4-Pentynoyl-Val-Ala-PAB - CAS 1956294-75-9

4-Pentynoyl-Val-Ala-PAB - CAS 1956294-75-9 Catalog number: BADC-01843

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4-Pentynoyl-Val-Ala-PAB is a click chemistry reagent containing an azide group.

Category
ADCs Linker
Product Name
4-Pentynoyl-Val-Ala-PAB
CAS
1956294-75-9
Catalog Number
BADC-01843
Molecular Formula
C20H27N3O4
Molecular Weight
373.45

Ordering Information

Catalog Number Size Price Quantity
BADC-01843 -- $-- Inquiry
Description
4-Pentynoyl-Val-Ala-PAB is a click chemistry reagent containing an azide group.
Synonyms
4-Pentynoyl-Val-Ala-PAB-OH
IUPAC Name
(2S)-N-[(2S)-1-[4-(hydroxymethyl)anilino]-1-oxopropan-2-yl]-3-methyl-2-(pent-4-ynoylamino)butanamide
Canonical SMILES
CC(C)C(C(=O)NC(C)C(=O)NC1=CC=C(C=C1)CO)NC(=O)CCC#C
InChI
InChI=1S/C20H27N3O4/c1-5-6-7-17(25)23-18(13(2)3)20(27)21-14(4)19(26)22-16-10-8-15(12-24)9-11-16/h1,8-11,13-14,18,24H,6-7,12H2,2-4H3,(H,21,27)(H,22,26)(H,23,25)/t14-,18-/m0/s1
InChIKey
ZCRVRFUMZRBARG-KSSFIOAISA-N

4-Pentynoyl-Val-Ala-PAB, a versatile compound renowned in biochemical and medical research, finds diverse applications. Here are four key applications utilizing high perplexity and burstiness:

Protease Inhibition Studies: Widely employed as a specific inhibitor in protease activity assays, 4-Pentynoyl-Val-Ala-PAB intricately binds to the active sites of target proteases, allowing for a deep dive into the enzyme's kinetics and inhibition mechanisms. This profound knowledge serves as the bedrock for crafting novel therapeutic inhibitors tailored for diseases stemming from protease dysregulation.

Drug Design: In the realm of pharmaceutical research, 4-Pentynoyl-Val-Ala-PAB emerges as a beacon guiding the development of cutting-edge protease inhibitors. Its adaptable structure facilitates enhancements that boost potency and selectivity towards specific proteases. Researchers leverage its potential to innovate and validate new drug candidates targeting a spectrum of conditions, ranging from cancer to infectious diseases, ushering in a new era of therapeutic possibilities.

Chemical Biology: The unique alkyne group present in 4-Pentynoyl-Val-Ala-PAB positions it as a prime contender for bioorthogonal chemistry reactions, notably in click chemistry. By integrating this compound into biological systems, researchers can adorn and monitor specific proteins or processes within live cells. This application stands as a cornerstone for visualizing dynamic cellular processes and investigating intricate protein interactions with unparalleled precision.

Proteomics: Unveiling its prowess in proteomics, 4-Pentynoyl-Val-Ala-PAB emerges as a tool for enriching and unveiling protease substrates alongside their cleavage sites. Through the inhibition of protease activity and the capture of protease-substrate complexes, researchers glean intricate insights into proteolytic pathways, deepening our understanding of the pivotal roles played by proteases in cellular processes and the pathogenesis of diseases.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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