SCHEMBL13868320

SCHEMBL13868320

CC1=CC(C)=C(C#N)C1

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
SCHEMBL8157414 0.64
SCHEMBL4652308 0.64
SCHEMBL1027102 0.64
SCHEMBL7051863 0.62
SCHEMBL9142020 0.61
SCHEMBL11586910 0.61
SCHEMBL20145982 0.61
SCHEMBL7002117 0.60
SCHEMBL14925894 0.59
SCHEMBL17581052 0.58

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7514563-B2 Producing cyano-substituted pyridine, pyrrole, furan, thiophene or benzene boranes by reacting a cyanoarene with a BH or a HBBH compound, especially 4,4,5,5-tetramethyl-1,3,2-dioxborolane or its dimer, in the presence of an organo-phosphorus or -nitrogen iridium complex; drug intermediates BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2009-04-07 US disclosed