SCHEMBL5117068

SCHEMBL5117068

Nc1cc(S(=O)(=O)CCOS(=O)(=O)O)ccc1S(=O)(=O)O

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 8/20 0.47
ALDH1A1 P00352 4/20 0.40
HSD17B10 Q99714 2/20 0.40
CASP6 P55212 2/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
GAA P10253 3/20 0.37
MAPT P10636 2/20 0.37
KDM4E B2RXH2 2/20 0.37
MEN1 O00255 1/20 0.37
PKM P14618 1/20 0.37
RAB9A P51151 1/20 0.37
KMT2A Q03164 1/20 0.37
THRB P10828 1/20 0.36
TSHR P16473 1/20 0.34
NT5E P21589 1/20 0.34
CA12 O43570 1/20 0.34
CA1 P00915 1/20 0.34
CA9 Q16790 1/20 0.34
NSD2 O96028 1/20 0.33

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
SCHEMBL7632384 0.92 CA2 (0.55) CA2ALDH1A1HSD17B10CASP6CYP2C9
SCHEMBL8694925 0.88 CA2 (0.54) CA2ALDH1A1HSD17B10CASP6CYP2C9
SCHEMBL872920 0.88 CTDSP1 (0.40) CA2ALDH1A1HSD17B10CASP6CYP2C9
SCHEMBL9776593 0.85 TTR (0.41) CA2ALDH1A1HSD17B10CASP6CYP2C9
SCHEMBL9776579 0.85 TTR (0.41) CA2ALDH1A1HSD17B10CASP6CYP2C9
SCHEMBL9558736 0.83 CA2 (0.41) CA2ALDH1A1HSD17B10GAAMAPT
SCHEMBL5673668 0.83 ALDH1A1 (0.57) CA2ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL9338995 0.83 CA2 (0.67) CA2ALDH1A1HSD17B10CASP6CYP2C9
SCHEMBL6936839 0.82 ALDH1A1 (0.44) CA2ALDH1A1HSD17B10CYP2C9CYP2C19
SCHEMBL8707661 0.82 CA2 (0.40) CA2ALDH1A1HSD17B10CASP6CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2441805-B1 Black disazo dyes, their preparation and their use REX TONE IND LTD (IN) 2016-07-20 EP disclosed
US-8834620-B2 Black disazo dyes, their preparation and use ILFORD IMAGING SWITZERLAND GMBH (CH) 2014-09-16 US disclosed
US-20120090503-A1 BLACK DISAZO DYES, THEIR PREPARATION AND USE ILFORD IMAGING SWITZERLAND GMBH 2012-04-19 US disclosed
EP-2441805-A1 Black disazo dyes, their preparation and their use ILFORD Imaging Switzerland GmbH (CH) 2012-04-18 EP disclosed
US-7371892-B2 Method for processing β-sulphatoethylsulphonylaniline-2-sulphonic acid BASF AKTIENGESELLSCHAFT (DE) 2008-05-13 US disclosed
US-20070173661-A1 Method for processing beta-sulphatoethylsulphonylaniline-2-sulphonic acid BASF AKTIENGESELLSCHAFT (DE) 2007-07-26 US disclosed
EP-1179034-A4 MIXTURES OF SYMMETRICAL AND UNSYMMETRICAL RED REACTIVE DYES EVERLIGHT USA INC (US) 2004-10-06 EP disclosed
EP-1013720-B1 Red-dyeing dye mixtures of water-soluble fiber-reactive azo dyes and their use DYSTAR TEXTILFARBEN GMBH & CO (DE) 2003-10-22 EP disclosed
EP-1090962-B1 Dye mixtures of fiber-reactive azo dyes and use thereof for dyeing material containing hydroxy- and/or carboxamido groups DYSTAR TEXTILFARBEN GMBH & CO (DE) 2003-05-14 EP disclosed
EP-1179034-A1 MIXTURES OF SYMMETRICAL AND UNSYMMETRICAL RED REACTIVE DYES Everlight USA, Inc. (US) 2002-02-13 EP disclosed
US-4730038-A Water-soluble disazo compounds of 1-amino-8-naphthal-3,6- or 4,6-disulfonic acid as bivalent coupling component, containing fiber-reactive groups suitable as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1988-03-08 US disclosed
US-4701523-A Water-soluble disazo compounds containing one or two (nitro-phenylamino)-phenylamino-chlorotriazinylamino groups, the nitro-phenylamino being additionally substituted by a fiber-reactive group of the vinylsulfone series, suitable as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1987-10-20 US disclosed
US-4659807-A Water-soluble pyridone monoazo compounds suitable as fiber reactive dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1987-04-21 US disclosed
US-4622390-A DYEING FIBERS OF CELLULOSE, POLYAMIDES, POLYURETHANES HOECHST AKTIENGESELLSCHAFT (DE) 1986-11-11 US disclosed
EP-0197366-A1 Water soluble mono and disazo compounds, process for their preparation and their use as dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1986-10-15 EP disclosed
US-4485041-A Water-soluble metal free or copper triazino-bis-[hydroxy-naphthylamino]-disazo dyestuffs containing fiber reactive groups, and a process for dyeing or printing cellulose fibers HOECHST AKTIENGESELLSCHAFT (DE) 1984-11-27 US disclosed
US-4394310-A DIAZOTIZATION, CYCLIZATION HOECHST AKTIENGESELLSCHAFT (DE) 1983-07-19 US disclosed
US-4378312-A CONTAINING 1,3,5-TRIAZINE RING(S); WILL FORM COMPLEX WITH COPPER, COBALT OR CHROMIUM HOECHST AKTIENGESELLSCHAFT (DE) 1983-03-29 US disclosed
US-4323497-A Water-soluble disazo dyestuffs HOECHST AKTIENGESELLSCHAFT (DE) 1982-04-06 US disclosed
US-4242258-A TETRAKISAZO, BLACK HOECHST AKTIENGESELLSCHAFT (DE) 1980-12-30 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 (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-20070173661-A1 Method for processing beta-sulphatoethylsulphonylaniline-2-sulphonic acid ARSA, STS, TST CA2 5/4885ALDH1A1 4084/4885HSD17B10 4040/4885

“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.