2-氨基-4,5-二氢-5-羟基-4,4-二甲基萘并1,2-
b:4,3-b’difuran-3-羧酸乙酯 2-Amino-4,5-dihydro-5-hydroxy-4,4-dimethyl-naphtho1,2-b:4,3-b’difuran-3-carboxylic acid ethyl ester 30119-43-8 **科研现货速达** ≥98% HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等- 询价
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
2-Amino-4,5-dihydro-5-hydroxy-4,4-dimethyl-naphtho1,2-b:4,3-b’difuran-3-carboxylic acid ethyl ester
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
30119-43-8
- 规格：
10mg/100mg/5515mg
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文献和实验Precolumn derivatization of amino acids followed by their resolution by reverse-phase high-performance liquid chromatography (RP-HPLC) is now the preferred method for quantitative amino acid analysis. The derivatization step introduces
Preparation of Unnatural Amino Acids with Ammonia-Lyases and 2,3-Aminomutases
of unnatural amino acids. Besides the synthesis of various unnatural α-amino acids with the aid of phenylalanine ammonia-lyases (PALs) utilizing the 3,5-dihydro-5-methylidene-4H-imidazol-4-one (MIO) prosthetic groups, the biotransformations leading to various
Synthesis of 3-Amino-l-CarboxymethyI-Benzodiazepine (BZA) Peptidomimetics
inhibitors of Ras famesyltransferase (FTase) (6 ,7 ). The central pair of amino acids in the CAAX tetrapeptide was replaced with the nonpeptide scaffold 3-methylamino-1-carboxymethyl-2,3-dihydro-5-phenyl-1H-1,4-benzodiazepin-2-one, (N -Me)BZA, shown below.
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