Dibenzyl 2-((R)-1-(((S)-3,3-Dimethyl-1-(Methylamino)-1-Oxobutan-2-Yl)Amino)-4-Methyl-1-Oxopentan-2-Yl)-2-Hydroxymalonate

95%

Reagent Code: #178862
fingerprint
CAS Number 191792-11-7

science Other reagents with same CAS 191792-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 540.65 g/mol
Formula C₃₀H₄₀N₂O₇
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral drugs such as those targeting HIV and hepatitis C virus. Its chiral structure enables selective interactions with enzyme active sites, making it valuable in creating highly specific pharmaceutical agents. Commonly employed in asymmetric synthesis to introduce stereochemical control in complex molecule assembly. Also utilized in research settings for designing enzyme inhibitors with improved binding affinity and metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,530.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Dibenzyl 2-((R)-1-(((S)-3,3-Dimethyl-1-(Methylamino)-1-Oxobutan-2-Yl)Amino)-4-Methyl-1-Oxopentan-2-Yl)-2-Hydroxymalonate
No image available

Used as a key intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral drugs such as those targeting HIV and hepatitis C virus. Its chiral structure enables selective interactions with enzyme active sites, making it valuable in creating highly specific pharmaceutical agents. Commonly employed in asymmetric synthesis to introduce stereochemical control in complex molecule assembly. Also utilized in research settings for designing enzyme inhibitors with improved bi

Used as a key intermediate in the synthesis of protease inhibitors, particularly in the development of antiviral drugs such as those targeting HIV and hepatitis C virus. Its chiral structure enables selective interactions with enzyme active sites, making it valuable in creating highly specific pharmaceutical agents. Commonly employed in asymmetric synthesis to introduce stereochemical control in complex molecule assembly. Also utilized in research settings for designing enzyme inhibitors with improved binding affinity and metabolic stability.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...