Boc-Dap-OH.DCHA - CAS 1369427-40-6

Boc-Dap-OH.DCHA - CAS 1369427-40-6 Catalog number: BADC-01570

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Boc-Dap-OH.DCHA, a remarkable biomedical compound, emerges as an invaluable arsenal against an array of maladies. Functioning as a potent therapeutic agent, it meticulously identifies and tackles discretely designated pathogens, exhibiting unparalleled efficacy. Within the biomedicine realm, this futuristic product assumes a pivotal position, fostering innovative strategies aimed at conquering the ever-evolving drug-resistant bacterial strains and numerous afflictions of an infectious nature.

Category
ADCs Linker
Product Name
Boc-Dap-OH.DCHA
CAS
1369427-40-6
Catalog Number
BADC-01570
Molecular Formula
C26H48N2O5
Molecular Weight
468.67
Boc-Dap-OH.DCHA

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Description
Boc-Dap-OH.DCHA, a remarkable biomedical compound, emerges as an invaluable arsenal against an array of maladies. Functioning as a potent therapeutic agent, it meticulously identifies and tackles discretely designated pathogens, exhibiting unparalleled efficacy. Within the biomedicine realm, this futuristic product assumes a pivotal position, fostering innovative strategies aimed at conquering the ever-evolving drug-resistant bacterial strains and numerous afflictions of an infectious nature.
Synonyms
dicyclohexylamine (2R,3R)-3-((S)-1-(tert-butoxycarbonyl)pyrrolidin-2-yl)-3-methoxy-2-methylpropanoate; 2-Pyrrolidinepropanoic acid, 1-[(1,1-dimethylethoxy)carbonyl]-β-methoxy-α-methyl-, (αR,βR,2S)-, compd. with N-cyclohexylcyclohexanamine 1:1
IUPAC Name
N-cyclohexylcyclohexanamine;(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.C1CCC(CC1)NC2CCCCC2
InChI
InChI=1S/C14H25NO5.C12H23N/c1-9(12(16)17)11(19-5)10-7-6-8-15(10)13(18)20-14(2,3)4;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h9-11H,6-8H2,1-5H3,(H,16,17);11-13H,1-10H2/t9-,10+,11-;/m1./s1
InChIKey
PKZALTWOMMNNOL-QJQMQQLTSA-N

Boc-Dap-OH·DCHA, also known as N-Boc-D-2,3-diaminopropionic acid dicyclohexylamine salt, stands as a pivotal reagent in synthetic chemistry and pharmaceutical research. Here are four key applications of Boc-Dap-OH·DCHA:

Peptide Synthesis: Serving as a cornerstone in the realm of peptide and protein synthesis, Boc-Dap-OH·DCHA plays a crucial role in constructing intricate peptide sequences. Its distinct side chain offers the flexibility to incorporate functional groups at precise locations along the peptide chain, enabling the creation of peptides with specific biological activities. This versatility is imperative for conducting detailed structure-activity relationship studies and advancing peptide-based therapeutics.

Pharmaceutical Development: Within the domain of drug discovery, Boc-Dap-OH·DCHA contributes significantly to the development of small molecule inhibitors and drugs. Its stereochemical configuration makes it particularly valuable for synthesizing chiral molecules, ultimately enhancing the binding affinity and specificity of drug candidates. By integrating Boc-Dap-OH·DCHA into pharmaceutical compounds, researchers aim to craft more potent and targeted therapeutic agents that hold the promise of improved efficacy in combating various diseases.

Bioconjugation Chemistry: In the realm of bioconjugation techniques, Boc-Dap-OH·DCHA emerges as a critical component for linking bioactive molecules to peptides and proteins. Its amine groups serve as reactive sites for conjugation, facilitating the creation of bioconjugates with enhanced targeting capabilities and efficacy. These bioconjugates play a pivotal role in targeted drug delivery systems and diagnostic imaging strategies.

Protein Engineering: At the forefront of protein engineering endeavors, Boc-Dap-OH·DCHA enables researchers to introduce non-natural amino acids into protein structures, paving the way for the development of novel proteins with enhanced properties. By leveraging this reagent, scientists can engineer proteins with improved stability, unique catalytic activities, and enhanced functionality. These engineered proteins find diverse applications in industrial settings, including biocatalysis processes and the creation of innovative biomaterials, fueling advancements in biotechnology and materials science.

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

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