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MC-AAA-NHCH2OCH2COOH

  CAS No.: 2414594-28-6   Cat No.: BADC-01508 4.5  

MC-AAA-NHCH2OCH2COOH is a remarkable biomedicine chemical, exhibits immense promise for addressing diverse diseases and disorders. Its potency lies in its exceptional ability to selectively target and modulate key enzymes or proteins implicated in the intricate pathogenesis of these ailments.

MC-AAA-NHCH2OCH2COOH

Structure of 2414594-28-6

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Molecular Formula
C22H33N5O9
Molecular Weight
511.53

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Synonyms
MC-AAA-NHCH2OCH2COOH
IUPAC Name
2-[[[(2S)-2-[[(2S)-2-[[(2S)-2-[6-(2,5-dioxopyrrol-1-yl)hexanoylamino]propanoyl]amino]propanoyl]amino]propanoyl]amino]methoxy]acetic acid
Canonical SMILES
CC(C(=O)NC(C)C(=O)NC(C)C(=O)NCOCC(=O)O)NC(=O)CCCCCN1C(=O)C=CC1=O
InChI
InChI=1S/C22H33N5O9/c1-13(20(33)23-12-36-11-19(31)32)25-22(35)15(3)26-21(34)14(2)24-16(28)7-5-4-6-10-27-17(29)8-9-18(27)30/h8-9,13-15H,4-7,10-12H2,1-3H3,(H,23,33)(H,24,28)(H,25,35)(H,26,34)(H,31,32)/t13-,14-,15-/m0/s1
InChIKey
YJKZVKCTHXSDDV-KKUMJFAQSA-N

MC-AAA-NHCH2OCH2COOH, a specialized compound with wide-ranging potential in bioscience, finds applications across various domains.

Peptide Synthesis: Serving as a fundamental building block in synthesizing intricate peptides, MC-AAA-NHCH2OCH2COOH exhibits a molecular structure endowed with unique functional groups that streamline coupling with diverse amino acid derivatives. This functionality is integral in crafting customized peptides tailored for both research and therapeutic endeavors, delving into the intricate realms of molecular interactions and biological activities.

Drug Delivery: Positioned at the forefront of pharmaceutical innovation, MC-AAA-NHCH2OCH2COOH plays a pivotal role in drug delivery systems by forming stable conjugates with therapeutic agents. By tethering pharmaceuticals to this compound, scientists can enhance drug solubility and bioavailability, elevating the efficacy and precision in drug delivery, particularly in the realm of cancer therapeutics.

Bioconjugation: At the interface of biology and synthetic chemistry, MC-AAA-NHCH2OCH2COOH takes center stage in bioconjugation techniques, fostering the creation of hybrid molecules amalgamating biological and synthetic components. This application is indispensable for advancing biomaterials, biosensors, and diagnostic tools, as it facilitates the attachment of biomolecules onto synthetic matrices.

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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