AR antagonist 1
CAS No. 1818885-54-9
AR antagonist 1 ( —— )
产品货号. M26059 CAS No. 1818885-54-9
AR 拮抗剂 1 是雄激素受体的有效拮抗剂。在 PROTAC ARD-266 的合成中,它与 E3 连接酶配体结合,对 VHL 蛋白具有弱结合亲和力。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥1159 | 有现货 |
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| 10MG | ¥1720 | 有现货 |
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| 25MG | ¥2678 | 有现货 |
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| 50MG | ¥3636 | 有现货 |
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| 100MG | ¥4725 | 有现货 |
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| 200MG | ¥6237 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥1036 | 有现货 |
|
生物学信息
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产品名称AR antagonist 1
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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
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产品简述AR 拮抗剂 1 是雄激素受体的有效拮抗剂。在 PROTAC ARD-266 的合成中,它与 E3 连接酶配体结合,对 VHL 蛋白具有弱结合亲和力。
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产品描述AR antagonist 1 is a potent antagonist of the androgen receptor. It binds to E3 ligase ligands with weak binding affinities to VHL protein in the synthesis of PROTAC ARD-266.(In Vitro):AR antagonist 1 (compound 29) is the ligand for the target ligase of ARD-266. ARD-266 is a highly potent and VHL E3 ligase-based androgen receptor (AR) PROTAC degrader. AR antagonist 1 exhibits micromolar binding affinity to its E3 ligase complex, it can be successfully employed for the design of highly potent and efficient PROTAC degraders.
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体外实验AR antagonist 1 (compound 29) is the ligand for target ligase ofARD-266. ARD-266 is a highly potent and VHL E3 ligase-based?androgen receptor (AR)?PROTAC degrader. AR antagonist 1 exhibits micromolar binding affinity to its E3 ligase complex, it can be successfully employed for the design of highly potent and efficient PROTAC degraders. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein.PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
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体内实验——
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同义词——
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通路Endocrinology/Hormones
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靶点Androgen Receptor (AR)
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number1818885-54-9
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分子量278.78
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分子式C15H19ClN2O
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纯度>98% (HPLC)
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溶解度——
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SMILESN#CC1=CC=C(O[C@H]2C(C)(C)[C@H](N)C2(C)C)C=C1Cl
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Grimshaw MJ, et al. Endothelin-2 is a macrophage chemoattractant: implications for macrophage distribution in tumors. Eur J Immunol. 2002 Sep;32(9):2393-400.
产品手册
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