SCHEMBL13839484

SCHEMBL13839484

O=C(c1ccccc1OP(Oc1ccc2ccccc2c1)Oc1ccc2ccccc2c1)c1ccccc1OP(Oc1ccc2ccccc2c1)Oc1ccc2ccccc2c1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 6/20 0.42
MEN1 O00255 5/20 0.42
PTPN7 P35236 1/20 0.42
MAPT P10636 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
ESR1 P03372 2/20 0.42
GAA P10253 1/20 0.40
RCE1 Q9Y256 1/20 0.40
L3MBTL1 Q9Y468 2/20 0.40
ESR2 Q92731 1/20 0.39
CNR2 P34972 1/20 0.39
ELANE P08246 1/20 0.39
CYP1A2 P05177 1/20 0.39
CYP2A6 P11509 1/20 0.39
CASP3 P42574 1/20 0.39
SENP8 Q96LD8 1/20 0.39
SENP7 Q9BQF6 1/20 0.39
SENP6 Q9GZR1 1/20 0.39
ALDH1A1 P00352 1/20 0.39
HSD17B10 Q99714 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
SCHEMBL13839548 0.89 NPC1 (0.49) KMT2AMEN1MAPTESR1CNR2
SCHEMBL13839514 0.86 CYP1A2 (0.51) KMT2AMEN1MAPTCYP1A2CYP2A6
SCHEMBL13839492 0.81 CTNNB1 (0.46) KMT2AMEN1MAPTTDP1ESR1
SCHEMBL3960261 0.80 CYP2A6 (0.56) KMT2AMEN1PTPN7MAPTTDP1
SCHEMBL13839483 0.77 CDC25B (0.50) KMT2AMEN1TDP1GAAL3MBTL1
SCHEMBL13839558 0.75 HPGD (0.51) KMT2AMEN1MAPTGAACYP1A2
SCHEMBL8487523 0.74 NCOA1 (0.42) KMT2AMEN1PTPN7MAPTTDP1
SCHEMBL13839545 0.74 MEN1 (0.50) KMT2AMEN1CNR2CYP1A2ALDH1A1
SCHEMBL14016499 0.73 ALOX5 (0.40) KMT2AMEN1PTPN7MAPTTDP1
SCHEMBL13839462 0.73 CYP1A2 (0.42) KMT2AMEN1MAPTTDP1GAA

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