SCHEMBL841244

SCHEMBL841244

O=S(=O)(Cl)c1cccc(Br)c1Br

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 5/20 0.46
CA1 P00915 4/20 0.46
CA4 P22748 2/20 0.46
CA6 P23280 2/20 0.46
PLCG1 P19174 1/20 0.43
ALDH1A1 P00352 1/20 0.36
HSD17B10 Q99714 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
MAPT P10636 1/20 0.34
CA9 Q16790 4/20 0.33
TRPV4 Q9HBA0 1/20 0.33
EDNRB P24530 1/20 0.33
EDNRA P25101 1/20 0.33
CA12 O43570 2/20 0.33
CA7 P43166 2/20 0.33
AKR1B1 P15121 1/20 0.33
CDK2 P24941 1/20 0.32
CA5A P35218 2/20 0.32
CYP2C9 P11712 1/20 0.32
CA14 Q9ULX7 1/20 0.32

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
SCHEMBL8071 0.81 CA1 (0.62) CA2CA1CA4CA6PLCG1
SCHEMBL29540971 0.81 CA1 (0.62) CA2CA1CA4CA6PLCG1
SCHEMBL10605529 0.81 CA2 (0.50) CA2CA1CA4CA6PLCG1
SCHEMBL31152920 0.80 CA2 (0.45) CA2CA1CA4CA6PLCG1
SCHEMBL25294557 0.80 CA2 (0.45) CA2CA1CA4CA6PLCG1
SCHEMBL528641 0.79 CA2 (0.67) CA2CA1CA4CA6PLCG1
SCHEMBL11257444 0.79 TRPV4 (0.34) CA2CA1CA4CA6PLCG1
SCHEMBL2163749 0.78 CA1 (0.43) CA2CA1CA4CA6PLCG1
SCHEMBL3234143 0.78 EDNRB (0.37) CA2CA1CA4CA6PLCG1
SCHEMBL2163747 0.78 EDNRB (0.36) CA2CA1CA4CA6PLCG1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0576229-B1 Low temperature process for preparing alpha-anomer enriched 2-deoxy-2, 2-difluoro-D-ribofuranosyl sulfonates LILLY CO ELI (US) 1997-12-17 EP claimed
US-5401861-A CONTACTING A LACTOL WITH AN AMINE BASE, COOLING AND ADDING A SULFONATING REAGENT ELI LILLY AND COMPANY (US) 1995-03-28 US claimed
EP-0576229-A1 Low temperature process for preparing alpha-anomer enriched 2-deoxy-2, 2-difluoro-D-ribofuranosyl sulfonates ELI LILLY AND COMPANY (US) 1993-12-29 EP claimed
EP-2176223-B1 MALONAMIDE DERIVATIVES WITH ANTITHROMBOTIC ACTIVITY SANOFI SA (FR) 2013-01-23 EP disclosed
US-8143242-B2 Malonamide derivatives with antithrombotic activity SANOFI-AVENTIS (FR) 2012-03-27 US disclosed
US-7910686-B2 Block copolymer and application thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-03-22 US disclosed
US-20100249101-A1 MALONAMIDE DERIVATIVES WITH ANTITHROMBOTIC ACTIVITY SANOFI-AVENTIS (FR) 2010-09-30 US disclosed
EP-2176223-A1 MALONAMIDE DERIVATIVES WITH ANTITHROMBOTIC ACTIVITY Sanofi-Aventis (FR) 2010-04-21 EP disclosed
US-20100047661-A1 POLYMER LAMINATE MEMBRANE, THE METHOD FOR PRODUCING THE MEMBRANE AND THE USE OF THE MEMBRANE SUMITOMO CHEMICAL COMPANY, LIMITED 2010-02-25 US disclosed
US-7638220-B2 Polymeric laminates, processes for producing the same, and use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-12-29 US disclosed
US-20090264431-A1 NOVEL CATHEPSIN C INHIBITORS AND THEIR USE GLAXO GROUP LIMITED (GB) 2009-10-22 US disclosed
US-20030050315-A1 Aryl sulfonyls as factor Xa inhibitors WEXLER RUTH R (US) 2003-03-13 US disclosed
US-20020187377-A1 Reacting an aromatic diol with a disulfonylamine compound; membrane for fuel cell SUMITOMO CHEMICAL COMPANY, LIMITED 2002-12-12 US disclosed
EP-1248313-A2 Polymer electrolyte and process for producing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-10-09 EP disclosed
US-6399644-B1 ANTICOAGULANTS DUPONT PHARMACEUTICALS COMPANY 2002-06-04 US disclosed
EP-1175419-A2 ARYL SULFONYLS AS FACTOR XA INHIBITORS Du Pont Pharmaceuticals Company (US) 2002-01-30 EP disclosed
EP-1163221-A1 SULFONAMIDE DERIVATIVES AS 5HT7 RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 2001-12-19 EP disclosed
WO-2000059902-A2 ARYL SULFONYLS AS FACTOR XA INHIBITORS DU PONT PHARMACEUTICALS COMPANY (US) 2000-10-12 WO disclosed
WO-2000056712-A1 SULFONAMIDE DERIVATIVES AS 5-HT7 RECEPTOR ANTAGONISTS SMITHKLINE BEECHAM PLC (GB) 2000-09-28 WO disclosed
US-4163005-A FOR USE IN POLYMER COMPOSITIONS VELSICOL CHEMICAL CORPORATION (US) 1979-07-31 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-20030050315-A1 Aryl sulfonyls as factor Xa inhibitors F12, F11, TFPI CA2 2573/4885CA1 2249/4885CA4 2380/4885
US-20100249101-A1 MALONAMIDE DERIVATIVES WITH ANTITHROMBOTIC ACTIVITY F7, F9, TFPI CA2 1258/4885CA1 1690/4885CA4 1140/4885
US-20090264431-A1 NOVEL CATHEPSIN C INHIBITORS AND THEIR USE CTSB, CTSS, CTSF CA2 212/4885CA1 1144/4885CA4 987/4885

“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.