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Enopeptin A Sale

(Synonyms: BRN 537924, NSC 657143) 目录号 : GC43612

A depsipeptide antibiotic

Enopeptin A Chemical Structure

Cas No.:139601-96-0

规格 价格 库存 购买数量
500μg
¥5,122.00
现货
2.5mg
¥16,652.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

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产品描述

Enopeptin A, originally isolated from a culture broth of Streptomyces sp. RK-1051, is a depsipeptide antibiotic that contains two unusual amino acids (N-methylalanine and 4-methylproline) and features a pentaenone side chain. It is effective against Gram-positive bacteria, including methicillin-resistant S. aureus (MIC = 25 µg/ml), and Gram-negative bacteria, including mutant forms of E. coli and P. aeruginosa (MICs = 200 µg/ml); however, it is not inhibitory to fungi.

Chemical Properties

Cas No. 139601-96-0 SDF
别名 BRN 537924, NSC 657143
Canonical SMILES O=C(N[C@@H](CC1=CC=CC=C1)C(N[C@@H](COC2=O)C(N3[C@H](C(N([C@@H](C)C(N[C@H](C(N4[C@H]2C[C@@H](C)C4)=O)C)=O)C)=O)CCC3)=O)=O)/C=C/C=C/C=C/C=C/C=C/C(NC5=C(O)CCC5=O)=O
分子式 C47H57N7O11 分子量 896
溶解度 DMF: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 1.1161 mL 5.5804 mL 11.1607 mL
5 mM 0.2232 mL 1.1161 mL 2.2321 mL
10 mM 0.1116 mL 0.558 mL 1.1161 mL
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Research Update

Solution conformation of Enopeptin A, a depsipeptide antibiotic, using 2D NMR and restrained molecular dynamics studies

J Antibiot (Tokyo) 1994 Aug;47(8):922-31.PMID:7928680DOI:10.7164/antibiotics.47.922.

Studies on the solution conformation of the cyclic depsipeptide antibiotic Enopeptin A have been carried out using 2D NMR and molecular modelling techniques. The proton resonances of the antibiotic in DMSO-d6 have been assigned by the use of TOCSY and ROESY experiments. The interproton distance information obtained from the ROESY experiments have been used as the basis for elucidating the probable structures in solution. The restrained molecular dynamics technique was applied to calculate the structures in solution, and six resultant structures with fewer distance constraint violations were obtained that satisfy the experimental restraints very well. The conformation of the cyclic moiety of the molecules is well defined whereas the aliphatic chain segment is disordered.