76808-16-7
Chemical Structure
Ebelactone A
- CAS No.: 76808-16-7
- Formula:C20H34O4
- Molecular Weight:338.48
IUPAC Name: (3S,4S)-4-((2S,6R,8S,9R,10R,E)-9-hydroxy-4,6,8,10-tetramethyl-7-oxododec-4-en-2-yl)-3-methyloxetan-2-one
InChIKey: WOISDAHQBUYEAF-QIQXJRRPSA-N
SMILES: CC[C@@H](C)[C@@H](O)[C@H](C)C([C@H](C)/C=C(C)/C[C@@H]([C@@]1([H])[C@@H](C(O1)=O)C)C)=O
Biological Activity: Ebelactone A is a mycolic acid β-lactone, which exhibits inhibitory activity for esterase, lipase, fMet aminopeptidase (fMet AP) and PNBase, with IC50s of 56, 3, 8 and 7.5 μM, respectively[1]. Ebelactone A inhibits cutinase, exhibits plants protective potency against Erysiphe graminis[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Ebelactone A | 98.28% | Ebelactone A is a mycolic acid β-lactone, which exhibits inhibitory activity for esterase, lipase, fMet aminopeptidase (fMet AP) and PNBase, with IC50s of 56, 3, 8 and 7.5 μM, respectively. Ebelactone A inhibits cutinase, exhibits plants protective potency against Erysiphe graminis. | ||||||||||||||||||||
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- [1]. Umezawa H, et al., Ebelactone, an inhibitor of esterase, produced by actinomycetes. J Antibiot (Tokyo). 1980 Dec;33(12):1594-6. [Content Brief]
- [2]. Francis S A, et al., The role of cutinase in germling development and infection byErysiphe graminisf. sp. hordei[J]. Physiological and Molecular Plant Pathology, 1996, 49(3): 201-211.
Keywords
