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Sku CI05974_250_G
Chem Impex
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Product Information

Product Name
D-Homoproline
Brand Name
Chem Impex
Product Number
05974
CAS
1723-00-8
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
736316
IUPAC Name
(2R)-piperidine-2-carboxylic acid
InChI Key
HXEACLLIILLPRG-RXMQYKEDSA-N
SMILES
C1CCNC@H(C1)C(=O)O

Application

D-Homoproline is widely utilized in research focused on:

Peptide Synthesis: It serves as a valuable building block in the synthesis of peptides, enhancing stability and bioactivity compared to traditional amino acids.

Drug Development: Researchers leverage its unique properties to design novel pharmaceutical compounds, particularly in developing treatments for neurological disorders.

Protein Engineering: D-Homoproline is used to modify protein structures, improving their functionality and resistance to degradation, which is crucial in biotechnological applications.

Biochemical Research: It plays a role in studying protein folding and interactions, providing insights into molecular mechanisms that can lead to breakthroughs in understanding diseases.

Cosmetic Formulations: The compound is also explored in the cosmetic industry for its potential benefits in skin care products, offering enhanced moisture retention and skin barrier protection.

References Data Source From Pubchem

Fermented distiller’s grains improve broiler immunity and antioxidant capacity by modulating cecal microbiota and cecal/plasma metabolomes

Publication Name: BMC Microbiology
Publication Date: 2025-10-22
DOI: 10.1186/s12866-025-04397-3

Revealing Diversity in NRPS Gene Clusters Across Six Pathogenic Colletotrichum Species

Publication Name: Current Microbiology
Publication Date: 2025-09-20
DOI: 10.1007/s00284-025-04440-6

Bio-inspired Ag3PO4-ZnO Nanocomposites: Investigation of its Antioxidant, Anticancer Activity and Photocatalytic Degradation of Methylene Blue Dye

Publication Name: Journal of Inorganic and Organometallic Polymers and Materials
Publication Date: 2025-06-16
DOI: 10.1007/s10904-025-03895-1

Mechanistic and enantioselectivity analysis of amino acid-catalyzed asymmetric aldol reactions: a theoretical study

Publication Name: Reaction Kinetics, Mechanisms and Catalysis
Publication Date: 2025-01-13
DOI: 10.1007/s11144-025-02799-y

Micro-scale screening of genetically modified Fusarium fujikuroi strain extends the apicidin family

Publication Name: Natural Products and Bioprospecting
Publication Date: 2024-08-23
DOI: 10.1007/s13659-024-00473-9