uspto-grants-1981_03 · 10.6084/m9.figshare.5104873.v1 · US04256736
查看IDENTITY
结构与身份
- 标准SMILES
- NC(=O)CC[C@H](NC(=O)OCc1ccccc1)C(=O)Oc1ccc([N+](=O)[O-])cc1
- InChIKey
- KIVQPDPRDVIJDJ-INIZCTEOSA-N
- 分子式
- C19H19N3O7
- 平均分子量
- 401.4 g/mol
- 单同位素质量
- 401.12229995
COMPUTED
结构计算性质
- XLogP
- 2
- 极性表面积
- 154 Ų
- 氢键供体
- 2
- 氢键受体
- 7
- 可旋转键
- 10
- 重原子
- 29
- 形式电荷
- 0
- 复杂度
- 579
物化、安全与法规信息正在同步。
ALIASES
名称与别名
Z-Gln-ONp7763-16-8(4-nitrophenyl) (2S)-5-amino-5-oxo-2-(phenylmethoxycarbonylamino)pentanoateMFCD00042812N2-Benzyl p-nitrophenyl N2-carboxy-L-(2-aminoglutaramate)EINECS 231-854-44-Nitrophenyl N~2~-[(benzyloxy)carbonyl]glutaminateSCHEMBL11867081DTXSID20228289AKOS016001531FD21563AS-56150FG111458NS00037933N-carbobenzoxy-l-glutamine p-nitro-phenyl ester4-Nitrophenyl N~2~-[(benzyloxy)carbonyl]-L-glutaminateNalpha -benzyloxycarbonyl-L-glutamine p-nitrophenyl ester(4-nitrophenyl) (2S)-5-amino-2-(benzyloxycarbonylamino)-5-oxo-pentanoateN-alpha-BenZyloxycarbonyl-L-glutamine p-nitrophenyl ester (CbZ-L-Gln-ONp)
REACTIONS
参与反应
uspto-grants-1978_06 · 10.6084/m9.figshare.5104873.v1 · US04093611
查看uspto-grants-1979_07 · 10.6084/m9.figshare.5104873.v1 · US04159981
查看uspto-grants-1979_07 · 10.6084/m9.figshare.5104873.v1 · US04159981
查看uspto-grants-1979_07 · 10.6084/m9.figshare.5104873.v1 · US04159981
查看uspto-grants-1976_01 · 10.6084/m9.figshare.5104873.v1 · US03934008
查看uspto-grants-1976_01 · 10.6084/m9.figshare.5104873.v1 · US03934008
查看uspto-grants-1981_06 · 10.6084/m9.figshare.5104873.v1 · US04271152
查看