Phosphine

Phosphine

SCHEMBL3755463

C=Cc1ccccn1.P

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

⚠ 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
SCHEMBL9359592 0.97 MEN1 (0.67)
SCHEMBL15193 0.97
SCHEMBL29371456 0.97
SCHEMBL11734134 0.95
Iodide SCHEMBL10987591 0.95 MEN1 (0.64)
Iodide SCHEMBL1274592 0.95
Iodide SCHEMBL10987579 0.95 MEN1 (0.64)
SCHEMBL17201491 0.95
SCHEMBL8716225 0.95 MEN1 (0.64)
SCHEMBL7621695 0.95

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-8604201-B2 Use of cyclovinyl phosphine/copper complexes as arylation catalysts CENTRE NATIONAL DE RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) 2013-12-10 US disclosed
US-20100298569-A1 USE OF CYCLOVINYL PHOSPHINE/COPPER COMPLEXES AS ARYLATION CATALYSTS CENTRE NATIONAL DE RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) 2010-11-25 US disclosed