메뉴 건너뛰기




Volumn 66, Issue 3, 2012, Pages 516-524

Anti-hyperlipidemic constituents from the bark of Shorea roxburghii

Author keywords

Anti hyperlipidemic activity; Dipterocarpaceae; Oligostilbenoid; Pancreatic lipase inhibitor; Phayomphenol; Shorea roxburghii

Indexed keywords

ALPHA VINIFERIN; AMPELOPSIN A; AMPELOPSIN H; ANTILIPEMIC AGENT; BALANNOCARPOL; BALANOCARPOL; HEMSLEYANOL D; HOPEAFURAN; HOPEAPHENOL; ISOHOPEAPHENOL; MALIBATOL A; MALIBATOL B; METHANOL; OLIVE OIL; PARVIFLOROL; PHAYOMPHENOL A1; PHAYOMPHENOL A2; PLANT EXTRACT; RESVERATROL; SHOREA ROXBURGHII EXTRACT; TETRAHYDROLIPSTATIN; TRANS RESVERATROL 10 C BETA D GLUCOPYRANOSIDE; TRIACYLGLYCEROL; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VATICANOL A; VATICANOL B; VATICANOL C; VATICANOL E; VATICANOL G;

EID: 84863503093     PISSN: 13403443     EISSN: 18610293     Source Type: Journal    
DOI: 10.1007/s11418-011-0619-6     Document Type: Article
Times cited : (43)

References (33)
  • 3
    • 61449114952 scopus 로고    scopus 로고
    • Structures of acetylated oleanane-type triterpene saponins, rarasaponins IV, V, and VI, and anti-hyperlipidemic constituents from the pericarps of Sapindus rarak
    • Asao Y, Morikawa T, Xie Y, Okamoto M, Hamao M, Matsuda H, Muraoka O, Yuan D, Yoshikawa M (2009) Structures of acetylated oleanane-type triterpene saponins, rarasaponins IV, V, and VI, and anti-hyperlipidemic constituents from the pericarps of Sapindus rarak. Chem Pharm Bull 57:198-203
    • (2009) Chem Pharm Bull , vol.57 , pp. 198-203
    • Asao, Y.1    Morikawa, T.2    Xie, Y.3    Okamoto, M.4    Hamao, M.5    Matsuda, H.6    Muraoka, O.7    Yuan, D.8    Yoshikawa, M.9
  • 5
    • 71749121016 scopus 로고    scopus 로고
    • Hepatoprotective amide constituents from the fruit of Piper chaba: Structural requirements, mode of action, and new amides
    • Matsuda H, Ninomiya K, Morikawa T, Yasuda D, Yamaguchi I, Yoshikawa M (2009) Hepatoprotective amide constituents from the fruit of Piper chaba: structural requirements, mode of action, and new amides. Bioorg Med Chem 17:7313-7323
    • (2009) Bioorg Med Chem , vol.17 , pp. 7313-7323
    • Matsuda, H.1    Ninomiya, K.2    Morikawa, T.3    Yasuda, D.4    Yamaguchi, I.5    Yoshikawa, M.6
  • 6
    • 78651412197 scopus 로고    scopus 로고
    • Quantitative analysis of neosalacinol and neokotalanol, another two potent a-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography
    • Muraoka O, Morikawa T, Miyake S, Akaki J, Ninomiya K, Pongpiriyadacha Y, Yoshikawa M (2011) Quantitative analysis of neosalacinol and neokotalanol, another two potent a-glucosidase inhibitors from Salacia species, by LC-MS with ion pair chromatography. J Nat Med 65:142-148
    • (2011) J Nat Med , vol.65 , pp. 142-148
    • Muraoka, O.1    Morikawa, T.2    Miyake, S.3    Akaki, J.4    Ninomiya, K.5    Pongpiriyadacha, Y.6    Yoshikawa, M.7
  • 7
    • 55249099101 scopus 로고    scopus 로고
    • Oligostilbenoids from Dipterocarpaceaeous plants: A new resveratrol tetramer from Vateria indica and the revised structure of isohopeaphenol
    • Ito T, Abe N, Oyama M, Iinuma M (2008) Oligostilbenoids from Dipterocarpaceaeous plants: a new resveratrol tetramer from Vateria indica and the revised structure of isohopeaphenol. Helv Chim Acta 91:1989-1998
    • (2008) Helv Chim Acta , vol.91 , pp. 1989-1998
    • Ito, T.1    Abe, N.2    Oyama, M.3    Iinuma, M.4
  • 15
    • 0034956715 scopus 로고    scopus 로고
    • Hopeafuran and a C-glucosyl resveratrol isolated from stem wood of Hopea utilis
    • Tanaka T, Ito T, Ido Y, Nakaya K, Iinuma M, Chelladurai V (2001) Hopeafuran and a C-glucosyl resveratrol isolated from stem wood of Hopea utilis. Chem Pharm Bull 49:785-787
    • (2001) Chem Pharm Bull , vol.49 , pp. 785-787
    • Tanaka, T.1    Ito, T.2    Ido, Y.3    Nakaya, K.4    Iinuma, M.5    Chelladurai, V.6
  • 18
    • 0000955159 scopus 로고    scopus 로고
    • HIVinhibitory and cytotoxic oligostilbenes from the leaves of Hopea malibato
    • Dai J-R, Hallock YF, Cardellina JH II, Boyd MR (1998) HIVinhibitory and cytotoxic oligostilbenes from the leaves of Hopea malibato. J Nat Prod 61:351-353
    • (1998) J Nat Prod , vol.61 , pp. 351-353
    • Dai, J.-R.1    Hallock, Y.F.2    Cardellina II, J.H.3    Boyd, M.R.4
  • 19
    • 0033913707 scopus 로고    scopus 로고
    • Isolation and characterization of novel stilbene derivatives from Riesling wine
    • Baderschneider B, Winterhalter P (2000) Isolation and characterization of novel stilbene derivatives from Riesling wine. J Agric Food Chem 48:2681-2686
    • (2000) J Agric Food Chem , vol.48 , pp. 2681-2686
    • Baderschneider, B.1    Winterhalter, P.2
  • 21
    • 49349138226 scopus 로고
    • Carbon-13 NMR studies of flavonoids-III naturally occurring flavonoid glycosides and their acylated derivatives
    • Markham KR, Ternai B, Stanley R, Geiger H, Mabry TJ (1978) Carbon-13 NMR studies of flavonoids-III naturally occurring flavonoid glycosides and their acylated derivatives. Tetrahedron 34:1389-1397
    • (1978) Tetrahedron , vol.34 , pp. 1389-1397
    • Markham, K.R.1    Ternai, B.2    Stanley, R.3    Geiger, H.4    Mabry, T.J.5
  • 22
    • 19644388728 scopus 로고    scopus 로고
    • Synthesis of optically active vomifoliol and roseoside stereoisomers
    • Yamano Y, Ito M (2005) Synthesis of optically active vomifoliol and roseoside stereoisomers. Chem Pharm Bull 53:541-546
    • (2005) Chem Pharm Bull , vol.53 , pp. 541-546
    • Yamano, Y.1    Ito, M.2
  • 25
    • 0000737542 scopus 로고
    • Three dihydroisocoumarin glucosides from Hydrangea macrophylla subsp. serrata
    • Hashimoto T, Tori M, Asakawa Y (1987) Three dihydroisocoumarin glucosides from Hydrangea macrophylla subsp. serrata. Phytochemistry 26:3323-3330
    • (1987) Phytochemistry , vol.26 , pp. 3323-3330
    • Hashimoto, T.1    Tori, M.2    Asakawa, Y.3
  • 29
    • 14844325803 scopus 로고    scopus 로고
    • Asymmetric synthesis of 3-substituted 3,4-dihydroisocoumarins via stereoselective addition of laterally lithiated chiral 2-(o-tolyl)oxazolines to aldehydes followed by diastereomer-selective lactonization
    • Kurosaki Y, Fukuda T, Iwao M (2005) Asymmetric synthesis of 3-substituted 3,4-dihydroisocoumarins via stereoselective addition of laterally lithiated chiral 2-(o-tolyl)oxazolines to aldehydes followed by diastereomer-selective lactonization. Tetrahedron 61:3289-3303
    • (2005) Tetrahedron , vol.61 , pp. 3289-3303
    • Kurosaki, Y.1    Fukuda, T.2    Iwao, M.3
  • 32
    • 45249105767 scopus 로고    scopus 로고
    • Perennisosides I-VII, acylated triterpene saponins with antihyperlipidemic activities from the flowers of Bellis perennis
    • Morikawa T, Li X, Nishida E, Ito Y, Matsuda H, Nakamura S, Muraoka O, Yoshikawa M (2008) Perennisosides I-VII, acylated triterpene saponins with antihyperlipidemic activities from the flowers of Bellis perennis. J Nat Prod 71:828-835
    • (2008) J Nat Prod , vol.71 , pp. 828-835
    • Morikawa, T.1    Li, X.2    Nishida, E.3    Ito, Y.4    Matsuda, H.5    Nakamura, S.6    Muraoka, O.7    Yoshikawa, M.8
  • 33
    • 77949501425 scopus 로고    scopus 로고
    • Medicinal flowers. Part 29. acylated oleanane-type triterpene bisdesmosides: Perennisaponins G, H, I, J, K, L, and M with pancreatic lipase inhibitory activity from the flowers of Bellis perennis
    • Morikawa T, Li X, Nishida E, Nakamura S, Ninomiya K, Matsuda H, Oda Y, Muraoka O, Yoshikawa M (2010) Medicinal flowers. Part 29. acylated oleanane-type triterpene bisdesmosides: perennisaponins G, H, I, J, K, L, and M with pancreatic lipase inhibitory activity from the flowers of Bellis perennis. Helv Chim Acta 93:573-586
    • (2010) Helv Chim Acta , vol.93 , pp. 573-586
    • Morikawa, T.1    Li, X.2    Nishida, E.3    Nakamura, S.4    Ninomiya, K.5    Matsuda, H.6    Oda, Y.7    Muraoka, O.8    Yoshikawa, M.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.