SCHEMBL15624230

SCHEMBL15624230

C[n+]1ccc(/C=C/c2ccc(-n3c4ccc(/C=C/c5ccncc5)cc4c4cc(/C=C/c5cc[n+](C)cc5)ccc43)cc2)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CHAT P28329 5/20 0.46
▸ RAB9A P51151 8/20 0.42
▸ MEN1 O00255 6/20 0.42
▸ KMT2A Q03164 6/20 0.42
▸ POLB P06746 4/20 0.42
▸ USP2 O75604 3/20 0.42
▸ GPR55 Q9Y2T6 2/20 0.42
▸ NOD2 Q9HC29 1/20 0.42
▸ SMN1; SMN2 Q16637 5/20 0.42
▸ ALDH1A1 P00352 4/20 0.42
▸ MAPT P10636 4/20 0.42
▸ GLA P06280 1/20 0.42
▸ HPGD P15428 3/20 0.40
▸ KDM4E B2RXH2 2/20 0.40
▸ CYP2C19 P33261 2/20 0.40
▸ NPC1 O15118 4/20 0.39
▸ RXFP1 Q9HBX9 1/20 0.39
▸ LMNA P02545 1/20 0.38
▸ ALPG P10696 1/20 0.38
▸ THRB P10828 1/20 0.38

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
SCHEMBL15624214 0.94 CHAT (0.46) CHATRAB9AMEN1KMT2APOLB
SCHEMBL15624213 0.92 CHAT (0.49) CHATRAB9AMEN1KMT2APOLB
SCHEMBL17890335 0.89 MAPT (0.44) RAB9AMEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL17890333 0.89 MAPT (0.44) RAB9AMEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL17905913 0.85 CHAT (0.54) CHATRAB9AMEN1KMT2APOLB
SCHEMBL17890344 0.81 KDM4E (0.43) RAB9AMEN1KMT2APOLBSMN1; SMN2
SCHEMBL31258284 0.81 KDM4E (0.43) RAB9AMEN1KMT2APOLBSMN1; SMN2
SCHEMBL17890345 0.81 KDM4E (0.43) RAB9AMEN1KMT2APOLBSMN1; SMN2
SCHEMBL10256978 0.77 CHAT (0.61) CHATRAB9AMEN1KMT2ASMN1; SMN2
Iodide SCHEMBL28417346 0.76 CHAT (0.56) CHATRAB9AMEN1KMT2AUSP2

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
WO-2014044757-A1 CATIONIC TRIPHENYLAMINE DERIVATIVES ACTIVABLE BY VISIBLE AND INFRA RED LIGHT FOR INDUCING AND IMAGING APOPTOSIS IN CANCER CELLS INSTITUT CURIE (FR) 2014-03-27 — — WO disclosed
EP-2711366-A1 Cationic triphenylamine derivatives activable by visible and Infra Red light for inducing and imaging apoptosis in cancer cells Institut Curie (FR) 2014-03-26 — — EP disclosed
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