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Famciclovir

Famciclovir Structure
CAS No.
104227-87-4
Chemical Name:
Famciclovir
Synonyms
FCV;Famvir;famcyclovir;Oravir;FaMtrex;FaMcivir;BRL-42810;Amciclovir;Famvir (TN);Famciclover
CBNumber:
CB0464901
Molecular Formula:
C14H19N5O4
Molecular Weight:
321.33
MOL File:
104227-87-4.mol
MSDS File:
SDS
Modify Date:
2024/4/26 17:21:34

Famciclovir Properties

Melting point 102-104°C
Boiling point 550.2±60.0 °C(Predicted)
Density 1.40±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO: ≥10mg/mL
pka 4.00±0.10(Predicted)
form solid
color White to Off-White
λmax 310nm(EtOH)(lit.)
InChIKey GGXKWVWZWMLJEH-UHFFFAOYSA-N
CAS DataBase Reference 104227-87-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Hazard Codes  T
Risk Statements  20/21/22-45-61
Safety Statements  36/37/39-45-53-24/25
WGK Germany  3
RTECS  TY3164000
HS Code  29335990
NFPA 704
0
2 0

Famciclovir price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) F7932 Famciclovir ≥98% (HPLC) 104227-87-4 10MG ₹8724.95 2022-06-14 Buy
Sigma-Aldrich(India) PHR1696 Famciclovir Pharmaceutical Secondary Standard; Certified Reference Material 104227-87-4 1G ₹22083 2022-06-14 Buy
Sigma-Aldrich(India) F7932 Famciclovir ≥98% (HPLC) 104227-87-4 50MG ₹34943.1 2022-06-14 Buy
TCI Chemicals (India) F0842 Famciclovir 104227-87-4 500MG ₹5700 2022-05-26 Buy
Product number Packaging Price Buy
F7932 10MG ₹8724.95 Buy
PHR1696 1G ₹22083 Buy
F7932 50MG ₹34943.1 Buy
F0842 500MG ₹5700 Buy

Famciclovir Chemical Properties,Uses,Production

Description

Famciclovir, an effective oral prodrug of the antiviral penciclovir, was launched in the UK and shortly after in the U.S.A. for the treatment of shingles (herpes zoster). As the diacetyl ester of the 6-deoxy- penciclovir, famciclovir has significantly improved oral absorption. It is converted to penciclovir in vivo with a bioavailability of 41 % in rats. Penciclovir is phosphorylated, and hence activated onty in herpesvirus infected cells. This stable metabolite, penciclovir-triphosphate, is a strong inhibitor of herpesvirus DNA polymerases and of viral DNA synthesis with long lasting effects. The high selectivity of famciclovir/penciclovir to herpes family of viruses and their rather low toxicity may make this agent superior to other existing drugs.

Chemical Properties

Off-White Powder

Uses

sterol absorption inhibitor.
Famciclovir Tablets
Famciclovir (Famvir) a synthetic acyclic purine analog derived from guanine. It is the diacetyl ester (prodrug) of penciclovir, which exhibits no antiviral activity until hydrolyzed to penciclovir and its active metabolites. It is indicated for the management of acute herpes zoster infections. It has been shown to relieve acute symptoms as well as to shorten the duration of postherpetic neuralgia. It is also used for the treatment or suppression of recurrent episodes of genital herpes in immunocompetent patients and in the treatment of recurrent herpes simplex types 1 and 2 infections in patients with human immunodeficiency virus.

Indications

Famciclovir (Famvir) is the diacetyl ester prodrug of the acyclic guanosine analogue 6-deoxypenciclovir (Denavir).

Definition

ChEBI: 2-Amino-9H-purine in which the hydrogen at position 9 is substituted by a 4-acetoxy-3-(acetoxymethyl)but-1-yl group. A prodrug of the antiviral penciclovir, it is used for the treatment of acute herpes zoster (shingles), for the treatmen or suppression of recurrent genital herpes in immunocompetent patients and for the treatment of recurrent mucocutaneous herpes simplex infections in HIV infected patients.

General Description

Famciclovir is a diacetyl prodrug of penciclovir.As a prodrug,it lacks antiviral activity. Penciclovir, 9-[4-hydroxy-3-hydroxymethylbut-1-yl] guanine, is an acyclic guanine nucleoside analog. The structure is similar to that of acyclovir,except in penciclovir, a side chain oxygen has beenreplaced by a carbon atom and an extra hydroxymethylgroup is present.
VSV-infected cells, penciclovir is first phosphorylated byviral thymidine kinase41 and then further elaborated to thetriphosphate by host cell kinases. Penciclovir triphosphate isa competitive inhibitor of viral DNA polymerase. The pharmacokineticparameters of penciclovir are quite different fromthose of acyclovir. Although penciclovir triphosphate is about100-fold less potent in inhibiting viral DNA polymerase thanacyclovir triphosphate, it is present in the tissues for longerperiods and in much higher concentrations than acyclovir.

Mechanism of action

Famciclovir is a synthetic purine nucleoside analogue related to guanine. It is the diacetyl 6-deoxy ester of penciclovir, which is structurally related to ganciclovir. Its pharmacological and microbiological activities are similar to those of acyclovir. Famciclovir is a prodrug of penciclovir, which is formed in vivo by hydrolysis of the acetyl groups and oxidation at the 6-position by mixed function oxidases. Penciclovir and its metabolite penciclovir triphosphate possess antiviral activity resulting from inhibition of viral DNA polymerase.

Pharmacokinetics

Famciclovir can be given with or without food. The most common adverse effects are headache and GI disturbances. Concomitant use of famciclovir with probenecid results in increased plasma concentrations of penciclovir. The recommended dose of famciclovir is 500 mg every 8 hours for 7 days. The absolute bioavailability of famciclovir is 77%, and the area under plasma concentration–time curve (AUC) is 86 μg/mL. Famciclovir with digoxin increased plasma concentration of digoxin to 19% as compared to digoxin given alone.

Pharmacology

Famciclovir (Famvir) undergoes extensive first-pass metabolism to penciclovir after oral administration. Penciclovir is another nucleoside analog that has a mechanism of action similar to that of acyclovir. Compared with oral acyclovir, famciclovir has improved bioavailability as well as a significantly prolonged intracellular half-life, allowing for less frequent dosing. Valacyclovir and famciclovir are similar in their high absorption, bioavailability, renal elimination, minimal drug interaction profiles, safety profiles, and efficacy.

Clinical Use

Famciclovir is indicated for the treatment of acute herpes zoster (shingles); it is at least as effective in reducing pain and healing time. Famciclovir is generally as effective as acyclovir in the treatment of HSV. In immunocompetent patients, famciclovir is approved for the treatment and prophylaxis of recurrent genital herpes. For HIV-infected individuals, famciclovir is approved for the treatment of all recurrent mucocutaneous HSV infections.

Side effects

Famciclovir may interact with probenecid or other drugs eliminated by renal tubular secretion. This interaction may result in increased blood levels of penciclovir or other agents.

Famciclovir Preparation Products And Raw materials

Global( 521)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
J S LABS +91-7330612784 +91-7330612784 Tamil Nadu, India 160 58 Inquiry
Hetero Drugs Limited +91-4023704923 +91-4023704923 Telangana, India 296 58 Inquiry
Macleods Pharmaceuticals Limited +91-2266762800 +91-2266762800 Maharashtra, India 116 58 Inquiry
HRV Global Life Sciences +91-9820219686 +91-9820219686 Telangana, India 379 58 Inquiry
Ralington Pharma +91-7948911722 +91-9687771722 Gujarat, India 1350 58 Inquiry
Aurobindo Pharma Limited +914066725000 Telangana, India 112 58 Inquiry
Cipla Ltd +912224826000 Maharashtra, India 133 58 Inquiry
OCEAN TRADING CORPORATION +91(22) 24921669 New Delhi, India 6211 58 Inquiry
AUROBINDO PHARMA LTD +91 (40) 6672 1200 New Delhi, India 209 58 Inquiry
HETERO DRUGS LTD +91 40 23704923 / 24 / 25 New Delhi, India 98 58 Inquiry

Famciclovir Spectrum

Famciclover Amciclovir FAMCICLOVIR [2-(acetyloxymethyl)-4-(2-aminopurin-9-yl)-butyl] acetate 2-[2-(2-AMINO-9H-PURIN-9-YL)ETHYL]-1,3-PROPANEDIOL, DIACETATE ESTER [2-(acetyloxymethyl)-4-(2-aminopurin-9-yl)butyl] ethanoate 2-(2-(2-Amino-9H-purin-9-yl)ethyl 2-(acetoxymethyl)-4-(2-amino-4,5-dihydro-9H-purin-9-yl)butyl acetate acetic acid [2-(acetoxymethyl)-4-(2-amino-9-purinyl)butyl] ester acetic acid [2-(acetoxymethyl)-4-(2-aminopurin-9-yl)butyl] ester Famvir (TN) Oravir FAMCICLOVIR, MORPURE HPLC PURIFIED, DELIVERED >= 98% PURE WITH HPLC UV CHROMATOGRAM FAMCICLOVER 98.5+% USP 2-(acetoxymethyl)-4-(2-amino-4,5-dihydro-9H-purin- 2-[2-(2-AMINO-9H-PURIN-9-YL)ETHYL]-1,3-PROPANEDIOL(FAMCICLOVIR) BRL-42810 1,3-Propanediol, 2-[2-(2-amino-9H-purin-9-yl)ethyl]-, diacetate (ester) 2-[2-(2-Amino-9H-purin-9-yl)ethyl]-1,3-propanediol diacetate Diacetic acid 2-[2-(2-amino-9H-purine-9-yl)ethyl]-1,3-propanediyl ester Diacetic acid 3-(2-amino-9H-purine-9-yl)propylidenebis(methylene) ester 2-[2-(2-Amino-9H-purin-9-y1)ethyl]-1,3-propanediol diacetate(ester) Famciclovir (200 mg) 2-[(acetyloxy)Methyl]-4-(2-aMino-9H-purin-9-yl)butyl acetate 9-[4-Acetoxy-3-(acetoxyMethyl)but-1-yl]-2-aMinopurine FaMcivir FaMtrex FaMciclovir API 2-(2-(2-AMino-9H-purin-9-yl)ethyl)propane-1,3-diyl diacetate 2-[2-(2-amino-9H-purin-9-yl)ethyl]-1,3-propanediol 1,3-diacetate [2-(acetoxymethyl)-4-(2-aminopurin-9-yl)butyl] acetate Famciclovir, 98%, Antiviral guanosine analog Famciclovir> Famciclovir Famciclovir Famciclovir HCL 1,3-Propanediol, 2-[2-(2-amino-9H-purin-9-yl)ethyl]-, 1,3-diacetate Famciclovir USP/EP/BP Famciclovir (BRL 42810) FamciclovirQ: What is Famciclovir Q: What is the CAS Number of Famciclovir Q: What is the storage condition of Famciclovir Q: What are the applications of Famciclovir Famciclovir D6 Famciclovir (1269152) famcyclovir Famvir FCV Fanciclovir Famciclovirum Famciclovir, ≥ 98.0% 104227-87-4 124227-87-4 C14H19N5O4 API ZETIA Bases & Related Reagents Heterocycles Nucleotides Intermediates & Fine Chemicals Pharmaceuticals API's