP-0119441-A2 Reactive dyes with substituted 4-fluoropyridaz-6-one groups BASF Aktiengesellschaft (DE) 1984-09-26 EP disclosed
US-4473498-A Water-soluble, fiber-reactive organic dyestuffs containing a β-chloro-ethylsulfonyl-methyl-benzoic acid amide group HOECHST AKTIENGESELLSCHAFT (DE) 1984-09-25 US disclosed
EP-0042108-B1 REACTIVE DYES, THEIR USE AND CELLULOSE FIBERS DYED THEREWITH SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1984-04-04 EP disclosed
EP-0012969-B1 WATER-SOLUBLE FIBRE-REACTIVE COMPOUNDS AND THEIR USE IN FIBRE FINISHING,ESPECIALLY AS DYESTUFFS,AND DIHALOGENO-PYRIDAZONYL-CARBOXYLIC AND SULFONIC ACID HALIDES AND THEIR USE AS FIBRE-REACTIVE ANCHORS,AS WELL AS PROCESS FOR THE PREPARATION OF THESE COMPOUND HOECHST AKTIENGESELLSCHAFT (DE) 1983-06-08 EP disclosed
EP-0045488-A2 Water-soluble fibre-reactive compounds and their use in finishing textiles, as well as the beta-chloroethyl-sulfonyl-methyl-benzoic-acid halogenides, and their use as a fibre-reactive anchor HOECHST AKTIENGESELLSCHAFT (DE) 1982-02-10 EP disclosed
EP-0042108-A1 Reactive dyes, their use and cellulose fibers dyed therewith SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1981-12-23 EP disclosed
EP-0012969-A2 Water-soluble fibre-reactive compounds and their use in fibre finishing,especially as dyestuffs,and dihalogeno-pyridazonyl-carboxylic and sulfonic acid halides and their use as fibre-reactive anchors,as well as process for the preparation of these compound HOECHST AKTIENGESELLSCHAFT (DE) 1980-07-09 EP disclosed
US-4163675-A CONTAINING NAPHTHALENE DERIVATIVES PILOT INK CO., LTD. (JP) 1979-08-07 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 (2 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-20250333472-A1 Binding Domain Mapping and Compounds, Compositions, Complexes, Methods, and Kits Related Thereto SNRPE, SSBP1, RPA1 HSD17B10 3628/4885ALDH1A1 4743/4885CYP2C9 4821/4885
US-12331096-B2 Binding domain mapping and compounds, compositions, complexes, methods, and kits related thereto SNRPE, SSBP1, RPA1 HSD17B10 3628/4885ALDH1A1 4743/4885CYP2C9 4821/4885

“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.