SCHEMBL1385761

SCHEMBL1385761

Oc1cc(CCc2cnc(Nc3cc(Cl)cc(C(F)(F)F)c3)c3ccccc23)ccn1

nearest known ligand 0.39

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ KDR P35968 7/20 0.39
▸ FLT1 P17948 6/20 0.39
▸ HDAC3 O15379 1/20 0.37
▸ HDAC1 Q13547 1/20 0.37
▸ HDAC2 Q92769 1/20 0.37
▸ HDAC6 Q9UBN7 1/20 0.37
▸ NAMPT P43490 1/20 0.35
▸ EGFR P00533 2/20 0.35
▸ ABCG2 Q9UNQ0 2/20 0.35
▸ TSHR P16473 1/20 0.34
▸ HTT P42858 1/20 0.34
▸ RAPGEF3 O95398 1/20 0.34
▸ NR3C2 P08235 2/20 0.34
▸ CTSC P53634 1/20 0.34
▸ BRAF P15056 1/20 0.34
▸ PDGFRB P09619 1/20 0.33
▸ KIT P10721 1/20 0.33
▸ RAPGEF4 Q8WZA2 1/20 0.33
▸ RAF1 P04049 1/20 0.33

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
SCHEMBL1382827 0.87 EGFR (0.48) KDRFLT1EGFRABCG2TSHR
SCHEMBL1383596 0.86 KDR (0.38) KDRFLT1HDAC3HDAC1HDAC2
SCHEMBL1385235 0.85 NAMPT (0.46) KDRFLT1HDAC3HDAC1HDAC2
SCHEMBL1383679 0.82 RAPGEF4 (0.38) KDRFLT1HDAC3HDAC1HDAC2
SCHEMBL1386811 0.77 KDR (0.44) KDRFLT1NAMPTEGFRABCG2
SCHEMBL1383615 0.74 KDR (0.48) KDRFLT1EGFRABCG2TSHR
SCHEMBL1383724 0.73 KDR (0.53) KDRFLT1NAMPTEGFRABCG2
SCHEMBL1386144 0.73 NR3C2 (0.34) KDRFLT1HDAC3HDAC1HDAC6
SCHEMBL1384331 0.72 NAMPT (0.36) KDRFLT1NAMPTNR3C2PDGFRB
SCHEMBL1383042 0.71 KIF11 (0.53) KDRFLT1NAMPTEGFRABCG2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-4837864-B2 — — 2011-12-14 — — JP claimed
US-7323474-B2 Pyridine derivatives inhibiting angiogenesis and/or VEGF receptor tyrosine kinase NOVARTIS AG (CH) 2008-01-29 — — US claimed
EP-1254138-B1 PYRIDINE DERIVATIVES INHIBITING ANGIOGENESIS AND/OR VEGF RECEPTOR TYROSINE KINASE NOVARTIS AG (CH) 2005-05-11 — — EP claimed
US-20040209894-A1 Pyridine derivatives inhibiting angiogenesis and/or VEGF receptor tyrosine kinase BOLD GUIDO 2004-10-21 — — US claimed
US-6706731-B2 WITH ISOQUINOLINE DERIVATIVES AS ANTITUMOR AGENTS NOVARTIS AG (CH) 2004-03-16 — — US claimed
US-20030158409-A1 Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase NOVARTIS AG (CH) 2003-08-21 — — US claimed
EP-1254138-A1 PYRIDINE DERIVATIVES INHIBITING ANGIOGENESIS AND/OR VEGF RECEPTOR TYROSINE KINASE Novartis AG (CH) 2002-11-06 — — EP claimed
WO-2001058899-A1 PYRIDINE DERIVATIVES INHIBITING ANGIOGENESIS AND/OR VEGF RECEPTOR TYROSINE KINASE NOVARTIS AG (CH) 2001-08-16 — — WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20040209894-A1 Pyridine derivatives inhibiting angiogenesis and/or VEGF receptor tyrosine kinase FLT1, FLT4, KDR KDR 3/4885FLT1 1/4885HDAC3 3237/4885
US-20030158409-A1 Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase FLT1, FLT4, KDR KDR 3/4885FLT1 1/4885HDAC3 3113/4885

“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.

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