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Cat. No.: 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.

For research use only. We do not sell to patients.

CAS No.: 128554-13-2
Formula: C₅₀H₈₂N₈O₁₅
Molecular Weight:1035.23

Storage:

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

Citropeptin Chemical Structure

CAS No.: 128554-13-2

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Use of MCE Products

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

Biological Activity
- Description
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
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Biological Activity

Description

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].

All Endogenous Metabolite Isoforms :

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 No. 128554-13-2
Molecular Weight 1035.23
Formula 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
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

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

Purity & Documentation

Handling Instructions (2659 KB)

References

[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.

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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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