SCHEMBL9961322

SCHEMBL9961322

[C-]#[N+]/C(C#N)=C1/C(C)=Cc2cc3c(cc21)C=C(C)/C3=C(/C#N)[N+]#[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
SCHEMBL11891080 0.79 MEN1 (0.33) —
SCHEMBL10028802 0.72 MEN1 (0.34) —
SCHEMBL11910087 0.70 — —
SCHEMBL9961318 0.69 USP8 (0.33) —
SCHEMBL9961320 0.67 USP8 (0.32) —
SCHEMBL18975441 0.67 — —
SCHEMBL11891076 0.66 LMNA (0.34) —
SCHEMBL15686201 0.66 — —
SCHEMBL11910095 0.66 MEN1 (0.31) —
SCHEMBL12111054 0.66 KMT2A (0.34) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8624232-B2 Ambipolar polymeric semiconductor materials and organic electronic devices AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2014-01-07 — — US disclosed
US-8431680-B2 Semiconductor materials based on thienothiophene-2,5-dione oligomers and polymers BASF SE (DE) 2013-04-30 — — US disclosed
US-20120296058-A1 SEMICONDUCTOR MATERIALS BASED ON THIENOTHIOPHENE-2,5-DIONE OLIGOMERS AND POLYMERS BASF SE (DE) 2012-11-22 — — US disclosed
US-20120153274-A1 AMBIPOLAR POLYMERIC SEMICONDUCTOR MATERIALS AND ORGANIC ELECTRONIC DEVICES AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2012-06-21 — — US disclosed
Send feedback