Triaziquone

Triaziquone

SCHEMBL9750708

CCCl.O=C1C=C(N2CC2)C(=O)C(N2CC2)=C1N1CC1.O=P(O)(O)O

nearest known ligand 0.37

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Triaziquone. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
TP53 P04637 1/20 0.37
MAPT P10636 1/20 0.37
STAT3 P40763 1/20 0.37
HTT P42858 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
DNMT1 P26358 1/20 0.36
NSD2 O96028 2/20 0.33
TTR P02766 1/20 0.33
APAF1 O14727 1/20 0.30
TDP2 O95551 1/20 0.30
HKDC1 Q2TB90 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
Triaziquone SCHEMBL62271 0.90 DNMT1 (0.42) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL3903553 0.90 DNMT1 (0.42) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL6225692 0.89 TP53 (0.38) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL10680234 0.89 DNMT1 (0.41) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL2146169 0.88 TP53 (0.37) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL21805756 0.87 MAPT (0.39) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL21625776 0.87 MAPT (0.41) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL9678206 0.85 DNMT1 (0.39) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL11350903 0.85 HTT (0.42) TP53MAPTSTAT3HTTSMN1; SMN2
Triaziquone SCHEMBL20994184 0.85 TP53 (0.36) TP53MAPTSTAT3HTTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5028355-A Conductive polyurethane foam containing picric acid and analog thereof CREST-FOAM CORPORATION (US) 1991-07-02 US disclosed
EP-0316446-A4 IMPROVED CONDUCTIVE POLYURETHANE FOAM COMPOSITIONS AND METHOD 1991-03-20 EP disclosed
US-4886626-A REDUCTION OF ELECTRICAL RESISTANCE CREST-FOAM CORPORATION (US) 1989-12-12 US disclosed
EP-0316446-A1 IMPROVED CONDUCTIVE POLYURETHANE FOAM COMPOSITIONS AND METHOD CREST-FOAM Corp. (US) 1989-05-24 EP disclosed
WO-1988009350-A1 IMPROVED CONDUCTIVE POLYURETHANE FOAM COMPOSITIONS AND METHOD CREST-FOAM COPORATION (US) 1988-12-01 WO disclosed