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H-L-Phe(4-NH-Poc)-OH HCl

  CAS No.: 2737202-66-1   Cat No.: BADC-01757   Purity: >99% 4.5  

H-Phe(4-NH-Poc) HCl is a phenylalanine-based ADC linker intermediate with orthogonal protecting groups, allowing selective payload conjugation and enhancing linker stability in antibody-drug conjugates. Keywords: ADC linker, amino acid linker, protecting groups, targeted drug delivery, bioconjugation.

H-L-Phe(4-NH-Poc)-OH HCl

Structure of 2737202-66-1

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ADC Linker
Molecular Formula
C13H15ClN2O4
Molecular Weight
298.72
Storage
Store at 2-8 °C

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
H-L-Aph(Poc)-OH HCl; H-Phe(4-NH-Poc).HCl; H-4Aph(Poc) HCl; H-L-4Aph(Poc)-OH HCl; H-L-4-Aph(Poc)-OH HCl; H-p-amino-Phe(Poc)-OH HCl; H-L-Phe(4-NH-Pryoc)-OH HCl; H-4Aph(Pryoc) HCl; H-L-4Aph(Pryoc)-OH HCl; H-L-4-Aph(Pryoc)-OH HCl; H-p-amino-Phe(Pryoc)-OH HCl; (1S)-1-carboxy-2-(4-{[(prop-2-yn-1-yloxy)carbonyl]amino}phenyl)ethan-1-aminium chloride; L-Phenylalanine, 4-[[(2-propyn-1-yloxy)carbonyl]amino]-, hydrochloride (1:1); 4-(Propargyloxycarbonyl)amino-L-phenylalanine hydrochloride; H-L-Phe(4-NH-Poc)-OH hydrochloride
IUPAC Name
(2S)-2-amino-3-[4-(prop-2-ynoxycarbonylamino)phenyl]propanoic acid;hydrochloride
Canonical SMILES
C#CCOC(=O)NC1=CC=C(C=C1)C[C@@H](C(=O)O)N.Cl
InChI
InChI=1S/C13H14N2O4.ClH/c1-2-7-19-13(18)15-10-5-3-9(4-6-10)8-11(14)12(16)17;/h1,3-6,11H,7-8,14H2,(H,15,18)(H,16,17);1H/t11-;/m0./s1
InChIKey
PKNZLMSSIPKCPT-MERQFXBCSA-N
Storage
Store at 2-8 °C

H-Phe(4-NH-Poc) HCl, a versatile chemical compound, finds diverse applications in the realm of bioscience. Here are four key applications of H-Phe(4-NH-Poc) HCl:

Peptide Synthesis: H-Phe(4-NH-Poc) HCl plays a crucial role in crafting peptides and oligopeptides. Serving as a protective shield for the amine group of phenylalanine, it shields against undesired reactions during peptide coupling. This meticulous process ensures the synthesis of peptides with exceptional purity and precise sequences, which are indispensable for both research and therapeutic endeavors.

Drug Development: In pharmaceuticals, H-Phe(4-NH-Poc) HCl emerges as a key player in peptide-based drug development. Essential for creating complex peptide sequences step by step, protective agents like H-Phe(4-NH-Poc) pave the way for innovative peptide therapeutics targeting a spectrum of diseases, from cancer and diabetes to infectious ailments. This intricate synthesis process holds promise for groundbreaking advancements in medical treatments.

Bioconjugation: Delving into bioconjugation techniques, H-Phe(4-NH-Poc) HCl facilitates the fusion of peptides with diverse molecules like proteins, antibodies, or nanoparticles. This fusion is pivotal for the development of cutting-edge diagnostic tools and precision-targeted drug delivery systems. Leveraging the stability and functional enhancement offered by H-Phe(4-NH-Poc) ensures the efficacy of these conjugated peptides in various biomedical applications.

Proteomic Research: At the forefront of proteomics, H-Phe(4-NH-Poc) HCl takes center stage in preparing labeled peptides for mass spectrometry analysis. Its protective group aids in the selective modification of peptides, enabling accurate identification and quantification of proteins in intricate biological samples. This application holds profound importance in deciphering protein functions, interactions, and dynamics within cellular environments, shedding light on the intricacies of biological systems.

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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