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S88556

H3B-5942

源叶(MedMol) 98%
  • 英文名:
  • H3B-5942
  • 别名:
  • CAS号:
  • 2052128-15-9
  • 分子式:
  • C31H34N4O2
  • 分子量:
  • 494.63
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) S88556-1mg 98% ¥410.00元 4 - - - EA 加入购物车
源叶(MedMol) S88556-5mg 98% ¥1330.00元 6 - - - EA 加入购物车
源叶(MedMol) S88556-10mg 98% ¥1850.00元 4 - - - EA 加入购物车
源叶(MedMol) S88556-25mg 98% ¥3700.00元 3 - - - EA 加入购物车
源叶(MedMol) S88556-50mg 98% ¥6179.00元 1 - - - EA 加入购物车
源叶(MedMol) S88556-100mg 98% ¥10300.00元 3 - - - EA 加入购物车
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参考文献

质检证书(COA)

摩尔浓度计算器

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  • 产品描述: H3B-5942 is a selective, irreversible and orally active estrogen receptor covalent antagonist, inactivates both wild-type and mutant ERα by targeting Cys530, with Kis of 1 nM and 0.41 nM, respectively. H3B-5942 reduces ERα target gene GREB1, shows potent antitumor activity both in multiple cell lines or animals bearing ERαWT or ERα mutations
  • 靶点: ERαY537S:0.41 nM (Ki);ERαWT:1 nM (Ki);EstrogenReceptor/ERR; Estrogen/progestogenReceptor
  • 体外研究:
    H3B-5942 is a selective and irreversible estrogen receptor covalent antagonist, inactivates both wild-type and mutant ERα by targeting Cys530, with Kis of 1 nM and 0.41 nM, respectively. H3B-5942 elevates ERα protein level distinct from SERMs/SERD, blocks ERα-dependent transcription in breast cancer cells. H3B-5942 (0.01-10 μM) reduces ERα target gene GREB1 in MCF7-ERαWT, various MCF7-ERαMUT lines, and the PDX-ERαY537S/WT line. H3B-5942 also decreases proliferation of MCF7-Parental, MCF7-LTED-ERαWT, and MCF7-LTED-ERαY537C lines with GI50s of 0.5, 2, and 30 nM, respectively. H3B-5942 (10-25 nM) in combination with CDK4/6 inhibitors (≥25 pM) has synergic inhibitory effect on multiple cell lines bearing ERαWT or clinically frequent ERα mutations
  • 体内研究:
    H3B-5942 (1, 3, 10, or 30 mg/kg, p.o, q.d. for 17 days) dose-dependently inhibits tumor growth in MCF7 xenograft model in athymic female nude mice. H3B-5942 (3, 10, 30, 100, and 200 mg/kg, p.o, q.d.) exhibits similar anti-tumor activity in the ERαY537S/WT ST941 model in athymic female nude mice. Animal Model: MCF7 xenograft model in athymic female nude mice Dosage: 1, 3, 10, or 30 mg/kg Administration: P.O. once a day (q.d.×1) for 17 days Result: Exhibited tumor growth inhibition (TGI) on day 17 of 19%, 41%, 68%, and 83%, respectively.
  • 参考文献:
    1. Puyang X, et al. Discovery of Selective Estrogen Receptor Covalent Antagonists for the Treatment of ERαWT and ERαMUT Breast Cancer. Cancer Discov. 2018 Sep;8(9):1176-1193.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20°C
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.022 ml 10.109 ml 20.217 ml
    5 mM 0.404 ml 2.022 ml 4.043 ml
    10 mM 0.202 ml 1.011 ml 2.022 ml
    50 mM 0.04 ml 0.202 ml 0.404 ml
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