SCHEMBL1385899

SCHEMBL1385899

CCc1ccc(Nc2ncc(CCc3ccnc(OC)c3)c3ccccc23)cc1Br

nearest known ligand 0.36

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
▸ EGFR P00533 4/20 0.36
▸ CYP1A2 P05177 1/20 0.36
▸ GAA P10253 1/20 0.36
▸ SMN1; SMN2 Q16637 1/20 0.36
▸ NR3C2 P08235 1/20 0.36
▸ PTK6 Q13882 2/20 0.35
▸ LOX P28300 1/20 0.34
▸ LOXL2 Q9Y4K0 1/20 0.34
▸ PLA2G7 Q13093 1/20 0.34
▸ MAPT P10636 3/20 0.34
▸ KDR P35968 3/20 0.33
▸ PDGFRB P09619 2/20 0.33
▸ KIT P10721 2/20 0.33
▸ FLT1 P17948 2/20 0.33
▸ TNF P01375 2/20 0.33
▸ TP53 P04637 1/20 0.33
▸ ABCG2 Q9UNQ0 1/20 0.33
▸ ERBB4 Q15303 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
SCHEMBL4824885 0.87 KDR (0.36) EGFRCYP1A2GAASMN1; SMN2NR3C2
SCHEMBL1386144 0.87 NR3C2 (0.34) EGFRCYP1A2GAASMN1; SMN2NR3C2
SCHEMBL1386555 0.82 MEN1 (0.39) EGFRCYP1A2MAPTKDRFLT1
SCHEMBL1929579 0.81 KDR (0.52) EGFRPTK6KDRPDGFRBKIT
SCHEMBL1386333 0.81 MAPT (0.36) EGFRCYP1A2GAASMN1; SMN2MAPT
SCHEMBL1383073 0.80 CCNK (0.35) EGFRCYP1A2GAASMN1; SMN2NR3C2
SCHEMBL1383615 0.79 KDR (0.48) EGFRPTK6MAPTKDRFLT1
SCHEMBL13955593 0.79 FLT1 (0.43) EGFRSMN1; SMN2PTK6MAPTKDR
SCHEMBL1383596 0.75 KDR (0.38) EGFRMAPTKDRFLT1TNF
SCHEMBL4832143 0.74 MEN1 (0.36) EGFR

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 EGFR 15/4885CYP1A2 269/4885GAA 1930/4885
US-20030158409-A1 Pyridine derivatives inhibiting angiogenesis and/or vegf receptor tyrosine kinase FLT1, FLT4, KDR EGFR 12/4885CYP1A2 374/4885GAA 1666/4885

“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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