P0035
Penciclovir
Manufacturer: Sigma Aldrich
CAS Number: 39809-25-1
Synonym(S): 2-Amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)butyl]-6H-purin-6-one, BRL-39123
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 100 MG | P0035-100-MG | In Stock | ₹ 19,517.48 |
P0035 - 100 MG
In Stock
Quantity
1
Base Price: ₹ 19,517.48
GST (18%): ₹ 3,513.146
Total Price: ₹ 23,030.626
form
powder
Quality Level
100
solubility
0.02 M potassium phosphate: soluble 2 mg/mL
antibiotic activity spectrum
viruses
Mode of action
DNA synthesis | interferesenzyme | inhibits
SMILES string
NC1=NC(=O)c2ncn(CCC(CO)CO)c2N1
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
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Penciclovir | Sigma Aldrich | ₹ 19,517.48 | |
 | Penciclovir | ChemScene | ₹ 1,026.72 - ₹ 49,197.00 | |
 | 39809-25-1 | Penciclovir | A2B Chem | ₹ 342.24 - ₹ 2,652.36 |
Related Products
Description
- 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)[1].
- 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[2].
- Other Notes: Keep container tightly closed in a dry and well-ventilated place.
SAFETY INFORMATION
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Compare Similar Items
Show Difference
form: powder
Quality Level: 100
solubility: 0.02 M potassium phosphate: soluble 2 mg/mL
antibiotic activity spectrum: viruses
Mode of action: DNA synthesis | interferesenzyme | inhibits
SMILES string: NC1=NC(=O)c2ncn(CCC(CO)CO)c2N1
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
form:
powder
Quality Level:
100
solubility:
0.02 M potassium phosphate: soluble 2 mg/mL
antibiotic activity spectrum:
viruses
Mode of action:
DNA synthesis | interferesenzyme | inhibits
SMILES string:
NC1=NC(=O)c2ncn(CCC(CO)CO)c2N1
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
form: powder
Quality Level: 100
solubility: water: insoluble
antibiotic activity spectrum: __
Mode of action: __
SMILES string: C[C@@]12C[C@@]3(O)O[C@@H](O1)[C@]5(COC(=O)c4ccccc4)[C@H]3C[C@]25O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O
InChI: __
InChI key: __
form:
powder
Quality Level:
100
solubility:
water: insoluble
antibiotic activity spectrum:
__
Mode of action:
__
SMILES string:
C[C@@]12C[C@@]3(O)O[C@@H](O1)[C@]5(COC(=O)c4ccccc4)[C@H]3C[C@]25O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O
InChI:
__
InChI key:
__
form: powder
Quality Level: 100
solubility: water: insoluble
antibiotic activity spectrum: __
Mode of action: __
SMILES string: C[C@@]12C[C@@]3(O)O[C@@H](O1)[C@]5(COC(=O)c4ccccc4)[C@H]3C[C@]25O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O
InChI: __
InChI key: __
form:
powder
Quality Level:
100
solubility:
water: insoluble
antibiotic activity spectrum:
__
Mode of action:
__
SMILES string:
C[C@@]12C[C@@]3(O)O[C@@H](O1)[C@]5(COC(=O)c4ccccc4)[C@H]3C[C@]25O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O
InChI:
__
InChI key:
__
form: buffered aqueous solution
Quality Level: 200
solubility: __
antibiotic activity spectrum: __
Mode of action: __
SMILES string: __
InChI: __
InChI key: __
form:
buffered aqueous solution
Quality Level:
200
solubility:
__
antibiotic activity spectrum:
__
Mode of action:
__
SMILES string:
__
InChI:
__
InChI key:
__