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.

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 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 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 impurity 7 is an impurity of Acyclovir.

Acyclovir impurity 10 is an impurity of Acyclovir.

Acyclovir impurity 5 is an impurity of Acyclovir.

Acyclovir impurity 6 is an impurity of Acyclovir.

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 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.

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.

Acyclovir impurity 2 (O-[(Guanin-7-yl)methyl] acyclovir) is an impurity of Acyclovir.

Acyclovir impurity 8 is an impurity of Acyclovir.

Acyclovir impurity 4 is an impurity of Acyclovir.

Acyclovir impurity 3 (Acyclovir N-methylene dimer) is an impurity of Acyclovir.

Acyclovir impurity 11 is an impurity of Acyclovir.

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.