BUTYROLACETONE 3
BUTYROLACETONE 3 Basic information
- Product Name:
- BUTYROLACETONE 3
- Synonyms:
-
- GCN5 INHIBITOR 1
- BUTYROLACETONE 3
- Butyrolactone 3
- 3-Furancarboxylic acid, tetrahydro-4-methylene-5-oxo-2-propyl-, (2R,3S)-rel-
- CAS:
- 778649-18-6
- MF:
- C9H12O4
- MW:
- 184.19
- Product Categories:
-
- Heterocycles
- Inhibitors
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Heterocycles, Inhibitors, Pharmaceuticals, Intermediates & Fine Chemicals
- Mol File:
- 778649-18-6.mol
BUTYROLACETONE 3 Chemical Properties
- storage temp.
- -20°C
- solubility
- ≤14mg/ml in ethanol;14mg/ml in DMSO;13mg/ml in dimethyl formamide
- form
- powder
- color
- white to off-white
- Stability:
- Light Sensitive
BUTYROLACETONE 3 Usage And Synthesis
Uses
Butyrolactone 3 is a selective inhibitor of histone acetyltransferase Gcn5 with affinity for the enzyme comparable to its natural substrate. Butyrolactone 3 is very useful tool in understanding and further studying the histone code.
Definition
ChEBI: (2S,3R)-4-methylene-5-oxo-2-propyl-3-oxolanecarboxylic acid is a gamma-lactone.
in vitro
the analogs of butyrolactone 3 only showed a weak inhibition of cbp, while butyrolactone 3 led to an inhibition of gcn5. it was important to see that in the presence of acetyl-coa the kd value for binding of histone h3 to gcn5 or pcaf was around 100 mm. moreover, the affinity of butyrolactone 3 to the gcn5 enzyme was found to be comparable to that of the natural substrate h3 and could provide an good starting point for the study of sar. in addition, a nonirreversible inhibition of gcn5 could be determine, and thus a michael addition of nucleophilic groups of the enzymebs active side was unlikely. therefore, the derivatization of gbutyrolactone 3 at position 2 might be a promising starting point for future sar studies [1].
IC 50
100 μm
References
1. m. biel, a. kretsovali, e. karatzali, et al. design, synthesis, and biological evaluation of a small-molecule inhibitor of the histone acetyltransferase gcn5. angewandte chemie international edition 43, 3974-3976 (2004).
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