SCHEMBL9915852

SCHEMBL9915852

CCN1C(=O)C(=Cc2cc(OC)c(/C=C/c3cc(OC)c(/C=C/c4cc(OC)c(C=C5C(=O)N(CC)C(=S)N(CC)C5=O)cc4OC)cc3OC)cc2OC)C(=O)N(CC)C1=S

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 9/20 0.51
MEN1 O00255 8/20 0.51
KMT2A Q03164 8/20 0.51
ALDH1A1 P00352 7/20 0.51
HTT P42858 3/20 0.51
KDM4E B2RXH2 4/20 0.48
LMNA P02545 3/20 0.48
TNFRSF1A P19438 6/20 0.46
HPGD P15428 3/20 0.46
POLB P06746 2/20 0.46
MAPK1 P28482 2/20 0.46
NPC1 O15118 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
ENPP3 O14638 1/20 0.42
NPSR1 Q6W5P4 2/20 0.42
MDM2 Q00987 3/20 0.41
THRB P10828 1/20 0.40
KDM4C Q9H3R0 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
PDE4B Q07343 2/20 0.39

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
SCHEMBL9915864 0.90 MEN1 (0.49) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL13559205 0.74 MEN1 (0.53) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL14712993 0.73 MEN1 (0.57) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL13559209 0.73 MEN1 (0.42) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL9329273 0.70 PDE4B (0.42) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL29165202 0.69 TNFRSF1A (0.50) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL30788739 0.69 TNFRSF1A (0.62) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL15592638 0.68 MAPT (0.63) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL10014431 0.67 MAPT (0.53) MAPTMEN1KMT2AALDH1A1HTT
SCHEMBL11149658 0.66 TNFRSF1A (0.56) MAPTMEN1KMT2AALDH1A1HTT

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-8197722-B2 Irradiating the compound (containing two electron donor groups and a bridge of pi-conjugated bonds containing electron donor groups) with light, and the compound is converted to a multi-photon electronically excited state THE CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2012-06-12 US disclosed