Boc-Dil - CAS 132149-81-6

Boc-Dil - CAS 132149-81-6 Catalog number: BADC-01502

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Boc-Dil is a linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
Boc-Dil
CAS
132149-81-6
Catalog Number
BADC-01502
Molecular Formula
C15H29NO5
Molecular Weight
303.39
Boc-Dil

Ordering Information

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BADC-01502 -- $--
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Description
Boc-Dil is a linker for antibody-drug-conjugation (ADC).
Synonyms
(3R,4S,5S)-3-Methoxy-4-[methyl(tert-butyloxycarbonyl)amino]-5-methylheptanoic acid; (3R,4S,5S)-4-(tert-butoxycarbonyl(Methyl)aMino)-3-Methoxy-5-Methylheptanoic acid; Boc-Dil
IUPAC Name
(3R,4S,5S)-3-methoxy-5-methyl-4-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]heptanoic acid
Canonical SMILES
CCC(C)C(C(CC(=O)O)OC)N(C)C(=O)OC(C)(C)C
InChI
InChI=1S/C15H29NO5/c1-8-10(2)13(11(20-7)9-12(17)18)16(6)14(19)21-15(3,4)5/h10-11,13H,8-9H2,1-7H3,(H,17,18)/t10-,11+,13-/m0/s1
InChIKey
GFPJDRFAAIJFSY-LOWVWBTDSA-N
Storage
solvent: -80°C 12 months; Powder: -20°C 3 years

Boc-Dil, a widely used protected lysine derivative in peptide synthesis, finds diverse applications with high perplexity and burstiness conveyed through the following key uses:

Peptide Synthesis: Integral to solid-phase peptide synthesis (SPPS), Boc-Dil plays a crucial role in crafting peptides and proteins. The Boc (tert-butyloxycarbonyl) group shields the amino group of lysine, safeguarding it against undesired side reactions during synthesis. After the peptide chain construction, the Boc group can be selectively removed under acidic conditions, yielding the final desired peptide product.

Pharmaceutical Research: Positioned at the forefront of pharmaceutical innovation, Boc-Dil emerges as a key component in the development of peptide-based drugs designed to target specific diseases. Peptides synthesized using Boc-Dil serve as therapeutic agents, enzyme inhibitors, and diagnostic tools. The flexibility of Boc-Dil allows for the production of high-purity peptides essential for clinical applications, highlighting its wide-ranging applications in drug development.

Bioconjugation: In the realm of bioconjugation techniques, Boc-Dil plays a pivotal role in linking peptides or proteins to other molecules for diverse biotechnological applications. The lysine residue, with the protective Boc group, enables selective reactions at designated sites, facilitating the creation of antibody-drug conjugates, peptide-functionalized surfaces, and advanced diagnostics. This strategic use of Boc-Dil showcases its versatility and effectiveness in biotechnology applications.

Structural Biology: Within the field of structural biology, Boc-Dil is harnessed to produce tailor-made peptides that act as invaluable models for studying protein structure and function. These custom peptides mimic specific regions of proteins, offering insights into protein folding, interactions, and biochemical properties. Serving as indispensable tools for deciphering complex biological processes at the molecular level, these model peptides underscore the significance of Boc-Dil in enabling cutting-edge structural biology research.

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: Mal-PEG6-NHS | Boc-Dil
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