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4-nitrophenyl N-[(benzyloxy)carbonyl]alanylprolylglycinate is a chemical compound belonging to the class of 4-nitrophenyl esters, characterized by the presence of a 4-nitrophenyl group, a benzyloxy carbonyl group, an alanylprolylglycinate group, and an N-terminal modification. It is widely utilized in biochemical and pharmaceutical research for its unique structure and reactivity, making it a valuable tool in studying proteolytic enzyme activity, drug development, and protein-protein interactions.

35006-34-9

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35006-34-9 Usage

Uses

Used in Biochemical Research:
4-nitrophenyl N-[(benzyloxy)carbonyl]alanylprolylglycinate is used as a colorimetric substrate for enzyme assays, particularly in the study of proteolytic enzyme activity. Its specific chemical structure allows for the monitoring of enzyme activity through color changes, providing a convenient and sensitive method for assessing enzyme function.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, 4-nitrophenyl N-[(benzyloxy)carbonyl]alanylprolylglycinate serves as a valuable tool for drug development. Its reactivity and interaction with proteolytic enzymes can be leveraged to design and optimize drugs targeting specific biological processes, potentially leading to the discovery of novel therapeutic agents.
Used in Understanding Protein-Protein Interactions:
4-nitrophenyl N-[(benzyloxy)carbonyl]alanylprolylglycinate is employed in the study of protein-protein interactions, providing insights into the molecular mechanisms underlying various biological processes. By examining the compound's interactions with different proteins, researchers can gain a deeper understanding of the roles these proteins play in cellular function and disease progression.
Overall, 4-nitrophenyl N-[(benzyloxy)carbonyl]alanylprolylglycinate is a versatile chemical compound with diverse applications in biochemical and pharmaceutical research, enzyme assays, drug development, and the study of protein-protein interactions. Its unique structure and reactivity make it an indispensable tool for advancing our understanding of biological processes and developing new therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 35006-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,0 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35006-34:
(7*3)+(6*5)+(5*0)+(4*0)+(3*6)+(2*3)+(1*4)=79
79 % 10 = 9
So 35006-34-9 is a valid CAS Registry Number.

35006-34-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(9H-pyrido[3,4-b]indol-1-yl)furan-2-yl]methanol

1.2 Other means of identification

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Other names -

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

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More Details:35006-34-9 SDS

35006-34-9Upstream product

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