SCHEMBL413640

SCHEMBL413640

[2H]OC1[C@@H](COP(OCC[N+]#[C-])N(C(C)C)C(C)C)O[C@@H](B)[C@H]1O[Si](C)(C)C(C)(C)C

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
SCHEMBL12920231 1.00 — —
SCHEMBL12583011 0.88 — —
SCHEMBL12920244 0.83 — —
SCHEMBL12990156 0.77 — —
SCHEMBL12931038 0.70 — —
SCHEMBL13818671 0.69 L3MBTL1 (0.33) —
SCHEMBL12583008 0.69 L3MBTL1 (0.33) —
SCHEMBL12583009 0.69 — —
SCHEMBL10311004 0.68 — —
SCHEMBL12931039 0.67 — —

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
US-20130072670-A1 RNA SYNTHESIS-PHOSPHORAMIDITES FOR SYNTHETIC RNA IN THE REVERSE DIRECTION, AND APPLICATION IN CONVENIENT INTRODUCTION OF LIGANDS, CHROMOPHORES AND MODIFICATIONS OF SYNTHETIC RNA AT THE 3'-END CHEMGENES CORPORATION (US) 2013-03-21 — — US disclosed
US-20120065386-A1 SYNTHESIS OF LABILE BASE PROTECTED - MODIFIED DEOXY &amp; MODIFIED RIBO NUCLEOSIDES, CORRESPONDING PHOSPHORAMIDITES AND SUPPORTS AND THEIR USE IN HIGH PURITY OLIGONUCLEOTIDE SYNTHESIS CHEMGENES CORPORATION 2012-03-15 — — US disclosed
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