标签归档：boc

抑胃酶氨酸-BOC CAS 58521-49-6 货号5101-AAT Bioquest荧光染料

发表于由

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品，欢迎访问AAT Bioquest荧光染料官网了解更多信息。

抑胃酶氨酸-BOC CAS 58521-49-6

抑胃酶氨酸-BOC CAS 58521-49-6

抑胃酶氨酸-BOC CAS 58521-49-6 货号5101 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

说明书
抑胃酶氨酸-BOC CAS 58521-49-6.pdf

胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC 货号13461-AAT Bioquest荧光染料

发表于由

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品，欢迎访问AAT Bioquest荧光染料官网了解更多信息。

胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC

胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC

胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC 货号13461 货号 13461 存储条件 在零下15度以下保存, 避免光照
规格 5 mg 价格 1272
Ex (nm) 341 Em (nm) 441
分子量 741.75 溶剂 DMSO
产品详细介绍

简要概述

产品基本信息

货号：13461

产品名称：胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC

规格：5mg

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：741.75

溶剂：DMSO

激发波长（nm）：351

发射波长（nm）：430

 

产品介绍

胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC是美国AAT Bioquest生产的荧光底物，BOC-Val-Pro-Arg-AMC是α-凝血酶的敏感荧光底物。非荧光基板产生亮蓝色荧光AMC产品，其具有Ex / Em = 351 / 430nm，并且可以使用DAPI滤光器组容易地检测。据报道，BOC-Val-Pro-Arg-AMC的α-凝血酶和α-凝血酶卟啉葡萄糖苷复合物的Km值分别为21和25μM。 BOC-Val-ProArg-AMC的α-凝血酶和α-凝血酶葡萄糖凝固酶复合物的Kcat值分别为105和89s-1。该底物也已用于MRSA（耐甲氧西林金黄色葡萄球菌）的快速检测。金畔生物是AAT Bioquest的中国代理商，为您提供最优质的胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC。 

点击查看光谱

 

参考文献

A fluorescence lifetime-based assay for protease inhibitor profiling on human kallikrein 7
Authors: Doering K, Meder G, Hinnenberger M, Woelcke J, Mayr LM, Hassiepen U.
Journal: J Biomol Screen (2009): 1

A fluorescence quenching assay to discriminate between specific and nonspecific inhibitors of dengue virus protease
Authors: Bodenreider C, Beer D, Keller TH, Sonntag S, Wen D, Yap L, Yau YH, Shochat SG, Huang D, Zhou T, Caflisch A, Su XC, Ozawa K, Otting G, Vasudevan SG, Lescar J, Lim SP.
Journal: Anal Biochem (2009): 195

A protease inhibitor discovery method using fluorescence correlation spectroscopy with position-specific labeled protein substrates
Authors: Nakata H, Ohtsuki T, Sisido M.
Journal: Anal Biochem (2009): 121

Dual-function probe to detect protease activity for fluorescence measurement and 19F MRI
Authors: Mizukami S, Takikawa R, Sugihara F, Shirakawa M, Kikuchi K.
Journal: Angew Chem Int Ed Engl (2009): 3641

Fluorescence resonance energy transfer-based assay for characterization of hepatitis C virus NS3-4A protease activity in live cells
Authors: Sabariegos R, Picazo F, Domingo B, Franco S, Martinez MA, Llopis J.
Journal: Antimicrob Agents Chemother (2009): 728

Improved detection of ovarian cancer metastases by intraoperative quantitative fluorescence protease imaging in a pre-clinical model
Authors: Sheth RA, Upadhyay R, Stangenberg L, Sheth R, Weissleder R, Mahmood U.
Journal: Gynecol Oncol (2009): 616

Label-free, homogeneous, and fluorescence “turn-on” detection of protease using conjugated polyelectrolytes
Authors: An L, Liu L, Wang S.
Journal: Biomacromolecules (2009): 454

Real-time detection of caspase-3-like protease activation in vivo using fluorescence resonance energy transfer during plant programmed cell death induced by ultraviolet C overexposure
Authors: Zhang L, Xu Q, Xing D, Gao C, Xiong H.
Journal: Plant Physiol (2009): 1773

Real-time monitoring of human enterovirus (HEV)-infected cells and anti-HEV 3C protease potency by fluorescence resonance energy transfer
Authors: Tsai MT, Cheng YH, Liu YN, Liao NC, Lu WW, Kung SH.
Journal: Antimicrob Agents Chemother (2009): 748

[Prokaryotic expression and Identification of dual-fluorescence fusion proteins of small ubiquitin-like modifier and sentrin-specific protease]
Authors: Wang X, Guo J, Wang J, Li S, Sun L, Lu J.
Journal: Sheng Wu Gong Cheng Xue Bao (2009): 701

 

相关产品

产品名称 货号
荧光底物BOC-Val-Pro-Arg-Aminoluciferin Cat#13002

说明书
胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC.pdf

荧光底物BOC-Val-Pro-Arg-Aminoluciferin 货号13002-AAT Bioquest荧光染料

发表于由

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品，欢迎访问AAT Bioquest荧光染料官网了解更多信息。

荧光底物BOC-Val-Pro-Arg-Aminoluciferin

荧光底物BOC-Val-Pro-Arg-Aminoluciferin

荧光底物BOC-Val-Pro-Arg-Aminoluciferin 货号13002 货号 13002 存储条件 在零下15度以下保存, 避免光照
规格 1 mg 价格 6564
Ex (nm) Em (nm)
分子量 845.91 溶剂 DMSO
产品详细介绍

简要概述

产品基本信息

货号：13002

产品名称：BOC-Val-Pro-Arg-氨基荧光素

规格：1mg

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：845.91

溶剂：DMSO

 

产品介绍

        BOC-Val-Pro-Arg-氨基荧光素是美国AAT Bioquest生产的荧光底物，BOC-Val-Pro-Arg-氨基荧光素是α-凝血酶的敏感发光底物。不发光底物产生明亮的发光产物氨基荧光素，其可以用荧光素酶容易地检测。该底物也已用于MRSA（耐甲氧西林金黄色葡萄球菌）的快速检测。金畔生物是AAT Bioquest的中国代理商，为您提供最优质的BOC-Val-Pro-Arg-氨基荧光素。 

 

参考文献

Endotoxin assay by bioluminescence using mutant firefly luciferase
Authors: Kenichi Noda, Hitoshi Goto, Yuji Murakami, Abo Bakr F Ahmed, Akio Kuroda
Journal: Analytical biochemistry (2010): 152–155

 

相关产品

产品名称 货号
胰凝乳蛋白酶荧光底物BOC-Val-Pro-Arg-AMC Cat#13461

说明书
荧光底物BOC-Val-Pro-Arg-Aminoluciferin.pdf

抑胃酶氨酸-BOC CAS 58521-49-6 货号5100-AAT Bioquest荧光染料

发表于由

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品，欢迎访问AAT Bioquest荧光染料官网了解更多信息。

抑胃酶氨酸-BOC CAS 58521-49-6

抑胃酶氨酸-BOC CAS 58521-49-6

抑胃酶氨酸-BOC CAS 58521-49-6 货号5100 货号 5100 存储条件 在零下15度以下保存
规格 1 g 价格 6564
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：5100

产品名称：抑胃酶氨酸-BOC

CAS：58521-49-6

规格：1g

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

说明书
抑胃酶氨酸-BOC CAS 58521-49-6.pdf

BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK] CAS 187389-53-3 货号5311-AAT Bioquest荧光染料

发表于由

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品，欢迎访问AAT Bioquest荧光染料官网了解更多信息。

BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK] CAS 187389-53-3

BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK] CAS 187389-53-3

BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK] CAS 187389-53-3 货号5311 货号 5311 存储条件
规格 10 mg 价格 6564
Ex (nm) Em (nm)
分子量 263.27 溶剂
产品详细介绍

简要概述

产品基本信息

货号：5311

产品名称：BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK]

CAS：187389-53-3

规格：10mg

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：263.27

溶剂：DMF

激发波长（nm）：N/A

发射波长（nm）：N/A

 

产品介绍

FMK肽是有效的，可透过细胞的，不可逆的capase抑制剂。它可用于检测和监测体外和体内应用中的细胞凋亡。BOC-ASP（OMe）-FMK是开发和制备基于FMK的capase抑制剂和探针的关键中间体。基于Asp（OMe）-FMK的半胱天冬酶抑制剂是细胞可渗透的并且不可逆地结合活化的半胱天冬酶以阻断细胞凋亡。作为分子链锯的胱天蛋白酶是细胞凋亡反应的核心组成部分。半胱天冬酶是半胱氨酸蛋白酶，其天冬氨酸残基在其底物中裂解。14种已知的哺乳动物半胱天冬酶中至少有7种在细胞凋亡中起重要作用。金畔生物是AAT Bioquest的中国代理商，为您提供最优质的BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK]。

 

参考文献

A glycine-leucine-rich peptide structurally related to the plasticins from skin secretions of the frog Leptodactylus laticeps (Leptodactylidae)
Authors: Conlon JM, Abdel-Wahab YH, Flatt PR, Leprince J, Vaudry H, Jouenne T, Condamine E.
Journal: Peptides (2009): 888

Design of nontoxic analogues of cathelicidin-derived bovine antimicrobial peptide BMAP-27: the role of leucine as well as phenylalanine zipper sequences in determining its toxicity
Authors: Ahmad A, Azmi S, Srivastava RM, Srivastava S, Pandey BK, Saxena R, Bajpai VK, Ghosh JK.
Journal: Biochemistry (2009): 10905

Leucine-rich amelogenin peptide induces osteogenesis by activation of the Wnt pathway
Authors: Warotayanont R, Frenkel B, Snead ML, Zhou Y.
Journal: Biochem Biophys Res Commun (2009): 558

Leucine-rich amelogenin peptide induces osteogenesis in mouse embryonic stem cells
Authors: Warotayanont R, Zhu D, Snead ML, Zhou Y.
Journal: Biochem Biophys Res Commun (2008): 1

Leucine-rich glioma inactivated 3 is involved in amyloid beta peptide uptake by astrocytes and endocytosis itself
Authors: Okabayashi S, Kimura N.
Journal: Neuroreport (2008): 1175

Leucine 7-proline 7 polymorphism in the signal peptide of neuropeptide Y is not a risk factor for exudative age-related macular degeneration
Authors: Kaarniranta K, Holopainen JM, Karvonen MK, Koulu M, Kallio J, Pesonen U, Terasvirta M, Uusitalo H, Immonen I.
Journal: Acta Ophthalmol Scand (2007): 188

Peptide-phospholipid cross-linking reactions: identification of leucine enkephalin-alka(e)nal-glycerophosphatidylcholine adducts by tandem mass spectrometry
Authors: Reis A, Domingues P, Ferrer-Correia AJ, Domingues MR.
Journal: J Am Soc Mass Spectrom (2006): 657

131I-Labeled arginine-arginine-leucine (RRL)-containing cyclic peptide (YCGGRRLGGC) for imaging prostate carcinoma
Authors: Shan L
Journal: (2004)

Leucine-rich amelogenin peptide: a candidate signaling molecule during cementogenesis
Authors: Boabaid F, Gibson CW, Kuehl MA, Berry JE, Snead ML, Nociti FH, Jr., Katchburian E, Somerman MJ.
Journal: J Periodontol (2004): 1126

Cloning the tomato curl3 gene highlights the putative dual role of the leucine-rich repeat receptor kinase tBRI1/SR160 in plant steroid hormone and peptide hormone signaling
Authors: Montoya T, Nomura T, Farrar K, Kaneta T, Yokota T, Bishop GJ.
Journal: Plant Cell (2002): 3163

说明书
BOC-Asp(OMe)-FMK [Boc-D(OMe)-FMK] CAS 187389-53-3.pdf