메뉴 건너뛰기




Volumn 10, Issue 4, 2012, Pages 307-310

Triterpenes from Isodon xerophilus

Author keywords

Biosynthetic pathway; Cytotoxicity; Isodon xerophilus; Labiatae; Triterpenes

Indexed keywords

2ALPHA 3ALPHA 24 TRIHYDROXYOLEAN 12 EN 28 OIC ACID; 2ALPHA 3ALPHA 24 TRIHYDROXYURS 12 EN 28 OIC ACID; 2ALPHA HYDROXYURSOLIC ACID; 3BETA 23 DIHYDROXY URS 12 EN 28 OIC ACID; ARJUNOLIC ACID; ASIATIC ACID; HEDERAGENIN; MASLINIC ACID; OLEANOLIC ACID; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG; URSOLIC ACID;

EID: 84863504426     PISSN: 20956975     EISSN: 18755364     Source Type: Journal    
DOI: 10.1016/S1875-5364(12)60063-6     Document Type: Article
Times cited : (11)

References (15)
  • 1
    • 0000567248 scopus 로고
    • Angiospermae dicotylednae Labiatae (2)
    • Beijing academic press, Beijing
    • Wu CY, Li HW Angiospermae dicotylednae Labiatae (2). Flora Republicae Popularis Sinicae [M] 1987, 66:494. Beijing academic press, Beijing.
    • (1987) Flora Republicae Popularis Sinicae [M] , vol.66 , pp. 494
    • Wu, C.Y.1    Li, H.W.2
  • 2
    • 34548617819 scopus 로고    scopus 로고
    • Cytotoxic ent-kauranoids from the medicinal plant Isodon xerophilus [J]
    • Li LM, Weng ZY, Sun HD, et al. Cytotoxic ent-kauranoids from the medicinal plant Isodon xerophilus [J]. J Nat Prod 2007, 70(8):1295-1301.
    • (2007) J Nat Prod , vol.70 , Issue.8 , pp. 1295-1301
    • Li, L.M.1    Weng, Z.Y.2    Sun, H.D.3
  • 3
    • 34547770931 scopus 로고    scopus 로고
    • Isolation of two bioactive ent-kauranoids from the leaves of Isodon xerophilus [J]
    • Weng ZY, Huang SX, Sun HD, et al. Isolation of two bioactive ent-kauranoids from the leaves of Isodon xerophilus [J]. J Agric Food Chem 2007, 55(15):6039-6043.
    • (2007) J Agric Food Chem , vol.55 , Issue.15 , pp. 6039-6043
    • Weng, Z.Y.1    Huang, S.X.2    Sun, H.D.3
  • 4
    • 79960213800 scopus 로고    scopus 로고
    • Ent-Abietane diterpenoids from Isodon xerophilus [J]
    • Li LM, Pu JX, Sun HD, et al. ent-Abietane diterpenoids from Isodon xerophilus [J]. Arch Pharm Res 2011, 34(6):875-879.
    • (2011) Arch Pharm Res , vol.34 , Issue.6 , pp. 875-879
    • Li, L.M.1    Pu, J.X.2    Sun, H.D.3
  • 5
    • 0029590133 scopus 로고
    • Studies on the constituents of Clematis species. VI. The constituents of Clematis stans Sieb. et Zucc [J]
    • Kizu H, Shimana H, Tomimori T Studies on the constituents of Clematis species. VI. The constituents of Clematis stans Sieb. et Zucc [J]. Chem Pharm Bull 1995, 43(12):2187-2194.
    • (1995) Chem Pharm Bull , vol.43 , Issue.12 , pp. 2187-2194
    • Kizu, H.1    Shimana, H.2    Tomimori, T.3
  • 6
    • 0345770801 scopus 로고    scopus 로고
    • Studies on the chemical constituents from Prunella vulgaris [J]
    • Wang ZJ, Zhao YY, Tu GZ, et al. Studies on the chemical constituents from Prunella vulgaris [J]. Acta Pharm Sin 1999, 34(9):679-681.
    • (1999) Acta Pharm Sin , vol.34 , Issue.9 , pp. 679-681
    • Wang, Z.J.1    Zhao, Y.Y.2    Tu, G.Z.3
  • 7
    • 85009521848 scopus 로고    scopus 로고
    • Studies on the constituents of Passiflora wilsonii [J]
    • Yu JH, Li GP, Zhao JF, et al. Studies on the constituents of Passiflora wilsonii [J]. Nat Prod Res Dev 2003, 15(1):27-28.
    • (2003) Nat Prod Res Dev , vol.15 , Issue.1 , pp. 27-28
    • Yu, J.H.1    Li, G.P.2    Zhao, J.F.3
  • 8
    • 77954066896 scopus 로고    scopus 로고
    • Chemical components of Isodon lophanthoides var. gerardianus and their anti-hepatitis B virus effects [J]
    • Hu YJ, Lai XP, Liu ZQ, et al. Chemical components of Isodon lophanthoides var. gerardianus and their anti-hepatitis B virus effects [J]. Chin Tradit Herb Drugs 2005, 36(11):1612-1615.
    • (2005) Chin Tradit Herb Drugs , vol.36 , Issue.11 , pp. 1612-1615
    • Hu, Y.J.1    Lai, X.P.2    Liu, Z.Q.3
  • 9
    • 45249129321 scopus 로고
    • Triterpenoid saponins from plants of Araliaceae [J]
    • Srivastava SK, Jain DC Triterpenoid saponins from plants of Araliaceae [J]. Phytochemistry 1989, 28(2):644-647.
    • (1989) Phytochemistry , vol.28 , Issue.2 , pp. 644-647
    • Srivastava, S.K.1    Jain, D.C.2
  • 10
    • 0028533863 scopus 로고
    • Oleanane and ursane glycosides from Schefflera octophylla [J]
    • Maeda C, Ohtani K, Kasai R, et al. Oleanane and ursane glycosides from Schefflera octophylla [J]. Phytochemistry 1994, 37(4):1131-1137.
    • (1994) Phytochemistry , vol.37 , Issue.4 , pp. 1131-1137
    • Maeda, C.1    Ohtani, K.2    Kasai, R.3
  • 11
    • 0029278873 scopus 로고
    • Triterpene saponins from Aster yunnanensis [J]
    • Shao Y, Zhou BN, Lin LZ, et al. Triterpene saponins from Aster yunnanensis [J]. Phytochemistry 1995, 38(6):1487-1492.
    • (1995) Phytochemistry , vol.38 , Issue.6 , pp. 1487-1492
    • Shao, Y.1    Zhou, B.N.2    Lin, L.Z.3
  • 12
    • 27844589051 scopus 로고    scopus 로고
    • Chemical investigation of Morina chinesis [J]
    • Zhang GL, Zhou ZZ, Li BG Chemical investigation of Morina chinesis [J]. Nat Prod Res Dev 1997, 9(4):10-13.
    • (1997) Nat Prod Res Dev , vol.9 , Issue.4 , pp. 10-13
    • Zhang, G.L.1    Zhou, Z.Z.2    Li, B.G.3
  • 13
    • 0000444442 scopus 로고
    • Pentacyclic triterpenoids from Prunella vulgaris [J]
    • Kojima H, Tominaga H, Sato S, et al. Pentacyclic triterpenoids from Prunella vulgaris [J]. Phytochemistry 1987, 26(4):1107-1111.
    • (1987) Phytochemistry , vol.26 , Issue.4 , pp. 1107-1111
    • Kojima, H.1    Tominaga, H.2    Sato, S.3
  • 14
    • 0034683034 scopus 로고    scopus 로고
    • Enzyme mechanisms for polycyclic triterpene formation [J]
    • Wendt KU, Schultz GE, Corey EJ, et al. Enzyme mechanisms for polycyclic triterpene formation [J]. Angew Chem Int Edn 2000, 39(16):2812-2833.
    • (2000) Angew Chem Int Edn , vol.39 , Issue.16 , pp. 2812-2833
    • Wendt, K.U.1    Schultz, G.E.2    Corey, E.J.3
  • 15
    • 33744906765 scopus 로고    scopus 로고
    • Pharmacological activities of natural triterpenoids and their therapeutic implications [J]
    • Dzubak P, Hajduch M, Vydra D, et al. Pharmacological activities of natural triterpenoids and their therapeutic implications [J]. Nat Prod Rep 2006, 23:394-411.
    • (2006) Nat Prod Rep , vol.23 , pp. 394-411
    • Dzubak, P.1    Hajduch, M.2    Vydra, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.