SCHEMBL16466926

SCHEMBL16466926

CCN(CC)CCNC(=O)c1c(C)[nH]c(C=C2C(=O)Nc3ccc(C(=O)O)cc32)c1C

nearest known ligand 0.80

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 14/20 0.80
PRKAA1 Q13131 13/20 0.80
PRKAA2 P54646 12/20 0.80
PDGFRB P09619 5/20 0.80
FGFR1 P11362 4/20 0.80
EGFR P00533 3/20 0.80
GRK5 P34947 3/20 0.80
FLT3 P36888 3/20 0.80
PLK4 O00444 2/20 0.80
DCLK1 O15075 2/20 0.80
PDPK1 O15530 2/20 0.80
DAPK3 O43293 2/20 0.80
ROCK2 O75116 2/20 0.80
RPS6KA5 O75582 2/20 0.80
RPS6KA4 O75676 2/20 0.80
MAP4K4 O95819 2/20 0.80
CHEK2 O96017 2/20 0.80
NTRK1 P04629 2/20 0.80
INSR P06213 2/20 0.80
LCK P06239 2/20 0.80

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
SCHEMBL16466924 1.00 KDR (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL31672467 0.93 PRKAA1 (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL2115444 0.93 PRKAA1 (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL13755240 0.93 PRKAA1 (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL19726319 0.93 KDR (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL16111834 0.92 KDR (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL16111830 0.92 KDR (0.80) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL12336826 0.92 KDR (0.77) KDRPRKAA1PRKAA2PDGFRBFGFR1
SCHEMBL15202704 0.90 KDR (0.84) KDRPRKAA1PRKAA2PDGFRBFGFR1
Sunitinib SCHEMBL2726689 0.90 KDR (0.88) KDRPRKAA1PRKAA2PDGFRBFGFR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9458463-B2 Method for treatment of diabetes by a small molecule inhibitor for GRK5 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2016-10-04 US claimed
WO-2015022437-A1 INDOLINONE DERIVATIVES AS GRK5 MODULATORS MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2015-02-19 WO claimed
EP-2837626-A1 Indolinone derivatives as GRK5 modulators Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2015-02-18 EP claimed
US-9458463-B2 Method for treatment of diabetes by a small molecule inhibitor for GRK5 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2016-10-04 US disclosed
US-20150079108-A1 KINASES AS TARGETS FOR ANTI-DIABETIC THERAPY MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2015-03-19 US disclosed
WO-2015022437-A1 INDOLINONE DERIVATIVES AS GRK5 MODULATORS MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2015-02-19 WO disclosed
EP-2837626-A1 Indolinone derivatives as GRK5 modulators Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2015-02-18 EP 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 (1 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-20150079108-A1 KINASES AS TARGETS FOR ANTI-DIABETIC THERAPY GCKR, GRK4, GRK5 KDR 1123/4885PRKAA1 205/4885PRKAA2 148/4885

“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.