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Penciclovir

SIGMA/P0035

Synonym: 2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one; BRL-39123

CAS Number: 39809-25-1
Empirical Formula (Hill Notation): C10H15N5O3
Molecular Weight: 253.26
MDL Number: MFCD15142866
Linear Formula: C10H15N5O3
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-P0035-100MG 100 mg
$287.00
1/EA
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antibiotic activity spectrum viruses
form powder
InChI 1S/C10H15N5O3/c11-10-13-8-7(9(18)14-10)12-5-15(8)2-1-6(3-16)4-17/h5-6,16-17H,1-4H2,(H3,11,13,14,18)
InChI key JNTOCHDNEULJHD-UHFFFAOYSA-N
mode of action DNA synthesis | interferes
  enzyme | inhibits
Quality Level 100 
SMILES string NC1=NC(=O)c2ncn(CCC(CO)CO)c2N1
solubility 0.02 M potassium phosphate: soluble 2 mg/mL
Application: 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).
Biochem/physiol Actions: 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.
Other Notes: Keep container tightly closed in a dry and well-ventilated place.
Packaging: 100 mg in glass bottle
Hazard Codes Xi
Risk Statements 36
Safety Statements 26
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
UNSPSC 51102829

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