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Antifungal agent 38 是一种环二硫化物,具有抗真菌和抗细菌活性。Antifungal agent 38 能诱导菌丝收缩,破坏质膜的完整性,并导致细胞内容物的破坏和渗漏。
Antifungal agent 38 是一种环二硫化物,具有抗真菌和抗细菌活性。Antifungal agent 38 能诱导菌丝收缩,破坏质膜的完整性,并导致细胞内容物的破坏和渗漏。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
25 mg | ¥ 10,600 | 10-14周 | |
50 mg | ¥ 13,800 | 10-14周 | |
100 mg | ¥ 17,500 | 10-14周 |
Antifungal agent 38 相关产品
产品描述 | Antifungal agent 38 is a geterocyclic disulfide with antifungal and antibacterial activity. Antifungal agent 38 induces the shrinkage of hyphae, disrupts the integrity of the plasma membrane, and causes the damage and leakage of cell contents [1]. |
体外活性 | Antifungal agent 38 (50 μg/mL) has anti-fungal activity against 10 pathogenic fungi with inhibition rates of 56.57% ( R. solani ), 100% ( S. sclerotiorum ), 55.09% ( B. cinerea ), 71.23% ( F. graminearum ), 37.32% ( M. oryzae ), 50.87% ( P. capsici ), 100% ( A. flavus ), 59.75% ( P. expansum ), 100% ( M. fructicola ), 65.78% ( R. stolonifer ), respectively [1]. Antifungal agent 38 (5 μg/mL) damages plasma membrane integrity of M. fructicola [1]. Antifungal agent 38 (100 μg/mL) displays excellent anti-bacterial activity against X. oryzae accc 11602, X. axonpodis [1]. Antifungal agent 38 inhibits fungus growth with EC 50 s of 17.09 μg/mL ( R. solani ), 6.34 μg/mL ( S. sclerotiorum ), 25.24 μg/mL ( F. graminearum ), >10 μg/mL ( A. flavus ), 10.42 μg/mL ( M. fructicola ), 45.71 μg/mL ( B. cinerea ), respectively [1]. Cell Viability Assay [1] Cell Line: M. fructicola Concentration: 10, 25, 50 μg/mL Incubation Time: 2, 4, 6 days Result: Inhibited M. fructicola growth. |
体内活性 | Antifungal agent 38 (compound S8) (200 μg/mL) shows equivalent curative and higher protective effects as the positive drug Thiophanate-Methyl in vivo [1]. Antifungal agent 38 (50, 100, 200 μg/mL, 30 mL; sprinkling) applies on pears and inhibits M. fructicola growth in vivo [1]. |
分子量 | 200.32 |
分子式 | C8H12N2S2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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