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新型荧光埃德曼试剂7-N,N-二甲基氨基磺酰基-4-(2,1,3-苯并恶二唑基)异硫氰酸酯(DBD-NCS)和7-氨基磺酰基-4-(2,1,3-苯并恶二唑基)异硫氰酸酯(ABD-NCS)的合成。

Synthesis of novel fluorogenic Edman reagents, 7-N,N-dimethylaminosulphonyl- 4-(2,1,3-benzoxadiazolyl)isothiocyanate (DBD-NCS) and 7-aminosulphonyl-4-(2,1,3-benzoxadiazolyl)isothiocyanate (ABD-NCS).

作者信息

Imai K, Uzu S, Nakashima K, Akiyama S

机构信息

Branch Hospital Pharmacy, University of Tokyo, Japan.

出版信息

Biomed Chromatogr. 1993 Jan-Feb;7(1):56-7. doi: 10.1002/bmc.1130070114.

Abstract

Novel fluorogenic Edman reagents, 7-N,N-dimethylaminosulphonyl-4- (2,1,3-benzoxadiazolyl)isothiocyanate (DBD-NCS) and 7-aminosulphonyl-4-(2,1,3-benzoxadiazolyl)isothiocyanate (ABD-NCS) having no fluorescence themselves were synthesized. The derivatives of amino acids with DBD-NCS fluorescence at 505 nm with excitation at 385 nm. They were separated on a reversed-phase HPLC column and detected at the sub-picomol level. Ala-Phe derivatized with DBD-NCS was cleaved by acid to generate DBD-thiocarbamyl-Ala.

摘要

合成了新型荧光埃德曼试剂,即本身无荧光的7-N,N-二甲基氨基磺酰基-4-(2,1,3-苯并恶二唑基)异硫氰酸酯(DBD-NCS)和7-氨基磺酰基-4-(2,1,3-苯并恶二唑基)异硫氰酸酯(ABD-NCS)。氨基酸与DBD-NCS的衍生物在385nm激发下于505nm处发出荧光。它们在反相高效液相色谱柱上分离,并在亚皮摩尔水平进行检测。用DBD-NCS衍生化的丙氨酰-苯丙氨酸经酸裂解生成DBD-硫代氨基甲酰基-丙氨酸。

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