(2S,4R)-1-((S)-2-(cyclopentyloxycarbonyl)-3,3-diMethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid

≥99%

Reagent Code: #235213
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CAS Number 877069-25-5

science Other reagents with same CAS 877069-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.4 g/mol
Formula C₁₇H₂₇NO₆
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in the synthesis of antiviral agents, particularly as an intermediate in the production of hepatitis C virus (HCV) protease inhibitors. Its stereochemistry and functional groups make it valuable for constructing complex peptide-like structures that target viral enzymes. Commonly employed in pharmaceutical research to develop orally active drugs with improved metabolic stability and bioavailability. Also utilized in structure-activity relationship (SAR) studies to optimize inhibitor potency and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
(2S,4R)-1-((S)-2-(cyclopentyloxycarbonyl)-3,3-diMethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid
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Used in the synthesis of antiviral agents, particularly as an intermediate in the production of hepatitis C virus (HCV) protease inhibitors. Its stereochemistry and functional groups make it valuable for constructing complex peptide-like structures that target viral enzymes. Commonly employed in pharmaceutical research to develop orally active drugs with improved metabolic stability and bioavailability. Also utilized in structure-activity relationship (SAR) studies to optimize inhibitor potency and selec

Used in the synthesis of antiviral agents, particularly as an intermediate in the production of hepatitis C virus (HCV) protease inhibitors. Its stereochemistry and functional groups make it valuable for constructing complex peptide-like structures that target viral enzymes. Commonly employed in pharmaceutical research to develop orally active drugs with improved metabolic stability and bioavailability. Also utilized in structure-activity relationship (SAR) studies to optimize inhibitor potency and selectivity.

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