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Chem Impex
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Product Information

Product Name
Fmoc-S-4-methoxybenzyl-L-cysteine
Brand Name
Chem Impex
Product Number
02400
CAS
141892-41-3
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11236605
IUPAC Name
(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-methoxyphenyl)methylsulfanylpropanoic acid
InChI Key
IWZGYHFOLFRYPK-DEOSSOPVSA-N
SMILES
COC1=CC=C(C=C1)CSCC@@H(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

Application

Fmoc-S-4-methoxybenzyl-L-cysteine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity.

Drug Development: Its unique properties make it valuable in the design of peptide-based drugs, especially those targeting specific receptors or enzymes, enhancing therapeutic efficacy.

Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to other biomolecules, facilitating the development of targeted drug delivery systems.

Research in Cancer Therapy: It plays a role in the development of novel anticancer agents, as its modifications can improve selectivity and reduce side effects in cancer treatments.

Protein Engineering: The compound is instrumental in engineering proteins with enhanced stability and functionality, which is crucial for various applications in biotechnology and pharmaceuticals.

References Data Source From Pubchem

Analysis of Matrix Metalloproteinase Activity and Inhibition in Cancer Spheroids

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2024
DOI: 10.1007/978-1-0716-3589-6_16

Amino Acids Bearing Aromatic or Heteroaromatic Substituents as a New Class of Ligands for the Lysosomal Sialic Acid Transporter Sialin

Publication Name: Journal of Medicinal Chemistry
Publication Date: 2020-07-01
DOI: 10.1021/acs.jmedchem.9b02119

QSPR modeling of optical rotation of amino acids using specific quantum chemical descriptors

Publication Name: Journal of Molecular Modeling
Publication Date: 2018-02-17
DOI: 10.1007/s00894-018-3593-z

Solid-phase synthesis of reduced selenocysteine tetrapeptides and their oxidized analogs containing selenenylsulfide eight-membered rings

Publication Name: Molecular Diversity
Publication Date: 2013-06-01
DOI: 10.1007/s11030-013-9454-x