Su-014813

Su-014813

SCHEMBL4500940

Cc1[nH]c(C=C2C(=O)Nc3ccc(F)cc32)c(C)c1C(=O)NC[C@@H](O)CN1CCOCC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FLT1FLT3FLT4KDRKITPDGFRAPDGFRB

The experimentally established mechanism targets of Su-014813. 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
KDR known ✓ P35968 13/20 1.00
PDGFRB known ✓ P09619 12/20 1.00
KIT known ✓ P10721 4/20 1.00
FLT1 known ✓ P17948 3/20 1.00
FLT4 known ✓ P35916 3/20 1.00
FLT3 known ✓ P36888 3/20 1.00
PDGFRA known ✓ P16234 2/20 1.00
FGFR1 P11362 8/20 1.00
PRKAA1 Q13131 8/20 1.00
PRKAA2 P54646 7/20 1.00
TLK2 Q86UE8 5/20 1.00
RIOK2 Q9BVS4 3/20 1.00
TLK1 Q9UKI8 3/20 1.00
RIPK1 Q13546 3/20 1.00
PLK4 O00444 3/20 1.00
DCLK1 O15075 3/20 1.00
PDPK1 O15530 3/20 1.00
DAPK3 O43293 3/20 1.00
ROCK2 O75116 3/20 1.00
RPS6KA5 O75582 3/20 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
Su-014813 SCHEMBL2334599 1.00 KDR (1.00) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL902507 1.00 KDR (1.00) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL4500929 1.00 KDR (1.00) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL2334610 1.00 KDR (1.00) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL1249521 1.00 KDR (1.00) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL30030129 0.96 KDR (0.93) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL3367375 0.96 KDR (0.93) KDRPDGFRBFGFR1PRKAA1PRKAA2
Su-014813 SCHEMBL3367367 0.96 KDR (0.93) KDRPDGFRBFGFR1PRKAA1PRKAA2
SCHEMBL13711974 0.92 PDGFRB (0.86) KDRPDGFRBFGFR1PRKAA1PRKAA2
SCHEMBL5527704 0.91 KDR (0.83) KDRPDGFRBFGFR1PRKAA1PRKAA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040152759-A1 Combination administration of an indolinone with a chemotherapeutic agent for cell proliferation disorders SUGEN, INC. 2004-08-05 US claimed
US-6653308-B2 Anticancer agents; antidiabetic agents; antiinflammatory agents SUGEN, INC. 2003-11-25 US claimed
US-7582756-B2 3-(4-amidopyrrol-2-ylmethylidene)-2-indolinone derivatives as protein kinase inhibitors SUGEN, INC. (US) 2009-09-01 US disclosed
EP-1536783-B1 SOLID FORMULATIONS COMPRISING AN INDOLINONE COMPOUND PFIZER ITALIA SRL (IT) 2008-08-06 EP disclosed
US-20080045709-A1 3-(4-AMIDOPYRROL-2-YLMETHYLIDENE)-2-INDOLINONE DERIVATIVES AS PROTEIN KINASE INHIBITORS SUGEN, INC. 2008-02-21 US disclosed
US-7256189-B2 3-(4-amidopyrrol-2-ylmethylidene)-2-indolinone der derivatives as protein kinase inhibitors SUGEN, INC. (US) 2007-08-14 US disclosed
US-7179910-B2 3-(4-amidopyrrol-2-ylmethlidene)-2-indolinone derivatives as protein kinase inhibitors AGOURON PHARMACEUTICALS, INC. (US) 2007-02-20 US disclosed
US-20070027149-A1 3-(4-amidopyrrol-2-ylmethylidene)-2-indolinone der derivatives as protein kinase inhibitors SUGEN, INC. 2007-02-01 US disclosed
US-7119209-B2 Process for preparing indolinone derivatives PHARMACIA & UPJOHN COMPANY (US) 2006-10-10 US disclosed
US-20050171357-A1 Process for preparing indolinone derivatives PHARMACIA & UPJOHN COMPANY 2005-08-04 US disclosed
EP-1476443-A2 PROCESS FOR PREPARING INDOLINONE DERIVATIVES PHARMACIA & UPJOHN COMPANY (US) 2004-11-17 EP disclosed
US-20040152759-A1 Combination administration of an indolinone with a chemotherapeutic agent for cell proliferation disorders SUGEN, INC. 2004-08-05 US disclosed
US-20030229229-A1 Process for preparing indolinone derivatives PHARMACIA & UPJOHN COMPANY 2003-12-11 US disclosed
US-6653308-B2 Anticancer agents; antidiabetic agents; antiinflammatory agents SUGEN, INC. 2003-11-25 US disclosed
WO-2003070725-A2 PROCESS FOR PREPARING INDOLINONE DERIVATIVES PHARMACIA & UPJOHN COMPANY (US) 2003-08-28 WO disclosed
US-20030130280-A1 Treatment of acute myeloid leukemia with indolinone compounds SUGEN, INC. 2003-07-10 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 (6 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-20050171357-A1 Process for preparing indolinone derivatives CYP2B6, CYP2D6, CYP3A4 KDR 3047/4885PDGFRB 1410/4885KIT 278/4885
US-20080045709-A1 3-(4-AMIDOPYRROL-2-YLMETHYLIDENE)-2-INDOLINONE DERIVATIVES AS PROTEIN KINASE INHIBITORS MAP4K2, MAP4K3, CDK2 KDR 762/4885PDGFRB 687/4885KIT 595/4885
US-20040152759-A1 Combination administration of an indolinone with a chemotherapeutic agent for cell proliferation disorders MKI67, CCNA1, CCNI KDR 3687/4885PDGFRB 3475/4885KIT 303/4885
US-20030130280-A1 Treatment of acute myeloid leukemia with indolinone compounds FLT3, FLI1, MCL1 KDR 71/4885PDGFRB 123/4885KIT 9/4885
US-20030229229-A1 Process for preparing indolinone derivatives CYP2B6, CYP2D6, CYP3A4 KDR 3047/4885PDGFRB 1410/4885KIT 278/4885
US-20070027149-A1 3-(4-amidopyrrol-2-ylmethylidene)-2-indolinone der derivatives as protein kinase inhibitors PDPK1, MAP4K2, MAP4K3 KDR 1334/4885PDGFRB 1062/4885KIT 1899/4885

“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.