SCHEMBL3660118

SCHEMBL3660118

CCCCCCCCCCCCCCCC(=O)OC(C)OCCCC

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.65
MAPT P10636 3/20 0.56
MAPK1 P28482 3/20 0.56
DGKA P23743 1/20 0.53
ALDH1A1 P00352 1/20 0.53
PRKCA P17252 1/20 0.49
PRKCE Q02156 1/20 0.49
PRKCQ Q04759 1/20 0.49
PRKCD Q05655 1/20 0.49
CYP1A2 P05177 2/20 0.45
MEN1 O00255 1/20 0.45
GMNN O75496 1/20 0.45
HSP90AA1 P07900 1/20 0.45
BLM P54132 1/20 0.45
KMT2A Q03164 1/20 0.45
NPSR1 Q6W5P4 1/20 0.45
NR1H4 Q96RI1 1/20 0.45
TP53 P04637 1/20 0.45
CYP2C9 P11712 1/20 0.45
TSHR P16473 1/20 0.45

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
SCHEMBL3657908 1.00 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL9615270 1.00 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL11213763 1.00 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL220639 1.00 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL3660798 1.00 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL15588350 0.98 LMNA (0.61) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL5562346 0.98 LMNA (0.61) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL11209242 0.98 LMNA (0.61) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL10626066 0.96 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1
SCHEMBL1091502 0.96 LMNA (0.65) LMNAMAPTMAPK1DGKAALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8425784-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2013-04-23 US claimed
US-5075167-A Two magnetic layers containing ferromagnetic powder and binder , first layer containing hydrocarbyl fatty acid ester and seco nd containing hydrocarbyloxyhydrocarbyl fatty acid ester FUJI PHOTO FILM CO., LTD. (JP) 1991-12-24 US claimed
EP-2209547-B1 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS UNIV KANSAS (US) 2018-06-20 EP disclosed
US-8801939-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2014-08-12 US disclosed
US-20130240781-A1 Ozonolysis Reactions in Liquid CO2 and CO2-Expanded Solvents ARCHER DANIELS MIDLAND COMPANY (US) 2013-09-19 US disclosed
US-8425784-B2 Ozonolysis reactions in liquid CO2 and CO2-expanded solvents UNIVERSITY OF KANSAS (US) 2013-04-23 US disclosed
EP-2209547-A2 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS University Of Kansas (US) 2010-07-28 EP disclosed
WO-2009061806-A2 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS UNIVERSITY OF KANSAS (US) 2009-05-14 WO disclosed
US-20090118498-A1 OZONOLYSIS REACTIONS IN LIQUID CO2 AND CO2-EXPANDED SOLVENTS ARCHER DANIELS MIDLAND COMPANY 2009-05-07 US disclosed
US-6777072-B2 Magnetic recording medium EMTEC MAGNETICS GMBH (DE) 2004-08-17 US disclosed
US-20030031896-A1 Lower layer contains a binder and an inorganic pigment, and the upper magnetic layer contains a fatty ester, such as isobutyl stearate, and a an oxyalkylene fatty ester ether with 1-4 units, such as butoxyethoxyethyl stearate. EMTEC MAGNETICS GMBH (DE) 2003-02-13 US disclosed
US-5387464-A Increasing the adhesion between a nonmagnetic supports and a magnetic layer by an anionic polyesters, polyurethanes or polyesterurethane copolymers; bonding strength, dispersion, wear resistance, nonabrasive FUJI PHOTO FILM CO., LTD. (JP) 1995-02-07 US disclosed
US-5116658-A Support and magnetic layer with specified surface waviness limits; durability, nonabrasive KONICA CORPORATION (JP) 1992-05-26 US disclosed
US-5091268-A Magnetic recording medium lubricated by a three component fatty acid ester-fatty acid amide composition FUJI PHOTO FILM CO., LTD. (JP) 1992-02-25 US disclosed
US-5082733-A Magnetic recording medium containing magnetic particles surface treated with a glycidyl compound FUJI PHOTO FILM CO., LTD. (JP) 1992-01-21 US disclosed
US-5034271-A Polyurethane-vinyl chloride copolymer FUJI PHOTO FILM CO., LTD. (JP) 1991-07-23 US disclosed
EP-0431858-A2 Magnetic recording medium KONICA CORPORATION (JP) 1991-06-12 EP disclosed
US-4970121-A BINDER MIXTURE OF POLYCARBONATE POLYURETHANE AND PHENOXY RESIN FUJI PHOTO FILM CO., LTD. (JP) 1990-11-13 US disclosed
US-4885208-A CONTAINING POLAR AROMATIC COMPOUND FUJI PHOTO FILM CO., LTD. (JP) 1989-12-05 US disclosed
US-4364743-A ESTER AND MIDDLE OIL ERNER WILLIAM E 1982-12-21 US disclosed