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Aspochracin Sale

目录号 : GC42862

Aspochracin is a cyclic tripeptide originally isolated from the pathogenic fungus A.

Aspochracin Chemical Structure

Cas No.:22029-09-0

规格 价格 库存 购买数量
500μg
¥2,141.00
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2.5mg
¥8,034.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

Aspochracin is a cyclic tripeptide originally isolated from the pathogenic fungus A. ochraceus, which infects insects. Aspochracin is toxic to fall webworms (LD50 = 100 µg/g) and to silkworms. Unlike other aspochracin-type cyclic tripeptides, it has no antifungal activity against C. albicans and does not have antimicrobial activity up to a concentration of 0.1 mg/ml.

Chemical Properties

Cas No. 22029-09-0 SDF
Canonical SMILES O=C(NCCC[C@H](NC(/C=C/C=C/C=C/C)=O)C(N(C)[C@H]1C(C)C)=O)[C@H](C)N(C)C1=O
分子式 C23H36N4O4 分子量 432.6
溶解度 DMF: soluble,DMSO: soluble,Ethanol: soluble,Methanol: soluble 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.3116 mL 11.558 mL 23.116 mL
5 mM 0.4623 mL 2.3116 mL 4.6232 mL
10 mM 0.2312 mL 1.1558 mL 2.3116 mL
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Research Update

JBIR-15, a new Aspochracin derivative, isolated from a sponge-derived fungus, Aspergillus sclerotiorum Huber Sp080903f04

Biosci Biotechnol Biochem 2009 Aug;73(8):1898-900.PMID:19661713DOI:10.1271/bbb.90228.

In the course of our chemical screening program for novel metabolites by LC-MS monitoring, we isolated a new Aspochracin derivative, JBIR-15 (1), together with Aspochracin, from the culture broth of a sponge-derived fungus, Aspergillus sclerotiorum Huber Sp080903f04. The structure of 1 was determined to be N-demethyl Aspochracin at the alanyl residue on the basis of extensive NMR and MS analyses.

Cyclic tripeptides from the halotolerant fungus Aspergillus sclerotiorum PT06-1

J Nat Prod 2010 Jun 25;73(6):1133-7.PMID:20503985DOI:10.1021/np100198h.

Eleven new aspochracin-type cyclic tripeptides, sclerotiotides A-K (1-11), together with three known compounds, JBIR-15 (12), Aspochracin (13), and penicillic acid, were isolated from the ethyl acetate extract of the fermentation broth of the halotolerant Aspergillus sclerotiorum PT06-1 in a hypersaline nutrient-rich medium. Their structures were elucidated by spectroscopic analysis and chemical methods. Chemical transformations of 12 and 13 proved that sclerotiotides D-K (4-11) were artifacts probably formed during the fermentation or subsequent isolation steps. All 13 cyclic tripeptides have been evaluated for their antimicrobial and cytotoxic effects. Only sclerotiotides A (1), B (2), F (6), and I (9) and JBIR-15 (12) showed selective antifungal activity against Candida albicans with MIC values of 7.5, 3.8, 30, 6.7, and 30 microM, respectively.