CAS: 52299-14-6; 4-(((S)-1-(((S)-1-(((S)-1-((4-Nitrophenyl)Amino)-1-Oxopropan-2-yl)Amino)-1-Oxopropan-2-yl)Amino)-1-Oxopropan-2-yl)Amino)-4-Oxobutanoic Acid
该化合物是一种铬基基质,通常用于对弹性体和其他蛋白解酶进行检测,该化合物由与三偏化物(Ala-Ala-Ala-Ala)相连的苏cci(Suc)组和半硝基亚尼(p-NA)离开组组成.在酶裂变后,p-NA的释放产生一种黄色的,可测量的可测量光谱光谱,在405纳米时进行定量分析,从而能够对酶活动进行定量分析.它对于弹性体的高度特殊性使它成为生物化学和药物研究的宝贵工具.在标准实验室条件下,该基质稳定,并提供可靠,可复制的结果,便利动力研究和抑制剂检测.它的水溶性进一步提高其在体外测量中的效用.
- 英文名称4-(((S)-1-(((S)-1-(((S)-1-((4-Nitrophenyl)Amino)-1-Oxopropan-2-yl)Amino)-1-Oxopropan-2-yl)Amino)-1-Oxopropan-2-yl)Amino)-4-Oxobutanoic Acid
- 中文名称Suc-丙氨酰-丙氨酰-丙氨酰-对硝基苯胺
- IUPAC名称4-(((S)-1-(((S)-1-(((S)-1-((4-nitrophenyl)amino)-1-oxopropan-2-yl)amino)-1-oxopropan-2-yl)amino)-1-oxopropan-2-yl)amino)-4-oxobutanoic acid
- 其它别名3-Carboxypropionyl-L-alanyl-L-alanyl-L-alaninep-nitroanilide; Chromozym ELA; N-Succinyl-L-alanyl-L-alanyl-L-alanine p-nitroanilide; Succinyl-L-alanyl-L-alanyl-L-alanine 4-nitroanilide; Succinyl-L-alanyl-L-alanyl-L-alanine p-nitroanilide; Succinyl-L-alanyl-L-alanyl-L-alanyl p-nitroanilide; Succinyl-L-trialaninep-nitroanilide
- CAS编号52299-14-6
- MFCD编号:MFCD00036774
- EINECS号:257-823-5
- FDA UNII编号:9MJ6NSX3KJ
- 分子式:C19H25N5O8分子量:451.44
- 产品CID: 2512968
- 产品分类生物化工 → 氨基酸及其衍生物 → 丙氨酸类衍生物
物理性质
MSDS等安全信息
上下游产品
CAS号2483-52-5 N-benzyloxycarb... | CAS号1668-13-9 L-丙氨酸4-硝基酰苯胺 | CAS号108-30-5 丁二酸酐 | CAS号60354-61-2 AAA-pNA | CAS号100-01-6 对硝基苯胺 | CAS号1668-13-9 L-丙氨酸4-硝基酰苯胺 | CAS号141509-27-5 4-[[(2S)-1-[[(1...合成工艺路线路线简述
📜Benzyl ((S)-1-(((S)-1-Hydrazinyl-1-Oxopropan-2-yl)Amino)-1-Oxopropan-2-yl)Carbamate置于盐酸,Zeolit G (Oh Form),氢溴酸,Sodium Nitrite体系中,用 溶剂黄146,N,N-二甲基甲酰胺 作为反应溶剂,化学反应 1.0H,反应生成 Suc-丙氨酰-丙氨酰-丙氨酰-对硝基苯胺
参考文献:Kasafirek,Evzen; Fric,Premysl; Slaby,Jan,Collection Of Czechoslovak Chemical Communications,1987,Vol. 52,# 6,P. 1625-1633
标题:Kasafirek,Evzen; Fric,Premysl; Slaby,Jan,Collection Of Czechoslovak Chemical Communications,1987,Vol. 52,# 6,P. 1625-1633
海关参考信息
- 2905121000-正丙醇
2905130000-正丁醇
2912110000-甲醛
2912120000-乙醛 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:US-10105313-B2
优先权日:2014-05-19
标 题 :Uses of rose pigment compounds
发明人：FUKUI YUKO; YOSHIMOTO YUKO; MATSUOKA TATSUO; KITAGAWA SAYURI
权利人:SUNTORY HOLDINGS LTD
摘要:An object of the present invention is to provide hyaluronidase inhibitors, collagenase inhibitors, elastase inhibitors, MMP-1 production suppressors, and collagen synthesis promoters that contain as an active component one or more pigment compounds that are obtained as extracted from plants of the family Rosaceae, as well as agents for cutaneous application, skin cosmetics, and quasi-drugs that contain such pigment compounds. The present invention provides hyaluronidase inhibitors, collagenase inhibitors, elastase inhibitors, MMP-1 production suppressors, collagen synthesis promoters, agents for cutaneous application, skin cosmetics, and quasi-drugs that contain one or more compounds in a class of rosacyanins or one or more compounds in a class of rosadelphins as an active component.
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
合成参考文献
参考文献:10.5625/lar.2015.31.3.148
摘要:Choi E, Guo H, Choi J, Jang S, Shin K, Cha Y, Choi Y, Seo D, Lee Y, Joo S, Kim Y. Extraction conditions of white rose petals for the inhibition of enzymes related to skin aging. Laboratory Animal Research. 2015 Jul;31(3):148–52. doi: 10.5625/lar.2015.31.3.148.
参考文献:10.1002/bit.10891
摘要:Yoshimoto M, Wang S, Fukunaga K, Treyer M, Walde P, Kuboi R, Nakao K. Enhancement of apparent substrate selectivity of proteinase K encapsulated in liposomes through a cholate-induced alteration of the bilayer permeability. Biotechnol Bioeng. 2004 Jan 20;85(2):222–33. doi: 10.1002/bit.10891.
参考文献:10.1007/s002530051554
摘要:Terashima M, Murai Y, Kawamura M, Nakanishi S, Stoltz T, Chen L, Drohan W, Rodriguez RL, Katoh S. Production of functional human alpha 1-antitrypsin by plant cell culture. Appl Microbiol Biotechnol. 1999 Oct;52(4):516–23. doi: 10.1007/s002530051554.
参考文献:10.1007/978-1-60327-058-8_21
摘要:Proudfoot M, Kuznetsova E, Sanders SA, Gonzalez CF, Brown G, Edwards AM, Arrowsmith CH, Yakunin AF. High throughput screening of purified proteins for enzymatic activity. Methods Mol Biol. 2008;426():331–41. doi: 10.1007/978-1-60327-058-8_21.
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