(3R,4S,5S)-4-((S)-2-((S)-2-(Dimethylamino)-3-methylbutanamido)-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoic acid

97%

Reagent Code: #228671
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CAS Number 133120-89-5

science Other reagents with same CAS 133120-89-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 429.59 g/mol
Formula C₂₂H₄₃N₃O₅
badge Registry Numbers
MDL Number MFCD28387095
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of protease inhibitors. Its stereochemistry makes it valuable in creating highly selective drug molecules, especially for antiviral therapies. Due to its functionalized backbone and chiral centers, it serves as a building block in peptidomimetic drugs, aiding in improved metabolic stability and target binding affinity. Commonly employed in research settings for designing enzyme inhibitors where precise molecular orientation is critical for activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,930.00
inventory 1g
10-20 days ฿18,850.00

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(3R,4S,5S)-4-((S)-2-((S)-2-(Dimethylamino)-3-methylbutanamido)-N,3-dimethylbutanamido)-3-methoxy-5-methylheptanoic acid
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Used primarily as an intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of protease inhibitors. Its stereochemistry makes it valuable in creating highly selective drug molecules, especially for antiviral therapies. Due to its functionalized backbone and chiral centers, it serves as a building block in peptidomimetic drugs, aiding in improved metabolic stability and target binding affinity. Commonly employed in research settings for designing enzyme inhibitors
Used primarily as an intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of protease inhibitors. Its stereochemistry makes it valuable in creating highly selective drug molecules, especially for antiviral therapies. Due to its functionalized backbone and chiral centers, it serves as a building block in peptidomimetic drugs, aiding in improved metabolic stability and target binding affinity. Commonly employed in research settings for designing enzyme inhibitors where precise molecular orientation is critical for activity.
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