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Fenhexamid
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Fenhexamid图片
规格:98%
分子量:302.2
包装与价格:
包装价格(元)
50mg电议
100mg电议

产品介绍
Fenhexamid 是一种杀菌剂,是一种甾醇生物合成抑制剂。
货号:ajcx26070
CAS:126833-17-8
分子式:C14H17Cl2NO2
分子量:302.2
溶解度:DMF: 5 mg/ml,DMSO: 3 mg/ml,Ethanol: slightly soluble
纯度:98%
存储:Store at -20°C
库存:现货

Background:


Fenhexamid is a fungicide.1,2It inhibits germ-tube elongation and mycelial growth of several strains of the plant pathogenic fungusB. cinerea(EC50s = 0.13-8.3 and 0.03-16.5 µM, respectively).1Fenhexamid inhibits 3-ketoreductase (IC50= 3 µM for theB. cinereaenzyme), is an estrogen receptor α (ERα) agonist (EC50= 9 µM in a yeast reporter assay), and inhibits the androgenic effect of dihydrotestosterone in MDA-kb2 cells (IC20= 2.02 µM).1,3,4It increases the proliferation and migration of BG1 ovarian cancer cells when used at a concentration of 10 µM.5In field studies, fenhexamid applied at 842 g AI/ha provides 27.3 and 13.9% disease control for lettuce drop caused byS. minororS. sclerotiorum, respectively.2Formulations containing fenhexamid have been used as fungicides in agriculture.


1.Debieu, D., Bach, J., Montesinos, E., et al.Role of sterol 3-ketoreductase sensitivity in susceptibility to the fungicide fenhexamid in Botrytis cinerea and other phytopathogenic fungiPest. Manag. Sci.69(5)642-651(2013) 2.Matheron, M.E., and Porchas, M.Activity of boscalid, fenhexamid, fluazinam, fludioxonil, and vinclozolin on growth of Sclerotinia minor and S. sclerotiorum and development of lettuce dropPlant Dis.88(6)665-668(2004) 3.Teng, Y., Manavalan, T.T., Hu, C., et al.Endocrine disruptors fludioxonil and fenhexamid stimulate miR-21 expression in breast cancer cellsToxicol. Sci.131(1)71-83(2013) 4.Orton, F., Rosivatz, E., Scholze, M., et al.Widely used pesticides with previously unknown endocrine activity revealed as in vitro antiandrogensEnviron. Health Perspect.119(6)794-800(2011) 5.Go, R.-E., Kim, C.-W., and Choi, K.-C.Effect of fenhexamid and cyprodinil on the expression of cell cycle- and metastasis-related genes via an estrogen receptor-dependent pathway in cellular and xenografted ovarian cancer modelsToxicol. Appl. Pharmacol.289(1)48-57(2015)