Name: 4-((S)-2-((S)-2-amino-3-methylbutanamido)-5-ureidopentanamido)benzyl 2-(pyridin-2-yldisulfanyl)ethylcarbamate
Brand: BOC Sciences
Rating: 5 (1 reviews)

Size

Price

Stock

Quantity

$--

In stock

Synonyms

[4-[[(2S)-2-[[(2S)-2-amino-3-methylbutanoyl]amino]-5-(carbamoylamino)pentanoyl]amino]phenyl]methyl N-[2-(pyridin-2-yldisulfanyl)ethyl]carbamate;

IUPAC Name

Canonical SMILES

CC(C)C(C(=O)NC(CCCNC(=O)N)C(=O)NC1=CC=C(C=C1)COC(=O)NCCSSC2=CC=CC=N2)N

InChI

InChI=1S/C26H37N7O5S2/c1-17(2)22(27)24(35)33-20(6-5-13-30-25(28)36)23(34)32-19-10-8-18(9-11-19)16-38-26(37)31-14-15-39-40-21-7-3-4-12-29-21/h3-4,7-12,17,20,22H,5-6,13-16,27H2,1-2H3,(H,31,37)(H,32,34)(H,33,35)(H3,28,30,36)/t20-,22-/m0/s1

InChIKey

YMBCOKQFJNGLRV-UNMCSNQZSA-N

Appearance

Soild powder

Shipping

Room temperature

4-((S)-2-((S)-2-amino-3-methylbutanamido)-5-ureidopentanamido)benzyl 2-(pyridin-2-yldisulfanyl)ethylcarbamate is a synthetic molecule with versatile applications in biomedical research and pharmaceutical development. Here are some key applications of this compound:

Cancer Research: This compound can be used to study the mechanisms of cancer cell proliferation and survival. Its unique structure allows it to interact with specific proteins involved in cancer pathways. Researchers can use it to develop targeted therapies aimed at inhibiting cancer cell growth and inducing apoptosis.

Drug Delivery Systems: This molecule can be employed in the design of advanced drug delivery systems. Its chemical properties enable it to act as a carrier for therapeutic agents, improving their stability and bioavailability. This application is crucial for enhancing the efficiency of drug delivery and minimizing side effects.

Enzyme Inhibition Studies: The compound is a valuable tool in enzyme inhibition research. By interacting with key enzymes, it helps scientists understand enzyme functions and regulatory mechanisms. This information is vital for designing drugs that can selectively inhibit or modulate enzyme activity in various diseases.

Protein Modification: This molecule can be used for site-specific protein modification in biochemical research. Its reactive groups enable it to form covalent bonds with target proteins, tagging them for further analysis. This application is essential for studying protein-protein interactions and understanding protein function.