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BAY-57-1293

BAY-57-1293 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:bay57-1293
CAS:348086-71-5
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: career henan chemical co
Tel: +86-0371-86658258
Email: sales@coreychem.com
Products Intro: Product Name:BAY-57-1293
CAS:348086-71-5
Purity:99% Package:1KG;7USD
Company Name: Biochempartner
Tel: 0086-13720134139
Email: candy@biochempartner.com
Products Intro: Product Name:BAY57-1293
CAS:348086-71-5
Purity:98% HPLC LCMS Package:10G;20G
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:Pritelivir
CAS:348086-71-5
Purity:99.42% Package:5mg;39USD|10mg;55USD|25mg;88USD Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: RongNa Biotechnology Co.,Ltd
Tel: +86-86-13583358881 +8618560316533
Email: Brad@rongnabiotech.com
Products Intro: Product Name:BAY-57-1293
CAS:348086-71-5
Purity:0.99

BAY-57-1293 manufacturers

  • Pritelivir
  • Pritelivir pictures
  • $30.00
  • 2026-07-14
  • CAS:348086-71-5
  • Purity: 99.42%
  • Supply Ability: 10g
  • BAY-57-1293
  • BAY-57-1293 pictures
  • 2025-04-04
  • CAS:348086-71-5
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1Ton
BAY-57-1293 Basic information
Product Name:BAY-57-1293
Synonyms:PRITELIVIR;AIC316;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;BAY571293(Pritelivir);BAY-57-1293;N-[5-(Aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamide
CAS:348086-71-5
MF:C18H18N4O3S2
MW:402.49
EINECS:
Product Categories:Inhibitors
Mol File:348086-71-5.mol
BAY-57-1293 Structure
BAY-57-1293 Chemical Properties
Boiling point 639.4±65.0 °C(Predicted)
density 1.396±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
solubility insoluble in H2O; insoluble in EtOH; ≥13.9 mg/mL in DMSO
form solid
pka9.31±0.60(Predicted)
color White to off-white
InChIInChI=1S/C18H18N4O3S2/c1-12-17(27(19,24)25)26-18(21-12)22(2)16(23)11-13-6-8-14(9-7-13)15-5-3-4-10-20-15/h3-10H,11H2,1-2H3,(H2,19,24,25)
InChIKeyIVZKZONQVYTCKC-UHFFFAOYSA-N
SMILESC1(CC(N(C2=NC(C)=C(S(N)(=O)=O)S2)C)=O)=CC=C(C2=NC=CC=C2)C=C1
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
MSDS Information
BAY-57-1293 Usage And Synthesis
UsesBAY 57-1293 is a potent inhibitor of herpes simplex virus (HSV) that target the virus helicase primase complex.
Biological Activitybay 57-1293 is a potent and safe inhibitor of hsv helicase-primase with ic50 value of 12nm [1].bay 57-1293 displays anti-herpes activity through inhibiting the helicase-primase and affecting the viral dna synthesis. in the in vitro viral replication assay, bay 57-1293 shows inhibition against hsv-1 f, hsv-2 g and acyclovir-resistant hsv-1 f mutant with ic50 value of 20nm. in the plaque reduction assay and the conventional cytopathogenicity assay, bay 57-1293 shows ic50 values of 0.01-0.02μm and 0.01-0.03μm, respectively. besides that, bay 57-1293 is active at an ic50 value of 10nm–30nm against all clinical isolates of hsv-1 and hsv-2. furthermore, bay 57-1293 is active in vivo. the oral administration of bay 57-1293 shows 10-fold more potent than valacyclovir in a murine model of disseminated herpes infection. in a rat lethal challenge model, bay 57-1293 exerts profound antiviral activity without toxic effects. [1, 2]
in vivo

Pritelivir is the first in a class of antiviral agents that inhibit HSV replication by targeting the viral helicase-primase enzyme complex[2].
Pritelivir (0.03-45 mg/kg) significantly increases survival. Pritelivir (0.3-30 mg/kg) reduces mortality against HSV-1, E-377. Pritelivir has potent and resistance-breaking antiviral efficacy with potential for the treatment of potentially life-threatening HSV type 1 and 2 infections, including herpes simplex encephalitis[3].
Combination therapies of Pritelivir at 0.1 or 0.3 mg/kg/dose with Acyclovir (10 mg/kg/dose) are protective when compared to the vehicle treated group against HSV-2, strain MS[3].

Animal Model:Female BALB/c mice[3]
Dosage:0.03 to 45 mg/kg
Administration:Administered orally, twice daily at approximately 12 h intervals, for 7 days
Result:Survival was significantly increased to 80-100% as compared to the vehicle treatment. Even the lowest dose of 0.3 mg/kg was effective in increasing survival to 53%.
IC 50HSV-1: 0.02 μM (IC50); HSV-2: 0.02 μM (IC50)
storageStore at -20°C
references[1] kleymann g, fischer r, betz u a k, et al. new helicase-primase inhibitors as drug candidates for the treatment of herpes simplex disease. nature medicine, 2002, 8(4): 392-398.
[2] betz u a k, fischer r, kleymann g, et al. potent in vivo antiviral activity of the herpes simplex virus primase-helicase inhibitor bay 57-1293. antimicrobial agents and chemotherapy, 2002, 46(6): 1766-1772.
BAY-57-1293 Preparation Products And Raw materials
Tag:BAY-57-1293(348086-71-5) Related Product Information
HN0037 BAY57-1293 mesylate BAY-57-1293 AIC316 mesylate hydrate (S)-HN0037 Reagent RK-33