Isolation and Characterization of Cancer Chemopreventive Compounds from Barringtonia maunwongyathiae

Aranya Jutiviboonsuk Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand

Hong-Jie Zhang Program for Collaborative Research in the Pharmaceutical Sciences, Department of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois at Chicago, Chicago, Illinois, USA

Tamara P. Kondratyuk College of Pharmacy, Nursing and Health Sciences Purdue University, West hafayette, Indiana, USA

Angkana Herunsalee Department of Medical Sciences, The Ministry of Public Health, Nontaburi, Thailand

Wongsatit Chaukul Department of Pharmaceutical Botany, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand

John M. Pezzuto College of Pharmacy, Nursing and Health Sciences Purdue University, West hafayette, Indiana, USA

Harry H.S. Fong Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand

Nuntavan Bunyapraphatsara Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand

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Figures & data

Figure. 1 Chemical structures of compounds 1–14.

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Isolation and Characterization of Cancer Chemopreventive Compounds from Barringtonia maunwongyathiae

Table 1. ¹H NMR spectral data of compounds 1–9 (400 MHz, J. in Hz, CDCl₃).

Table 2. ¹³C-NMR spectral data of compounds 1–9 and 14 (100 MHz, CDCl₃).

Table 3. Biological activity of compounds 1–14.

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Isolation and Characterization of Cancer Chemopreventive Compounds from Barringtonia maunwongyathiae

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Table 1. 1H NMR spectral data of compounds 1–9 (400 MHz, J. in Hz, CDCl3).

Table 2. 13C-NMR spectral data of compounds 1–9 and 14 (100 MHz, CDCl3).

Table 3. Biological activity of compounds 1–14.

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Table 1. ¹H NMR spectral data of compounds 1–9 (400 MHz, J. in Hz, CDCl₃).

Table 2. ¹³C-NMR spectral data of compounds 1–9 and 14 (100 MHz, CDCl₃).