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Emeguisin A Sale

目录号 : GC48546

A fungal metabolite

Emeguisin A Chemical Structure

Cas No.:117032-54-9

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100µg
¥2,552.00
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500µg
¥8,292.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Emeguisin A is a depsidone fungal metabolite originally isolated from E. unguis.1 It is active against the bacteria S. aureus and methicillin-resistant S. aureus (MRSA; MIC = 0.5 µg/ml for both), the fungus C. neoformans (MIC = 0.5 µg/ml), and the protozoan P. falciparum (IC50 = 2.2 µM).2

1.Kawahara, N., Nozawa, K., Nakajima, S., et al.Isolation and structures of novel fungal depsidones, emeguisins A, B, and C, from Emericella unguisJ. Chem. Soc., Perkin Trans. 12611-2614(1988) 2.Klaiklay, S., Rukachaisirikul, V., Aungphao, W., et al.Depsidone and phthalide derivatives from the soil-derived fungus Aspergillus unguis PSU-RSPG199Tetrahedron Lett.57(39)4348-4351(2016)

Chemical Properties

Cas No. 117032-54-9 SDF
Canonical SMILES O=C1OC2=C(C(C(C)=CC)=C(C(O)=C2C)Cl)OC3=C1C(C(C)=CC)=CC(O)=C3C
分子式 C23H23ClO5 分子量 414.9
溶解度 储存条件 -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 2.4102 mL 12.0511 mL 24.1022 mL
5 mM 0.482 mL 2.4102 mL 4.8204 mL
10 mM 0.241 mL 1.2051 mL 2.4102 mL
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Research Update

Antibacterial and Antifungal Polyketides from the Fungus Aspergillus unguis PSU-MF16

J Nat Prod 2021 May 28;84(5):1498-1506.PMID:33861594DOI:10.1021/acs.jnatprod.0c01308

Seven new polyketides including a phenol (1), two diphenyl ethers (2 and 3), two depsidones (4 and 5), and two phthalides (6 and 7) were isolated from the fungus Aspergillus unguis PSU-MF16 along with 27 known compounds. Their structures were determined by extensive spectroscopic analysis. The absolute configurations of 1 and 4-7 were established using comparative analyses of calculated and experimental ECD spectra. Among the new metabolites, 2 exhibited the best antimicrobial activity against Staphylococcus aureus, methicillin-resistant S. aureus, and Microsporum gypseum with equal MIC values of 16 μg/mL. In addition, known Emeguisin A displayed potent antimicrobial activity against S. aureus, methicillin-resistant S. aureus, and Cryptococcus neoformans with equal MIC values of 0.5 μg/mL, compared with the standard drugs, vancomycin and amphotericin B. The structure-activity relationship study of the isolated compounds for antimicrobial activity is discussed.