SCHEMBL5653136

SCHEMBL5653136

Cc1cc(S(=O)(=O)N=C=O)ccc1N=C=S

nearest known ligand 0.45

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.45
LMNA P02545 2/20 0.45
CA1 P00915 1/20 0.36
CA2 P00918 1/20 0.36
POLB P06746 1/20 0.35
CYP3A4 P08684 3/20 0.33
TRPA1 O75762 1/20 0.33
TDP1 Q9NUW8 3/20 0.32
KDM4E B2RXH2 2/20 0.31
USP2 O75604 2/20 0.31
LTA P01374 2/20 0.31
MAPT P10636 2/20 0.31
HPGD P15428 2/20 0.31
P2RX3 P56373 2/20 0.31
RAD51 Q06609 2/20 0.31
HSD17B10 Q99714 2/20 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
SCHEMBL7464876 0.79 LMNA (0.52) ALDH1A1LMNAPOLBTDP1
SCHEMBL8102004 0.78 ALDH1A1 (0.39) ALDH1A1LMNACA1CA2POLB
SCHEMBL5653049 0.76 CYP3A4 (0.54) ALDH1A1LMNACYP3A4TRPA1TDP1
SCHEMBL5655949 0.76 LMNA (0.36) ALDH1A1LMNACYP3A4TRPA1TDP1
SCHEMBL5654352 0.74 CA1 (0.59) ALDH1A1LMNACA1CA2POLB
SCHEMBL11191599 0.74 CYP3A4 (0.46) ALDH1A1LMNAPOLBCYP3A4TRPA1
SCHEMBL5654372 0.72 LMNA (0.43) ALDH1A1LMNAPOLBCYP3A4TRPA1
SCHEMBL9795474 0.72 ALDH1A1 (0.46) ALDH1A1LMNACA1CA2POLB
SCHEMBL6517286 0.72 MIF (0.41) ALDH1A1CA1CA2CYP3A4TDP1
SCHEMBL5655635 0.71 TDP1 (0.38) ALDH1A1LMNACA1CA2POLB

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 13 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
EP-0232541-B1 POLYISOCYANATE COMPOSITIONS CONTAINING LATENT TIN-CATALYSTS, THEIR USE IN THE PREPARATION OF POLYURETHANE RESINS AND REACTION PRODUCTS OF SULFONYL ISOCYANATES WITH SELECTED TIN COMPOUNDS BAYER AG (DE) 1990-10-24 EP 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
EP-0232541-A2 Polyisocyanate compositions containing latent tin-catalysts, their use in the preparation of polyurethane resins and reaction products of sulfonyl isocyanates with selected tin compounds BAYER AG (DE) 1987-08-19 EP disclosed
US-4614785-A TERTIARY PHOSPHINE OR PERALKYLATED PHOSPHORUS ACID TRIAMIDE CATALYST BAYER AKTIENGESELLSCHAFT (DE) 1986-09-30 US disclosed
EP-0172379-A1 Material for orthopaedic bandages BAYER AG (DE) 1986-02-26 EP disclosed
EP-0132675-A2 Preparations of polyisocynate containing reversibly blocked catalysts, process for their production, their use in the production of polyurethanes, and addition products of sulfonylisocyanates on catalysts with a structure of carboxylates of tin II or IV BAYER AG (DE) 1985-02-13 EP disclosed