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S81394

Lificiguat (YC-1)

源叶(MedMol) 99%
  • 英文名:
  • 3-(5-Hydroxymethyl-2-Furyl)-1-Benzylindazole
  • 别名:
  • 2-Furanmethanol,5-[1-(phenylmethyl)-1H-indazol-3-yl]; 1-benzyl-3-(5-hydroxymethyl-furan-2-yl)indazole; 5-[1-(PHENYLMETHYL)-1H-INDAZOL-3-YL]-2-FURANMETHANOL; (5-(1-Benzyl-1H-indazol-3-yl)furan-2-yl)Met
  • CAS号:
  • 170632-47-0
  • 分子式:
  • C19H16N2O2
  • 分子量:
  • 304.343
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S81394-2mg 99% ¥208.00元 4 - - - EA 加入购物车
源叶(MedMol) S81394-5mg 99% ¥360.00元 1 - - - EA 加入购物车
源叶(MedMol) S81394-10mg 99% ¥480.00元 4 - - - EA 加入购物车
源叶(MedMol) S81394-25mg 99% ¥1040.00元 5 - - - EA 加入购物车
源叶(MedMol) S81394-50mg 99% ¥1920.00元 3 - - - EA 加入购物车
源叶(MedMol) S81394-100mg 99% ¥3200.00元 预计交期:2-3天 - - - EA 加入购物车
源叶(MedMol) S81394-250mg 99% ¥5120.00元 预计交期:2-3天 - - - EA 加入购物车
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产品介绍

参考文献

质检证书(COA)

摩尔浓度计算器

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  • 提示:详情请下载说明书。
  • 产品描述: Lificiguat binds to the β subunit of soluble guanylyl cyclase(sGC) with Kd of 0.6-1.1 μM in the presence of CO.
  • 靶点: Kd: 0.6-1.1 μM (sGC, in the presence of CO);Others; Guanylatecyclase; HIF
  • 体内研究:
    Lificiguat (YC-1) (30 or 60 mg/kg, i.p.) inhibits MDA-MB-468 tumor growth in a dose-dependent manner. The effect of the prodrug formulation of Lificiguat (YC-1), YC-1-S, in MDA-MB-468 tumor-bearing mice is also investigated. In vivo pharmacokinetic analysis reveal that YC-1-S is quickly converted into its active form. Mice are administered 20, 40 or 80 mg/kg YC-1-S p.o. YC-1-S also displays dose-dependent inhibition of MDA-MB468 tumor growth. Both Lificiguat (YC-1) and YC-1-S dose-dependently reduce tumor weight. Moreover, the mean body weight of mice is not affected by Lificiguat (YC-1) or YC-1-S compare with vehicle-treated groups. Lificiguat (YC-1) is a potent NO-GC activator reported to improve rodent learning behavior when examined with the Morris water maze (MWM) and avoidance tests. Lificiguat (YC-1) enhances long-term potentiation (LTP) in hippocampal Schafer collateral-CA1 synapse via the NO-cGMP-PKG-dependent pathway and potentiated LTP induction in the amygdala, increases the activation of ERK, and potentiated the expression of brain-derived neurotrophic factor (BDNF) cAMP response element-binding protein (CREB) in response to fear memory test.
  • 参考文献:
    1. Purohit R, et al. YC-1 binding to the β subunit of soluble guanylyl cyclase overcomes allosteric inhibition by the α subunit. Biochemistry. 2014 Jan 14;53(1):101-14. 2. Kong J, et al. YC-1 enhances the anti-tumor activity of sorafenib through inhibition of signal transducer and activator of transcription 3 (STAT3) in hepatocellular carcinoma. Mol Cancer. 2014 Jan 13;13:7. 3. Chang LC, et al. YC-1 inhibits proliferation of breast cancer cells by down-regulating EZH2 expression via activation of c-Cbl and ERK. Br J Pharmacol. 2014 Sep;171(17):4010-25. 4. Komsuoglu Celikyurt I, et al. Effects of YC-1 on Learning and Memory Functions of Aged Rats. Med Sci Monit Basic Res. 2014 Aug 21;20:130-7.
  • 溶解性: DMSO  :  ≥  100  mg/mL  (328.58  mM)
  • 保存条件: 2-8℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 3.286 ml 16.429 ml 32.858 ml
    5 mM 0.657 ml 3.286 ml 6.572 ml
    10 mM 0.329 ml 1.643 ml 3.286 ml
    50 mM 0.066 ml 0.329 ml 0.657 ml
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