SCHEMBL3911054

SCHEMBL3911054

COCCOS(=O)(=O)c1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 2/20 0.50
PSIP1 O75475 1/20 0.43
CA2 P00918 2/20 0.43
PARL Q9H300 1/20 0.43
KMT2A Q03164 2/20 0.41
MEN1 O00255 1/20 0.41
HPGD P15428 2/20 0.40
PABPC1 P11940 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
HSD17B10 Q99714 1/20 0.40
ALDH1A1 P00352 4/20 0.40
TDP1 Q9NUW8 2/20 0.40
CA12 O43570 1/20 0.40
CA1 P00915 1/20 0.40
CA4 P22748 1/20 0.40
CA5A P35218 1/20 0.40
CA7 P43166 1/20 0.40
CA9 Q16790 1/20 0.40
CA5B Q9Y2D0 1/20 0.40
HSP90AA1 P07900 1/20 0.40

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
SCHEMBL3397901 0.94 MAPK1 (0.46) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL12882875 0.94 MAPK1 (0.46) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL28319664 0.94 MAPK1 (0.46) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL20745410 0.94 MAPK1 (0.46) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL3449015 0.89 PARL (0.50) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL30011527 0.83 ALDH1A1 (0.50) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL85631 0.82 ALDH1A1 (0.50) CA2HPGDSMN1; SMN2ALDH1A1CA12
SCHEMBL3133897 0.82 PSIP1 (0.45) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL778545 0.82 PSIP1 (0.50) MAPK1PSIP1CA2PARLKMT2A
SCHEMBL5945104 0.81 PARL (0.47) MAPK1PSIP1CA2PARLKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-8311324-A None JP disclosed
US-8921515-B2 Methods and compositions of preparation for proteome analysis CASE WESTERN RESERVE UNIVERSITY (US) 2014-12-30 US disclosed
CN-103880697-A N-dimethoxyethyl-m-aminoacetanilide synthesis process JIANGSU DAOBO CHEMICAL CO LTD 2014-06-25 CN disclosed
US-20130172539-A1 METHODS AND COMPOSITIONS OF PREPARATION FOR PROTEOME ANALYSIS CASE WESTERN RESERVE UNIVERSITY (US) 2013-07-04 US disclosed
EP-1686188-B1 Thin membrane for measuring protease activity FUJIFILM CORP (JP) 2009-03-18 EP disclosed
EP-1270736-B1 FILMS FOR ASSAYING PROTEASE ACTIVITY FUJIFILM CORP (JP) 2009-03-11 EP disclosed
EP-1686188-A1 Thin membrane for measuring protease activity Fuji Photo Film Co. Ltd. (JP) 2006-08-02 EP disclosed
US-7067272-B2 Thin membrane for measuring protease activity FUJI PHOTO FILM CO., LTD. (JP) 2006-06-27 US disclosed
US-6727294-B2 RADIATION TRANSPARENT MOLDING MATERIALS MITSUBISHI ENGINEERING-PLASTICS CORPORATION (JP) 2004-04-27 US disclosed
EP-0794218-B1 Polycarbonate resin composition stabilized against radiation MITSUBISHI ENG PLASTICS CORP (JP) 2003-10-15 EP disclosed
US-5455218-A Supported dye layer containing binder and substituted pyrrolopyrazoles, for transferring high density colorfast images AGFA-GEVAERT N.V. (BE) 1995-10-03 US disclosed
EP-0670225-A1 A dye donor element for use in a thermal dye transfer process AGFA-GEVAERT N.V. (BE) 1995-09-06 EP disclosed
US-5432182-A Inhibitors of gastric acid secretion SMITHKLINE BEECHAM INTERCREDIT B.V. (NL) 1995-07-11 US disclosed
CN-1100414-A Preparation of pharmaceutical compound containing novel derivative of leukol SMITHKLINE BECKMAN INTERCREDIT (NL) 1995-03-22 CN disclosed
CN-1027368-C Process for preparing substituted quinoline derivatives SMITHKLINE BECKMAN INTERCREDIT (NL) 1995-01-11 CN disclosed
EP-0330485-B1 4-AMINO-3-ACYL QUINOLINE DERIVATIVES AND THEIR USE AS INHIBITORS OF GASTRIC ACID SECRETION SmithKline Beecham Intercredit B.V. (NL) 1993-05-26 EP disclosed
US-5089504-A SUBSTITUTED 4-AMINOQUINOLINE DERIVATIVES AS GASTRIC ACID SECRETION INHIBITORS SMITHKLINE BECKMAN INTERCREDIT B.V. (NL) 1992-02-18 US disclosed
CN-1035501-A PROCESS FOR PREPARING SUBSTITUTED QUINOLINE DERIVATIVES SMITHKLINE BECKMAN INTERCREDIT (NL) 1989-09-13 CN disclosed
WO-1989008104-A1 4-AMINO-3-ACYLQUINOLINE DERIVATIVES AND THEIR USE AS INHIBITORS OF GASTRIC SECRETION SMITHKLINE BECKMAN INTERCREDIT B.V. (NL) 1989-09-08 WO disclosed
EP-0330485-A1 4-Amino-3-acyl quinoline derivatives and their use as inhibitors of gastric acid secretion SmithKline Beecham Intercredit B.V. (NL) 1989-08-30 EP disclosed