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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
≤ 4 °C.避光
- 英文名:
7-AMINO-4-METHYLCOUMARIN, N-CBZ-L-PHENYL 10201
- 库存:
99
- 供应商:
Biotium
- CAS号:
65417-22-0
Z-FR-AMC is a substrate for serine proteases, including cathepsins, kallikrein and plasmin.
- λEx/λEm of substrate = 330/390 nm (weak fluorescence)
- λEx/λEm of end product (AMC) = 342/441 nm (strong fluorescence)
- Off-white solid soluble in DMSO
- Store at 4°C and protect from light
- C33H37ClN6O6
- MW: 649.14
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文献和实验Enzymatic Production of D-Amino Acids
to obtain either D- or L-amino acids from D,L-mono-substituted hydantoin derivatives. The initial enzymatic reaction step of D,L-mono-substituted hydantoin hydrolysis is catalyzed by a D-hydantoinase after the subsequent racemization of L-isomer to D-isomer
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.
CarbonCarbon Bond-Forming Enzymes for the Synthesis of Non-natural Amino Acids
An enzymatic methodology for the preparation of β-hydroxy-α-amino acid derivatives is described. The method consists of the stereoselective aldol addition reaction of glycine to N -Cbz-amino aldehydes furnishing 3-hydroxy-2,4-diaminobutyric












