Acyl is an antiviral drug, a synthetic nucleoside analogue, that has inhibitory activity (interferes with viral replication) against the herpes viruses, including herpes simplex 1 and 2 (cold sores and genital herpes), varicella-zoster (shingles and chickenpox), and Epstein-Barr virus (mononucleosis). Viruses take over living cells and reproduce themselves, often at the expense of the host cell. The Acyl is converted to an active form by the virus itself, and the virus then uses the active form of Acyl rather than the nucleoside it normally uses to manufacture DNA, a critical component of viral replication. Incorporation of active Acyl into new viral DNA stops the production of the DNA. Virally infected cells absorb more Acyl than normal cells and convert more of it to the active form, which prolongs its antiviral activity. The FDA approved Acyl in March 1982.
Other names for this medication:
Acyclovir,
Abduce,
Acic,
Aciclobeta,
Aciclomed,
Aciclostad,
Aciclovirum,
Acifar,
Acihexal,
Aciklovir,
Acitop,
Acivir,
Acivirex,
Acivision,
Acix,
Actios,
Activir,
Acycloguanosine,
Acyl,
Acyrax,
Acyvir,
Aklovir,
Antivir,
Asiviral,
Avir,
Aviral,
Avix,
Avorax,
Blistex,
Cicloferon,
Cicloviral,
Clinovir,
Clirbest,
Clopes,
Clovate,
Clovir,
Cusiviral,
Cyclomed,
Cyclovax,
Cyclovex,
Cyclovir,
Danovir,
Declovir,
Epsin,
Eurovir,
Hascovir,
Hernovir,
Herperax,
Herpesil,
Herpesin,
Herpex,
Herpin,
Herplex,
Heviran,
Immunovir,
Lisovyr,
Lovir,
Lovire,
Lovrak,
Medovir,
Menova,
Ocuvir,
Poviral,
Ranvir,
Remex,
Rexan,
Scanovir,
Sitavig,
Sophivir,
Soviclor,
Supraviran,
Telviran,
Uniplex,
Vilerm,
Viraban,
Viralex,
Viratac,
Viratop,
Virest,
Virestat,
Virex,
Virless,
Virolex,
Viromed,
Virosil,
Virostatic,
Virovir,
Virucid,
Viruderm,
Virustat,
Virux,
Vivorax,
Xiclovir,
Xorox,
Zevin,
Ziverone,
Zoral,
Zorax,
Zoraxin,
Zovirax,
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Dizole,
Dalfaz,
Firin,
Valtrex,
Victrelis,
Virless,
Ulpax,
Pediazole,
Efferven,
Baktar,
Spirono,
Farcet,
Xylar,
Sporidex,
Amfebutamone,
Virest,
Mahacef,
Xorox,
Viraban,
Ultramox,
Clopes,
Multigram,
Esertia,
Cefix,
Avir,
Kailasa,
Finpecia,
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S-Adenosylmethionine:nocardicin 3-amino-3-carboxypropyltransferase catalyzes the biosynthetically rare transfer of the 3-amino-3-carboxypropyl moiety from S-adenosylmethionine to a phenolic site in the beta-lactam substrates nocardicin E, F, and G, a late step of the biosynthesis of the monocyclic beta-lactam antibiotic nocardicin A. Human and murine FDC converted IC into potent immunogens (specific antibody increased from background to clarithromycin for tonsillitis dosage of pepto thousands of ng / ml). This is the first report of successful use of self-hypnosis for the treatment of polysomnogram-proven disorders of arousal in the pediatric population.