SCHEMBL2156185

SCHEMBL2156185

NC(=O)NN(C(=O)Nc1ccc(Cl)cc1)c1ccc([N+](=O)[O-])cc1Cl

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 8/20 0.47
SMN1; SMN2 Q16637 3/20 0.47
NPC1 O15118 2/20 0.47
RAB9A P51151 1/20 0.47
MCL1 Q07820 1/20 0.47
KMT2A Q03164 8/20 0.47
MEN1 O00255 6/20 0.47
HTT P42858 3/20 0.47
GAA P10253 3/20 0.45
PKM P14618 2/20 0.45
ALDH1A1 P00352 2/20 0.44
CNR1 P21554 2/20 0.44
PTGES O14684 1/20 0.43
POLB P06746 1/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42
CA9 Q16790 1/20 0.42
FLT1 P17948 1/20 0.41

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
SCHEMBL2156773 0.77 MAPT (0.47) MAPTSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL2156952 0.73 GAA (0.52) MAPTSMN1; SMN2NPC1RAB9AKMT2A
Urea SCHEMBL2156179 0.72 KMT2A (0.69) MAPTSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL28099900 0.72 KMT2A (0.51) MAPTSMN1; SMN2NPC1RAB9AMCL1
SCHEMBL4956157 0.70 KMT2A (0.74) MAPTSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL18147432 0.69 RORC (0.80) MAPTSMN1; SMN2NPC1RAB9AMCL1
SCHEMBL18825691 0.68 MEN1 (0.82) MAPTSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL1102071 0.66 KMT2A (0.71) MAPTSMN1; SMN2NPC1RAB9AKMT2A
SCHEMBL28044831 0.66 MAPT (0.84) MAPTSMN1; SMN2NPC1RAB9AMCL1
SCHEMBL2061203 0.65 P2RX1 (0.71) MAPTSMN1; SMN2NPC1RAB9AKMT2A

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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7973034-B2 Ameliorating toxic effects of such as cancer therapy drugs or addictive drug overdose ST. JUDE CHILDREN'S RESEARCH HOSPITAL (US) 2011-07-05 US disclosed
US-20080146548-A1 AMIDE, ARYL SULFONAMIDE, ARYL UREA, AND a,b-DIKETONE DERIVED CARBOXYLESTERASE INHIBITORS, AND THEIR METHODS OF USE ST. JUDE CHILDREN'S RESEARCH HOSPITAL (US) 2008-06-19 US disclosed
US-20050054691-A1 Carboxylesterase inhibitors ST. JUDE CHILDREN'S RESEARCH HOSPITAL (US) 2005-03-10 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050054691-A1 Carboxylesterase inhibitors CES1, CES2, BCHE MAPT 3726/4885SMN1; SMN2 4443/4885NPC1 1377/4885
US-20080146548-A1 AMIDE, ARYL SULFONAMIDE, ARYL UREA, AND a,b-DIKETONE DERIVED CARBOXYLESTERASE INHIBITORS, AND THEIR METHODS OF USE CES1, BCHE, CES2 MAPT 4046/4885SMN1; SMN2 3998/4885NPC1 2012/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.