SCHEMBL13839636

SCHEMBL13839636

CC(C)c1ccccc1OP(Oc1ccccc1C(C)C)Oc1cccc2c1Oc1c(cccc1OP(Oc1ccccc1C(C)C)Oc1ccccc1C(C)C)C2

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NISCH Q9Y2I1 2/20 0.33
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
CYP1A2 P05177 2/20 0.33
CYP3A4 P08684 2/20 0.33
CYP2C9 P11712 1/20 0.33
CYP2C19 P33261 1/20 0.33
RECQL P46063 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
ADRA2A P08913 1/20 0.33
ADRA2B P18089 1/20 0.33
ADRA2C P18825 1/20 0.33
ADRB2 P07550 2/20 0.32
ADRB1 P08588 2/20 0.32
ADRB3 P13945 2/20 0.32
P2RX3 P56373 1/20 0.31
P2RX2 Q9UBL9 1/20 0.31
ALDH1A1 P00352 1/20 0.31
PLA2G1B P04054 1/20 0.31
ATG4B Q9Y4P1 1/20 0.31

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
SCHEMBL13839623 0.85 ATM (0.38) MEN1KMT2AL3MBTL1ALDH1A1LMNA
SCHEMBL13839629 0.81 CA12 (0.41) KMT2ACYP3A4L3MBTL1ALDH1A1CA1
SCHEMBL13839619 0.81 ALDH1A1 (0.35) MEN1KMT2AALDH1A1HPGDTSHR
SCHEMBL2861909 0.79 GABRA1 (0.43) NISCHMEN1KMT2ACYP1A2CYP3A4
SCHEMBL29636737 0.79 GABRA1 (0.43) NISCHMEN1KMT2ACYP1A2CYP3A4
SCHEMBL13839632 0.79 MAOA (0.33) MAOAMAOB
SCHEMBL13839595 0.79 KMT2A (0.38) NISCHMEN1KMT2ACYP1A2CYP3A4
SCHEMBL13839621 0.77 CYP1A2 (0.34) NISCHCYP1A2CYP2C19L3MBTL1ALDH1A1
SCHEMBL13839626 0.77 HTR1B (0.35) MEN1KMT2ACYP1A2CYP3A4CYP2C9
SCHEMBL13839620 0.75 HRH1 (0.35) ADRA2AADRA2BADRA2CLMNA

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