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抑胃酶氨酸-BOC CAS 58521-49-6
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货号 | 5101 | 存储条件 | 在零下15度以下保存 |
| 规格 | 10 g | 价格 | 33036 | |
| Ex (nm) | Em (nm) | |||
| 分子量 | 275.34 | 溶剂 | DMF | |
| 产品详细介绍 | ||||
简要概述
产品基本信息
货号：5101
产品名称：抑胃酶氨酸-BOC
CAS：58521-49-6
规格：10g
储存条件：-15℃避光防潮
保质期：12个月
产品物理化学光谱特性
分子量：275.34
溶剂：DMF
激发波长（nm）：N/A
发射波长（nm）：N/A
产品介绍
（3S，4S）-Statine是胃蛋白酶抑制剂的新型氨基酸，胃蛋白酶抑制剂是酸性蛋白酶的低分子量抑制剂。这种BOC-Statine构建锁是使用标准BOC化学制备用于药物应用的蛋白酶抗性肽的非常有用的前体。金畔生物是AAT Bioquest的中国代理商，为您提供最优质的赖氨酸Lys 5-FITC标记。
参考文献
Investigation of the synthetic route to pepstatin analogues by SPPS using O-protected and O-unprotected statine as building blocks
Authors: Cadicamo CD, Asante V, Abu Ammar M, Borelli C, Korting HC, Koksch B.
Journal: J Pept Sci (2009): 272
[Drug (statine)-induced hepatitis]
Authors: Lazebnik LB, Zvenigorodskaia LA, Khomeriki SG, Efremov LI, Cherkashova EA.
Journal: Eksp Klin Gastroenterol (2009): 110
A simple microscale method for determining the relative stereochemistry of statine units
Authors: Preciado A, Williams PG.
Journal: J Org Chem (2008): 9228
Atovaquone-statine “double-drugs” with high antiplasmodial activity
Authors: Romeo S, Parapini S, Dell’Agli M, Vaiana N, Magrone P, Galli G, Sparatore A, Taramelli D, Bosisio E.
Journal: ChemMedChem (2008): 418
Design, synthesis and SAR of potent statine-based BACE-1 inhibitors: exploration of P1 phenoxy and benzyloxy residues
Authors: Back M, Nyhlen J, Kvarnstrom I, Appelgren S, Borkakoti N, Jansson K, Lindberg J, Nystrom S, Hallberg A, Rosenquist S, Samuelsson B.
Journal: Bioorg Med Chem (2008): 9471
Macrocyclic statine-based inhibitors of BACE-1
Authors: Barazza A, Gotz M, Cadamuro SA, Goettig P, Willem M, Steuber H, Kohler T, Jestel A, Reinemer P, Renner C, Bode W, Moroder L.
Journal: Chembiochem (2007): 2078
Stereocontrolled synthesis of 2,4-diamino-3-hydroxyacids starting from diketopiperazines: a new route for the preparation of statine analogues
Authors: Farran D, Toupet L, Martinez J, Dewynter G.
Journal: Org Lett (2007): 4833
A novel approach to identifying beta-secretase inhibitors: bis-statine peptide mimetics discovered using structure and spot synthesis
Authors: Bridges KG, Chopra R, Lin L, Svenson K, Tam A, Jin G, Cowling R, Lovering F, Akopian TN, DiBlasio-Smith E, Annis-Freeman B, Marvell TH, LaVallie ER, Zollner RS, Bard J, Somers WS, Stahl ML, Kriz RW.
Journal: Peptides (2006): 1877
Molecular docking and 3D-QSAR studies on the binding mechanism of statine-based peptidomimetics with beta-secretase
Authors: Zuo Z, Luo X, Zhu W, Shen J, Shen X, Jiang H, Chen K.
Journal: Bioorg Med Chem (2005): 2121
Design and synthesis of potent inhibitors of the malaria aspartyl proteases plasmepsin I and II. Use of solid-phase synthesis to explore novel statine motifs
Authors: Johansson PO, Chen Y, Belfrage AK, Blackman MJ, Kvarnstrom I, Jansson K, Vrang L, Hamelink E, Hallberg A, Rosenquist A, Samuelsson B.
Journal: J Med Chem (2004): 3353
