SCHEMBL2885158

SCHEMBL2885158

Cc1[c]c(-c2[c]c(C)cc3ccccc23)c2ccccc2c1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 7/20 0.45
CYP2A6 P11509 7/20 0.45
ALDH1A1 P00352 6/20 0.44
HSD17B10 Q99714 4/20 0.44
HPGD P15428 2/20 0.44
HIF1A Q16665 1/20 0.41
CYP1B1 Q16678 1/20 0.41
KDM4E B2RXH2 2/20 0.39
GAA P10253 1/20 0.39
TSHR P16473 2/20 0.37
TRPM4 Q8TD43 1/20 0.37
TDP1 Q9NUW8 2/20 0.36
HTR2A P28223 1/20 0.35
NQO2 P16083 1/20 0.35
L3MBTL1 Q9Y468 1/20 0.35
BRD4 O60885 1/20 0.35
MEN1 O00255 1/20 0.34
GLA P06280 1/20 0.34
CYP2C19 P33261 1/20 0.34
KMT2A Q03164 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
SCHEMBL7943109 0.87 ALDH1A1 (0.40) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL11574890 0.83 TRPM4 (0.43) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL2172611 0.82 CYP2A6 (0.45) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL1699462 0.78 CRHR1 (0.43) ALDH1A1HPGDKDM4EL3MBTL1
SCHEMBL27921773 0.74 CA1 (0.40) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL21812138 0.73 ALDH1A1 (0.41) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL5832994 0.72 ALDH1A1 (0.38) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL2882999 0.72 ALDH1A1 (0.37) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL2885777 0.72 ALDH1A1 (0.43) CYP1A2CYP2A6ALDH1A1HSD17B10HPGD
SCHEMBL18317628 0.70 MAPK1 (0.45) CYP1A2ALDH1A1HSD17B10HPGDHIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
US-6265620-B1 REACTING OLEFINIC COMPOUND WITH CARBON MONOXIDE AND HYDROGEN IN PRESENCE OF CATALYST CONTAINING METAL OF GROUP 8 TO 10 AND TRIVALENT ORANIC PHOSPHORUS COMPOUND TO PRODUCE ALDEHYDE MITSUBISHI CHEMICAL CORPORATION (JP) 2001-07-24 US disclosed