HCID65028

Oseltamivir

ethyl (3R,4R,5S)-4-acetamido-5-amino-3-pentan-3-yloxycyclohexene-1-carboxylate

C16H28N2O4312.4 g/molCAS 196618-13-0

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IDENTITY

结构与身份

标准SMILES: CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1
InChIKey: VSZGPKBBMSAYNT-RRFJBIMHSA-N
分子式: C16H28N2O4
平均分子量: 312.4 g/mol
单同位素质量: 312.20490738

COMPUTED

结构计算性质

等待补全

XLogP: 1.1
极性表面积: 90.7 Å²
氢键供体: 2
氢键受体: 5
可旋转键: 8
重原子: 22
形式电荷: 0
复杂度: 418

物化、安全与法规信息正在同步。

ALIASES

名称与别名

共 104 条

oseltamivir196618-13-0Tamvir(-)-oseltamivirGS-4104ebilfuminGS 4104oseltamivirumGS4104HSDB 7433ethyl (3R,4R,5S)-4-acetamido-5-amino-3-pentan-3-yloxycyclohexene-1-carboxylateRo-640796Ro-64-0796Ethyl (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylateRo 640796GS-4071 ETHYL ESTER20O93L6F9H1-Cyclohexene-1-carboxylic acid, 4-(acetylamino)-5-amino-3-(1-ethylpropoxy)-, ethyl ester, (3R-(3alpha,4beta,5alpha))-ethyl (3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylateRO64-0796

REACTIONS

参与反应

11 条

uspto-grants-2010_06 · 10.6084/m9.figshare.5104873.v1 · US07732632B2

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uspto-grants-2010_06 · 10.6084/m9.figshare.5104873.v1 · US07732632B2

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uspto-grants-2009_05 · 10.6084/m9.figshare.5104873.v1 · US07531687B2

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uspto-grants-2002_10 · 10.6084/m9.figshare.5104873.v1 · US06462226B1

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uspto-grants-2003_02 · 10.6084/m9.figshare.5104873.v1 · US06518048B2

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uspto-grants-2016_02 · 10.6084/m9.figshare.5104873.v1 · US09250238B2

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uspto-grants-2016_02 · 10.6084/m9.figshare.5104873.v1 · US09250238B2

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uspto-grants-2016_02 · 10.6084/m9.figshare.5104873.v1 · US09250238B2

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