SCHEMBL7148663

SCHEMBL7148663

CN1C=CC(C2(Cl)c3ccc([nH]3)C(c3ccccc3)=C3C=CC(=N3)C(c3ccccc3)=c3ccc([nH]3)=C(c3ccccc3)C3=NC2(Cl)C=C3)=CC1

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
SCHEMBL7149929 0.96 — —
SCHEMBL7147334 0.96 — —
SCHEMBL5947696 0.95 — —
SCHEMBL8182068 0.88 — —
SCHEMBL8182744 0.88 — —
SCHEMBL8182556 0.87 — —
SCHEMBL8184161 0.84 — —
SCHEMBL9641187 0.83 — —
SCHEMBL3190937 0.83 — —
SCHEMBL8183373 0.79 — —

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-1347679-A1 METHOD OF INACTIVATING VIRAL PARTICLES IN A BLOOD PRODUCT Photobiochem N.V. (NL) 2003-10-01 — — EP disclosed
WO-2002030190-A1 METHOD OF INACTIVATING VIRAL PARTICLES IN A BLOOD PRODUCT PHOTOBIOCHEM N.V. (NL) 2002-04-18 — — WO disclosed
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