| Weight | 253.262 g/mol |
|---|---|
| Formula | C10H15N5O3 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
penciclovir (39809-25-1)
Denavir · SB-CH brand of penciclovir · Vectavir
Score:
#113 in Microbiology
,
#1227 in Biology
,
#1410 in Chemistry
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- Herpes Simplex Virus Resistance to Acyclovir and Penciclovir after Two Decades of Antiviral Therapy (Clinical Microbiology Reviews, 2003)
- Mode of antiviral action of penciclovir in MRC-5 cells infected with herpes simplex virus type 1 (HSV-1), HSV-2, and varicella-zoster virus. (Antimicrobial Agents and Chemotherapy, 1992)
- Selection of an oral prodrug (BRL 42810; famciclovir) for the antiherpesvirus agent BRL 39123 [9-(4-hydroxy-3-hydroxymethylbut-l-yl)guanine; penciclovir]. (Antimicrobial Agents and Chemotherapy, 1989)
- Penciclovir Cream for the Treatment of Herpes Simplex Labialis: A Randomized, Multicenter, Double-blind, Placebo-Controlled Trial (JAMA, 1997)
- Famciclovir and Penciclovir. The Mode of Action of Famciclovir Including Its Conversion to Penciclovir (Antiviral Chemistry & Chemotherapy, 1993)
- Inhibition of the replication of the DNA polymerase M550V mutation variant of human hepatitis B virus by adefovir, tenofovir, L-FMAU, DAPD, penciclovir and lobucavir. (Journal of Viral Hepatitis, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Denavir
- SB-CH brand of penciclovir
- Vectavir
- BRL 39123
- penciclovir, monosodium salt
- penciclovir, monosodium salt, monohydrate
- Novartis brand of penciclovir
- BRL-39123
- Visfarm brand of penciclovir
- 9-(4-hydroxy-3-hydroxymethylbut-1-yl)guanine
- Penciclovir Visfarm
-
SMILESC1=NC2=C(N1CCC(CO)CO)NC(=NC2=O)N
-
InChIKeyJNTOCHDNEULJHD-UHFFFAOYSA-N
- Pubchem - penciclovir
- Wikipedia - penciclovir
Penciclovir is a guanosine analogue antiviral drug used for the treatment of various herpesvirus infections. It is a nucleoside analogue which exhibits low toxicity and good selectivity. Because penciclovir is absorbed poorly when given orally (by mouth) it is more often used as a topical treatment.
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penciclovir
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