SCHEMBL1838470

SCHEMBL1838470

O=C(Nc1nc2ccc(Sc3cnc4ncccn34)cc2s1)C1CCOCC1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CASP3 P42574 1/20 0.45
SENP8 Q96LD8 1/20 0.45
SENP7 Q9BQF6 1/20 0.45
SENP6 Q9GZR1 1/20 0.45
ABL1 P00519 6/20 0.44
MAOA P21397 1/20 0.43
MAOB P27338 1/20 0.43
RIPK1 Q13546 2/20 0.43
NPC1 O15118 4/20 0.43
RAB9A P51151 4/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
GFER P55789 1/20 0.43
MET P08581 1/20 0.42
HSP90AA1 P07900 1/20 0.42
KIT P10721 1/20 0.42
PDGFRA P16234 1/20 0.42
LMNA P02545 2/20 0.41
CLK1 P49759 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
SCHEMBL1841257 0.95 CASP3 (0.50) CASP3SENP8SENP7SENP6ABL1
SCHEMBL2544077 0.88 MET (0.45) NPC1RAB9AMEN1KMT2ASMN1; SMN2
SCHEMBL2539011 0.88 NPC1 (0.42) CASP3SENP8SENP7SENP6ABL1
SCHEMBL2542595 0.85 ALDH1A1 (0.57) NPC1RAB9AMEN1KMT2ASMN1; SMN2
SCHEMBL2538170 0.85 PIK3CA (0.49) NPC1RAB9ASMN1; SMN2DYRK1A
SCHEMBL27818351 0.84 LCK (0.45) ABL1MEN1KMT2ASMN1; SMN2MET
SCHEMBL2540992 0.84 ALDH1A1 (0.48) MEN1KMT2ASMN1; SMN2LMNACLK1
SCHEMBL2544044 0.84 MET (0.48) ABL1RAB9AMEN1KMT2ASMN1; SMN2
SCHEMBL1842687 0.82 MET (0.62) ABL1METDYRK1A
SCHEMBL1836150 0.82 MAPT (0.42) NPC1RAB9AMEN1KMT2ASMN1; SMN2

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-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
EP-2318414-A2 IMIDAZO [1,2-A] PYRIMIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION, USE AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND USE AS MET INHIBITORS Sanofi-Aventis (FR) 2011-05-11 EP disclosed
WO-2010007318-A2 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) 2010-01-21 WO 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 CASP3 3573/4885SENP8 2677/4885SENP7 3564/4885

“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.