186023-44-9
中文名称
(9H-Fluoren-9-yl)MethOxy]Carbonyl Ala-Pro-OH
英文名称
(9H-Fluoren-9-yl)MethOxy]Carbonyl Ala-Pro-OH
CAS
186023-44-9
分子式
C23H24N2O5
分子量
408.45
MOL 文件
186023-44-9.mol
更新日期
2025/05/16 08:27:49
186023-44-9 结构式
基本信息
中文别名
N-芴甲氧羰基-丙氨酰-脯氨酸N-FMOC-L-丙氨酰-L-脯氨酸
N-[(9H-芴-9-甲氧基)羰基]-L-丙氨酰基-L-脯氨酸
英文别名
N-Fmoc-L-Alanyl-L-prolineFmoc-Ala-Pro-OH (B-4415.0001)
(9H-Fluoren-9-yl)MethOxy]Carbonyl Ala-Pro-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-alanyl-L-proline
L-Proline, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanyl-
(2S)-1-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoyl]pyrrolidine-2-carboxylic acid
所属类别
生物化工：氨基酸及其衍生物物理化学性质
沸点674.0±55.0 °C(Predicted)
密度1.318±0.06 g/cm3(Predicted)
酸度系数(pKa)3.51±0.20(Predicted)
InChIKeyHLFCRSYTJCARCY-XOBRGWDASA-N
SMILESC(O)(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O
应用领域
用途一
Fmoc-Ala-Pro-OH is a linker with an Fmoc-protected amine and a terminal carboxylic acid. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.