메뉴 건너뛰기




Volumn 12, Issue , 2015, Pages 282-286

Triterpenoids from the seedpods of Holarrhena curtisii King and Gamble

Author keywords

11 Hydroperoxy; Apocynaceae; Holarrhena curtisii King and Gamble; Pentacyclic triterpenoids; Glucosidase inhibitory activity

Indexed keywords

24 METHYLENEPOLLINASTANOL; 3BETA HYDROXY 11ALPHA HYDROPEROXYOLEAN 12 EN 28 OIC; 3BETA HYDROXY 11ALPHA HYDROPEROXYURSAN 12 EN 28 OIC; ACARBOSE; ALPHA AMYRIN; ALPHA GLUCOSIDASE; BETA AMYRIN; CATECHIN; CYCLOEUCALENOL; GALLOCATECHIN; LANOSTA 7,24 DIEN 3 BETA OL; LUPEOL; LUPEOL ACETATE; METHANOL; OLEANOLIC ACID; SQUALENE; TRITERPENOID; UNCLASSIFIED DRUG; URSOLIC ACID;

EID: 84931262804     PISSN: 18743900     EISSN: 18767486     Source Type: Journal    
DOI: 10.1016/j.phytol.2015.04.013     Document Type: Article
Times cited : (9)

References (32)
  • 1
    • 77953461954 scopus 로고    scopus 로고
    • Attenuation of diabetic disorders in experimentally induced diabetic rat by methanol extract of seed of Holarrhena antidysenterica
    • K.M. Ali, T.K. Bera, S. Mandal, B.R. Barik, and D. Ghosh Attenuation of diabetic disorders in experimentally induced diabetic rat by methanol extract of seed of Holarrhena antidysenterica Int. J. Pharm. Tech. Res. 1 2009 1205 1211
    • (2009) Int. J. Pharm. Tech. Res. , vol.1 , pp. 1205-1211
    • Ali, K.M.1    Bera, T.K.2    Mandal, S.3    Barik, B.R.4    Ghosh, D.5
  • 2
    • 79955466721 scopus 로고    scopus 로고
    • Inhibitory effect of hydro-methanolic extract of seed of Holarrhena antidysenterica on alpha-glucosidase activity and postprandial blood glucose level in normoglycemic rat
    • K.M. Ali, K. Chatterjee, D. De, K. Jana, T.K. Bera, and D. Ghosh Inhibitory effect of hydro-methanolic extract of seed of Holarrhena antidysenterica on alpha-glucosidase activity and postprandial blood glucose level in normoglycemic rat J. Ethnopharmacol. 135 2011 194 196
    • (2011) J. Ethnopharmacol. , vol.135 , pp. 194-196
    • Ali, K.M.1    Chatterjee, K.2    De, D.3    Jana, K.4    Bera, T.K.5    Ghosh, D.6
  • 3
    • 0037030814 scopus 로고    scopus 로고
    • Inhibition of α-glucosidase by oleanolic acid and its synthetic derivatives
    • M.S. Ali, M. Jahangir, S.S. Hussan, and M.I. Choudhary Inhibition of α-glucosidase by oleanolic acid and its synthetic derivatives Phytochemistry 60 2002 295 299
    • (2002) Phytochemistry , vol.60 , pp. 295-299
    • Ali, M.S.1    Jahangir, M.2    Hussan, S.S.3    Choudhary, M.I.4
  • 4
    • 84878228478 scopus 로고    scopus 로고
    • Biochemical basis of the antidiabetic activity of oleanolic acid and related pentacyclic triterpenes
    • J.M. Castellano, A. Guinda, T. Delgado, M. Rada, and J.A. Cayuela Biochemical basis of the antidiabetic activity of oleanolic acid and related pentacyclic triterpenes Diabetes 62 2013 1791 1799
    • (2013) Diabetes , vol.62 , pp. 1791-1799
    • Castellano, J.M.1    Guinda, A.2    Delgado, T.3    Rada, M.4    Cayuela, J.A.5
  • 5
    • 0032738770 scopus 로고    scopus 로고
    • Antibacterial steroid alkaloids from the stem bark of Holarrhena pubescens
    • A. Chakraborty, and A.H. Brantner Antibacterial steroid alkaloids from the stem bark of Holarrhena pubescens J. Ethnopharmacol. 68 1999 339 344
    • (1999) J. Ethnopharmacol. , vol.68 , pp. 339-344
    • Chakraborty, A.1    Brantner, A.H.2
  • 6
    • 0028231321 scopus 로고
    • Isolation and relay synthesis of 11α-hydroperoxy diacetyl hederagenin, a novel triterpenoid derivative from Serjania triquetra (Sapindaceae)
    • M.I. Chávez, and G. Delgado Isolation and relay synthesis of 11α-hydroperoxy diacetyl hederagenin, a novel triterpenoid derivative from Serjania triquetra (Sapindaceae) Biogenet. Implic. Tetrahedron 50 1994 3869 3878
    • (1994) Biogenet. Implic. Tetrahedron , vol.50 , pp. 3869-3878
    • Chávez, M.I.1    Delgado, G.2
  • 9
    • 0031731290 scopus 로고    scopus 로고
    • Cytotoxic and leishmanicidal aminoglycosteroids and aminosteroids from Holarrhena curtisii
    • T.-S. Kam, K.-M. Sim, T. Koyano, M. Toyoshima, M. Hayashi, and K. Komiyama Cytotoxic and leishmanicidal aminoglycosteroids and aminosteroids from Holarrhena curtisii J. Nat. Prod. 61 1998 1332 1336
    • (1998) J. Nat. Prod. , vol.61 , pp. 1332-1336
    • Kam, T.-S.1    Sim, K.-M.2    Koyano, T.3    Toyoshima, M.4    Hayashi, M.5    Komiyama, K.6
  • 12
    • 0034108906 scopus 로고    scopus 로고
    • Six new ursane- and oleanane-type triterpenes from the aerial roots of Ficus microcarpa
    • Y.-H. Kuo, and Y.-M. Chiang Six new ursane- and oleanane-type triterpenes from the aerial roots of Ficus microcarpa Chem. Pharm. Bull. 48 2000 593 596
    • (2000) Chem. Pharm. Bull. , vol.48 , pp. 593-596
    • Kuo, Y.-H.1    Chiang, Y.-M.2
  • 16
    • 0028278958 scopus 로고
    • An NMR and molecular mechanics study of squalene and squalene derivatives
    • L. Pogliani, M. Ceruti, G. Ricchiardi, and D. Viterbo An NMR and molecular mechanics study of squalene and squalene derivatives Chem. Phys. Lipids 70 1994 21 34
    • (1994) Chem. Phys. Lipids , vol.70 , pp. 21-34
    • Pogliani, L.1    Ceruti, M.2    Ricchiardi, G.3    Viterbo, D.4
  • 20
    • 84881099698 scopus 로고    scopus 로고
    • Triterpenoids and steroids from Holarrhena pubescens seeds
    • B. Sanjib, T. Saswati, and S.C. Nath Triterpenoids and steroids from Holarrhena pubescens seeds Pharmacogn. Mag. 5 2009 407 411
    • (2009) Pharmacogn. Mag. , vol.5 , pp. 407-411
    • Sanjib, B.1    Saswati, T.2    Nath, S.C.3
  • 21
    • 34247159943 scopus 로고    scopus 로고
    • Oligomeric procyanidins of French maritime pine bark extract (Pycnogenol®) effectively inhibit α-glucosidase
    • A. Schäfer, and P. Högger Oligomeric procyanidins of French maritime pine bark extract (Pycnogenol®) effectively inhibit α-glucosidase Diabetes Res. Clin. Pract. 77 2007 41 46
    • (2007) Diabetes Res. Clin. Pract. , vol.77 , pp. 41-46
    • Schäfer, A.1    Högger, P.2
  • 22
    • 0142087956 scopus 로고    scopus 로고
    • Complete assignments of 1H and 13C NMR resonances of oleanolic acid 18α-oleanolic acid, ursolic acid and their 11-oxo derivatives
    • W. Seebacher, N. Simic, R. Weis, R. Saf, and O. Kunert Complete assignments of 1H and 13C NMR resonances of oleanolic acid 18α-oleanolic acid, ursolic acid and their 11-oxo derivatives Magn. Reson. Chem. 41 2003 636 638
    • (2003) Magn. Reson. Chem. , vol.41 , pp. 636-638
    • Seebacher, W.1    Simic, N.2    Weis, R.3    Saf, R.4    Kunert, O.5
  • 26
    • 33947473539 scopus 로고
    • The nuclear magnetic resonance spectra of pentacyclic triterpenes
    • M. Shamma, R.E. Glick, and R.O. Mumma The nuclear magnetic resonance spectra of pentacyclic triterpenes J. Org. Chem. 27 1962 4512 4517
    • (1962) J. Org. Chem. , vol.27 , pp. 4512-4517
    • Shamma, M.1    Glick, R.E.2    Mumma, R.O.3
  • 27
    • 0000358216 scopus 로고
    • Steroidal alkaloids and an androstane derivative from the bark of Holarrhena pubescens
    • B.S. Siddiqui, S.B. Usmani, S. Begum, and S. Siddiqui Steroidal alkaloids and an androstane derivative from the bark of Holarrhena pubescens Phytochemistry 33 1993 925 928
    • (1993) Phytochemistry , vol.33 , pp. 925-928
    • Siddiqui, B.S.1    Usmani, S.B.2    Begum, S.3    Siddiqui, S.4
  • 30
    • 40549121927 scopus 로고    scopus 로고
    • Speciosaperoxide, a new triterpene acid, and other terpenoids from Chaenomeles speciosa
    • Y.L. Song, L. Zhang, J.M. Gao, G.H. Du, and Y.X. Cheng Speciosaperoxide, a new triterpene acid, and other terpenoids from Chaenomeles speciosa J. Asian Nat. Prod. Res. 10 2008 214 217
    • (2008) J. Asian Nat. Prod. Res. , vol.10 , pp. 214-217
    • Song, Y.L.1    Zhang, L.2    Gao, J.M.3    Du, G.H.4    Cheng, Y.X.5
  • 32
    • 78650912369 scopus 로고    scopus 로고
    • Triterpenoids from the fruits of Forsythia suspensa
    • J. Xue, L. Xie, B.-R. Liu, and L.-X. Yu Triterpenoids from the fruits of Forsythia suspensa Chin. J. Nat. Med. 8 2010 414 418
    • (2010) Chin. J. Nat. Med. , vol.8 , pp. 414-418
    • Xue, J.1    Xie, L.2    Liu, B.-R.3    Yu, L.-X.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.