• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Tebuconazole

CAS No. 107534-96-3

Tebuconazole ( —— )

产品货号. M23283 CAS No. 107534-96-3

戊唑醇是一种农用唑类杀菌剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
50MG ¥154 有现货
100MG ¥201 有现货
500MG ¥431 有现货
1G ¥581 有现货
1 mL x 10 mM in DMSO ¥185 有现货

生物学信息

  • 产品名称
    Tebuconazole
  • 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
    戊唑醇是一种农用唑类杀菌剂。
  • 产品描述
    Tebuconazole is an agricultural azole fungicide. It can also inhibit CYP51 (IC50s: 0.9 and 1.3 μM for Candida albicans CYP51 and truncated Homo sapiens CYP51, respectively).
  • 体外实验
    Western Blot Analysis Cell Line:HepG2 cells Concentration:20,40,80 μM Incubation Time:1–12 hours Result:Increased the nuclear translocation of peroxisome proliferator-activated receptors and the expression of cluster of differentiation 36, fatty acid transport protein (FATP) 2, FATP5, and carnitine palmitoyltransferase 1. Apoptosis AnalysisCell Line:Bovine mammary gland epithelial cells (MAC-T cells Concentration: 100,150,200,250,500,750 μM Incubation Time:24 hours Result:Decreased cells viability and proliferation and activates apoptotic cell death via the upregulation of pro-apoptotic proteins, such as cleaved caspases 3 and 8 and BAX.Induced loss of mitochondrial membrane potential in MAC-T cells.Induced mitochondria-mediated apoptotic MAC-T cell death by activating ER stress.Induced endoplasmic reticulum (ER) stress via the upregulation of Bip/GRP78; PDI; ATF4; CHOP; and ERO1-Lα.
  • 体内实验
    Animal Model:Male Wistar ratsDosage:10, 25, and 50 mg/kg Administration:p. o. once daily for 28 days Result:Induced CYP1A1/2, CYP2B1/2, CYP2E1, and CYP3A proteins in liver.Decreased glutathione content and increased glutathione S-transferase, superoxide dismutase, catalase, and glutathione peroxidase activities in liver . Increased superoxide dismutase activities in kidney and testis.Decreased glutathione S-transferase activity in testis .Decreased serum testosterone concentration and cauda epididymal sperm count .Animal Model:Male and female Sprague-Dawley ratsDosage:25, 50, and 100 mg/kg Administration:Oral gavage (p.o.), for 10 days Result:Increased fetal serum testosterone and progesterone levels.Increased the number of fetal Leydig cells per testis without inducing cell aggregation. Up-regulated the expression levels of Star, Cyp11a1, Hsd17b3, and Fshr.Increased phosphorylation of AKT1, ERK1/2, and mTOR, the level of BCL2, as well as the decrease of Beclin1, LC3B, and BAX.
  • 同义词
    ——
  • 通路
    Metabolic Enzyme/Protease
  • 靶点
    P450
  • 受体
    CYP51
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    107534-96-3
  • 分子量
    307.82
  • 分子式
    C16H22ClN3O
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:50 mg/mL (162.43 mM)
  • SMILES
    CC(C)(C)C(CCc(cc1)ccc1Cl)(Cn1ncnc1)O
  • 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.Warrilow AG, et al. Azole affinity of sterol 14α-demethylase (CYP51) enzymes from Candida albicans and Homo sapiens. Antimicrob Agents Chemother. 2013 Mar;57(3):1352-60.
产品手册
关联产品
  • N-Nornuciferine hydr...

    N-Nornuciferine 是荷叶中的一种阿朴啡生物碱,显着抑制 CYP2D6(IC50:3.76 μM,Ki:2.34 μM)。N-Nornuciferine 强烈抑制 CYP2D6 活性,但对其他四种 P450 同工酶(CYP2C19、CYP3A4、 CYP2E1、CYP2C9)。 N-Nornuciferine 竞争性抑制 CYP2D6 催化的右美沙芬 O-去甲基化 (Ki: 2.34 μM)。

  • MS-PPOH

    MS-PPOH 是一种有效的选择性细胞色素 P450 (CYP) 环氧化酶抑制剂。MS-PPOH 抑制 CYP2C8 和 CYP2C9,IC50 分别为 15 和 11 μM。MS-PPOH 是一种点击化学试剂。它含有 Alkyne 基团,可以和含有 Azide 基团的分子发生铜催化的叠氮-炔环加成反应 (CuAAc)。

  • PF-4981517

    CYP3cide (PF-4981517) 是一种有效,选择性和时间依赖性细胞色素P4503A4 (CYP3A4) 抑制剂。对于 CYP3A4,CYP3A5 和 CYP3A7,抑制 Midazolam 1'-羟化酶活性的 IC50 值分别为 0.03 μM,17 μM 和 71μM。CYP3cide 可用于区分 CYP3A4 和 CYP3A5 在活性分子代谢中的作用。