ALS-8112

≥99%

Reagent Code: #99508
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CAS Number 1445379-92-9

science Other reagents with same CAS 1445379-92-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.68 g/mol
Formula C₁₀H₁₃ClFN₃O₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

ALS-8112 is an investigational antiviral nucleoside analog primarily developed for the treatment of chronic hepatitis C virus (HCV) infections. It is phosphorylated intracellularly to its active triphosphate form, ALS-8112-TP, which selectively inhibits the HCV NS5B RNA-dependent RNA polymerase, thereby blocking viral RNA replication. This mechanism makes it a promising candidate for anti-HCV therapy, particularly against genotype 1. Preclinical and Phase I clinical studies have demonstrated potent antiviral activity and a favorable safety profile, with ongoing research evaluating its efficacy in combination regimens and potential for broader clinical use.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿35,910.00
inventory 1mg
10-20 days ฿15,390.00

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ALS-8112
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ALS-8112 is an investigational antiviral nucleoside analog primarily developed for the treatment of chronic hepatitis C virus (HCV) infections. It is phosphorylated intracellularly to its active triphosphate form, ALS-8112-TP, which selectively inhibits the HCV NS5B RNA-dependent RNA polymerase, thereby blocking viral RNA replication. This mechanism makes it a promising candidate for anti-HCV therapy, particularly against genotype 1. Preclinical and Phase I clinical studies have demonstrated potent antiv

ALS-8112 is an investigational antiviral nucleoside analog primarily developed for the treatment of chronic hepatitis C virus (HCV) infections. It is phosphorylated intracellularly to its active triphosphate form, ALS-8112-TP, which selectively inhibits the HCV NS5B RNA-dependent RNA polymerase, thereby blocking viral RNA replication. This mechanism makes it a promising candidate for anti-HCV therapy, particularly against genotype 1. Preclinical and Phase I clinical studies have demonstrated potent antiviral activity and a favorable safety profile, with ongoing research evaluating its efficacy in combination regimens and potential for broader clinical use.

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