(S)-2-Amino-5-((2,2,10,10-Tetramethyl-4,8-Dioxo-3,9-Dioxa-5,7-Diazaundecan-6-Ylidene)Amino)Pentanoic Acid

98%

Reagent Code: #236145
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CAS Number 145315-38-4

science Other reagents with same CAS 145315-38-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 374.43 g/mol
Formula C₁₆H₃₀N₄O₆
inventory_2 Storage & Handling
Storage 2-8℃, away from light, dry

description Product Description

Used in the synthesis of peptide-based pharmaceuticals, this compound serves as a chiral building block for developing enzyme inhibitors and bioactive peptides. Its functionalized structure allows for selective conjugation in drug design, particularly in targeting proteases and other nitrogen-containing biomolecule interactions. It is also employed in solid-phase peptide synthesis due to its protected imino and carboxyl functionalities, enabling controlled coupling and deprotection steps. Additionally, it finds use in creating peptidomimetic compounds with enhanced metabolic stability and receptor specificity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 1g
10-20 days ฿18,670.00
(S)-2-Amino-5-((2,2,10,10-Tetramethyl-4,8-Dioxo-3,9-Dioxa-5,7-Diazaundecan-6-Ylidene)Amino)Pentanoic Acid
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Used in the synthesis of peptide-based pharmaceuticals, this compound serves as a chiral building block for developing enzyme inhibitors and bioactive peptides. Its functionalized structure allows for selective conjugation in drug design, particularly in targeting proteases and other nitrogen-containing biomolecule interactions. It is also employed in solid-phase peptide synthesis due to its protected imino and carboxyl functionalities, enabling controlled coupling and deprotection steps. Additionally, i

Used in the synthesis of peptide-based pharmaceuticals, this compound serves as a chiral building block for developing enzyme inhibitors and bioactive peptides. Its functionalized structure allows for selective conjugation in drug design, particularly in targeting proteases and other nitrogen-containing biomolecule interactions. It is also employed in solid-phase peptide synthesis due to its protected imino and carboxyl functionalities, enabling controlled coupling and deprotection steps. Additionally, it finds use in creating peptidomimetic compounds with enhanced metabolic stability and receptor specificity.

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