SCHEMBL13839558

SCHEMBL13839558

COc1ccc(C(=O)c2ccccc2OP(Oc2ccccc2)Oc2ccccc2)c(OP(Oc2ccccc2)Oc2ccccc2)c1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 4/20 0.51
LMNA P02545 4/20 0.51
CYP1A2 P05177 3/20 0.51
CYP2C19 P33261 3/20 0.51
PGR P06401 2/20 0.51
SLC6A2 P23975 2/20 0.51
CYP3A4 P08684 2/20 0.51
ADORA3 P0DMS8 1/20 0.51
AR P10275 1/20 0.51
CHRM1 P11229 1/20 0.51
ALOX15 P16050 1/20 0.51
TBXA2R P21731 1/20 0.51
ADRA1A P35348 1/20 0.51
HIF1A Q16665 1/20 0.51
NPC1 O15118 4/20 0.49
MEN1 O00255 4/20 0.47
KMT2A Q03164 4/20 0.47
POLB P06746 2/20 0.47
ALDH1A1 P00352 3/20 0.47
HTT P42858 2/20 0.47

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
SCHEMBL13839518 0.97 NPC1 (0.51) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839550 0.90 NPC1 (0.54) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13841151 0.89 HPGD (0.51) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13841191 0.89 HPGD (0.51) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839517 0.89 NPC1 (0.55) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839548 0.88 NPC1 (0.49) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839526 0.88 HPGD (0.50) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839528 0.87 TAS1R3 (0.49) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839553 0.86 CYP1A2 (0.47) HPGDLMNACYP1A2CYP2C19PGR
SCHEMBL13839500 0.86 NPC1 (0.49) HPGDLMNACYP1A2CYP2C19PGR

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