SCHEMBL2879306

SCHEMBL2879306

Pc1c(-c2ccccc2)ccc(Cl)c1Cl

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 3/20 0.50
CSNK2A1 P68400 2/20 0.41
AHR P35869 2/20 0.40
CTRC Q99895 2/20 0.39
CLCN2 P51788 1/20 0.39
CYP1A2 P05177 2/20 0.37
ALDH1A1 P00352 5/20 0.37
HSD17B10 Q99714 3/20 0.37
HPGD P15428 2/20 0.37
NPC1 O15118 1/20 0.37
TP53 P04637 1/20 0.37
TSHR P16473 1/20 0.37
RAB9A P51151 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
BACE1 P56817 1/20 0.36
FEN1 P39748 1/20 0.36
ALOX5 P09917 1/20 0.35
BCL2L1 Q07817 1/20 0.34
MAPK1 P28482 1/20 0.34

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
SCHEMBL2884227 0.84 CYP2A6 (0.48) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL29983843 0.81 AHR (0.60) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL381602 0.81 AHR (0.60) CYP2A6CSNK2A1AHRCTRCCLCN2
Water SCHEMBL7043753 0.79 AHR (0.58) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL1696360 0.77 CYP2A6 (0.50) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL28755845 0.76 CYP2A6 (0.48) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL932320 0.76 CYP2A6 (0.48) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL28895884 0.76 CYP2A6 (0.48) CYP2A6CSNK2A1AHRCTRCCLCN2
SCHEMBL6005208 0.74 CYP2A6 (0.46) CYP2A6CSNK2A1AHRCTRCCLCN2
Hydrochloric Acid SCHEMBL28115567 0.74 CYP2A6 (0.46) CYP2A6CSNK2A1AHRCTRCCLCN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1354886-B1 Process for the preparation of tertiary phosphines SALTIGO GMBH (DE) 2009-08-26 EP claimed
US-7230136-B2 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2007-06-12 US claimed
US-20030229240-A1 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2003-12-11 US claimed
EP-1354886-A1 Process for the preparation of tertiary phosphines Bayer Aktiengesellschaft (DE) 2003-10-22 EP claimed
US-7847126-B2 prepared by reacting phosphorus halide with organomagnesium compound in presence of copper compound; di(tert-butyl)phenylphosphonium tetrafluoroborate, for example LANXESS DEUTSCHLAND GMBH (DE) 2010-12-07 US disclosed
EP-1354886-B1 Process for the preparation of tertiary phosphines SALTIGO GMBH (DE) 2009-08-26 EP disclosed
US-20070299273-A1 prepared by reacting phosphorus halide with organomagnesium compound in presence of copper compound; di(tert-butyl)phenylphosphonium tetrafluoroborate, for example LANXESS DEUTSCHLAND GMBH (DE) 2007-12-27 US disclosed
US-7230136-B2 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2007-06-12 US disclosed
US-20030229240-A1 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2003-12-11 US disclosed
EP-1354886-A1 Process for the preparation of tertiary phosphines Bayer Aktiengesellschaft (DE) 2003-10-22 EP disclosed