SCHEMBL13839643

SCHEMBL13839643

O=P(c1ccccc1)(c1ccccc1OP(Oc1ccccc1-c1ccccc1)Oc1ccccc1-c1ccccc1)c1ccccc1OP(Oc1ccccc1-c1ccccc1)Oc1ccccc1-c1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 3/20 0.43
ALDH1A1 P00352 2/20 0.43
POLB P06746 1/20 0.43
NPSR1 Q6W5P4 1/20 0.39
MAPK1 P28482 2/20 0.37
TP53 P04637 1/20 0.37
RAB9A P51151 1/20 0.37
MEN1 O00255 3/20 0.36
KMT2A Q03164 3/20 0.36
ADRB2 P07550 2/20 0.36
KDM4E B2RXH2 3/20 0.35
L3MBTL1 Q9Y468 3/20 0.35
TDP1 Q9NUW8 2/20 0.35
NCOA1 Q15788 1/20 0.34
NCOA3 Q9Y6Q9 1/20 0.34
LMNA P02545 2/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
RXRA P19793 1/20 0.33
RXRB P28702 1/20 0.33
RXRG P48443 1/20 0.33

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
SCHEMBL13839657 0.83 ALDH1A1 (0.46) HTTALDH1A1POLBNPSR1MEN1
SCHEMBL13839642 0.80 POLB (0.44) HTTALDH1A1POLBNPSR1MEN1
SCHEMBL13839653 0.80 KMT2A (0.47) HTTALDH1A1POLBNPSR1MAPK1
SCHEMBL674709 0.80 MAPK1 (0.47) ALDH1A1MAPK1TP53RAB9AADRB2
SCHEMBL13841234 0.78 SRC (0.44) HTTALDH1A1POLBNPSR1MEN1
SCHEMBL14424039 0.78 ALDH1A1 (0.42) HTTALDH1A1POLBNPSR1MAPK1
SCHEMBL13839664 0.77 ALDH1A1 (0.41) HTTALDH1A1POLBNPSR1TP53
SCHEMBL13839644 0.77 NPSR1 (0.51) HTTALDH1A1POLBNPSR1MAPK1
SCHEMBL13839650 0.75 ALDH1A1 (0.40) HTTALDH1A1POLBNPSR1RAB9A
SCHEMBL13839655 0.75 ALDH1A1 (0.43) HTTALDH1A1POLBNPSR1MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7531682-B2 Method for making nitrile compounds from ethylenically unsaturated compounds RHODIA POLYAMIDE INTERMEDIATES (FR) 2009-05-12 US disclosed
US-7531682-B2 Method for making nitrile compounds from ethylenically unsaturated compounds RHODIA POLYAMIDE INTERMEDIATES (FR) 2009-05-12 US disclosed
US-7253298-B2 Hydrocyanating an unsaturated aliphatic nitrile, or a linear pentenenitrile in a liquid medium with hydrogen cyanide in the presence of a Nickel catalyst with an triaryl phosphite ligand; isomerization RHODIA POLYAMIDE INTERMEDIATES (FR) 2007-08-07 US disclosed
US-7253298-B2 Hydrocyanating an unsaturated aliphatic nitrile, or a linear pentenenitrile in a liquid medium with hydrogen cyanide in the presence of a Nickel catalyst with an triaryl phosphite ligand; isomerization RHODIA POLYAMIDE INTERMEDIATES (FR) 2007-08-07 US disclosed