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Art. -Nr.: HY-N21827

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Citropeptin

Citropeptin is a cyclic hexadepsipeptide antitumor compound belonging to the Azinothricin family, which is found in Streptomyces flavidovirens. Citropeptin can be used in cancer research.

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CAS. Nr.: 128554-13-2
Formel: C₅₀H₈₂N₈O₁₅
Molecular Weight:1035.23

Speicherung:

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

Citropeptin Chemical Structure

CAS. Nr.: 128554-13-2

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Use of MCE Products

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

Biologische Aktivität
- Beschreibung
- In Vitro
Chemical Information
Reinheit & Dokumentation
Verweise
Calculators
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

Citropeptin is a cyclic hexadepsipeptide antitumor compound belonging to the Azinothricin family, which is found in Streptomyces flavidovirens. Citropeptin can be used in cancer research^[1]^[2].

Alle Endogenous Metabolite Isoform-spezifische Produkte anzeigen :

In Vitro

Citropeptin (5 days) is a cyclic hexadepsipeptide isolated from Streptomyces flavidovirens K3619. Its structure differs from Azinothricin and A83586C (HY-P2599) in specific amino acid and side chain substitutions, while its stereochemical characteristics are completely identical to those of A83586C and Azinothricin^[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS. Nr. 128554-13-2
Molecular Weight 1035.23
Formel C₅₀H₈₂N₈O₁₅
SMILES

O=C(N[C@H](C(O)C)C(O[C@H]([C@H](NC([C@@](C)(O)[C@](CC[C@@H]1C)(O)O[C@]1([H])/C(C)=C/[C@H](C)C(/C(C)=C/C)=O)=O)C(N2NCCC[C@@H]2C(N(O)[C@@H](COC)C(N(C)[C@@H]3CC(C)C)=O)=O)=O)C(C)C)=O)C4CCCNN4C3=O
Structure Classification
- Antibiotics
Initial Source
- Microorganisms
Streptomyces flavidovirens
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

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

Reinheit & Dokumentation

Handling Instructions (2659 KB)

Verweise

[1]. Hale KJ, et al. Synthetic studies on the azinothricin family of antibiotics. 4. Enantioselective synthesis of the northern half of antitumour antibiotics A83586C and citropeptin. Tetrahedron Letters. 1995 Sep 18;36(38):6965‑6968.

[2]. Nakagawa M, et al. Structural studies on new depsipeptide antibiotics, variapeptin and citropeptin. The Journal of antibiotics. 1990 May;43(5):477-84.

Calculators

Molaritätsrechner

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

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

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.

Bioz

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MOQ

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100 mg

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