AC-SER-GLN-ASN-TYR-PRO-VAL-VAL-NH2

Modify Date: 2024-01-05 17:07:02

AC-SER-GLN-ASN-TYR-PRO-VAL-VAL-NH2 Structure
AC-SER-GLN-ASN-TYR-PRO-VAL-VAL-NH2 structure
Common Name AC-SER-GLN-ASN-TYR-PRO-VAL-VAL-NH2
CAS Number 121822-32-0 Molecular Weight 846.92700
Density N/A Boiling Point N/A
Molecular Formula C38H58N10O12 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of AC-SER-GLN-ASN-TYR-PRO-VAL-VAL-NH2


Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2 is a substrato peptídico of HIV-1 protease.Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2 acts as the variable substrate in a peptidolytic assay to quantify the inhibition of the protease[1][2].

 Names

Name 2-[(2-acetamido-3-hydroxypropanoyl)amino]-N-[4-amino-1-[[1-[2-[[1-[(1-amino-3-methyl-1-oxobutan-2-yl)amino]-3-methyl-1-oxobutan-2-yl]carbamoyl]pyrrolidin-1-yl]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-1,4-dioxobutan-2-yl]pentanediamide
Synonym More Synonyms

 AC-SER-GLN-ASN-TYR-PRO-VAL-VAL-NH2 Biological Activity

Description Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2 is a substrato peptídico of HIV-1 protease.Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2 acts as the variable substrate in a peptidolytic assay to quantify the inhibition of the protease[1][2].
Related Catalog
References

[1]. Ana C. R. Sodero, et al. Mecanismo Catalítico e Estado de Protonação do Sítio Ativo de Aspartil Proteases Pepsina-Símiles.Revista Virtual de Química, v. 1 n. 2 (2009).

[2]. G B Dreyer, et al. Inhibition of human immunodeficiency virus 1 protease in vitro: rational design of substrate analogue inhibitors. Proc Natl Acad Sci U S A. 1989 Dec;86(24):9752-6.  

 Chemical & Physical Properties

Molecular Formula C38H58N10O12
Molecular Weight 846.92700
Exact Mass 846.42400
PSA 364.64000
LogP 0.16910

 Synonyms

Acetyl-Ser-Gln-Asn-Tyr-Pro-Val-Val amide
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