Golvatinib

Golvatinib

SCHEMBL4249254

Br.CN1CCN(C2CCN(C(=O)Nc3cc(Oc4ccc(NC(=O)C5(C(=O)Nc6ccc(F)cc6)CC5)c(F)c4)ccn3)CC2)CC1

nearest known ligand 0.99

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

KDRMET

The experimentally established mechanism targets of Golvatinib. 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
MET known ✓ P08581 10/20 0.99
KDR known ✓ P35968 8/20 0.99
NTRK1 P04629 2/20 0.99
EPHB6 O15197 1/20 0.99
RIPK2 O43353 1/20 0.99
ABL1 P00519 1/20 0.99
LCK P06239 1/20 0.99
LYN P07948 1/20 0.99
RET P07949 1/20 0.99
HCK P08631 1/20 0.99
PDGFRB P09619 1/20 0.99
BCR P11274 1/20 0.99
EPHA2 P29317 1/20 0.99
EPHB2 P29323 1/20 0.99
FLT3 P36888 1/20 0.99
ABL2 P42684 1/20 0.99
FRK P42685 1/20 0.99
LIMK1 P53667 1/20 0.99
EPHB3 P54753 1/20 0.99
EPHA5 P54756 1/20 0.99

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
Golvatinib SCHEMBL30498608 0.99 MET (1.00) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL1727298 0.99 MET (1.00) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL30498607 0.99 MET (1.00) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL1727167 0.99 MET (0.99) METKDRNTRK1EPHB6RIPK2
SCHEMBL2250771 0.97 MET (0.96) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL4245713 0.96 MET (0.94) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL4251976 0.95 MET (0.92) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL4248644 0.95 MET (0.92) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL4248648 0.95 MET (0.92) METKDRNTRK1EPHB6RIPK2
Golvatinib SCHEMBL1728754 0.95 MET (0.92) METKDRNTRK1EPHB6RIPK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2062886-A1 SALT OF PHENOXYPYRIDINE DERIVATIVE OR CRYSTAL THEREOF AND PROCESS FOR PRODUCING THE SAME Eisai R&D Management Co., Ltd. (JP) 2009-05-27 EP disclosed
US-20080318924-A1 PHENOXYPYRIDINE DERIVATIVE SALTS AND CRYSTALS THEREOF, AND PROCESS FOR PREPARING THE SAME EISAI R&D MANAGEMENT CO., LTD (JP) 2008-12-25 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 (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-20080318924-A1 PHENOXYPYRIDINE DERIVATIVE SALTS AND CRYSTALS THEREOF, AND PROCESS FOR PREPARING THE SAME HGF, MET, FLT1 MET 2/4885KDR 9/4885NTRK1 206/4885

“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.