SCHEMBL13839490

SCHEMBL13839490

O=C(c1ccccc1OP(Oc1ccccn1)Oc1ccccn1)c1ccccc1OP(Oc1ccccn1)Oc1ccccn1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 4/20 0.39
NPC1 O15118 2/20 0.39
KMT2A Q03164 2/20 0.39
MEN1 O00255 1/20 0.39
TP53 P04637 1/20 0.39
GAA P10253 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
ELANE P08246 1/20 0.39
KDM4E B2RXH2 2/20 0.37
SGMS2 Q8NHU3 1/20 0.36
CES2 O00748 1/20 0.35
CES1 P23141 1/20 0.35
CDK5 Q00535 1/20 0.35
CDK5R1 Q15078 1/20 0.35
GRM4 Q14833 1/20 0.35
ALDH1A1 P00352 1/20 0.35
CYP2C9 P11712 1/20 0.35
CYP2C19 P33261 1/20 0.35
HSD17B10 Q99714 1/20 0.35
LMNA P02545 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
SCHEMBL13839551 0.86 RAB9A (0.48) RAB9ANPC1KMT2AMEN1TP53
SCHEMBL13839520 0.82 RAB9A (0.50) RAB9ANPC1KMT2AMEN1KDM4E
SCHEMBL7629364 0.80 KDM4E (0.48) RAB9ANPC1KMT2AMEN1TP53
SCHEMBL13839465 0.74 KDM4E (0.37) KMT2AMEN1GAAKDM4ELMNA
SCHEMBL13839492 0.74 CTNNB1 (0.46) RAB9AKMT2AMEN1SMN1; SMN2ELANE
SCHEMBL14016572 0.74 KDM4E (0.38) KDM4E
SCHEMBL28012790 0.73 SRC (0.51) RAB9ANPC1KMT2AMEN1GAA
SCHEMBL14016487 0.73 KDM4E (0.36) NPC1KDM4EALDH1A1CYP2C19LMNA
SCHEMBL13839611 0.73 KCNA3 (0.40) RAB9AKMT2AMEN1GAASMN1; SMN2
SCHEMBL13839473 0.73 ELANE (0.47) RAB9AKMT2AMEN1ELANEKDM4E

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