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Pyribencarb

CAS No. 799247-52-2

Pyribencarb ( ZINC43065336 )

产品货号. M28112 CAS No. 799247-52-2

Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥786 有现货
10MG ¥1320 有现货
25MG ¥2608 有现货
50MG ¥4026 有现货
100MG ¥5856 有现货
500MG ¥12312 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Pyribencarb
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi.
  • 产品描述
    Pyribencarb is a benzylcarbamate-type fungicide, which is active against a wide range of plant pathogenic fungi. Pyribencarb is a potent Qo inhibitor of cytochrome b. Pyribencarb is especially active against Botrytis cinerea and Sclerotinia sclerotirum.(In Vitro):Pyribencarb potently inhibits succinate-cytochrome c reductase (SCR) activities of Botrytis cinerea (cucumber gray mold), Corynespora cassiicola (leaf spot) and decylubiquinol-cytochrome c reductase (UCR) activity of B. cinerea. Pyribencarb inhibits the UCR of B. cinerea in an uncompetitive manner, and the substrate-dependent inhibition constant is found from calculation to be 13 nM. The target site of Pyribencarb is cytochrome b of complex III in the electron transport system of the respiratory chain. The inhibitory potency of pyribencarb on SCR activities of plants, rats and carp is relatively weak compared with that of strobilurin fungicides.
  • 同义词
    ZINC43065336
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    ——
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    799247-52-2
  • 分子量
    361.8
  • 分子式
    C18H20ClN3O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    C(=N\OCC=1N=C(C)C=CC1)(\C)/C2=CC(CNC(OC)=O)=C(Cl)C=C2
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Pribylova M, et al. Paclitaxel conjugation with the analog of the gonadotropin-releasing hormone as a targeting moiety. Int J Pharm. 2011 Aug 30;415(1-2):175-80.
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