SCHEMBL7198239

SCHEMBL7198239

O=C1CON=C1CCCCCc1ccccc1

nearest known ligand 0.42

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 1/20 0.42
▸ RXFP1 Q9HBX9 1/20 0.42
▸ GSK3A P49840 1/20 0.41
▸ GSK3B P49841 1/20 0.41
▸ SIGMAR1 Q99720 3/20 0.41
▸ TDP1 Q9NUW8 1/20 0.41
▸ L3MBTL1 Q9Y468 1/20 0.41
▸ NAAA Q02083 6/20 0.40
▸ FAAH O00519 3/20 0.40
▸ MIF P14174 1/20 0.39
▸ MGLL Q99685 1/20 0.39
▸ MAOA P21397 1/20 0.39

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
SCHEMBL8096690 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL1226782 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL8860760 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL347066 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL2822511 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL2823250 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL8099665 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL8100057 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL8086519 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA
SCHEMBL8095284 0.70 SIGMAR1 (0.71) MAPTRXFP1SIGMAR1L3MBTL1MAOA

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101113137-B Intermidiate for preparing 1,2-oxygen nitrogen heterocyclic-2-alkene acylbenzene and its preparation BASF AG 2010-12-29 — — CN disclosed
CN-100516030-C Intermidiate for preparing 1,2-oxygen nitrogen heterocyclic-2-alkene acylbenzene and its preparation BASF AG (DE) 2009-07-22 — — CN disclosed
CN-1255377-C Intermediate for preparing isoxazoline-3-yl acyl benzene and process for preparing intermediate BASF AG (DE) 2006-05-10 — — CN disclosed
CN-1757634-A Intermidiate for preparing 1,2-oxygen nitrogen heterocyclic-2-alkene acylbenzene and its preparation BASF AG (DE) 2006-04-12 — — CN disclosed
CN-1210269-C Preparation of 4-thioalkylbromobenzene derivatives BASF AG (DE) 2005-07-13 — — CN disclosed
CN-1182124-C Method for producing 4-bromine-aniline derivatives �����ɷ� 2004-12-29 — — CN disclosed
CN-1495158-A Intermediate for preparing isoxazoline-3-yl acyl benzene and process for preparing intermediate �����ɷ� 2004-05-12 — — CN disclosed
CN-1139578-C Preparation of isoxazolin-3-yl-acylbenzenes �����ɷ� 2004-02-25 — — CN disclosed
CN-1139578-C Preparation of isoxazolin-3-yl-acylbenzenes �����ɷ� 2004-02-25 — — CN disclosed
CN-1443156-A Preparation of 4-sulfanylbromide derivatives BASF AG (DE) 2003-09-17 — — CN disclosed
CN-1438995-A Method for producing 4-bromine-aniline derivatives BASF AG (DE) 2003-08-27 — — CN disclosed
US-6525204-B1 Oximination reaction of nitro-o-methylphenyl compound with organic nitrite; cyclization with alkene in basic catalyst presence; reduction, bromination, oxidation, carboxylation BASF AKTIENGESELLSCHAFT (DE) 2003-02-25 — — US disclosed
CN-1300284-A Preparation of isoxazolin-3-yl-acylbenzenes BASF AG (DE) 2001-06-20 — — CN disclosed
CN-1300284-A Preparation of isoxazolin-3-yl-acylbenzenes BASF AG (DE) 2001-06-20 — — CN disclosed
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