SCHEMBL13839656

SCHEMBL13839656

O=P(c1ccccc1)(c1ccccc1OP(Oc1cccnc1)Oc1cccnc1)c1ccccc1OP(Oc1cccnc1)Oc1cccnc1

nearest known ligand 0.43

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.39
POLB P06746 1/20 0.39
HTT P42858 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.38
KCNA5 P22460 7/20 0.38
KCNN4 O15554 4/20 0.38
MAPK1 P28482 1/20 0.36
HSD17B10 Q99714 1/20 0.36
NPSR1 Q6W5P4 1/20 0.36
LMNA P02545 3/20 0.34
NOTUM Q6P988 1/20 0.33
NAMPT P43490 1/20 0.33
CYP11B1 P15538 1/20 0.33
CYP11B2 P19099 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
NPC1 O15118 1/20 0.33
TP53 P04637 1/20 0.33
RECQL P46063 1/20 0.33
RAB9A P51151 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 0.86 ALDH1A1 (0.46) ALDH1A1POLBHTTNPSR1LMNA
SCHEMBL13839655 0.76 ALDH1A1 (0.43) ALDH1A1POLBHTTKCNA5NPSR1
SCHEMBL13839650 0.76 ALDH1A1 (0.40) ALDH1A1POLBHTTHSD17B10NPSR1
SCHEMBL13839653 0.75 KMT2A (0.47) ALDH1A1POLBHTTSMN1; SMN2MAPK1
SCHEMBL13839642 0.75 POLB (0.44) ALDH1A1POLBHTTSMN1; SMN2NPSR1
SCHEMBL1449085 0.74 LMNA (0.54) ALDH1A1HTTSMN1; SMN2LMNACYP11B1
SCHEMBL13839491 0.73 ALDH1A1 (0.47) ALDH1A1POLBHTTSMN1; SMN2MAPK1
SCHEMBL13839643 0.73 HTT (0.43) ALDH1A1POLBHTTSMN1; SMN2MAPK1
SCHEMBL14424039 0.72 ALDH1A1 (0.42) ALDH1A1POLBHTTMAPK1HSD17B10
SCHEMBL13841234 0.72 SRC (0.44) ALDH1A1POLBHTTSMN1; SMN2NPSR1

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