SCHEMBL13839600

SCHEMBL13839600

Cc1ccccc1OP(Oc1ccccc1C)Oc1cccc2c1C(=O)c1c(OP(Oc3ccccc3C)Oc3ccccc3C)cccc1C2=O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ELANE P08246 6/20 0.49
▸ EGFR P00533 1/20 0.43
▸ PIM1 P11309 1/20 0.43
▸ RAB9A P51151 3/20 0.41
▸ NPC1 O15118 2/20 0.41
▸ TSHR P16473 2/20 0.41
▸ HPGD P15428 2/20 0.41
▸ KMT2A Q03164 4/20 0.41
▸ MEN1 O00255 3/20 0.41
▸ ALDH1A1 P00352 5/20 0.40
▸ MAPT P10636 4/20 0.40
▸ SMN1; SMN2 Q16637 3/20 0.40
▸ KCNA3 P22001 1/20 0.40
▸ LMNA P02545 2/20 0.40
▸ HTT P42858 2/20 0.40
▸ CTSG P08311 1/20 0.40
▸ APAF1 O14727 1/20 0.40
▸ MITF O75030 1/20 0.40
▸ MAPK1 P28482 2/20 0.39
▸ CASP3 P42574 2/20 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
SCHEMBL13839610 0.84 EGFR (0.54) ELANEEGFRPIM1RAB9ANPC1
SCHEMBL13839613 0.82 KCNA3 (0.51) ELANEEGFRPIM1RAB9ATSHR
SCHEMBL13839572 0.81 KMT2A (0.41) ELANERAB9ANPC1TSHRHPGD
SCHEMBL13839601 0.81 KCNA3 (0.43) ELANEEGFRPIM1RAB9ATSHR
SCHEMBL13839617 0.80 ELANE (0.40) ELANEEGFRPIM1RAB9ANPC1
SCHEMBL13839602 0.80 EGFR (0.40) ELANEEGFRPIM1RAB9ANPC1
SCHEMBL13839607 0.79 ALDH1A1 (0.52) ELANEEGFRPIM1RAB9ATSHR
SCHEMBL29405565 0.78 TSHR (0.46) RAB9ANPC1TSHRHPGDKMT2A
SCHEMBL215848 0.78 TSHR (0.46) RAB9ANPC1TSHRHPGDKMT2A
SCHEMBL27387712 0.78 TSHR (0.46) RAB9ANPC1TSHRHPGDKMT2A

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
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