A new triterpenoid glycoside from the leaves and stems of Duranta repens

References

• Ahmad N, Zeb F, Ahmad I, Wang F. 2009. Repenins A–D, four new antioxidative coumarinolignoids from Duranta repens Linn. Bioorg Med Chem Lett. 19:3521–3524, doi:10.1016/j.bmcl.2009.05.006.
   PubMed Web of Science ®Google Scholar
• Ahmed WS, Mohamed MA, EI-Dib RA, Hamed M. 2009. New triterpene saponins from Duranta repens Linn. and their cytotoxic activity. Molecules. 14:1952–1965.
   PubMed Web of Science ®Google Scholar
• Anis I, Anis E, Ahmed S, Mustafa G, Malik A, Amtul Z, Atta-ur-rahman. 2001. Thrombin inhibitory constituents from Duranta repens. Helv Chim Acta. 84:649–655, doi:10.1002/1522-2675(20010321)84:3 < 649:AID-HLCA649>3.0.CO;2-5.
   Web of Science ®Google Scholar
• Anis I, Ahmed S, Malik A, Yasin A, Choudary MI. 2002. Enzyme inhibitory constituents from Duranta repens. Chem Pharm Bull. 50:515–518, https://doi.org/10.1248/cpb.50.515.
   PubMed Web of Science ®Google Scholar
• Castro VH, Ramirez E, Mora GA, Iwase Y, Nagao T, Okabe H, Matsunaga H, Katano M, Mori M. 1997. Structures and antiproliferative activity of saponins from Sechium pittieri and S. talamancense. Chem Pharm Bull. 45:349–358, doi:10.1248/cpb.45.349.
   PubMed Web of Science ®Google Scholar
• Fujioka T, Iwamoto M, Iwase Y, Hachiyama S, Okabe H, Yamauchi T, Mihashi K. 1989. Studies on the constituents of Actinostemma lobatum MAXIM. V. Structure of lobatosides B, E, F and G, the dicrotalic acid esters of bayogenin bisdesmosides isolated from the herb. Chem Pharm Bull. 37:2325–2360.
   Google Scholar
• Hiradate S, Yada H, Ishii T, Nakajima N, Ohnishi-kameyama M, Sugie H, Zungsontiporn S, Fujii Y. 1999. Three plant growth inhibiting saponins from Duranta repens. Phytochemistry. 52:1223–1228, doi:10.1016/S0031-9422(99)00408-2.
   Web of Science ®Google Scholar
• Iqbal K, Malik A, Mukhtar N, Anis I, Khan SN, Choudhary MI. 2004. α-Glucosidase inhibitory constituents from Duranta repens. Chem Pharm Bull. 52:785–789, https://doi.org/10.1248/cpb.52.785.
   PubMed Web of Science ®Google Scholar
• Ishii H, Kitagawa I, Matsushita K, Shirakawa K, Tori K, Tozyo T, Yoshikawa M, Yoshimura Y. 1981. The configuration and conformation of the arabinose moiety in platycodins, saponins isolated from Platycodon grandiflorum, and mi-saponins from Madhuca logifolia based on Carbon-13 and hydrogen-1 NMR spectroscopic evidence: the total structures of saponins. Tetrahedron Lett. 22:1529–1532, doi:10.1016/S0040-4039(01)90369-7.
   Web of Science ®Google Scholar
• Junior P. 1985. Weitere iridoidglucoside Aus Penstemon strictus. Planta Med. 51:229–232, doi:10.1055/s-2007-969465.
   Web of Science ®Google Scholar
• Kasai R, Suzuo M, Asakawa J, Tanaka O. 1977. Carbon-13 chemical shifts of isoprenoid-β-d-glucopyranosides and -β-d-mannopyranosides. Stereochemical influences of aglycone alchols. Tetrahedron Lett. 18:175–178, doi:10.1016/S0040-4039(01)92581-X.
   Google Scholar
• Kitagawa I, Inada A, Yosioka I. 1975. Saponin and sapogenol. XII. Mi-saponin A and Mi-saponin B, two major bisdesmosides from the seed kernels of Madhuca longifolia (L.) Macbride. Chem Pharm Bull. 23:2268–2278, doi:10.1248/cpb.23.2268.
   Web of Science ®Google Scholar
• Kuo YH, Chen ZS, Lin YL. 1996. Chemical components of the leaves of Duranta repens Linn.. Chem Pharm Bull. 44:429–436, doi:10.1248/cpb.44.429.
   Web of Science ®Google Scholar
• Mahato SB, Kundu AP. 1994. 13C NMR spectra of pentacyclic triterpenoids-a compilation and some salient features. Phytochemistry. 37:1517–1575, doi:10.1016/S0031-9422(00)89569-2.
   Web of Science ®Google Scholar
• Takeda Y, Morimoto Y, Matsumoto T, Ogimi C, Hirata E, Takushi A, Otsuka H. 1995. Iridoid glucosides from the leaves and stems of Duranta erecta. Phytochemistry. 39:829–833, doi:10.1016/0031-9422(95)00024-2.
   PubMed Web of Science ®Google Scholar
• Ono M, Koto M, Komatsu H, Igoshi K, Kobayashi H, Ito Y, Nohara T. 2004. Cytotoxic triterpenes and sterol from the fruit of rabbiteye blueberry (Vaccinium ashei). Food Sci Technol Res. 10:56–59, doi:10.3136/fstr.10.56.
   Web of Science ®Google Scholar
• Ono M, Oishi K, Abe H, Masuoka C, Okawa M, Ikeda T, Nohara T. 2006. New iridoid glucosides from the aerial parts of Verbena brasiliensis. Chem Pharm Bull. 54:1421–1424, doi:10.1248/cpb.54.1421.
   PubMed Web of Science ®Google Scholar
• Ono M, Sugita F, Shigematsu S, Takamura C, Yoshimitsu H, Miyashita H, Ikeda T, Nohara T. 2007. Three new steroid glycosides from the underground parts of Trillium kamtschaticum. Chem Pharm Bull. 55:1093–1096, doi:10.1248/cpb.55.1093.
   PubMed Web of Science ®Google Scholar
• Ono M, Oda E, Tanaka T, Iida Y, Yamasaki T, Masuoka C, Ikeda T, Nohara T. 2008. DPPH radical-scavenging effect on some constituents from the aerial parts of Lippia triphylla. J Nat Med. 62:101–106, doi:10.1007/s11418-007-0197-9.
   PubMed Web of Science ®Google Scholar
• Ono M, Toyohisa D, Morishita T, Horita H, Yasuda S, Nishida Y, Tanaka T, Okawa M, Kinjo J, Yoshimitsu H, Nohara T. 2011. Three new nortriterpene glycosides and two new triterpene glycosides from the bulbs of Scilla scilloides. Chem Pharm Bull. 59:1348–1354, doi:10.1248/cpb.59.1348.
   PubMed Web of Science ®Google Scholar
• Ono M, Furusawa C, Matsumura K, Noguchi S, Yasuda S, Okawa M, Kinjo J, Eto M, Yamaguchi K, Yoshimitsu H, Nohara T. 2013a. A new diterpenoid from the leaves of Clerodendron trichotomum. J Nat Med. 67:404–409, doi:10.1007/s11418-012-0690-7.
   PubMed Web of Science ®Google Scholar
• Ono M, Ochiai T, Yasuda S, Nishida Y, Tanaka T, Okawa M, Kinjo J, Yoshimitsu H, Nohara T. 2013b. Five new nortriterpenoid glycosides from the bulbs of Scilla scilloides. Chem Pharm Bull. 61:592–598, https://doi.org/10.1248/cpb.c13-00116.
   PubMed Web of Science ®Google Scholar
• Sasaki H, Nishimura H, Chin (chen zhengxiong) M, Mitsuhashi H. 1989. Hydroxycinnamic acid esters of phenethylalcohol glycosides from Rehmannia glutinosa var. Purpurea. Phytochemistry. 28:875–879, doi:10.1016/0031-9422(89)80134-7.
   Web of Science ®Google Scholar
• Seo S, Tomita Y, Tori K, Yoshimura Y. 1978. Determination of the absolute configuration of a secondary hydroxy group in a chiral secondary alcohol using glycosidation shifts in Carbon-13 nuclear magnetic resonance spectroscopy. J Am Chem Soc. 100:3331–3339, doi:10.1021/ja00479a014.
   Web of Science ®Google Scholar
• Shahat AA, Nazif NM, Abousetta LM, Ibrahim NA, Cos P, Miert SV, Pieters L, Vlietinck AJ. 2005. Phytochemical investigation and antioxidant activity of Duranta repens. Phytother Res. 19:1071–1073, doi:10.1002/ptr.1766.
   PubMed Web of Science ®Google Scholar
• Tori K, Seo S, Yoshimura Y, Arita H, Tomita Y. 1977. Carbon-13 chemical shifts of isoprenoid-β-d-glucopyranosides and -β-d-mannopyrnanosides. Tetrahedron Lett. 18:179–182, doi:10.1016/S0040-4039(01)92582-1.
   Google Scholar
• Verotta L, Caldiroli S, Gariboldi P, Tatò M. 1996. 600 MHz 1H and 13C NMR full assignments of two saponins from Nothapodytes foetida. Phytochem Anal. 7:245–252, doi:10.1002/(SICI)1099-1565(199609)7:5 < 245:AID-PCA312>3.0.CO;2-L.
   Web of Science ®Google Scholar