1315451-94-5
Chemical Structure
Chevalone E
Synonym(s): Deacetylchevalone C
- CAS No.: 1315451-94-5
- Formula:C26H38O4
- Molecular Weight:414.58
IUPAC Name: (2S,4aR,4bR,6aS,12aS,12bR,14aR)-2-hydroxy-1,1,4a,6a,9,12b-hexamethyl-2,3,4,4a,4b,5,6,6a,12,12a,12b,13,14,14a-tetradecahydro-1H,11H-naphtho[2,1-f]pyrano[2,3-b]chromen-11-one
InChIKey: PSHUZQHBLAPAMD-KFCOXGNHSA-N
SMILES: C[C@]12[C@@](CC[C@]3([C@@]2([H])CC4=C(OC(C)=CC4=O)O3)C)([H])[C@@]5([C@@](C(C)([C@H](CC5)O)C)([H])CC1)C
Biological Activity: Chevalone E (Deacetylchevalone C) (Compound 3) is a meroditerpenoid. Chevalone E can be isolated from the fungus Aspergillus similanensis sp. Chevalone E has a synergic effect with Oxacillin (HY-B0925A) and Ampicillin (HY-B0522) against MRSA[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Chevalone E | Chevalone E (Deacetylchevalone C) (Compound 3) is a meroditerpenoid. Chevalone E can be isolated from the fungus Aspergillus similanensis sp. Chevalone E has a synergic effect with Oxacillin (HY-B0925A) and Ampicillin (HY-B0522) against MRSA. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Prompanya C, et al. New isocoumarin derivatives and meroterpenoids from the marine sponge-associated fungus Aspergillus similanensis sp. nov. KUFA 0013. Mar Drugs. 2014 Oct 14;12(10):5160-73. [Content Brief]
- [2]. Xiao Z H, et al. Biocatalytic and chemical derivatization of the fungal meroditerpenoid chevalone E[J]. Organic Chemistry Frontiers, 2022, 9(7): 1837-1843.
