(R)-piperidine-4-carboxylic acid (acetyl-{3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamoyloxy)-methyl ester hydrochloride 分子结构式
HCID11753752

(R)-piperidine-4-carboxylic acid (acetyl-{3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamoyloxy)-methyl ester hydrochloride

[acetyl-[[(5R)-3-[4-(1,1-dioxothian-4-yl)-3-fluorophenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]carbamoyl]oxymethyl piperidine-4-carboxylate;hydrochloride

C25H33ClFN3O9S606.1 g/mol

IDENTITY

结构与身份

标准SMILES
CC(=O)N(C[C@H]1CN(c2ccc(C3CCS(=O)(=O)CC3)c(F)c2)C(=O)O1)C(=O)OCOC(=O)C1CCNCC1.Cl
InChIKey
QKCXOPOQXDGKKY-BDQAORGHSA-N
分子式
C25H33ClFN3O9S
平均分子量
606.1 g/mol
单同位素质量
605.1610067

COMPUTED

结构计算性质

已同步
极性表面积
157 Ų
氢键供体
2
氢键受体
11
可旋转键
9
重原子
40
形式电荷
0
复杂度
1,020

ALIASES

名称与别名

共 2 条
QKCXOPOQXDGKKY-BDQAORGHSA-N(R)-piperidine-4-carboxylic acid (acetyl-{3-[4-(1,1-dioxo-hexahydro-1lambda6-thiopyran-4-yl)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-carbamoyloxy)-methyl ester hydrochloride

REACTIONS

参与反应

1
HRID 915289 反应方程式

uspto-grants-2007_09 · 10.6084/m9.figshare.5104873.v1 · US07265140B2

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