SCHEMBL2114209

SCHEMBL2114209

Cc1cc(C(=O)O)[nH]c1/C=C1\C(=O)Nc2ccccc21

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 11/20 0.73
FLT1 P17948 5/20 0.70
FGFR1 P11362 5/20 0.70
RET P07949 5/20 0.70
PDGFRB P09619 5/20 0.70
FLT3 P36888 4/20 0.70
CSF1R P07333 3/20 0.70
SRC P12931 3/20 0.70
FGFR3 P22607 3/20 0.70
FLT4 P35916 3/20 0.70
ALK Q9UM73 3/20 0.70
AURKA O14965 3/20 0.70
MAP4K2 Q12851 3/20 0.70
STK3 Q13188 3/20 0.70
AURKB Q96GD4 3/20 0.70
PDPK1 O15530 3/20 0.70
MAPK1 P28482 2/20 0.70
ZAP70 P43403 2/20 0.70
PLK4 O00444 2/20 0.70
JAK2 O60674 2/20 0.70

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
SCHEMBL31672504 1.00 KDR (0.73) KDRFLT1FGFR1RETPDGFRB
SCHEMBL2114210 1.00 KDR (0.73) KDRFLT1FGFR1RETPDGFRB
SCHEMBL2117299 0.87 KDR (0.80) KDRFLT1FGFR1RETPDGFRB
SCHEMBL2117305 0.87 KDR (0.80) KDRFLT1FGFR1RETPDGFRB
SCHEMBL5465253 0.85 KDR (1.00) KDRFLT1FGFR1RETPDGFRB
SCHEMBL5465247 0.85 KDR (1.00) KDRFLT1FGFR1RETPDGFRB
SCHEMBL2114990 0.84 RET (0.72) KDRFLT1FGFR1RETPDGFRB
SCHEMBL2114988 0.84 RET (0.72) KDRFLT1FGFR1RETPDGFRB
SCHEMBL3797925 0.84 RET (0.72) KDRFLT1FGFR1RETPDGFRB
SCHEMBL3797926 0.84 RET (0.72) KDRFLT1FGFR1RETPDGFRB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070167488-A1 Novel therapeutic use LEO PHARMA A/S (DK) 2007-07-19 US claimed
EP-1259234-B9 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN INC (US) 2007-02-14 EP claimed
EP-1696906-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES Leo Pharma A/S (DK) 2006-09-06 EP claimed
EP-1259234-B1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN INC (US) 2006-08-16 EP claimed
WO-2005058309-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES LEO PHARMA A/S (DK) 2005-06-30 WO claimed
US-20030191162-A1 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy SUGEN INC. 2003-10-09 US claimed
US-20030073837-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN, INC. 2003-04-17 US claimed
EP-1259234-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY Sugen, Inc. (US) 2002-11-27 EP claimed
WO-2001049287-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN, INC. (US) 2001-07-12 WO claimed
EP-3789027-A1 BOSUTINIB, SUNITINIB, TIVOZANIB, IMATINIB, NILOTINIB, REBASTINIB OR BAFETINIB FOR PREVENTING AND/OR TREATING AMYOTROPHIC LATERAL SCLEROSIS KYOTO UNIVERSITY (JP) 2021-03-10 EP disclosed
US-20180000771-A1 AGENT FOR PREVENTING AND/OR TREATING AMYOTROPHIC LATERAL SCLEROSIS KYOTO UNIVERSITY (JP) 2018-01-04 US disclosed
US-20180000771-A1 AGENT FOR PREVENTING AND/OR TREATING AMYOTROPHIC LATERAL SCLEROSIS KYOTO UNIVERSITY (JP) 2018-01-04 US disclosed
US-20120094998-A1 Oligomer-Protein Tyrosine Kinase Inhibitor Conjugates NEKTAR THERAPEUTICS (US) 2012-04-19 US disclosed
WO-2010120387-A1 OLIGOMER-PROTEIN TYROSINE KINASE INHIBITOR CONJUGATES NEKTAR THERAPEUTICS (US) 2010-10-21 WO disclosed
US-20030100555-A1 Prodrugs of a 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives SUGEN. INC. 2003-05-29 US disclosed
US-20030073837-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN, INC. 2003-04-17 US disclosed
WO-2003015608-A2 COMBINATION THERAPY FOR THE TREATMENT OF CANCER SUGEN, INC. (US) 2003-02-27 WO disclosed
EP-1259234-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY Sugen, Inc. (US) 2002-11-27 EP disclosed
US-20020156292-A1 Pyrrole substituted 2-indolinone protein kinase inhibitors PHARMACIA & UPJOHN COMPANY LLC 2002-10-24 US disclosed
WO-2001049287-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN, INC. (US) 2001-07-12 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 (7 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-20180000771-A1 AGENT FOR PREVENTING AND/OR TREATING AMYOTROPHIC LATERAL SCLEROSIS WEE2, WEE1, ERBB2 KDR 648/4885FLT1 659/4885FGFR1 48/4885
US-20030100555-A1 Prodrugs of a 3-(pyrrol-2-ylmethylidene)-2-indolinone derivatives PLK2, CDK2, PDPK1 KDR 1081/4885FLT1 1354/4885FGFR1 1037/4885
US-20070167488-A1 Novel therapeutic use MAG, PMP22, MYT1 KDR 4334/4885FLT1 4247/4885FGFR1 4752/4885
US-20030073837-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY DCK, TNK2, MKNK1 KDR 2091/4885FLT1 2549/4885FGFR1 1576/4885
US-20120094998-A1 Oligomer-Protein Tyrosine Kinase Inhibitor Conjugates PTK2B, ERBB2, FRK KDR 395/4885FLT1 305/4885FGFR1 462/4885
US-20030191162-A1 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy DCK, TNK2, MKNK1 KDR 2091/4885FLT1 2549/4885FGFR1 1576/4885
US-20020156292-A1 Pyrrole substituted 2-indolinone protein kinase inhibitors PDPK1, MAP3K20, PLK2 KDR 1372/4885FLT1 1532/4885FGFR1 1091/4885

“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.