NMR-based stability evaluation of (E)-1-(3',4'-dimethoxyphenyl)butadiene (DMPBD) from Zingiber cassumunar Roxb. rhizome.

DMPBD NMR Z. cassumunar stability evaluation

Journal

Phytochemical analysis : PCA
ISSN: 1099-1565
Titre abrégé: Phytochem Anal
Pays: England
ID NLM: 9200492

Informations de publication

Date de publication:
22 Dec 2023
Historique:
revised: 26 09 2023
received: 25 07 2023
accepted: 05 12 2023
medline: 22 12 2023
pubmed: 22 12 2023
entrez: 22 12 2023
Statut: aheadofprint

Résumé

The active compound (E)-1-(3',4'-dimethoxyphenyl)butadiene (DMPBD) isolated from the rhizomes of Zingiber cassumunar Roxb. has potent anti-inflammatory and anticancer activities. Although DMPBD is one of the promising drug candidates for phytomedicine, its limited stability impedes its widespread use. For the development of new drugs, the assessment of their chemical stability is essential, ensuring they maintain their properties within specified limits throughout the period from production until use. In the present study, we aimed to evaluate the stability of DMPBD under various conditions, including different solvents, temperatures, and lighting conditions, to identify the factors affecting stability and optimize the storage and handling conditions. DMPBD samples subjected to the different conditions tested were monitored by quantitative Significant decomposition of DMPBD was observed in chloroform-d For pharmacological/therapeutic applications, DMPBD should be stored in the form of the crude extract or as a purified material in methanolic solution. Ideally, the storage temperature should be below 4°C and O

Identifiants

pubmed: 38130156
doi: 10.1002/pca.3314
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Thammasat University Research Fund
ID : TUFT 41/2564
Organisme : Thammasat University Research Unit in Cannabis and Herbal Products Innovation.
Organisme : The Thailand Science Research and Innovation Fundamental Fund fiscal year 2023

Informations de copyright

© 2023 John Wiley & Sons Ltd.

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Auteurs

Boonwiset Seaho (B)

Department of Chemistry, Faculty of Science and Technology, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.

Chatkamon Lekwongphaiboon (C)

Department of Chemistry, Faculty of Science and Technology, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.

Wichayasith Inthakusol (W)

Drug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.
Thammasat University Research Unit in Cannabis and Herbal Products Innovation, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.

Saisuree Prateeptongkum (S)

Department of Chemistry, Faculty of Science and Technology, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.

Wacharee Harnying (W)

Department of Chemistry (Organic Chemistry), University of Cologne, Cologne, Germany.

Albrecht Berkessel (A)

Department of Chemistry (Organic Chemistry), University of Cologne, Cologne, Germany.

Nongnaphat Duangdee (N)

Drug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.
Thammasat University Research Unit in Cannabis and Herbal Products Innovation, Thammasat University (Rangsit Campus), Pathum Thani, Thailand.

Classifications MeSH