• 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

Goitrin

CAS No. 13190-34-6

Goitrin ( —— )

产品货号. M17945 CAS No. 13190-34-6

甲状腺激素是一种有效的抗甲状腺化合物,天然存在于十字花科植物中。 Goitrin 负责诱导谷胱甘肽 S-转移酶。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥591 有现货
10MG ¥931 有现货
25MG ¥1544 有现货
50MG ¥2297 有现货
100MG ¥3285 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥396 有现货

生物学信息

  • 产品名称
    Goitrin
  • 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
    甲状腺激素是一种有效的抗甲状腺化合物,天然存在于十字花科植物中。 Goitrin 负责诱导谷胱甘肽 S-转移酶。
  • 产品描述
    Goitrin is a potent antithyroid compound found naturally in crucifers. Goitrin is responsible for the induction of glutathione S-transferases.Goitrin is a moderate inhibitor of purified bovine adrenal dopamine beta-hydroxylase, leads to a depression of brain norepinephrine and to an elevation of heart and adrenal dopamine.
  • 体外实验
    The active ingredients according to the report table Spring is the anti-influenza virus, according to the spring report not only without the active, more reported having certain toxicity.
  • 体内实验
    ——
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Others
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    13190-34-6
  • 分子量
    129.17
  • 分子式
    C5H7NOS
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (774.11 mM)
  • SMILES
    C=CC1CNC(=S)O1
  • 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

产品手册
关联产品
  • pTH-Related Protein ...

    pTH-Related Protein (1-40) (human, mouse, rat) 通过 PTHR1 受体和 PKCα/β 信号通路刺激大鼠肠细胞钙摄取。pTH-Related Protein (1-40) 上调甲状旁腺激素 1 受体 (PTHR1) 蛋白、四种跨细胞钙转运蛋白、潜在香草素成员 6 (TRPV6)、钙结合蛋白-D9k (CaBP-D9k)、钠钙交换剂 1 (NCX1) 和质膜钙 ATP 酶 1 (PMCA1)。

  • Mulberrofuran Q

    Mulberrofuran Q is an active compound that inhibits the formation of 12-hydroxy-5,8,10-heptadecatrienoic acid (HHT) and thromboxane B2 (cyclooxygenase product) , which protects neuronal cells from hypoxia-glycorrhoea-deficiency (OGD)-induced oxidative stress.

  • LEM-14-1189 B

    Lem-14-1189, a LEM-14 derivative, is a potent NSD inhibitor of the nuclear receptor binding SET domain, and has inhibitory effects on NSD1, NSD2, and NSD3, with IC50 of 418 μM, 111 μM, and 60 μM, respectively. LEM-14-1189 has potential anticancer activity and can be used to study multiple myeloma (MM) and diseases of the blood system.