SCHEMBL8865378

SCHEMBL8865378

C=C(c1ccc(F)cc1)c1ccc(F)cc1

nearest known ligand 0.55

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.55
HTT P42858 1/20 0.55
GFER P55789 1/20 0.55
HSD17B10 Q99714 1/20 0.55
GPR55 Q9Y2T6 1/20 0.55
CES2 O00748 1/20 0.52
CES1 P23141 1/20 0.52
MAOA P21397 2/20 0.48
MAOB P27338 2/20 0.48
CA1 P00915 2/20 0.48
CA2 P00918 2/20 0.48
BCL2L1 Q07817 1/20 0.44
BAD Q92934 1/20 0.44
PTPN1 P18031 1/20 0.42
NPC1 O15118 1/20 0.42
RAB9A P51151 1/20 0.42
LTA4H P09960 1/20 0.41
MEN1 O00255 1/20 0.39
KMT2A Q03164 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
SCHEMBL13461740 0.89 MAPT (0.75) MAPTHTTGFERHSD17B10GPR55
SCHEMBL7907022 0.89 MEN1 (0.54) MAPTHTTGFERHSD17B10GPR55
SCHEMBL8618039 0.87 MAOB (0.45) MAPTHTTGFERHSD17B10GPR55
SCHEMBL10705376 0.87 HTT (0.46) MAPTHTTGFERHSD17B10GPR55
SCHEMBL13811433 0.87 ACHE (0.62) MAPTHTTGFERHSD17B10GPR55
SCHEMBL24398858 0.83 BCL2L1 (0.54) MAPTHTTGFERHSD17B10GPR55
SCHEMBL18689505 0.81 CES2 (0.52) CES2CES1MAOAMAOBCA1
SCHEMBL10946523 0.80 MAOA (0.40) MAPTHTTGFERHSD17B10GPR55
SCHEMBL9208657 0.80 LTA4H (0.52) MAPTBCL2L1BADRAB9ALTA4H
SCHEMBL10363954 0.79 CES2 (0.50) CES2CES1MAOAMAOBCA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115197036-A Method for carrying out anti-Ma hydrocarboxylation reaction on olefin compound and carbon dioxide by photocatalysis 中国科学院理化技术研究所 2022-10-18 CN disclosed
CN-109265311-B Phenyl fluorene derivative and preparation method and application thereof 上海兆维科技发展有限公司 2021-06-04 CN disclosed
CN-108623425-A Method for constructing four-membered ring by visible light catalysis [2+2] reaction 中国科学院理化技术研究所 2018-10-09 CN disclosed
WO-2017216129-A1 FORMULATION OF AN ORGANIC FUNCTIONAL MATERIAL MERCK PATENT GMBH (DE) 2017-12-21 WO disclosed
EP-2780326-A1 METHOD FOR INHIBITION OF DEUBIQUITINATING ACTIVITY Vivolux Ab (SE) 2014-09-24 EP disclosed
WO-2013058691-A1 METHOD FOR INHIBITION OF DEUBIQUITINATING ACTIVITY VIVOLUX AB (SE) 2013-04-25 WO disclosed
US-5631264-A NEUROLOGICAL DISORDERS SANOFI WINTHROP, INC. (US) 1997-05-20 US disclosed
US-5604224-A NEURODEGENERATIVE DISORDERS STERLING WINTHROP INC. (US) 1997-02-18 US disclosed
US-5569655-A Substituted heterocyclylisoquinolinium salts and compositions and method of use thereof STERLING WINTHROP INC. (US) 1996-10-29 US disclosed
US-5554620-A Substituted 6,11-ethano-6,11-dihydrobenzo[b] quinolizinium salts and compositions and methods of use thereof STERLING WINTHROP INC. (US) 1996-09-10 US disclosed
EP-0656359-A1 Substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts and compositionsand methods of use thereof STERLING WINTHROP INC. (US) 1995-06-07 EP disclosed
EP-0647641-A1 Substituted heterocyclylisoquinolinium salts and compositions and methods of usethereof STERLING WINTHROP INC. (US) 1995-04-12 EP disclosed
EP-0065354-B1 PROCESS FOR THE PREPARATION OF 1,1-BIS PHENYL-2-HALOALKAN-1-OLS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1985-07-03 EP disclosed
US-4431852-A HALOGENATION OF A 1,1-DIPHENYL ETHANOL OR -ETHENE IN WATER AT A PH OF 7 OR LOWER IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1984-02-14 US disclosed
EP-0065354-A1 Process for the preparation of 1,1-bis phenyl-2-haloalkan-1-ols IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1982-11-24 EP disclosed