Fmoc-Val-Ala-OH - CAS 150114-97-9

Fmoc-Val-Ala-OH - CAS 150114-97-9 Catalog number: BADC-01482

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Fmoc-Val-Ala-OH is a widely used cleavable peptide linker that can conveniently serve as a building block for the careful construction of peptide-directed therapeutics and pharmaceuticals. Its multifaceted nature holds great promise in combating a range of diseases, including but not limited to neoplastic diseases, autoimmune diseases, and potential infections.

Category
ADCs Linker
Product Name
Fmoc-Val-Ala-OH
CAS
150114-97-9
Catalog Number
BADC-01482
Molecular Formula
C23H26N2O5
Molecular Weight
410.46
Purity
≥ 95%
Fmoc-Val-Ala-OH

Ordering Information

Catalog Number Size Price Quantity
BADC-01482 500 mg $298 Inquiry
Description
Fmoc-Val-Ala-OH is a widely used cleavable peptide linker that can conveniently serve as a building block for the careful construction of peptide-directed therapeutics and pharmaceuticals. Its multifaceted nature holds great promise in combating a range of diseases, including but not limited to neoplastic diseases, autoimmune diseases, and potential infections.
Synonyms
(S)-2-((S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-methylbutanamido)propanoic acid; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-valyl-L-alanine
IUPAC Name
(2S)-2-[[(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-methylbutanoyl]amino]propanoic acid
Canonical SMILES
CC(C)C(C(=O)NC(C)C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChI
InChI=1S/C23H26N2O5/c1-13(2)20(21(26)24-14(3)22(27)28)25-23(29)30-12-19-17-10-6-4-8-15(17)16-9-5-7-11-18(16)19/h4-11,13-14,19-20H,12H2,1-3H3,(H,24,26)(H,25,29)(H,27,28)/t14-,20-/m0/s1
InChIKey
KQZMZNLKVKGMJS-XOBRGWDASA-N
Density
1.2±0.1 g/cm3
Solubility
Soluble in DMF (Slightly), DMSO (Slightly)
Appearance
White to Off-White Solid
Boiling Point
676.7±45.0 °C at 760 mmHg

Fmoc-Val-Ala-OH, also known as N-[(9-Fluorenylmethoxycarbonyl)-L-valyl]-L-alanine, is a protected dipeptide utilized in peptide synthesis and biochemical research. Here are four key applications of this compound:

Peptide Synthesis: Serving as a cornerstone in solid-phase peptide synthesis (SPPS), Fmoc-Val-Ala-OH plays a pivotal role in crafting precise peptide sequences. Its Fmoc protective group enables methodical deprotection steps, ensuring the meticulous assembly of peptides. This dipeptide is essential for constructing intricate peptides utilized in pharmaceutical research and diagnostics, contributing to advancements in therapeutic development.

Protein Engineering: In the realm of protein engineering, researchers leverage Fmoc-Val-Ala-OH to introduce specific amino acid sequences into target proteins. By incorporating this dipeptide, scientists can manipulate the structure and functionality of proteins, facilitating the study of their properties or the design of novel proteins with unique characteristics.

Biophysical Studies: Delving into biophysical studies, Fmoc-Val-Ala-OH serves as a tool for investigating peptide folding, stability, and interactions. By synthesizing peptides containing this dipeptide, researchers can explore their conformational dynamics under diverse conditions. This in-depth understanding is crucial for unravelling the complexities of protein folding disorders and formulating effective therapeutic strategies.

Drug Discovery: Through the creation of peptide libraries using combinatorial chemistry, researchers can screen for peptides exhibiting high affinity and specificity towards target molecules. These peptide drugs hold the potential to function as inhibitors, activators, or signaling molecules in therapeutic contexts, offering promising avenues for innovative drug interventions.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Historical Records: Fmoc-Val-Ala-OH
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