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Cat. No.: HY-N13920

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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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CAS No.: 69787-80-0
Formule: C₆₁H₉₀Cl₂O₃₂
Masse moléculaire:1406.25

Stockage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (268 KB)

Avilamycin C Chemical Structure

CAS No.: 69787-80-0

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Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique

Description

Avilamycin C is an avilamycin-type antibiotic. Avilamycin C has antibacterial activity and can inhibit Gram-positive bacteria^[1]^[2].

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Chemical Information

CAS No. 69787-80-0
Masse moléculaire 1406.25
Formule C₆₁H₉₀Cl₂O₃₂
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
Structure Classification
- Antibiotics
- Other Antibiotics
- Others
Initial Source
- Microorganisms
Streptomyces viridochromogenes
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (268 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instruction de manipulation (2659 KB)

Références

[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]

Calculators

Calculateur de molarité

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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Activité biologique
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Chemical Information
Pureté et documentation
Références

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Avilamycin C

Voir tous les produits spécifiques à Isoform Antibiotic

Activité biologique

Chemical Information

Pureté et documentation

Références

Calculators

Help & FAQs

Avilamycin C Related Classifications

HY-N13920 Related Classifications