Boc-NMe-Val-Val-Dil-Dap-OH - CAS 1352202-13-1

Boc-NMe-Val-Val-Dil-Dap-OH - CAS 1352202-13-1 Catalog number: BADC-00586

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Boc-NMe-Val-Val-Dil-Dap-OH is a Lyn-derived linker for antibody-drug-conjugation (ADC).

Category
ADCs Linker
Product Name
Boc-NMe-Val-Val-Dil-Dap-OH
CAS
1352202-13-1
Catalog Number
BADC-00586
Molecular Formula
C45H66N4O9
Molecular Weight
807.03

Ordering Information

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BADC-00586 -- $--
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Description
Boc-NMe-Val-Val-Dil-Dap-OH is a Lyn-derived linker for antibody-drug-conjugation (ADC).
Synonyms
(2R,3R)-3-[(2S)-1-[(3R,4S,5S)-4-[[(2S)-1-[[(2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylbutanoyl]amino]-3-methyl-1-oxobutan-2-yl]-methylamino]-3-methoxy-5-methylheptanoyl]pyrrolidin-2-yl]-3-methoxy-2-methylpropanoic acid
IUPAC Name
(2R,3R)-3-[(2S)-1-[(3R,4S,5S)-4-[[(2S)-1-[[(2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-3-methylbutanoyl]amino]-3-methyl-1-oxobutan-2-yl]-methylamino]-3-methoxy-5-methylheptanoyl]pyrrolidin-2-yl]-3-methoxy-2-methylpropanoic acid
Canonical SMILES
CCC(C)C(C(CC(=O)N1CCCC1C(C(C)C(=O)O)OC)OC)N(C)C(C(C)C)C(=O)NC(=O)C(C(C)C)N(C)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
InChI
InChI=1S/C45H66N4O9/c1-12-28(6)40(36(56-10)24-37(50)49-23-17-22-35(49)41(57-11)29(7)44(53)54)47(8)38(26(2)3)42(51)46-43(52)39(27(4)5)48(9)45(55)58-25-34-32-20-15-13-18-30(32)31-19-14-16-21-33(31)34/h13-16,18-21,26-29,34-36,38-41H,12,17,22-25H2,1-11H3,(H,53,54)(H,46,51,52)/t28-,29+,35-,36+,38-,39-,40-,41+/m0/s1
InChIKey
XRRKONJQRPJXFK-HXHBLSAESA-N
Solubility
10 mm in DMSO
Purity
>98.0%
Shelf Life
≥ 2 years
Shipping
Room temperature
Storage
Store at -20 °C, keep in dry and avoid sunlight.

Boc-NMe-Val-Val-Dil-Dap-OH is a synthetic peptide compound that is utilized in various biochemical applications.

The primary application of Boc-NMe-Val-Val-Dil-Dap-OH lies in its utility within the field of peptide synthesis and biochemical research. Peptides are short chains of amino acids linked by peptide bonds and they play crucial roles in biological processes, serving as hormones, enzymes, and structural components. Boc-NMe-Val-Val-Dil-Dap-OH is particularly valuable in studying protein interactions and functions due to its specific sequence and protective groups. Its structure allows researchers to investigate specific amino acid sequences and functional groups in a controlled environment, facilitating the study of their biochemical properties and interactions with other molecules.

In pharmaceutical research, Boc-NMe-Val-Val-Dil-Dap-OH can be employed in the development and characterization of novel therapeutic agents. As a part of peptide-based drug design, its unique sequence can act as a lead compound, offering insights into binding affinities, stability, and bioavailability of potential drug candidates. The ability to manipulate its sequence and protective groups enables the design of peptides with enhanced specificity and efficacy. Additionally, its structural attributes may also contribute to optimizing drug delivery mechanisms by targeting specific cellular pathways or receptors, which is crucial in the design of targeted therapies.

Moreover, Boc-NMe-Val-Val-Dil-Dap-OH is used in the investigation of enzyme-substrate interactions. Enzymes, being biological catalysts, interact closely with peptides and proteins to perform their functions. By modifying and analyzing peptides like Boc-NMe-Val-Val-Dil-Dap-OH, biochemists can elucidate mechanisms of enzymatic activities, identify how substrate modifications affect catalysis, and design specific inhibitors that can regulate enzyme functions. These studies contribute significantly to fields like metabolic engineering, disease treatment, and biotechnology, where understanding enzyme behavior is essential.

In addition to its applications in research and drug development, Boc-NMe-Val-Val-Dil-Dap-OH is also a valuable tool in the field of material science. Peptides are increasingly being used in the design of novel materials due to their biological compatibility and ability to form structured assemblies. This peptide’s distinct properties can be harnessed to create materials with unique mechanical or chemical characteristics, useful in creating biosensors, hydrogels, and other innovative biomaterials. Such materials can have applications ranging from medical implants and tissue engineering to environmental sensors and smart materials.

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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