SCHEMBL5203211

SCHEMBL5203211

Cc1cc(C)c(C=C2C(=O)Nc3ccc(O)cc32)[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDPK1 O15530 5/20 1.00
KDR P35968 4/20 1.00
RET P07949 10/20 0.77
PDGFRB P09619 3/20 0.76
FLT3 P36888 4/20 0.73
ALK Q9UM73 4/20 0.73
TLK2 Q86UE8 1/20 0.72
CSF1R P07333 2/20 0.70
FGFR1 P11362 2/20 0.70
SRC P12931 2/20 0.70
FLT1 P17948 2/20 0.70
FGFR3 P22607 2/20 0.70
MAPK1 P28482 2/20 0.70
FLT4 P35916 2/20 0.70
ABL1 P00519 2/20 0.70
NTRK1 P04629 2/20 0.70
MEN1 O00255 1/20 0.70
NPC1 O15118 1/20 0.70
GMNN O75496 1/20 0.70
USP2 O75604 1/20 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
SCHEMBL5478517 1.00 PDPK1 (1.00) PDPK1KDRRETPDGFRBFLT3
SCHEMBL17480337 0.90 KDR (0.80) PDPK1KDRRETPDGFRBFLT3
SCHEMBL13081086 0.87 RET (1.00) PDPK1KDRRETPDGFRBFLT3
SCHEMBL5475962 0.84 PDGFRB (0.81) PDPK1KDRRETPDGFRBFLT3
SCHEMBL29394706 0.84 RET (1.00) PDPK1KDRRETPDGFRBFLT3
SCHEMBL31726696 0.84 RET (0.76) PDPK1KDRRETPDGFRBFLT3
SCHEMBL5475963 0.84 PDGFRB (0.81) PDPK1KDRRETPDGFRBFLT3
SCHEMBL19979 0.84 RET (1.00) PDPK1KDRRETPDGFRBFLT3
SCHEMBL19978 0.84 RET (1.00) PDPK1KDRRETPDGFRBFLT3
SCHEMBL4416658 0.84 RET (1.00) PDPK1KDRRETPDGFRBFLT3

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 25 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
EP-1680401-A2 INDOLINONE DERIVATIVES AND THEIR USE IN TREATING DISEASE-STATES SUCH AS CANCER Schering Aktiengesellschaft (DE) 2006-07-19 EP claimed
WO-2005058309-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES LEO PHARMA A/S (DK) 2005-06-30 WO claimed
WO-2005040116-A2 INDOLINONE DERIVATIVES AND THEIR USE IN TREATING DISEASE-STATES SUCH AS CANCER SCHERING AKTIENGESELLSCHAFT (DE) 2005-05-06 WO claimed
US-20050090541-A1 Indolinone derivatives and their use in treating disease-states such as cancer SCHERING AKTIENGESELLSCHAFT (DE) 2005-04-28 US 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
US-20070167488-A1 Novel therapeutic use LEO PHARMA A/S (DK) 2007-07-19 US disclosed
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 disclosed
US-7105563-B2 Indolinone derivatives and their use in treating disease-states such as cancer SCHERING AKTIENGESELLSCHAFT (DE) 2006-09-12 US disclosed
EP-1696906-A1 NOVEL THERAPEUTIC USE OF INDOLINONE DERIVATIVES Leo Pharma A/S (DK) 2006-09-06 EP disclosed
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 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
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
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 (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-20050090541-A1 Indolinone derivatives and their use in treating disease-states such as cancer PDK3, PDK2, PDK4 PDPK1 4/4885KDR 2521/4885RET 1754/4885
US-20070167488-A1 Novel therapeutic use MAG, PMP22, MYT1 PDPK1 1635/4885KDR 4334/4885RET 3720/4885
US-20030073837-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY DCK, TNK2, MKNK1 PDPK1 4/4885KDR 2091/4885RET 882/4885
US-20030191162-A1 3-heteroarylidenyl-2-indolinone compounds for modulating protein kinase activity and for use in cancer chemotherapy DCK, TNK2, MKNK1 PDPK1 4/4885KDR 2091/4885RET 882/4885

“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.