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Palmarumycin C3 Sale

目录号 : GC48703

A fungal metabolite

Palmarumycin C3 Chemical Structure

Cas No.:159934-11-9

规格 价格 库存 购买数量
500µg
¥2,381.00
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2.5mg
¥8,342.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Palmarumycin C3 is a spirobisnaphthalene fungal metabolite that has been found in C. palmarum and has diverse biological activities.1,2 It is active against the bacteria A. tumefaciens, B. subtilis, P. lachrymans, R. solanacearum, S. haemolyticus, and X. vesicatoria (MICs = 6.25, 6.25, 12.5, 12.5, 6.25, and 6.25 µg/ml, respectively).2 Palmarumycin C3 is also active against the fungi M. microspora and E. repens, as well as the plant pathogenic fungi F. oxysporum and U. violacea, in agar diffusion assays when used at a concentration of 0.5 mg/disc.1 It scavenges DPPH radicals in cell-free assays and has antioxidant activity in a β-carotene-linoleic acid bleaching assay (IC50s = 37.57 and 7.41 µg/ml, respectively).

1.Krohn, K., Michel, A., FlÖrke, U., et al.Biologically active metabolites from fungi, 5. Palmarumycins C1-C16 from Coniothyrium sp.: Isolation, structure elucidation, and biological activityEur. J. Org. Chem.1994(11)1099-1108(1994) 2.Mou, Y., Meng, J., Fu, X., et al.Antimicrobial and antioxidant activities and effect of 1-hexadecene addition on palmarumycin C2 and C3 yields in liquid culture of endophytic fungus Berkleasmium sp. Dzf12Molecules18(12)15587-15599(2013)

Chemical Properties

Cas No. 159934-11-9 SDF
Canonical SMILES OC1=C2C3(OC4=CC=CC5=C4C(O3)=CC=C5)[C@@]6([H])[C@](C(C2=C(C=C1)O)=O)([H])O6
分子式 C20H12O6 分子量 348.3
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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1 mg 5 mg 10 mg
1 mM 2.8711 mL 14.3554 mL 28.7109 mL
5 mM 0.5742 mL 2.8711 mL 5.7422 mL
10 mM 0.2871 mL 1.4355 mL 2.8711 mL
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Research Update

Antimicrobial and antioxidant activities and effect of 1-hexadecene addition on palmarumycin C2 and C3 yields in liquid culture of endophytic fungus Berkleasmium sp. Dzf12

Molecules 2013 Dec 13;18(12):15587-99.PMID:24352015DOI:PMC6270283

Two spirobisnaphthalenes, namely palmarumycins C2 and C3, were isolated from cultures of the endophytic fungus Berkleasmium sp. Dzf12 after treatment with 1-hexadecene. After addition of 1-hexadecene at 10% to the medium on day 6 of culture, the maximal yields of palmarumycins C2 and C3 were obtained as 0.40 g/L and 1.19 g/L, which were 40.00 fold and 59.50 fold higher, respectively, in comparison with those of the control (0.01 g/L and 0.02 g/L). The results indicated that addition of 1-hexadecene can be an effective strategy for enhancing the production of palmarumycins C2 and C3 in liquid culture of endophytic fungus Berkleasmium sp. Dzf12. Palmarumycin C3 exhibited stronger antimicrobial and antioxidant activities than palmarumycin C2.