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Postion:Product Catalog >Biochemical Engineering>Biochemical Reagents>Agonist Inhibitors>BAY-57-1293
BAY-57-1293
  • BAY-57-1293

BAY-57-1293

Price $7
Package 1KG
Min. Order: 1KG
Supply Ability: 100KG
Update Time: 2019-07-10

Product Details

Product Name: BAY-57-1293 CAS No.: 348086-71-5
Min. Order: 1KG Purity: 99%
Supply Ability: 100KG Release date: 2019/07/10

JD 607 100

Product Name: BAY-57-1293
Synonyms: BAY-57-1293;Pritelivir;N-[5-(Aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide;Pritelivir,BAY-57-1293;Benzeneacetamide, N-[5-(aminosulfonyl)-4-methyl-2-thiazolyl]-N-methyl-4-(2-pyridinyl)-;AIC316;N-[5-(Aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide BAY57-1293 Pritelivir;2-METHYL-2-PROPANYL [4-(CHLOROSULFONYL)PHENYL]CARBAMATE
CAS: 348086-71-5
MF: C18H18N4O3S2
MW: 402.49052
EINECS:  
Product Categories: Inhibitors
Mol File: 348086-71-5.mol
Article illustration
 
BAY-57-1293 Chemical Properties
 
Safety Information
MSDS Information
 
 
BAY-57-1293 Usage And Synthesis
Enzyme inhibitor This antiviral (FW = 402.49 g/mol; CAS 348086-71-5), also named BAY 57-1293 and N-methyl-N-(4-methyl-5-sulfamoyl-1,3-thiazol-2-yl)-2-[4- (pyridin-2-yl)phenyl]acetamide, inhibits replication of herpes simplex virus (HSV) types 1 and 2 by blocking the enzymatic activity of the viral primase-helicase complex (IC50 ≈ 20 nM)). Although pritelivir is highly active against HSV-1 and superior to acyclovir in Vero cells, drug resistance has been detected in two different strains of HSV at 10-4 to 10-5, and resistant variants are present, even before the selection was applied. Resistant variants did not readily revert to a drug-sensitive phenotype in the absence of the inhibitor, and representative pritelivir-resistant variants were cross-resistant to BILS-22-BS, another helicase-primase inhibitor (HPI). Notably, variants resistant to BAY 57-1293 retained sensitivity to the nucleoside analogue, ACV. Two HSV-1 mutants, that are 100x and >3000x resistant to ritelivir, have substitutions in the UL5 helicase protein (e.g., one with A4V and K356Q mutations, and the other with a single G352R mutation). Marker transfer experiments confirmed that K356Q and G352R (near the predicted functional domain of HSV-1 helicase)) are the drug-resistance mutations that are directly associated with differences in virus growth in tissue culture. Moreover, to achieve maximum potency, pritelivir interacts with both components (UL5 and UL52) of the helicaseprimase complex, but BILS-22-BS does not. Herpes simplex type 1 (HSV1) infected cells form β-amyloid (Aβ) and abnormally phosphorylated Tau (P-Tau) in vitro, and pritelivir is more effective that acyclovir in preventing these Alzheimer-associated proteins.
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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