acyclovir

Acyclovir (Aciclovir) is a guanine analog and orally active antiviral agent characterized by a narrow antiviral spectrum, high selectivity, and low toxicity. Acyclovir exhibits activity against HSV-1 (IC50 = 0.85 μM), HSV-2 (IC50 = 0.86 μM), and varicella-zoster virus. Acyclovir can be used for herpesvirus treatment research.

Acyclovir L-isoleucinate is an acyclovir impurity. It also is an Acyclovir amino acid ester prodrug.

Acyclovir alanine is a pro-drug of Acyclovir. Acyclovir works by decreasing the production of DNA of the virus and it shows very low cytotoxicity.

Acyclovir mixture with hydrocortisone is used for Herpes simplex labialis.

Acyclovir sodium is a guanosine nucleoside analogue and viral DNA polymerase inhibitor with antiviral activity, used to treat skin and mucous membrane HSV infections, exhibiting significant activity against HSV-1, HSV-2, and VZV.

Acyclovir-D4 (Standard) is a reference standard of Acyclovir-D4 intended for quantitative analysis, quality control, and related biochemical research applications. Acyclovir-d4 is a deuterated compound of Acyclovir. Acyclovir has a CAS number of 59277-89-3. Acyclovir is a synthetic analog of the purine nucleoside, guanosine, with potent antiviral activity against herpes simplex viruses type 1 and 2, varicella-zoster virus and other viruses of the herpesvirus family.

Desciclovir (DCV), a prodrug of the antiherpetic agent acyclovir (ACV), is converted in humans to ACV, presumably by xanthine oxidase.

Acyclovir (Aciclovir) hydrochloride is an effective oral antiviral agent with potent anti-herpetic activity. It exhibits IC50 values of 0.85 μM for HSV-1 and 0.86 μM for HSV-2, indicating strong inhibitory effects against these strains. Additionally, Acyclovir hydrochloride induces cell cycle disturbances and apoptosis. This compound also prevents bacterial infections during induction therapy for acute leukemia.

Acyclovir monophosphate is a potent anti-Herpes Simplex Virus (HSV) agent with antitumor activity, blocking DNA synthesis by inhibiting viral DNA polymerase and terminating viral DNA chain elongation [1] [2].

Acyclovir triphosphate sodium, a labeled modified deoxyoligonucleotide (dNTP), is capable of releasing pyrophosphate to generate fluorescence and is specifically utilized in applications such as gene synthesis and sequencing.

N2-Acetyl acyclovir benzoate-d5 is the deuterium-labeled version of N2-Acetyl acyclovir benzoate.

Acyclovir-D4 is a deuterated compound of Acyclovir. Acyclovir (T1454) has a CAS number of 59277-89-3. Acyclovir (T1454) is a synthetic analog of the purine nucleoside, guanosine, with potent antiviral activity against herpes simplex viruses type 1 and 2, varicella-zoster virus and other viruses of the herpesvirus family.

N2-Acetyl acyclovir benzoate-d4 is the deuterium-labeled version of N2-Acetyl acyclovir benzoate.

Valacyclovir hydrochloride (Valaciclovir hydrochloride) is an acyclovir prodrug that, upon metabolism, inhibits viral DNA replication.

Valacyclovir hydrochloride hydrate is a potent antiviral agent and prodrug rapidly converted to acyclovir in vivo, used to formulate ocular inserts for treating ocular herpes, and for the treatment of herpes simplex, herpes zoster, and herpes b.

Valacyclovir hydrochloride (Standard) is the standard substance of Valacyclovir hydrochloride, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Valacyclovir hydrochloride (Valaciclovir hydrochloride) is an acyclovir prodrug that, upon metabolism, inhibits viral DNA replication.

Benzyloxycarbonyl valacyclovir is a biochemical.

Valacyclovir Related Compound D is a bioactive chemical.

Diacetylacyclovir is a useful organic compound for research related to life sciences. The catalog number is T65324 and the CAS number is 75128-73-3.

Valacyclovir-[D4] (Standard) is a reference standard of Valacyclovir-[D4] intended for quantitative analysis, quality control, and related biochemical research applications.

Valacyclovir-[D8] Hcl (L-Valine-D8) (Standard) is a reference standard of Valacyclovir-[D8] Hcl (L-Valine-D8) intended for quantitative analysis, quality control, and related biochemical research applications.

Eprociclovir (A-5021) is a novel acyclovir analog that is a potent inhibitor of EHV1 replication and may be used for the treatment and/or prevention of infections with this virus.Eprociclovir has potent anti-herpetic activity against most human herpesviruses.

Ganciclovir (2'-Nor-2'-deoxyguanosine) is an ACYCLOVIR analog that is a potent inhibitor of the Herpesvirus family including cytomegalovirus. Ganciclovir is used to treat complications from AIDS-associated cytomegalovirus infections.

Hexanoic anhydride is a reactive chemical compound utilized as a key reactant in the synthetic pathway for acremomannolipin A. Applied in the green synthesis of acyclovir ester prodrugs to enhance bioavailability, and employed in the preparation of hexanoyl-modified chitosan nanoparticles through N-acylation reactions to create chitosan-based polymeric surfactants and drug delivery systems.