SCHEMBL12294163

SCHEMBL12294163

[C-]#[N+]/C(C(=O)O)=C1/C=C(C)OC(/C=C/c2ccc(N(c3ccccc3)c3ccc(-c4ccc(N(c5ccccc5)c5ccc(/C=C/C6=C/C(=C(\C#N)C(=O)O)C=C(C)O6)cc5)cc4)cc3)cc2)=C1

nearest known ligand 0.38

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.32
SLC16A3 O15427 1/20 0.31
SLC16A1 P53985 1/20 0.31
CTDSP1 Q9GZU7 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL12328173 0.92 MAPT (0.36) MAPTSLC16A3SLC16A1CTDSP1
SCHEMBL12294112 0.89 CTDSP1 (0.37) MAPTSLC16A3SLC16A1CTDSP1
SCHEMBL14331474 0.80 CTDSP1 (0.35) MAPTCTDSP1
SCHEMBL5448210 0.78 RELA (0.34) MAPTSLC16A3SLC16A1CTDSP1
SCHEMBL5448209 0.78 RELA (0.34) MAPTSLC16A3SLC16A1CTDSP1
SCHEMBL440302 0.78 KDM4E (0.37) MAPTCTDSP1
SCHEMBL12294115 0.77 SLC16A3 (0.35) MAPTSLC16A3SLC16A1CTDSP1
SCHEMBL10058508 0.77 MEN1 (0.38) MAPTSLC16A3SLC16A1CTDSP1
SCHEMBL13931184 0.76 SLC16A3 (0.32) SLC16A3SLC16A1
SCHEMBL12327832 0.74 SLC16A3 (0.33) MAPTSLC16A3SLC16A1CTDSP1

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-8022293-B2 Using oxide semiconductor particles sensitized with an N,N,N*,N*-tetraphenyl-p-phenylenediamine derivative methine dye; solar cells with high stability and conversion efficiency NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2011-09-20 US disclosed
US-20080067476-A1 Dye-Sensitized Photoelectic Conversion Devices NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2008-03-20 US disclosed