SCHEMBL2547101

SCHEMBL2547101

O=C(Nc1nc2ccc(Sc3cnc4ncccn34)cc2s1)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LRRK2 Q5S007 1/20 0.52
SCD O00767 8/20 0.49
SMN1; SMN2 Q16637 3/20 0.49
MAPT P10636 3/20 0.49
TP53 P04637 1/20 0.49
NPC1 O15118 4/20 0.49
RAB9A P51151 4/20 0.49
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
ABL1 P00519 1/20 0.48
OPRK1 P41145 2/20 0.47
HTT P42858 2/20 0.47
POLB P06746 1/20 0.47
PKM P14618 1/20 0.47
AGTR1 P30556 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
CASP3 P42574 1/20 0.45
SENP8 Q96LD8 1/20 0.45
SENP7 Q9BQF6 1/20 0.45
SENP6 Q9GZR1 1/20 0.45

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
SCHEMBL2538170 0.88 PIK3CA (0.49) SMN1; SMN2NPC1RAB9AHTTDYRK1A
SCHEMBL1841257 0.85 CASP3 (0.50) SMN1; SMN2NPC1RAB9AMEN1KMT2A
SCHEMBL1836150 0.85 MAPT (0.42) SMN1; SMN2MAPTTP53NPC1RAB9A
SCHEMBL1828695 0.85 MAPT (0.42) SMN1; SMN2MAPTTP53NPC1RAB9A
Hydrochloric Acid SCHEMBL2547151 0.84 MAPT (0.42) SMN1; SMN2MAPTTP53NPC1RAB9A
SCHEMBL2547102 0.83 NPC1 (0.46) SMN1; SMN2MAPTTP53NPC1RAB9A
SCHEMBL2540705 0.83 RAB9A (0.42) SMN1; SMN2MAPTTP53NPC1RAB9A
SCHEMBL2539011 0.82 NPC1 (0.42) SMN1; SMN2MAPTNPC1RAB9AMEN1
SCHEMBL1838470 0.82 CASP3 (0.45) SMN1; SMN2NPC1RAB9AMEN1KMT2A
SCHEMBL2543283 0.81 RAB9A (0.41) SMN1; SMN2MAPTTP53NPC1RAB9A

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-20110263593-A1 NOVEL IMIDAZO[1,2-a]PYRIMIDINE DERIVATIVES, METHOD FOR THE PREPARATION THEREOF, USE THEREOF AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND NOVEL USE, IN PARTICULAR AS MET INHIBITORS SANOFI-AVENTIS (FR) 2011-10-27 US claimed
US-20110263593-A1 NOVEL IMIDAZO[1,2-a]PYRIMIDINE DERIVATIVES, METHOD FOR THE PREPARATION THEREOF, USE THEREOF AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND NOVEL USE, IN PARTICULAR AS MET INHIBITORS SANOFI-AVENTIS (FR) 2011-10-27 US disclosed
CN-102159577-A Imidazo [1,2-a ] pyrimidine derivatives, process for their preparation, their use as medicaments, pharmaceutical compositions and as MET inhibitors SANOFI AVENTIS 2011-08-17 CN 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 (1 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-20110263593-A1 NOVEL IMIDAZO[1,2-a]PYRIMIDINE DERIVATIVES, METHOD FOR THE PREPARATION THEREOF, USE THEREOF AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND NOVEL USE, IN PARTICULAR AS MET INHIBITORS TPMT, MET, PAICS LRRK2 2321/4885SCD 4869/4885SMN1; SMN2 2888/4885

“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.