Masitinib

Masitinib

SCHEMBL2297143

CS(=O)(=O)O.CS(=O)(=O)O.Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Nc1nc(-c2cccnc2)cs1

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FGFR3KITPDGFRAPDGFRB

The experimentally established mechanism targets of Masitinib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KIT known ✓ P10721 13/20 0.94
PDGFRA known ✓ P16234 4/20 0.94
PDGFRB known ✓ P09619 4/20 0.94
ABL1 P00519 19/20 0.94
BCR P11274 14/20 0.94
ABL2 P42684 7/20 0.94
SRC P12931 3/20 0.94
EGFR P00533 2/20 0.94
ERBB2 P04626 2/20 0.94
LCK P06239 2/20 0.94
FYN P06241 2/20 0.94
CSF1R P07333 2/20 0.94
LYN P07948 2/20 0.94
FGR P09769 2/20 0.94
BRAF P15056 2/20 0.94
NQO2 P16083 2/20 0.94
EPHA8 P29322 2/20 0.94
FRK P42685 2/20 0.94
BLK P51451 2/20 0.94
DDR1 Q08345 2/20 0.94

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
Masitinib SCHEMBL30024483 1.00 ABL1 (0.94) ABL1BCRKITABL2PDGFRA
Masitinib SCHEMBL1096348 1.00 ABL1 (0.94) ABL1BCRKITABL2PDGFRA
Masitinib SCHEMBL29353195 0.97 ABL1 (1.00) ABL1BCRKITABL2PDGFRA
Masitinib SCHEMBL29355443 0.97 ABL1 (1.00) ABL1BCRKITABL2PDGFRA
Masitinib SCHEMBL717239 0.97 ABL1 (1.00) ABL1BCRKITABL2PDGFRA
SCHEMBL5515053 0.93 ABL1 (0.84) ABL1BCRKITABL2PDGFRA
SCHEMBL3301373 0.93 ABL1 (0.91) ABL1BCRKITABL2PDGFRA
SCHEMBL16085058 0.91 ABL1 (0.89) ABL1BCRKITABL2PDGFRA
SCHEMBL717173 0.91 ABL1 (0.88) ABL1BCRKITABL2PDGFRA
SCHEMBL17177780 0.91 ABL1 (0.88) ABL1BCRKITABL2PDGFRA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140100215-A1 Methods of Using PI3K and MEK Modulators EXELIXIS, INC. (US) 2014-04-10 US disclosed
US-8642584-B2 Method of using PI3K and MEK modulators EXELIXIS, INC. (US) 2014-02-04 US disclosed
US-8450302-B2 2-(3-aminoaryl) amino-4-aryl-thiazoles and their use as c-kit inhibitors AB SCIENCE (FR) 2013-05-28 US disclosed
US-20120302545-A1 Method of Using PI3K and MEK Modulators EXELIXIS, INC. (US) 2012-11-29 US disclosed
US-20120302577-A1 TREATMENT OF GIST WITH MASITINIB AB SCIENCE (FR) 2012-11-29 US disclosed
US-20110201620-A1 2-(3-AMINOARYL) AMINO-4-ARYL-THIAZOLES AND THEIR USE AS C-KIT INHIBITORS AB SCIENCE (FR) 2011-08-18 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 (4 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-20110201620-A1 2-(3-AMINOARYL) AMINO-4-ARYL-THIAZOLES AND THEIR USE AS C-KIT INHIBITORS KIT, ABL1, MUSK KIT 1/4885PDGFRA 52/4885PDGFRB 89/4885
US-20140100215-A1 Methods of Using PI3K and MEK Modulators PIK3CA, PIK3CD, PIK3R1 KIT 711/4885PDGFRA 889/4885PDGFRB 683/4885
US-20120302545-A1 Method of Using PI3K and MEK Modulators PIK3CA, PIK3CD, PIK3R1 KIT 623/4885PDGFRA 1052/4885PDGFRB 779/4885
US-20120302577-A1 TREATMENT OF GIST WITH MASITINIB ABL1, KIT, MYLK KIT 2/4885PDGFRA 41/4885PDGFRB 86/4885

“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.