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118584-90-0

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  • L-Lysine,N6-[[5-(dimethylamino)-1-naphthalenyl]sulfonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-/ LIDE PHARMA- Factory supply / Best price

    Cas No: 118584-90-0

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118584-90-0 Usage

Description

FMOC-L-LYS(DANSYL)-OH, also known as Fmoc-Lysine(Dansyl), is a dansylated peptide derivative that serves as a valuable tool in the field of biochemistry and molecular biology. It is characterized by its white powder form and exhibits unique fluorescent properties due to the dansyl group attached to the lysine residue. This modification allows for the sensitive detection and quantification of proteolytic enzyme activity, making it a versatile reagent for various applications.

Uses

Used in Biochemistry Research:
FMOC-L-LYS(DANSYL)-OH is used as a substrate for fluorometric proteolytic enzyme assays, providing a means to study enzyme kinetics, specificity, and activity. The dansyl group's fluorescence allows for the real-time monitoring of enzymatic reactions, offering a sensitive and quantitative approach to enzyme analysis.
Used in Drug Discovery and Development:
In the pharmaceutical industry, FMOC-L-LYS(DANSYL)-OH can be employed as a tool for the identification and optimization of potential drug candidates targeting proteolytic enzymes. By monitoring the fluorescence changes upon enzyme cleavage, researchers can screen for compounds that modulate enzyme activity, leading to the development of novel therapeutic agents.
Used in Diagnostic Applications:
FMOC-L-LYS(DANSYL)-OH can be utilized in the development of diagnostic assays for various diseases, particularly those involving abnormal proteolytic activity. The dansyl group's fluorescence can be harnessed to create sensitive and specific tests for the detection and monitoring of disease biomarkers, aiding in early diagnosis and treatment.
Used in Education and Training:
In academic settings, FMOC-L-LYS(DANSYL)-OH serves as an educational tool for teaching students about enzyme kinetics, mechanisms, and the principles of fluorescence-based assays. It provides a hands-on experience in conducting experiments and understanding the fundamental concepts of biochemistry and molecular biology.

Check Digit Verification of cas no

The CAS Registry Mumber 118584-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,8 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 118584-90:
(8*1)+(7*1)+(6*8)+(5*5)+(4*8)+(3*4)+(2*9)+(1*0)=150
150 % 10 = 0
So 118584-90-0 is a valid CAS Registry Number.

118584-90-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-6-[[5-(dimethylamino)naphthalen-1-yl]sulfonylamino]-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid

1.2 Other means of identification

Product number -
Other names AmbotzFAA1446

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:118584-90-0 SDS

118584-90-0Downstream Products

118584-90-0Relevant articles and documents

Efficient N-terminal labeling of proteins by use of sortase

Williamson, Daniel J.,Fascione, Martin A.,Webb, Michael E.,Turnbull, W. Bruce

supporting information, p. 9377 - 9380 (2012/11/06)

"Sorting out" N-terminal labeling: The reversibility of transpeptidase reactions makes protein N-terminal labeling challenging. Depsipeptide substrates for sortase A release alcohol by-products, which are poor nucleophiles for the reverse reaction, during ligation. Proteins with an unhindered N-terminal glycine residue can be labeled efficiently with only a minimal excess of the labeling reagent (see scheme).

Synthese Bor-reicher Lysindendrimere zur Proteinmarkierung in der Elektronenmikroskopie

Qualmann, Britta,Kessels, Michael Manfred,Musiol, Hans-Juergen,Sierralta, Walter Daniel,Jungblut, Peter Wilhelm,Moroder, Luis

, p. 970 - 973 (2007/10/03)

Keywords: Borverbindungen; Dendrimere; Elektronenmikroskopie; Festphasensynthese; Peptide

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