SCHEMBL180417

SCHEMBL180417

C1=NC=C2ON=NC=C2N1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL9839360 0.53 — —
SCHEMBL9384920 0.50 — —
SCHEMBL3188857 0.50 — —
SCHEMBL442655 0.41 — —
SCHEMBL26660960 0.25 — —
SCHEMBL25434707 0.20 — —
SCHEMBL5134016 0.20 — —
SCHEMBL6559802 0.20 — —
SCHEMBL11498741 0.20 — —
SCHEMBL157229 0.20 — —

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 44 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9896730-B2 Use of EMT gene signatures in cancer drug discovery, diagnostics, and treatment OSI Pharmaceuticals, LLC (US) 2018-02-20 — — US disclosed
EP-2702173-A1 USE OF EMT GENE SIGNATURES IN CANCER DRUG DISCOVERY, DIAGNOSTICS, AND TREATMENT OSI Pharmaceuticals, LLC (US) 2014-03-05 — — EP disclosed
US-20140057352-A1 METHODS FOR THE IDENTIFICATION OF AGENTS THAT INHIBIT MESENCHYMAL-LIKE TUMOR CELLS OR THEIR FORMATION OSI PHARMACEUTICALS LLC (US) 2014-02-27 — — US disclosed
US-8642834-B2 Methods for the identification of agents that inhibit mesenchymal-like tumor cells or their formation OSI Pharmaceuticals, LLC (US) 2014-02-04 — — US disclosed
WO-2013152252-A1 COMBINATION ANTI-CANCER THERAPY OSI Pharmaceuticals, LLC (US) 2013-10-10 — — WO disclosed
US-20130210026-A1 BIOLOGICAL MARKERS PREDICTIVE OF ANTI-CANCER RESPONSE TO KINASE INHIBITORS OSI Pharmaceuticals, LLC 2013-08-15 — — US disclosed
US-8465912-B2 Methods for the identification of agents that inhibit mesenchymal-like tumor cells or their formation OSI Pharmaceuticals, LLC (US) 2013-06-18 — — US disclosed
US-8377636-B2 Biological markers predictive of anti-cancer response to kinase inhibitors OSI Pharmaceuticals, LLC (US) 2013-02-19 — — US disclosed
US-20120302572-A1 USE OF EMT GENE SIGNATURES IN CANCER DRUG DISCOVERY, DIAGNOSTICS, AND TREATMENT AVEO PHARMACEUTICALS, INC. (US) 2012-11-29 — — US disclosed
WO-2012149014-A1 USE OF EMT GENE SIGNATURES IN CANCER DRUG DISCOVERY, DIAGNOSTICS, AND TREATMENT OSI Pharmaceuticals, LLC (US) 2012-11-01 — — WO disclosed
EP-1565475-B1 DIAZINOPYRIMIDINES AND THEIR USE AS PROTEIN KINASE INHIBITORS HOFFMANN LA ROCHE (CH) 2009-04-08 — — EP disclosed
WO-2009009016-A1 COMBINATION ANTI-CANCER THERAPY OSI PHARMACEUTICALS, INC. (US) 2009-01-15 — — WO disclosed
WO-2009008992-A2 COMBINATION ANTI-CANCER THERAPY COMPRISING AN INHIBITOR OF BOTH MTORC1 AND MT0RC2 OSI PHARMACEUTICALS INC. (US) 2009-01-15 — — WO disclosed
US-20080312260-A1 Biological markers predictive of anti-cancer response to kinase inhibitors HALEY JOHN D 2008-12-18 — — US disclosed
WO-2008127719-A1 BIOLOGICAL MARKERS PREDICTIVE OF ANTI-CANCER RESPONSE TO KINASE INHIBITORS OSI PHARMACEUTICALS, INC. (US) 2008-10-23 — — WO disclosed
US-20050261284-A1 Diazinopyrimidines CHEN JIAN J 2005-11-24 — — US disclosed
US-6943158-B2 Diazinopyrimidines ROCHE PALO ALTO LLC (US) 2005-09-13 — — US disclosed
EP-1565475-A1 DIAZINOPYRIMIDINES F. HOFFMANN-LA ROCHE AG (CH) 2005-08-24 — — EP disclosed
WO-2004046152-A1 DIAZINOPYRIMIDINES F. HOFFMANN LA ROCHE AG (CH) 2004-06-03 — — WO disclosed
US-20040097493-A1 For preparing medicaments useful for the therapy of the p38 MAP kinase and FGFR kinase mediated diseases and conditions HOFFMANN-LA ROCHE INC. 2004-05-20 — — US disclosed
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