69787-80-0
69787-80-0
Chemical Structure
Avilamycin C
- CAS No.: 69787-80-0
- Formula:C61H90Cl2O32
- Molecular Weight:1406.25
InChIKey: AEIFATUAVHHRBC-UHFFFAOYSA-N
SMILES: CC1=C(C(OC)=C(C(O)=C1Cl)Cl)C(O[C@@H]2[C@@H](C)O[C@@H](O[C@@H]3[C@@H](C)O[C@]4(O[C@]([C@@H]5O4)(C)C[C@H](O[C@H]6[C@@H](OC)[C@@H](C)O[C@@H](O[C@@H]7[C@@H](COC)O[C@@H](O[C@H]8[C@H](OC(C(C)C)=O)[C@H]9[C@@H](O[C@@]%10(O9)[C@H]%11[C@@H](OCO%11)[C@@]([C@@H](C)O%10)(C(C)O)O)CO8)[C@@H](OC)[C@H]7O)[C@@H]6O)O[C@@H]5C)C[C@H]3O)C[C@H]2O)=O
Biological Activity: Avilamycin C is an avilamycin-type antibiotic. Avilamycin C has antibacterial activity and can inhibit Gram-positive bacteria[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Avilamycin C | Avilamycin C is an avilamycin-type antibiotic. Avilamycin C has antibacterial activity and can inhibit Gram-positive bacteria. | |||||||||||||||||||||
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References
- [1]. Zhang D, et al. An NADH/NAD+-favored aldo-keto reductase facilitates avilamycin A biosynthesis by primarily catalyzing oxidation of avilamycin C. Appl Environ Microbiol. 2024 Apr 17;90(4):e0015024. [Content Brief]
- [2]. Weitnauer G, et al. Biosynthesis of the orthosomycin antibiotic avilamycin A: deductions from the molecular analysis of the avi biosynthetic gene cluster of Streptomyces viridochromogenes Tü57 and production of new antibiotics. Chem Biol. 2001 Jun;8(6):569-81. [Content Brief]
