Boc-Dap-OH - CAS 120205-50-7

Boc-Dap-OH - CAS 120205-50-7 Catalog number: BADC-01591

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Boc-Dap-OH is a pivotal compound extensively utilized in the biomedical sector. It assumes a fundamental function in the amalgamation of diverse pharmaceutical remedies and peptides. This indispensable product profoundly contributes to the progression of therapeutics targeting ailments like cancer and viral infections.

Category
ADCs Linker
Product Name
Boc-Dap-OH
CAS
120205-50-7
Catalog Number
BADC-01591
Molecular Formula
C14H25NO5
Molecular Weight
287.35
Purity
95%
Boc-Dap-OH

Ordering Information

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Related Molecules

Boc-Dap-OH.DCHA Inquiry
Description
Boc-Dap-OH is a pivotal compound extensively utilized in the biomedical sector. It assumes a fundamental function in the amalgamation of diverse pharmaceutical remedies and peptides. This indispensable product profoundly contributes to the progression of therapeutics targeting ailments like cancer and viral infections.
Synonyms
N-Boc-dolaproine; BOC-DAP; (2R,3R)-BOC-dolaproine; (2R,3R)-3-((S)-1-(tertbutoxycarbonyl)pyrrolidin-2-yl)-3-methoxy-2-methylpropanoic acid
IUPAC Name
(2R,3R)-3-methoxy-2-methyl-3-[(2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidin-2-yl]propanoic acid
Canonical SMILES
CC(C(C1CCCN1C(=O)OC(C)(C)C)OC)C(=O)O
InChI
InChI=1S/C14H25NO5/c1-9(12(16)17)11(19-5)10-7-6-8-15(10)13(18)20-14(2,3)4/h9-11H,6-8H2,1-5H3,(H,16,17)/t9-,10+,11-/m1/s1
InChIKey
LNEHHTWYEBGHBY-OUAUKWLOSA-N
Quantity
Data not available, please inquire.

Boc-Dap-OH, a derivative of lysine, finds widespread use in peptide synthesis and biochemical research. Here are four key applications, presented with high perplexity and burstiness:

1. Peptide Synthesis: Central to peptide and protein synthesis, Boc-Dap-OH acts as a critical building block. Its tert-butyloxycarbonyl (Boc) protective moiety effectively shields against undesirable side reactions, ensuring the synthesis process yields highly pure peptides with optimal efficiency.

2. Drug Development: In the dynamic landscape of pharmaceutical innovation, Boc-Dap-OH plays a pivotal role in crafting peptide-based therapeutics. These novel drugs, known for their specificity and reduced side effects compared to small molecules, can be synthesized with remarkable efficiency using Boc-Dap-OH, thus shaping the future of medication development across various disease domains.

3. Bioconjugation: At the intersection of biomolecular sciences, Boc-Dap-OH shines in bioconjugation applications, enabling the linkage of peptides or proteins to diverse entities like fluorescent probes, drugs, or polymers. The resulting conjugates serve as invaluable tools for investigating biological processes, facilitating imaging studies, and advancing targeted drug delivery strategies, thereby broadening the horizons of research and therapeutic possibilities.

4. Proteomics Research: Unveiling the intricacies of proteomics, Boc-Dap-OH emerges as a key reagent for protein modification and labeling. This enables researchers to enhance the identification and quantification of proteins within complex biological samples, enriching the precision and sensitivity of mass spectrometry-based proteomics analyses through the strategic incorporation of Boc-Dap-OH into peptides.

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: Boc-Dap-OH
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