Ledipasvir
CAS No. 1256388-51-8
Ledipasvir ( GS5885; GS-5885; GS 5885; Ledipasvir )
产品货号. M17226 CAS No. 1256388-51-8
Ledipasvir is a Hepatitis C Virus NS5A Inhibitor. The mechanism of action of ledipasvir is as a P-Glycoprotein Inhibitor, and Breast Cancer Resistance Protein Inhibitor.
纯度: 98%
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥365 | 有现货 |
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5MG | ¥583 | 有现货 |
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10MG | ¥729 | 有现货 |
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25MG | ¥1312 | 有现货 |
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50MG | ¥2187 | 有现货 |
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100MG | ¥3791 | 有现货 |
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500MG | ¥8667 | 有现货 |
|
1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Ledipasvir
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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Ledipasvir is a Hepatitis C Virus NS5A Inhibitor. The mechanism of action of ledipasvir is as a P-Glycoprotein Inhibitor, and Breast Cancer Resistance Protein Inhibitor.
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产品描述Ledipasvir, also known as GS-5885; is an inhibitor of the hepatitis C virus NS5A protein and is a drug for the treatment of hepatitis C that was developed by Gilead Sciences. On October 10, 2014 the FDA approved the combination product ledipasvir 90 mg/sofosbuvir 400 mg (trade name Harvoni). The ledipasvir/sofosbuvir combination is a direct-acting antiviral agent that interferes with HCV replication and can be used to treat patients with genotypes 1a or 1b without PEG-interferon or ribavirin.
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同义词GS5885; GS-5885; GS 5885; Ledipasvir
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通路Cell Cycle/DNA Damage
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靶点HDAC
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受体GT1a; GT1b
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研究领域Infection
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适应症——
化学信息
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CAS Number1256388-51-8
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分子量889
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分子式C49H54F2N8O6
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纯度98%
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溶解度DMSO : 50 mg/mL. 56.24 mM;H2O : < 0.1 mg/mL
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SMILESO=C(OC)N[C@H](C(=O)N1[C@H](c2ncc(c3cc4C(F)(F)c5c(ccc(c6ccc7nc([C@H]8N(C(=O)[C@@H](NC(=O)OC)C(C)C)[C@@H]9CC[C@H]8C9)[nH]c7c6)c5)c4cc3)[nH]2)CC2(C1)CC2)C(C)C
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化学全称Methyl N-[(2S)-1-[(6S)-6-[5-[9,9-Difluoro-7-[2-[(1S,2S,4R)-3-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]-3-azabicyclo[2.2.1]heptan-2-yl]-3H-benzimidazol-5-yl]fluoren-2-yl]-1H-imidazol-2-yl]-5-azaspiro[2.4]heptan-5-yl]-3-methyl-1-oxobutan-2-yl]carbamate
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. Smith MA, et al. Ann Pharmacother. 2015 Mar;49(3):343-50.