SCHEMBL2884958

SCHEMBL2884958

COc1c(-c2[c]ccc(Cl)c2OC)[c]ccc1Cl

nearest known ligand 0.39

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.39
KDM4E B2RXH2 2/20 0.39
HSD17B10 Q99714 1/20 0.39
HTR1A P08908 1/20 0.33
HTR1D P28221 1/20 0.33
HTR2C P28335 1/20 0.33
HTR7 P34969 1/20 0.33
HTR5A P47898 1/20 0.33
TSHR P16473 1/20 0.33
MAPK1 P28482 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32

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
SCHEMBL159595 0.82 ALDH1A1 (0.39) ALDH1A1KDM4EHSD17B10HTR1AHTR1D
SCHEMBL8682848 0.80 ALDH1A1 (0.38) ALDH1A1KDM4EHSD17B10TSHRMAPK1
SCHEMBL831500 0.80 ALDH1A1 (0.38) ALDH1A1KDM4EHSD17B10TSHRMAPK1
SCHEMBL719277 0.78 ALDH1A1 (0.37) ALDH1A1KDM4EHSD17B10TSHRMAPK1
SCHEMBL2355429 0.70 ALDH1A1 (0.50) ALDH1A1KDM4EHSD17B10HTR1AHTR1D
SCHEMBL29536407 0.70 ALDH1A1 (0.50) ALDH1A1KDM4EHSD17B10HTR1AHTR1D
SCHEMBL2884395 0.69 ALDH1A1 (0.36) ALDH1A1
SCHEMBL11484541 0.69 ALDH1A1 (0.48) ALDH1A1KDM4EHSD17B10HTR1AHTR1D
SCHEMBL221144 0.68
SCHEMBL8531806 0.67 CYP1B1 (0.40) ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7057061-B2 Chiral monophosphorus compounds BAYER AKTIENGESELLSCHAFT (DE) 2006-06-06 US claimed
US-20030119664-A1 Chiral monophosphorus compounds LANXESS DEUTSCHLAND GMBH (DE) 2003-06-26 US 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
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-7057061-B2 Chiral monophosphorus compounds BAYER AKTIENGESELLSCHAFT (DE) 2006-06-06 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-20030119664-A1 Chiral monophosphorus compounds LANXESS DEUTSCHLAND GMBH (DE) 2003-06-26 US disclosed