N-β-(9-Fluorenylmethoxycarbonyl)-γ-(3-benzothienyl)-D-β-homoalanine
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N-β-(9-Fluorenylmethoxycarbonyl)-γ-(3-benzothienyl)-D-β-homoalanine

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Category
Fmoc-Amino Acids
Catalog number
BAT-004695
CAS number
269396-51-2
Molecular Formula
C27H23NO4S
Molecular Weight
457.54
N-β-(9-Fluorenylmethoxycarbonyl)-γ-(3-benzothienyl)-D-β-homoalanine
IUPAC Name
(3R)-4-(1-benzothiophen-3-yl)-3-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid
Synonyms
Fmoc-D-Ala(3-Bzt)-(C#CH2)OH; (R)-3-[(9-Fluorenylmethoxycarbonyl)amino]-4-(3-benzothienyl)butanoic acid
Purity
95%
Density
1.331±0.06 g/cm3(Predicted)
Boiling Point
702.4±60.0 °C(Predicted)
Storage
Store at 2-8 °C
InChI
InChI=1S/C27H23NO4S/c29-26(30)14-18(13-17-16-33-25-12-6-5-7-19(17)25)28-27(31)32-15-24-22-10-3-1-8-20(22)21-9-2-4-11-23(21)24/h1-12,16,18,24H,13-15H2,(H,28,31)(H,29,30)/t18-/m1/s1
InChI Key
AOUNLYYDVNQRKT-GOSISDBHSA-N
Canonical SMILES
C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CSC5=CC=CC=C54)CC(=O)O

N-β-(9-Fluorenylmethoxycarbonyl)-γ-(3-benzothienyl)-D-β-homoalanine, an advanced synthetic compound utilized in peptide synthesis and research, possesses unique chemical properties that enable a wide array of applications. Here are the key applications of this compound, expressed with high perplexity and burstiness:

Peptide Synthesis: A cornerstone in the world of peptide synthesis, this compound serves as a vital building block for constructing intricate peptide structures. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective shield, facilitating the methodical creation of peptides with specific amino acid sequences, crucial for diverse biochemical investigations. Its role in peptide assembly is fundamental in advancing our understanding of complex biological processes.

Drug Development: In the realm of therapeutic innovation, N-β-(9-Fluorenylmethoxycarbonyl)-γ-(3-benzothienyl)-D-β-homoalanine plays a pivotal role in designing and synthesizing peptide-based drugs. By integrating this compound into peptide chains, researchers pave the way for novel therapeutic agents targeting a myriad of diseases. This compound's contribution to the development of stable and biologically active peptides expands the horizons of drug formulation, fostering groundbreaking advancements in pharmaceutical science.

Structural Biology: At the intersection of protein structure and function studies, this compound emerges as a key player, aiding researchers in unraveling the intricacies of protein behavior. When harnessed for preparing peptides for structural analysis, it illuminates the nuances of protein folding, binding interactions, and conformational changes. This knowledge is indispensable for deciphering the underlying mechanisms of protein-mediated biological processes, pushing the boundaries of structural biology research.

Material Science: The unique molecular structure of N-β-(9-Fluorenylmethoxycarbonyl)-γ-(3-benzothienyl)-D-β-homoalanine grants it a pivotal role in the realm of biomaterial development. This compound's versatility lends itself to crafting novel biomaterials with tailored functionalities for diverse applications in biocompatible devices, drug delivery systems, and tissue engineering. By harnessing its chemical properties, researchers can create materials with customized characteristics, opening new possibilities in advanced biomedical material science.

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