59277-89-3

Acyclovir Chemical Structure
59277-89-3

Chemical Structure

Acyclovir

Synonym(s): Aciclovir; Acycloguanosine

  • CAS No.: 59277-89-3
  • Formula:C8H11N5O3
  • Molecular Weight:225.21

IUPAC Name: 2-amino-9-((2-hydroxyethoxy)methyl)-1,9-dihydro-6H-purin-6-one

InChIKey: MKUXAQIIEYXACX-UHFFFAOYSA-N

SMILES: O=C1NC(N)=NC2=C1N=CN2COCCO

Biological Activity: Acyclovir (Aciclovir) is a potent, orally active antiviral agent. Acyclovir has antiherpetic activity with IC50 values of 0.85 μM and 0.86 μM for HSV-1 and HSV-2, respectively. Acyclovir induces cell cycle perturbation and apoptosis. Acyclovir prevents bacterial infections during induction therapy for acute leukaemia[1][2][3][4].

Cat. No. Product Name Purity Description Pricing
HY-17422
Acyclovir 99.18% Acyclovir (Aciclovir) is a potent, orally active antiviral agent. Acyclovir has antiherpetic activity with IC50 values of 0.85 μM and 0.86 μM for HSV-1 and HSV-2, respectively. Acyclovir induces cell cycle perturbation and apoptosis. Acyclovir prevents bacterial infections during induction therapy for acute leukaemia.
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HY-17422R
Acyclovir (Standard) 99.72% Acyclovir (Standard) is the analytical standard of Acyclovir. This product is intended for research and analytical applications. Acyclovir (Aciclovir) is a potent, orally active antiviral agent. Acyclovir has antiherpetic activity with IC50 values of 0.85 μM and 0.86 μM for HSV-1 and HSV-2, respectively. Acyclovir induces cell cycle perturbation and apoptosis. Acyclovir prevents bacterial infections during induction therapy for acute leukaemia.
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HY-17422S1
Acyclovir-d4 98.15% Acyclovir-d4 is the deuterium labeled Acyclovir. Acyclovir (Aciclovir) is a guanosine analogue and an orally active antiviral agent. Acyclovir inhibits HSV-1 (IC50 of 0.85 μM), HSV-2 (IC50 of 0.86 μM) and varicella-zoster virus. Acyclovir can be phosphorylated by viral thymidine kinase (TK), and Acyclovir triphosphate interferes with viral DNA polymerization through competitive inhibition with guanosine triphosphate and obligatory chain termination. Acyclovir prevents bacterial infections during induction therapy for acute leukaemia.
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