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Sku CI00645_250_G
Chem Impex
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Product Information

Product Name
Na-Boc-Nin-formyl-L-tryptophan
Brand Name
Chem Impex
Product Number
00645
CAS
47355-10-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
7017963
IUPAC Name
(2S)-3-(1-formylindol-3-yl)-2-(2-methylpropan-2-yl)oxycarbonylaminopropanoic acid
InChI Key
IHXHBYFWSOYYTR-ZDUSSCGKSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CN(C2=CC=CC=C21)C=O)C(=O)O

Description

Na-Boc-Nin-formyl-L-tryptophan is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require specific modifications for enhanced stability and bioactivity.

Drug Development: Its unique structure allows for the design of novel pharmaceuticals targeting neurological disorders, leveraging the properties of tryptophan derivatives.

Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to drugs or imaging agents, which is crucial in targeted therapy.

Research in Neuroscience: It plays a role in studies related to serotonin pathways, aiding researchers in understanding mood regulation and potential treatments for depression.

Food Industry Applications: The compound can be explored for enhancing flavor profiles in food products due to its tryptophan content, which is linked to the production of serotonin.

References Data Source From Pubchem

In Situ Neutralization Protocols for Boc-SPPS

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2020
DOI: 10.1007/978-1-0716-0227-0_3

A recombinant human stromelysin catalytic domain identifying tryptophan derivatives as human stromelysin inhibitors

Publication Name: Journal of Medicinal Chemistry
Publication Date: 1994-01-07
DOI: 10.1021/jm00027a027

Structure-activity relationship of Ac-CCK-7: Analogs with o-, m- and p-tyrosine sulfate and phosphate

Publication Name: Peptides
Publication Date: 1990
DOI: 10.1007/978-94-010-9060-5_39