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Literature summary for 2.3.1.48 extracted from

  • Costi, R.; Di Santo, R.; Artico, M.; Miele, G.; Valentini, P.; Novellino, E.; Cereseto, A.
    Cinnamoyl compounds as simple molecules that inhibit p300 histone acetyltransferase (2007), J. Med. Chem., 50, 1973-1977.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
1,7-bis(3-bromo-4-hydroxyphenyl)-1,6-heptadiene-3,5-dione
-
Homo sapiens
2,6-bis(3-bromo-4-hydroxybenzylidene)cyclohexanone
-
Homo sapiens
curcumin
-
Homo sapiens
Lys-CoA
-
Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
HeLa cell
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
HAT
-
Homo sapiens
histone acetyltransferase
-
Homo sapiens
p300
-
Homo sapiens

IC50 Value

IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
0.005
-
-
Homo sapiens 1,7-bis(3-bromo-4-hydroxyphenyl)-1,6-heptadiene-3,5-dione
0.03
-
-
Homo sapiens Lys-CoA
0.033
-
-
Homo sapiens 2,6-bis(3-bromo-4-hydroxybenzylidene)cyclohexanone
0.4
-
value above 0.4 Homo sapiens curcumin