SCHEMBL691337

SCHEMBL691337

CNC(=O)c1ccccc1Nc1cc(Cl)ncc1Br

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPK10 P53779 5/20 0.51
MAPK8 P45983 1/20 0.51
ULK1 O75385 3/20 0.50
MAPK9 P45984 4/20 0.49
MAPK3 P27361 1/20 0.48
MAPK1 P28482 1/20 0.48
PTK2 Q05397 3/20 0.47
TYK2 P29597 5/20 0.46
JAK2 O60674 4/20 0.46
JAK1 P23458 4/20 0.46
PDE4D Q08499 1/20 0.43
CDK7 P50613 1/20 0.43
CDK9 P50750 1/20 0.43
MET P08581 1/20 0.42
ALK Q9UM73 1/20 0.42
FGFR1 P11362 1/20 0.42
FGFR2 P21802 1/20 0.42
FGFR4 P22455 1/20 0.42
FGFR3 P22607 1/20 0.42
EGFR P00533 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
Hydrochloric Acid SCHEMBL3405374 0.99 MAPK10 (0.50) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL690590 0.87 MAPK10 (0.65) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL1230901 0.87 MAPK10 (0.51) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL29777593 0.87 MAPK10 (0.65) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL719807 0.86 PTGS2 (0.50) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL12887553 0.86 MAPK10 (0.52) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL14068247 0.85 MAPK10 (0.49) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL13060634 0.85 MAPK10 (0.51) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL1558027 0.85 MAPK10 (0.51) MAPK10MAPK8ULK1MAPK9MAPK3
SCHEMBL3775946 0.82 ULK1 (0.51) MAPK10MAPK8ULK1MAPK9MAPK3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9446034-B2 Pyrazolylaminopyridines as inhibitors of FAK GLAXOSMITHKLINE LLC (US) 2016-09-20 US disclosed
US-20160095841-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2016-04-07 US disclosed
US-20150265589-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2015-09-24 US disclosed
US-9012479-B2 Pyrazolylaminopyridines as inhibitors of FAK GLAXOSMITHKLINE LLC (US) 2015-04-21 US disclosed
US-20140155410-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC (US) 2014-06-05 US disclosed
US-20140107131-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC (US) 2014-04-17 US disclosed
CN-102264371-B Pyrazolylaminopyridines as inhibitors of FAK GLAXOSMITHKLINE LLC 2013-10-02 CN disclosed
EP-2421537-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GlaxoSmithKline LLC (US) 2012-02-29 EP disclosed
CN-102264371-A Pyrazolylaminopyridines as inhibitors of fak 2011-11-30 CN disclosed
US-20110269774-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2011-11-03 US disclosed
US-20110207743-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2011-08-25 US disclosed
US-20100317663-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2010-12-16 US disclosed
US-20100317663-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2010-12-16 US disclosed
US-20100317663-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2010-12-16 US disclosed
EP-2249650-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK GlaxoSmithKline LLC (US) 2010-11-17 EP disclosed
WO-2010062578-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC (US) 2010-06-03 WO disclosed
US-20100113475-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK GLAXOSMITHKLINE LLC 2010-05-06 US disclosed
WO-2009105498-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK SMITHKLINE BEECHAM CORPORATION (US) 2009-08-27 WO disclosed
WO-2009105498-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK SMITHKLINE BEECHAM CORPORATION (US) 2009-08-27 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 (8 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-20100317663-A1 ANILINOPYRIDINES AS INHIBITORS OF FAK PTK2, JAK2, SRC MAPK10 386/4885MAPK8 779/4885ULK1 3788/4885
US-20110269774-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885
US-20160095841-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885
US-20150265589-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885
US-20100113475-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885
US-20110207743-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885
US-20140107131-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885
US-20140155410-A1 PYRAZOLYLAMINOPYRIDINES AS INHIBITORS OF FAK PTK2, PAK1, CTTN MAPK10 656/4885MAPK8 912/4885ULK1 2443/4885

“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.