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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Recommended Temperature controlled NMT30℃ for storage
- 英文名：
2,3-dihydro-1-benzofuran-5-amine
- 供应商：
南京鼎石
- CAS号：
42933-43-7
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///15554kg
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文献和实验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.
Immunochemical Method for Ochratoxin A
Ochratoxin A (7-L-β-phenylalanylcarbonyl-5-chloro-8-hydroxy-3,4-dihydro-3-R-methylisocoumarin, Fig. 1 ) was first isolated in 1965 from A. ochraceus (1 ). Meanwhile several Aspergillus and Penicillium species are known to produce
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
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