SCHEMBL5024952

SCHEMBL5024952

C=C(C)C(=O)OC(C)N(CC)S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

nearest known ligand 0.40

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
MMP1 P03956 9/20 0.40
MMP2 P08253 9/20 0.40
MMP9 P14780 9/20 0.40
MMP8 P22894 9/20 0.40
MMP13 P45452 9/20 0.40
CA1 P00915 6/20 0.40
CA2 P00918 6/20 0.40
F2 P00734 2/20 0.31
PRSS1 P07477 2/20 0.31
PRSS2 P07478 2/20 0.31
PRSS3 P35030 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
SCHEMBL6685817 0.88 MMP1 (0.38) MMP1MMP2MMP9MMP8MMP13
SCHEMBL6681417 0.83 MMP1 (0.34) MMP1MMP2MMP9MMP8MMP13
SCHEMBL2744930 0.82 MMP1 (0.40) MMP1MMP2MMP9MMP8MMP13
SCHEMBL2127580 0.82 MMP1 (0.35) MMP1MMP2MMP9MMP8MMP13
SCHEMBL4234133 0.79 MMP1 (0.39) MMP1MMP2MMP9MMP8MMP13
SCHEMBL8209698 0.78 MMP1 (0.34) MMP1MMP2MMP9MMP8MMP13
SCHEMBL6259411 0.76 MMP1 (0.46) MMP1MMP2MMP9MMP8MMP13
SCHEMBL3459497 0.76 MMP1 (0.34) MMP1MMP2MMP9MMP8MMP13
SCHEMBL9237820 0.76 CA1 (0.31) MMP1MMP2MMP9MMP8MMP13
SCHEMBL8947839 0.75 MMP1 (0.38) MMP1MMP2MMP9MMP8MMP13

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023165378-A1 INK, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 深圳市国华光电科技有限公司 2023-09-07 WO claimed
EP-0463805-B1 Carbamate modified sulfonated and non-sulfonated hydroxy-functional polyurethane macroiniferter compounds, copolymers made therewith, and magnetic recording media prepared therefrom MINNESOTA MINING & MFG (US) 1998-10-21 EP claimed
EP-0463806-B1 Vinyl-sulfonated and non-sulfonated hydroxy functional polyurethane copolymers prepared from macromonomers and their use in magnetic recording media MINNESOTA MINING & MFG (US) 1997-08-27 EP claimed
EP-0465070-B1 Sulfonated and non-sulfonated, thiol, and hydroxy functional polyurethanes and graft copolymers made therewith MINNESOTA MINING & MFG (US) 1996-08-14 EP claimed
US-5384362-A Graft polymers formed from diols and polyisocyanates and sulfonate groups on the polyurethane MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1995-01-24 US claimed
US-5240972-A Carbamate modified sulfonated and non-sulfonated hydroxy-functional polyurethane macroiniferter compounds, copolymers made therewith, and magnetic recording media prepared therefrom MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1993-08-31 US claimed
US-5218072-A Binders for magnetic recording media MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1993-06-08 US claimed
EP-0465070-A2 Sulfonated and non-sulfonated, thiol, and hydroxy functional polyurethanes and graft copolymers made therewith MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-08 EP claimed
EP-0463806-A2 Vinyl-sulfonated and non-sulfonated hydroxy functional polyurethane copolymers prepared from macromonomers and their use in magnetic recording media MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-02 EP claimed
EP-0463805-A2 Carbamate modified sulfonated and non-sulfonated hydroxy-functional polyurethane macroiniferter compounds, copolymers made therewith, and magnetic recording media prepared therefrom MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-02 EP claimed
WO-2023165378-A1 INK, PREPARATION METHOD THEREFOR, AND APPLICATION THEREOF 深圳市国华光电科技有限公司 2023-09-07 WO disclosed
EP-0966503-B2 CURE-ON-DEMAND, MOISTURE-CURABLE COMPOSITIONS HAVING REACTIVE SILANE FUNCTIONALITY MINNESOTA MINING & MFG (US) 2008-01-09 EP disclosed
US-20030045630-A1 Carboxylic acid functional polyurethane polymers and blends thereof used in magnetic recording media MINNESOTA MINING AND MANUFACTURING COMPANY 2003-03-06 US disclosed
EP-0869981-B1 CARBOXYLIC ACID FUNCTIONAL POLYURETHANE POLYMERS AND BLENDS THEREOF USED IN MAGNETIC RECORDING MEDIA MINNESOTA MINING & MFG (US) 2001-10-04 EP disclosed
US-6204350-B1 POLYMER HAVING REACTIVE END GROUPS 3M INNOVATIVE PROPERTIES COMPANY 2001-03-20 US disclosed
US-5118580-A Dissociate forming free radical MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-06-02 US disclosed
EP-0465070-A2 Sulfonated and non-sulfonated, thiol, and hydroxy functional polyurethanes and graft copolymers made therewith MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-08 EP disclosed
EP-0463806-A2 Vinyl-sulfonated and non-sulfonated hydroxy functional polyurethane copolymers prepared from macromonomers and their use in magnetic recording media MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-02 EP disclosed
EP-0463805-A2 Carbamate modified sulfonated and non-sulfonated hydroxy-functional polyurethane macroiniferter compounds, copolymers made therewith, and magnetic recording media prepared therefrom MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-02 EP disclosed
US-4972002-A Process for producing cellular plastics by the polyisocyanate polyaddition method by means of stable emulsions containing blowing agents, and such emulsions BASF AKTIENGESELLSCHAFT (DE) 1990-11-20 US disclosed