Boc-β-(3-thienyl)-D-alanine dicyclohexylammonium salt
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Boc-β-(3-thienyl)-D-alanine dicyclohexylammonium salt

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Category
BOC-Amino Acids
Catalog number
BAT-007181
CAS number
226880-86-0
Molecular Formula
C12H17NO4S·C12H23N
Molecular Weight
452.30
Boc-β-(3-thienyl)-D-alanine dicyclohexylammonium salt
Synonyms
Boc-3-D-Ala(3-thienyl)-OH DCHA
Appearance
White powder
Purity
≥ 99% (HPLC, Chiral purtiy)
Boiling Point
434.7°C at 760mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H17NO4S/c1-12(2,3)17-11(16)13-9(10(14)15)6-8-4-5-18-7-8/h4-5,7,9H,6H2,1-3H3,(H,13,16)(H,14,15)/t9-/m1/s1
InChI Key
SIQSLARNSCAXSF-SECBINFHSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CSC=C1)C(=O)O

Boc-β-(3-thienyl)-D-alanine dicyclohexylammonium salt, a specialized chemical reagent with diverse applications in various fields, is a key player in scientific and industrial realms. Here are the significant applications each presented with a high degree of perplexity and burstiness:

Peptide Synthesis: Engrained in solid-phase peptide synthesis, Boc-β-(3-thienyl)-D-alanine dicyclohexylammonium salt emerges as a crucial component serving as a shielded amino acid derivative. It meticulously orchestrates the synthesis process warding off unwanted side reactions. The acid-labile Boc group upon removal under acidic conditions paves the way for seamless coupling with other amino acids ensuring precise peptide assembly.

Pharmaceutical Development: A cornerstone in pharmaceutical innovation, this compound propels the creation of novel drug entities by acting as a foundational element for peptide-based therapeutic candidates. It facilitates the crafting of peptide sequences boasting heightened biological potency and stability particularly advantageous in targeting specific protein pathways and interactions fostering the emergence of tailored pharmaceutical solutions.

Structural Biology: Delving into the realms of structural biology, Boc-β-(3-thienyl)-D-alanine dicyclohexylammonium salt finds its place in elucidating protein structure-function dynamics. By integrating this compound into peptides, researchers unravel the intricate web of protein folding stability and interactions. Through targeted modifications of residues a profound exploration into the molecular underpinnings of protein functionality unfolds laying the groundwork for the design of cutting-edge therapeutic interventions.

Chemical Biology: Embraced in the domain of chemical biology, this compound assumes a pivotal role in fashioning peptide mimetics and analogs enriching the arsenal of tools for biological inquiry. It empowers the infusion of distinct chemical functionalities into peptides enabling the probing of intricate biological systems. These bespoke peptides engineered with tailored modifications serve as potent instruments for dissecting enzyme mechanisms unraveling cellular processes and modeling disease scenarios facilitating groundbreaking discoveries in biological research.

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