SCHEMBL5656809

SCHEMBL5656809

O=C=Nc1ccc(-c2ccc(S(=O)(=O)N=C=O)cc2)cc1

nearest known ligand 0.42

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 2/20 0.42
TSHR P16473 1/20 0.42
CA2 P00918 5/20 0.38
CA1 P00915 4/20 0.38
MAPK1 P28482 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
CA12 O43570 4/20 0.34
CA9 Q16790 4/20 0.34
TRPA1 O75762 1/20 0.34
EPHX2 P34913 1/20 0.33
CYP1A2 P05177 1/20 0.33
CA14 Q9ULX7 1/20 0.31

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
SCHEMBL182964 0.94 CYP3A4 (0.47) CYP3A4TSHRCA2CA1MAPK1
SCHEMBL5652661 0.84 CYP3A4 (0.67) CYP3A4TSHRCA2CA1MAPK1
SCHEMBL5653955 0.82 F2 (0.37) CYP3A4CYP1A2
SCHEMBL5654352 0.81 CA1 (0.59) CYP3A4TSHRCA2CA1TDP1
SCHEMBL7824474 0.81 CA12 (0.50) TSHRCA2CA1CA12CA9
SCHEMBL23721668 0.79 CYP3A4 (0.61) CYP3A4TSHRCA2CA1MAPK1
SCHEMBL241534 0.79 CYP3A4 (0.61) CYP3A4TSHRCA2CA1MAPK1
Water SCHEMBL3898007 0.77 CYP3A4 (0.58) CYP3A4TSHRCA2CA1MAPK1
Hydrogen Sulfide SCHEMBL3894665 0.77 CYP3A4 (0.58) CYP3A4TSHRCA2CA1MAPK1
SCHEMBL278353 0.76 CYP3A4 (0.52) CYP3A4TSHRCA2CA1MAPK1

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7030274-B2 Process for the production of carbodiimide modified organic isocyanates BAYER MATERIALSCIENCE LLC (US) 2006-04-18 US disclosed
US-20050282993-A1 Process for the production of carbodiimide modified organic isocyanates COVESTRO LLC 2005-12-22 US disclosed
EP-1607425-A1 Process for the production of carboiimide modified organic isocyanates Bayer MaterialScience LLC (US) 2005-12-21 EP disclosed
US-6362247-B1 DEACTIVATION PHOSPHOLENE CATALYSTS ROHM AND HAAS COMPANY 2002-03-26 US disclosed
EP-1054029-A1 Method of improving stability of aromatic polycarbodimides ROHM AND HAAS COMPANY (US) 2000-11-22 EP disclosed
US-5045226-A Reaction product of tin compound with sulfonyl isocyanate, storage stability, polyurethanes BAYER AKTIENGESELLSCHAFT (DE) 1991-09-03 US disclosed
US-4824595-A Polyisocyanate compositions containing reversibly blocked catalysts and addition products of sulfonyl isocyanates with catalysts having a tin(II)- or tin(IV)-carboxylate structure BAYER AKTIENGESELLSCHAFT (DE) 1989-04-25 US disclosed
EP-0172379-B1 MATERIAL FOR ORTHOPAEDIC BANDAGES BAYER AG (DE) 1989-04-19 EP disclosed
US-4638795-A FOR MEDICAL AND VETERINARY USE; BASED ON POLYURETHANES BAYER AKTIENGESELLSCHAFT (DE) 1987-01-27 US disclosed
US-4614785-A TERTIARY PHOSPHINE OR PERALKYLATED PHOSPHORUS ACID TRIAMIDE CATALYST BAYER AKTIENGESELLSCHAFT (DE) 1986-09-30 US disclosed