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Pharmaceutical Biology Volume 54, 2016 - Issue 1
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Original Article

Chemical constituents and biological activities of Albizia myriophylla wood

Nantiya JoycharatFaculty of Traditional Thai Medicine, Prince of Songkla University, Songkhla, Thailand, ;Natural Products Research Center of Excellence, Faculty of Science, Prince of Songkla University, Songkhla, Thailand, Correspondence[email protected]
,
Chancheera BoonmaFaculty of Traditional Thai Medicine, Prince of Songkla University, Songkhla, Thailand,
,
Sonesay ThammavongFaculty of Pharmacy, University of Health Sciences, Vientiane, Lao PDR,
,
Boon-ek YingyongnarongkulDepartment of Chemistry, Faculty of Science, Ramkhamhaeng University, Bangkok, Thailand, and
,
Surasak LimsuwanFaculty of Traditional Thai Medicine, Prince of Songkla University, Songkhla, Thailand, ;Natural Products Research Center of Excellence, Faculty of Science, Prince of Songkla University, Songkhla, Thailand,
&
Supayang Piyawan VoravuthikunchaiNatural Products Research Center of Excellence, Faculty of Science, Prince of Songkla University, Songkhla, Thailand, ;Department of Microbiology, Faculty of Science, Prince of Songkla University, Songkhla, Thailand
Pages 62-73 | Received 07 Jun 2014, Accepted 23 Jan 2015, Published online: 20 Apr 2015

Figures & data

Figure 1. Chemical structures of isolated compounds from Albizia myriophylla Benth.

Figure 1. Chemical structures of isolated compounds from Albizia myriophylla Benth.

Figure 2. IR spectrum of compound 1.

Figure 2. IR spectrum of compound 1.

Figure 3. 1H NMR (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 3. 1H NMR (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 4. 13C NMR (100 MHz, DMSO-d6) spectrum of compound 1.

Figure 4. 13C NMR (100 MHz, DMSO-d6) spectrum of compound 1.

Figure 5. COSY (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 5. COSY (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 6. HMQC (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 6. HMQC (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 7. HMBC (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 7. HMBC (400 MHz, DMSO-d6) spectrum of compound 1.

Figure 8. HRESIMS spectrum of compound 1.

Figure 8. HRESIMS spectrum of compound 1.

Table 1. The NMR spectral data of 3,4,7,3′-tetrahydroxyflavan (1) (in DMSO-d6, 400 MHz).

Table 2. Antibacterial activity of extracts and the isolated compounds from two different collections of A. myriophylla.

Table 3. Anticancer activity of the isolated compounds from A. myriophylla.

Figure 9. HPLC chromatogram of standard lupinifolin.

Figure 9. HPLC chromatogram of standard lupinifolin.

Table 4. Lupinifolin content and anti-cariogenic activity against S. mutans ATCC 25175 of two different collections of A. myriophylla.

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