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ILCPA > Volume 16 > Chemical Constituents from the Roots of Furcraea...
Chemical Constituents from the Roots of <i>Furcraea bedinghausii</i> Koch
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Chemical Constituents from the Roots of Furcraea bedinghausii Koch

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Abstract:

Phytochemical investigation of the roots of Furcraea bedinghausii Koch. Led to the isolation of a mixture of two new homoisoflavones, 5,7-dihydroxy-3-(3,4-methylenedioxybenzyl)-chromone (4a) and 5,7-dihydroxy-3-(4-methoxybenzyl)-chromone (4b), together with the known β-sitosterol (1), 7,4'-dihydroxyhomoisoflavane (2), dihydrobonducellin (3), kaempferol (5), 5,7-dihydroxy-3-(4-hydroxybenzyl)-chromone (6), 1-linoleylglycerol (7), 6’-linoleyl-3-O-β-D-glucopyranosyl-β-sitosterol (8), trans-3,3’,5,5’-tetrahydroxy-4’-methoxystilbene (9), yuccaol C (10), yuccaol D (11), 3-O-b-D-glucopyranosyl-b-sitosterol (12), 4-[6-O-(4-hydroxy-3,5-dimethoxybenzoyl)-β-D-glucopyranosyloxy]-3-methoxybenzoic acid (13) and two pairs of steroidal saponins: (25R)-2α-3β–dihydroxy-5α-spirostan-12-one 3-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (14a) and (25R)-2α-3β–dihydroxy-5α-spirost-9-en-12-one 3-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (14b), (25R)-3β–hydroxy-5α-spirostan-12-one 3-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (15a) and (25R)-3β–hydroxy-5α-spirost-9-en-12-one 3-O-β-D-glucopyranosyl-(1→2)-O-[β-D-xylopyranosyl-(1→3)]-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (15b). Their structures were elucidated by interpretation of spectral data and by comparison with literature.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 16)
Pages:
9-19
DOI:
https://doi.org/10.18052/www.scipress.com/ILCPA.16.9
Citation:
R. B. Teponno et al., "Chemical Constituents from the Roots of Furcraea bedinghausii Koch", International Letters of Chemistry, Physics and Astronomy, Vol. 16, pp. 9-19, 2013
Online since:
September 2013
Authors:
Rémy B. Teponno, Beaudelaire K. Ponou, Dennis Fiorini, Luciano Barboni, Léon A. Tapondjou
Keywords:
Agavaceae, Chemotaxonomy, Flavonoids, Furcraea bedinghausi, Phenolic Compounds, Steroidal Saponins
Export:
RIS, BibTeX, Text
Distribution:
Open Access

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References:

[1] A. Plock, G. Beyer, K. Hiller, E. Grundemann, E. Krause, M. Nimtz, V. Wray, Phytochemistry 57 (2001) 489-496.

[2] J. C. David, Hanburyana 4 (2009) 23-32.

[3] J. L. Simmons-Boyce, W. F. Tinto, S. McLean, W. F. Reynolds, Fitoterapia 75 (2004) 634-638.

[4] A. Yokosuka, T. Sano, K. Hashimoto, H. Sakagami, Y. Mimaki, Chem. Pharm. Bull. 57 (2009) 1161-1166.

[5] W. Oleszek, M. Sitek, A. Stochmal, S. Piacente, C. Pizza, P. Cheeke, J. Agric. Food Chem. 49 (2001) 747-752.

DOI: https://doi.org/10.1021/jf010598+

[6] S. Piacente, P. Montoro, W. Oleszek, C. Pizza, J. Nat. Prod. 67 (2004) 882-885.

[7] R. B. Teponno, A. L. Tapondjou, D. Gatsing, J. D. Djoukeng, E. Abou-Mansour, R. Tabacchi, P. Tane, H. Stoekli-Evans, D. Lontsi, H. -J. Park, Phytochemistry 67 (2006) 1957-(1963).

DOI: https://doi.org/10.1016/j.phytochem.2007.01.023

[8] Y. Luo, H. Wang, X. Xu, W. Mei, H. Dai, Molecules 15 (2010), 8904-8914.

[9] P. Y. Chen, Y. C. Kuo, C. H. Chen, Y. H. Kuo, C. K. Lee, Molecules 14 (2009) 1789-1795.

[10] N. Jain, S. Alam, M. Kamil, M. Ilyas, M. Niwa, A. Sakae, Phytochemistry 29 (1990) 3988-3991.

DOI: https://doi.org/10.1016/0031-9422(90)85389-w

[11] A. G. References and further reading may be available for this article. To view references and further reading you must purchase this article. Gonzalez, F. Léon, L. Sanchez-Pinto, J. I. Padron, J. Bermejo, J. Nat. Prod. 63 (2000) 1297-1299.

[12] B. Thanomsub, T. Watcharachaipong, K. Chotelersak, P. Arunrattiyakorn, T. Nitoda, H. Kanzaki, J. Appl. Microbiol. 96 (2004) 588-592.

DOI: https://doi.org/10.1111/j.1365-2672.2004.02202.x

[13] S. Ghosal, Phytochemistry 24 (1985) 1807-1810.

[14] Y. Mizushina, R. I., Nakanishi, K. Kamiya, T. Satake, N. Shimazaki, O. Koiwai, Y. Uchiyama, Y. Yonezawa, M. Takemura, K. Sakaguchi, H. Yoshida, J. Steroid. Biochem. Mol. Biol. 99 (2006) 100-107.

DOI: https://doi.org/10.1016/j.jsbmb.2005.12.007

[15] A. Yokosuka, Y. Mimaki, Chem. Pharm. Bull. 55 (2007) 273-279.

[16] Y. Mimaki, M. Kuroda, A. Kameyama, A. Yokosuka, Y. Sashida, Phytochemistry 48 (1998) 1361-1369.

[17] A. Yokosuka, Y. Mimaki, M. Kuroda, Y. Sashida, Planta Med. 66 (2000) 393-395. MEYUTA.

[18] M. Masaoud, H. Ripperger, A. Porzel, G. Adam, Phytochemistry 38 (1995) 745-749.

DOI: https://doi.org/10.1016/0031-9422(94)00738-f

[19] E. C. N. Nono, P. Mkounga, V. Kuete, K. Marat, P. G. Hultin, A. E. Nkengfack, J. Nat. Prod. 73 (2010) 213-216.

DOI: https://doi.org/10.1021/np9007393

[20] A. Yokosuka, T. Sano, K. Hashimoto, H. Sakagami, Y. Mimaki, Chem. Pharm. Bull. 57 (2009) 1161-1166.

[21] S. Piacente, C. Pizza, W. Oleszek, Phytochem. Rev. 4 (2005) 177-190.

[22] J. A. Morales-Serna, A. Jiménez, R. Estrada-Reyes, C. Marquez, J. Cárdenas, M. Salmón, Molecules 15 (2010) 3295-3301.

DOI: https://doi.org/10.3390/molecules15053295

[23] The Angiosperm Phylogeny Group, Bot. J. Linn. Soc. 161 (2009) 105-121.

[24] J. L. Reveal, M.W. Chase, Phytotaxa 19 (2011) 71-134.

[26] S. Piacente, G. Bifulco, C. Pizza, A. Stochmal, W. Oleszek, Tetrahedron Let. 43 (2002) 9133-9136.

DOI: https://doi.org/10.1016/s0040-4039(02)02244-x

[26] P. Torres, J. G. Avila, A. Romo de Vivar, A. M. Garcia, J. C. Marin, E. Aranda, C. L. Cespedes, Phytochemistry 64 (2003) 463-473. ( Received 05 July 2013; accepted 09 July 2013 ).

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