SCHEMBL1593817

SCHEMBL1593817

C=CCC(=O)OC1CCCCC1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 1/20 0.49
NAAA Q02083 2/20 0.47
HTT P42858 2/20 0.46
CYP19A1 P11511 2/20 0.44
EPHX1 P07099 2/20 0.43
ALDH1A1 P00352 5/20 0.36
CA12 O43570 2/20 0.36
CA1 P00915 2/20 0.36
CA2 P00918 2/20 0.36
CA9 Q16790 2/20 0.36
GAA P10253 1/20 0.36
KDM4E B2RXH2 3/20 0.35
HPGD P15428 2/20 0.35
HSD17B10 Q99714 1/20 0.35
LMNA P02545 2/20 0.34
RAB9A P51151 1/20 0.34
MIF P14174 1/20 0.34
SMN1; SMN2 Q16637 2/20 0.33
NPSR1 Q6W5P4 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33

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
SCHEMBL17470137 1.00 CYP2C19 (0.49) CYP2C19NAAAHTTCYP19A1EPHX1
SCHEMBL27615579 0.90
SCHEMBL6711347 0.83 CYP2C19 (0.52) CYP2C19NAAAHTTCYP19A1EPHX1
SCHEMBL6650101 0.83 CYP2C19 (0.52) CYP2C19NAAAHTTCYP19A1EPHX1
SCHEMBL21357996 0.82 NAAA (0.33) CYP2C19NAAAHTTCYP19A1
SCHEMBL28131502 0.82 SMYD3 (0.33) CYP2C19NAAAHTTCYP19A1
SCHEMBL3964894 0.82 CYP2C19 (0.50) CYP2C19NAAAHTTCYP19A1EPHX1
SCHEMBL1378849 0.81 NAAA (0.53) CYP2C19NAAAHTTCYP19A1EPHX1
SCHEMBL112347 0.81 EPHX1 (0.41) CYP2C19NAAAHTTCYP19A1EPHX1
SCHEMBL25401219 0.80 NAAA (0.51) CYP2C19NAAAHTTCYP19A1EPHX1

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-3974196-A Method for disproportionating ethylenically unsaturated compounds having functional ester groups JAPAN SYNTHETIC RUBBER CO., LTD. (JA) 1976-08-10 US claimed
US-7960476-B2 Acrylic resin composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-06-14 US disclosed
US-20110091818-A1 PROCESS FOR PRODUCING PHOTORESIST PATTERN SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-04-21 US disclosed
US-7585570-B2 A curable adhesive comprising acrylic ester polymers, a polysilsesquioxane or polysilicate, and a disisocyanate crosslinking agent; liquid crystal displays; glass substrates; films; durability; antipeeling agents; haze-free, nonblistering; antifoam agents; resistant to repeated cycles of heating/cooling SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-09-08 US disclosed
US-20080131640-A1 ACRYLIC RESIN COMPOSITION KAWAMURA AKIRA 2008-06-05 US disclosed
US-20060252863-A1 A curable adhesive comprising acrylic ester polymers, a polysilsesquioxane or polysilicate, and a disisocyanate crosslinking agent; liquid crystal displays; glass substrates; films; durability; antipeeling agents; haze-free, nonblistering; antifoam agents; resistant to repeated cycles of heating/cooling SUMITOMO CHEMICHAL COMPANY, LIMITED 2006-11-09 US disclosed
US-20060036040-A1 Adhesive SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-02-16 US disclosed
US-20050261433-A1 Acrylic resin SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-11-24 US disclosed
US-20050244657-A1 Acrylic resin composition SUMITOMO CHEMICAL COMPANY, LIMITED 2005-11-03 US disclosed
US-20050215743-A1 Acrylic resin SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-09-29 US disclosed
JP-2000235263-A POSITIVE TYPE RESIST COMPOSITION AND ACID DISSOCIABLE GROUP-CONTAINING MONOMER USED IN SAME TOKYO OHKA KOGYO CO LTD 2000-08-29 JP disclosed
US-5731383-A USED FOR HIGH DENSITY POLYESTERS, POLYAMIDES, POLYUREAS, POLYURETHANES AMOCO CORPORATION (US) 1998-03-24 US disclosed
US-5589548-A Process for preparing difunctional telechelic linear non-crosslinked polyolefins AMOCO CORPORATION (US) 1996-12-31 US disclosed
US-5559190-A Difunctional telechelic linear non-crosslinked polyolefins AMOCO CORPORATION (US) 1996-09-24 US disclosed
US-5512635-A OLEFIN METATHESIS PROCESS; CROSSLINKING INHIBITION AMOCO CORPORATION (US) 1996-04-30 US disclosed
US-5403904-A Process for preparation of telechelic difunctional unsaturated oligomers or polymers by acyclic olefin metathesis AMOCO CORPORATION (US) 1995-04-04 US disclosed
EP-0626402-A2 Process for preparing linear monofunctional and telechelic difunctional polymers and compositions obtained thereby AMOCO CORPORATION (US) 1994-11-30 EP disclosed
US-4770810-A Organic compound having a smectic phase A, and a mixture comprising this compound THOMSON-CSF (FR) 1988-09-13 US disclosed
US-4217299-A Method for converting unsaturated compound having functional group JAPAN SYNTHETIC RUBBER CO., LTD. (JP) 1980-08-12 US disclosed
US-3974196-A Method for disproportionating ethylenically unsaturated compounds having functional ester groups JAPAN SYNTHETIC RUBBER CO., LTD. (JA) 1976-08-10 US disclosed