SCHEMBL378979

SCHEMBL378979

CCOC(=O)c1c(C)[nH]c(/C=C2\C(=O)Nc3ccccc32)c1C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FGFR1 P11362 6/20 1.00
FLT3 P36888 6/20 1.00
PDGFRB P09619 5/20 1.00
RET P07949 5/20 1.00
ALK Q9UM73 5/20 1.00
ABL1 P00519 2/20 1.00
KDR P35968 11/20 0.67
PRKAA1 Q13131 2/20 0.63
PRKAA2 P54646 1/20 0.63
FLT1 P17948 4/20 0.61
CSF1R P07333 4/20 0.61
FLT4 P35916 4/20 0.61
AURKA O14965 3/20 0.61
MAP4K2 Q12851 3/20 0.61
STK3 Q13188 3/20 0.61
AURKB Q96GD4 3/20 0.61
FGFR3 P22607 3/20 0.61
ZAP70 P43403 2/20 0.61
PLK4 O00444 2/20 0.61
PDPK1 O15530 2/20 0.61

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
SCHEMBL6001446 1.00 FGFR1 (1.00) FGFR1FLT3PDGFRBRETALK
SCHEMBL5390359 1.00 FGFR1 (1.00) FGFR1FLT3PDGFRBRETALK
SCHEMBL19255670 0.87 PDGFRB (0.77) FGFR1FLT3PDGFRBRETALK
SCHEMBL5373629 0.86 PDGFRB (0.76) FGFR1FLT3PDGFRBRETALK
SCHEMBL6391018 0.85 PDGFRB (0.74) FGFR1FLT3PDGFRBRETALK
SCHEMBL6389339 0.85 PDGFRB (0.74) FGFR1FLT3PDGFRBRETALK
SCHEMBL5376617 0.85 PDGFRB (0.74) FGFR1FLT3PDGFRBRETALK
SCHEMBL5567713 0.85 ALK (0.76) FGFR1FLT3PDGFRBRETALK
SCHEMBL31727052 0.85 FLT3 (0.74) FGFR1FLT3PDGFRBRETALK
SCHEMBL31727096 0.85 PDGFRB (0.74) FGFR1FLT3PDGFRBRETALK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20170172989-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS BAYER HEALTHCARE LLC (US) 2017-06-22 US claimed
US-20100173954-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS BAYER HEALTHCARE LLC (US) 2010-07-08 US claimed
EP-2114403-A2 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS Bayer Healthcare, LLC (US) 2009-11-11 EP claimed
WO-2008089388-A2 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS BAYER HEALTHCARE LLC (US) 2008-07-24 WO claimed
US-20070167488-A1 Novel therapeutic use LEO PHARMA A/S (DK) 2007-07-19 US claimed
EP-1696906-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES Leo Pharma A/S (DK) 2006-09-06 EP claimed
WO-2005058309-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES LEO PHARMA A/S (DK) 2005-06-30 WO claimed
US-5792783-A CAPABLE OF MODULATING TYROSINE KINASE SIGNAL TRANSDUCTION IN ORDER TO REGULATE, MODULATE AND/OR INHIBIT ABNORMAL CELL PROLIFERATION SUGEN, INC. (US) 1998-08-11 US claimed
WO-2017133517-A1 PHOSPHAMIDE DERIVATIVE, METHOD FOR MANUFACTURING THE SAME, AND USES THEREOF 四川海思科制药有限公司 2017-08-10 WO disclosed
US-20170172989-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS BAYER HEALTHCARE LLC (US) 2017-06-22 US disclosed
US-9439961-B2 Pharmaceutical composition for treating ischemic events NIIGATA UNIVERSITY (JP) 2016-09-13 US disclosed
US-20140127233-A1 PHARMACEUTICAL COMPOSITION FOR TREATING ISCHEMIC EVENTS NIIGATA UNIVERSITY (JP) 2014-05-08 US disclosed
US-20120295965-A1 FUSED THIOPHENES AS DUAL INHIBITORS OF EGFR/VEGFR AND THEIR USE IN THE TREATMENT OF CANCER CORNING INCORPORATED 2012-11-22 US disclosed
EP-1981851-B1 KINASE INHIBITORS AND METHODS OF USE THEREOF ARRAY BIOPHARMA INC (US) 2012-01-25 EP disclosed
EP-1981851-A1 KINASE INHIBITORS AND METHODS OF USE THEREOF Array Biopharma, Inc. (US) 2008-10-22 EP disclosed
WO-2008089388-A2 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS BAYER HEALTHCARE LLC (US) 2008-07-24 WO disclosed
WO-2007089646-A1 KINASE INHIBITORS AND METHODS OF USE THEREOF ARRAY BIOPHARMA INC. (US) 2007-08-09 WO disclosed
US-20070167488-A1 Novel therapeutic use LEO PHARMA A/S (DK) 2007-07-19 US disclosed
EP-1696906-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES Leo Pharma A/S (DK) 2006-09-06 EP disclosed
WO-2005058309-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES LEO PHARMA A/S (DK) 2005-06-30 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 (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-20170172989-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS CDK4, TP53, ABCC1 FGFR1 350/4885FLT3 526/4885PDGFRB 2508/4885
US-20070167488-A1 Novel therapeutic use MAG, PMP22, MYT1 FGFR1 4752/4885FLT3 4311/4885PDGFRB 4421/4885
US-20120295965-A1 FUSED THIOPHENES AS DUAL INHIBITORS OF EGFR/VEGFR AND THEIR USE IN THE TREATMENT OF CANCER EGFR, ERBB2, KDR FGFR1 21/4885FLT3 30/4885PDGFRB 13/4885
US-20100173954-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS CDK4, TP53, ABCC1 FGFR1 350/4885FLT3 526/4885PDGFRB 2508/4885

“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.