Penciclovir

Synonyms: BRL-39123, VSA 671,NSC-759624

Penciclovir (BRL-39123, VSA 671,NSC-759624) is a purine acyclic nucleoside analogue with potent antiviral activity.

Penciclovir Chemical Structure

Penciclovir Chemical Structure

CAS: 39809-25-1

Selleck's Penciclovir has been cited by 6 publications

Purity & Quality Control

Batch: S418401 DMSO] 34 mg/mL] false] Water] 1 mg/mL] false] Ethanol] Insoluble] false Purity: 99.94%
99.94

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Biological Activity

Description Penciclovir (BRL-39123, VSA 671,NSC-759624) is a purine acyclic nucleoside analogue with potent antiviral activity.
In vitro
In vitro

Penciclovir is a guanine analogue antiviral drug used for the treatment of various herpesvirus infections. It is a nucleoside analogue which exhibits low toxicity and good selectivity. Penciclovir is a selective antiherpesvirus agent, particularly against herpes simplex virus types 1 and 2 (HSV-1 and HSV-2) and varicella-zoster virus (VZV). Penciclovir is converted to its active form, penciclovir triphosphate, by cellular kinases. It inhibits viral DNA polymerase by competing with deoxyguanosine triphosphate. It inhibits DNA synthesis of virus-infected cells. Penciclovir has in vitro activity against herpes simplex virus types 1 (HSV-1) and 2 (HSV-2). It does not inhibit DNA synthesis in non-infected cells. Mode of resistance is via qualitative changes in viral thymidine kinase or DNA polymerase. [1] Penciclovir has activity against several herpes viruses with IC50 of 37.9 μM for HHV-6A and 77.8 μM for HHV-6B. [2] Herpes simplex virus-1 studies indicate that Penciclovir induces apoptosis without causing much genotoxicity. [3]

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT00878072 Completed
Herpes Labialis
Novartis Pharmaceuticals|Novartis
March 25 2009 Phase 2|Phase 3
NCT00098059 Completed
Herpes Simplex
Novartis Pharmaceuticals|Novartis
February 2005 Phase 3

Chemical Information & Solubility

Molecular Weight 253.26 Formula

C10H15N5O3

CAS No. 39809-25-1 SDF Download Penciclovir SDF
Smiles C1=NC2=C(N1CCC(CO)CO)N=C(NC2=O)N
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 34 mg/mL ( (134.24 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 1 mg/mL

Ethanol : Insoluble


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In vivo
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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