SCHEMBL256712

SCHEMBL256712

CSc1cccc(Nc2ncc3cc(-c4c(Cl)cccc4Cl)c(=O)n(C)c3n2)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FGFR1 P11362 12/20 1.00
SRC P12931 12/20 1.00
ABL1 P00519 11/20 1.00
EGFR P00533 10/20 1.00
PDGFRB P09619 10/20 1.00
PDGFRA P16234 10/20 1.00
MAPK14 Q16539 10/20 1.00
KIT P10721 4/20 1.00
FGFR2 P21802 2/20 1.00
FGFR4 P22455 2/20 1.00
FGFR3 P22607 2/20 1.00
WEE1 P30291 2/20 1.00
RIPK2 O43353 2/20 1.00
ACVR1 Q04771 2/20 1.00
BMPR1B O00238 1/20 1.00
STK25 O00506 1/20 1.00
GAK O14976 1/20 1.00
EPHB6 O15197 1/20 1.00
JAK2 O60674 1/20 1.00
STK10 O94804 1/20 1.00

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
SCHEMBL29468190 1.00 FGFR1 (1.00) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL29571986 1.00 FGFR1 (1.00) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL22681324 0.91 FGFR1 (0.84) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL20033384 0.91 FGFR1 (0.84) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL18813993 0.91 FGFR1 (0.84) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL23879897 0.88 FGFR1 (0.79) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL1249524 0.88 FGFR1 (1.00) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL2252904 0.88 FGFR1 (0.78) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL13498143 0.87 FGFR1 (0.83) FGFR1SRCABL1EGFRPDGFRB
SCHEMBL5762318 0.86 FGFR1 (1.00) FGFR1SRCABL1EGFRPDGFRB

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 182 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230149415-A1 METHODS AND COMPOSITIONS FOR TREATING CANCER ENGINE BIOSCIENCES PTE. LTD. (SG) 2023-05-18 US claimed
WO-2020242910-A1 COMPOSITIONS AND METHODS FOR TREATING CANCER THE REGENTS OF THE UNIVERSITY OFCALIFORNIA (US) 2020-12-03 WO claimed
EP-2233174-B1 Compositions and use of tyrosine kinase inhibitors to treat pathogenic infection UNIV EMORY (US) 2016-07-20 EP claimed
US-20080220497-A1 Modulation of protein functionalities DECIPHERA PHARMACEUTICALS LLC 2008-09-11 US claimed
EP-1907411-A2 MODULATION OF PROTEIN FUNCTIONALITIES Deciphera Pharmaceuticals, LLC. (US) 2008-04-09 EP claimed
EP-1835934-A2 ENZYME MODULATORS AND TREATMENTS Deciphera Pharmaceuticals, LLC (US) 2007-09-26 EP claimed
US-20070078121-A1 Enzyme modulators and treatments DECIPHERA PHARMACEUTICALS, LLC 2007-04-05 US claimed
EP-1744735-A2 METHOD OF TREATMENT OF MYOCARDIAL INFARCTION The Scripps Research Institute (US) 2007-01-24 EP claimed
WO-2007008917-A2 MODULATION OF PROTEIN FUNCTIONALITIES DECIPHERA PHARMACEUTICALS, LLC (US) 2007-01-18 WO claimed
WO-2006071940-A2 ENZYME MODULATORS AND TREATMENTS DECIPHERA PHARMACEUTICALS, LLC (US) 2006-07-06 WO claimed
JP-2005533604-A 2005-11-10 JP claimed
WO-2005089366-A2 METHOD OF TREATMENT OF MYOCARDIAL INFARCTION THE SCRIPPS RESEARCH INSTITUTE (US) 2005-09-29 WO claimed
US-20050203612-A1 Luminal prostheses which allow for programmed and controlled delivery of mycophenolic acid or derivatives with increased efficacy to selected locations within a patient's vasculature to inhibit restenosis and hyperplasia AVANTEC VASCULAR CORPORATION (US) 2005-09-15 US claimed
EP-1539041-A1 DEVICES DELIVERING THERAPEUTIC AGENTS AND METHODS REGARDING THE SAME Avantec Vascular Corporation (US) 2005-06-15 EP claimed
WO-2005051229-A2 DEVICES DELIVERING THERAPEUTIC AGENTS AND METHODS REGARDING THE SAME AVANTEC VASCULAR CORPORATION (US) 2005-06-09 WO claimed
US-20050125054-A1 Devices delivering therapeutic agents and methods regarding the same AVANTEC VASCULAR CORPORATION (US) 2005-06-09 US claimed
US-20040214836-A1 Method of treatment of myocardial infarction NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-10-28 US claimed
WO-2004010900-A1 DEVICES DELIVERING THERAPEUTIC AGENTS AND METHODS REGARDING THE SAME AVANTEC VASCULAR CORPORATION (US) 2004-02-05 WO claimed
WO-2026087699-A1 NEW TREATMENT OF NON-SMALL CELL LUNG CANCER PIERRE FABRE MEDICAMENT (FR) 2026-04-30 WO disclosed
WO-2004010900-A1 DEVICES DELIVERING THERAPEUTIC AGENTS AND METHODS REGARDING THE SAME AVANTEC VASCULAR CORPORATION (US) 2004-02-05 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 (3 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-20040214836-A1 Method of treatment of myocardial infarction SRC, LCK, DSTYK FGFR1 914/4885SRC 1/4885ABL1 5/4885
US-20080220497-A1 Modulation of protein functionalities C1QBP, SERPINA6, CD2BP2 FGFR1 4698/4885SRC 2604/4885ABL1 3158/4885
US-20070078121-A1 Enzyme modulators and treatments ABL1, ABL2, LCK FGFR1 118/4885SRC 9/4885ABL1 1/4885

“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.