SCHEMBL2061609

SCHEMBL2061609

CNC(=O)c1cnn(C)c1N

nearest known ligand 0.44

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
MAPK14 Q16539 5/20 0.44
MAPK11 Q15759 2/20 0.44
POLB P06746 1/20 0.41
BAZ2B Q9UIF8 1/20 0.40
SMN1; SMN2 Q16637 2/20 0.39
NPC1 O15118 1/20 0.39
RAB9A P51151 1/20 0.39
ALDH1A1 P00352 1/20 0.39
SPR P35270 1/20 0.38
BRD4 O60885 1/20 0.36
GAA P10253 1/20 0.35
PROKR1 Q8TCW9 1/20 0.35
KDR P35968 1/20 0.35
ACACB O00763 1/20 0.35
CREBBP Q92793 1/20 0.35
LMNA P02545 1/20 0.34

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
SCHEMBL9921391 0.82 POLB (0.39) MAPK14MAPK11POLBSMN1; SMN2NPC1
SCHEMBL3902859 0.82 ALOX5 (0.45) MAPK14MAPK11POLBSMN1; SMN2NPC1
SCHEMBL353273 0.79 NPC1 (0.58) BAZ2BSMN1; SMN2NPC1RAB9AALDH1A1
SCHEMBL535661 0.79 KDM4E (0.44) MAPK14POLBSMN1; SMN2NPC1RAB9A
SCHEMBL11965637 0.79 MAPK1 (0.40) MAPK14POLBSMN1; SMN2NPC1RAB9A
SCHEMBL174225 0.79 RIPK2 (0.51) MAPK14POLBSMN1; SMN2NPC1RAB9A
SCHEMBL10452886 0.78 PROKR1 (0.35) MAPK14POLBSMN1; SMN2NPC1RAB9A
SCHEMBL3436120 0.78 CYP1A2 (0.51) NPC1RAB9AALDH1A1GAALMNA
SCHEMBL939409 0.77 NPC1 (0.52) POLBSMN1; SMN2NPC1RAB9AALDH1A1
SCHEMBL27714949 0.77 PROKR1 (0.39) MAPK14POLBSMN1; SMN2NPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2684874-B1 Fused bicyclic derivatives of 2,4-diaminopyrimidine as alk and C-met inhibitors CEPHALON INC (US) 2017-05-17 EP disclosed
EP-2222647-B1 FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND C-MET INHIBITORS CEPHALON INC (US) 2015-08-05 EP disclosed
EP-2684874-A1 Fused bicyclic derivatives of 2,4-diaminopyrimidine as alk and C-met inhibitors Cephalon, Inc. (US) 2014-01-15 EP disclosed
US-8552186-B2 Fused bicyclic derivatives of 2,4-diaminopyrimidine as ALK and c-MET inhibitors CEPHALON, INC. (US) 2013-10-08 US disclosed
US-20120165519-A1 Fused Bicyclic Derivatives of 2,4-Diaminopyrimidine as ALK and c-MET Inhibitors CEPHALON, INC. (US) 2012-06-28 US disclosed
US-8148391-B2 Fused bicyclic derivatives of 2,4-diaminopyrimidine as ALK and c-Met inhibitors CEPHALON, INC. (US) 2012-04-03 US disclosed
EP-2222647-A1 FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND C-MET INHIBITORS Cephalon, Inc. (US) 2010-09-01 EP disclosed
US-20090221555-A1 FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND c-MET INHIBITORS CEPHALON, INC. (US) 2009-09-03 US disclosed
WO-2008051547-A1 FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND C-MET INHIBITORS CEPHALON, INC. (US) 2008-05-02 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 (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-20090221555-A1 FUSED BICYCLIC DERIVATIVES OF 2,4-DIAMINOPYRIMIDINE AS ALK AND c-MET INHIBITORS ALK, MET, RET MAPK14 869/4885MAPK11 1098/4885POLB 2680/4885
US-20120165519-A1 Fused Bicyclic Derivatives of 2,4-Diaminopyrimidine as ALK and c-MET Inhibitors ALK, MET, RET MAPK14 869/4885MAPK11 1098/4885POLB 2680/4885

“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.