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Volumn , Issue , 2013, Pages 3225-3250

Plant steroidal saponins: A focus on open-chain glycosides

Author keywords

Cholestane glycosides; Furostanol; Open chain steroidal glycosides; Spirostanol; Stereochemistry; Steroidal saponins; Structure elucidation

Indexed keywords


EID: 84927529675     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1007/978-3-642-22144-6_139     Document Type: Chapter
Times cited : (6)

References (129)
  • 1
    • 33846219958 scopus 로고    scopus 로고
    • Saponins, classification and occurrence in the plant kingdom
    • Vinçken JP, Heng L, de Groot A, Grnppen H (2007) Saponins, classification and occurrence in the plant kingdom. Phytochemistry 68:275-297. doi:10.1016/j.phytochem.2006.10.008
    • (2007) Phytochemistry , vol.68 , pp. 275-297
    • Vinçken, J.P.1    Heng, L.2    De Groot, A.3    Grnppen, H.4
  • 2
    • 35748949934 scopus 로고    scopus 로고
    • The Dioscorea genus: A review of bioactive steroid saponins
    • Sautour M, Mitaine-Offer AC, Lacaille-Dubois MA (2007) The Dioscorea genus: A review of bioactive steroid saponins. J Nat Med 61:91-101. doi:10.1007/s11418-006-0126-3
    • (2007) J Nat Med , vol.61 , pp. 91-101
    • Sautour, M.1    Mitaine-Offer, A.C.2    Lacaille-Dubois, M.A.3
  • 3
    • 4344587843 scopus 로고    scopus 로고
    • Biological activities and distribution of plant saponins
    • Sparg SG, Light ME, van Staden J (2004) Biological activities and distribution of plant saponins. J Ethnopharmacol 94:219-243. doi:10.1016/j.jep.2004.05.016
    • (2004) J Ethnopharmacol , vol.94 , pp. 219-243
    • Sparg, S.G.1    Light, M.E.2    Van Staden, J.3
  • 5
    • 85008107977 scopus 로고
    • Comparative studies on the constituents of ophiopogonis tuber and its congeners. I. Studies of the constituents of the subterranean part of Liriope platyphylla Wang et Tang. (1)
    • Watanabe Y, Sanada S, Ida Y, Shoji J (1983) Comparative studies on the constituents of ophiopogonis tuber and its congeners. I. Studies of the constituents of the subterranean part of Liriope platyphylla Wang et Tang. (1). Chem Pharm Bull 31:1980-1990
    • (1983) Chem Pharm Bull , vol.31 , pp. 1980-1990
    • Watanabe, Y.1    Sanada, S.2    Ida, Y.3    Shoji, J.4
  • 6
    • 0031002622 scopus 로고    scopus 로고
    • Antineoplastic agents. Part 2. Four furostanol glycosides from rhizomes of Dioscorea collettii var. Hypoglauca
    • Hu K, Dong AJ, Yao XS, Kobayashi H, Iwasaki S (1997) Antineoplastic agents. Part 2. Four furostanol glycosides from rhizomes of Dioscorea collettii var. hypoglauca. Planta Med 63:161-165
    • (1997) Planta Med , vol.63 , pp. 161-165
    • Hu, K.1    Dong, A.J.2    Yao, X.S.3    Kobayashi, H.4    Iwasaki, S.5
  • 8
    • 33847001683 scopus 로고    scopus 로고
    • Medicinal flowers. XII. New spirostane-type steroid saponins with antidiabetogenic activity from Borassus flabellifer
    • Yoshikawa M, Xu F, Morikawa T, Pongpiriyadacha Y, Nakamura S, Asao Y et al (2007) Medicinal flowers. XII. New spirostane-type steroid saponins with antidiabetogenic activity from Borassus flabellifer. Chem Pharm Bull 55:308-316
    • (2007) Chem Pharm Bull , vol.55 , pp. 308-316
    • Yoshikawa, M.1    Xu, F.2    Morikawa, T.3    Pongpiriyadacha, Y.4    Nakamura, S.5    Asao, Y.6
  • 9
    • 0041713610 scopus 로고
    • Identification and isolation of steroidal saponins of Dioscorea zingiberensis Wright
    • Tang S, Wu Y, Pang Z (1983) Identification and isolation of steroidal saponins of Dioscorea zingiberensis Wright. Zhiwu Xuebao 25:556-562
    • (1983) Zhiwu Xuebao , vol.25 , pp. 556-562
    • Tang, S.1    Wu, Y.2    Pang, Z.3
  • 12
    • 84982334910 scopus 로고
    • Saponins of the spirostanol series. XII. Parillin, a saponin with a highly branched sugar chain
    • Tschesche R, Kottler R, Wulff G (1966) Saponins of the spirostanol series. XII. Parillin, a saponin with a highly branched sugar chain. Justus Liebigs Ann Chem 699:212-222
    • (1966) Justus Liebigs Ann Chem , vol.699 , pp. 212-222
    • Tschesche, R.1    Kottler, R.2    Wulff, G.3
  • 13
    • 21844479495 scopus 로고
    • Sarsaparilloside, a saponin derivative with bisglycosidic furostanol structure
    • Tschesche R, Luedke G, Wulff G (1967) Sarsaparilloside, a saponin derivative with bisglycosidic furostanol structure. Tetrahedron Lett 8:2785-2790
    • (1967) Tetrahedron Lett , vol.8 , pp. 2785-2790
    • Tschesche, R.1    Luedke, G.2    Wulff, G.3
  • 14
    • 0014455746 scopus 로고
    • Steroid saponins with more than one sugar chain. II. Sarsaparilloside, a bisdesmosidic 22-hydroxyfurostanol saponin
    • Tschesche R, Luedke G, Wulff G (1969) Steroid saponins with more than one sugar chain. II. Sarsaparilloside, a bisdesmosidic 22-hydroxyfurostanol saponin. Chem Ber 102:1253-1269
    • (1969) Chem Ber , vol.102 , pp. 1253-1269
    • Tschesche, R.1    Luedke, G.2    Wulff, G.3
  • 15
  • 17
    • 46549094776 scopus 로고
    • 13C NMR spectral investigations.10. 13C NMR spectroscopy of steroidal sapogenins and steroidal saponins
    • Agrawal PK, Jain DC, Gupta RK, Thakur RS (1985) 13C NMR spectral investigations.10. 13C NMR spectroscopy of steroidal sapogenins and steroidal saponins. Phytochemistry 24:2479-2496
    • (1985) Phytochemistry , vol.24 , pp. 2479-2496
    • Agrawal, P.K.1    Jain, D.C.2    Gupta, R.K.3    Thakur, R.S.4
  • 19
    • 85038233410 scopus 로고    scopus 로고
    • Steroidal saponins compounds in Tupistra: Structures and 13 C NMR features
    • Liu C, Xue Y, Cuo Z, Zou K, Li X (2011) Steroidal saponins compounds in Tupistra: structures and 13 C NMR features. Bopuxue Zazhi 28:115-126
    • (2011) Bopuxue Zazhi , vol.28 , pp. 115-126
    • Liu, C.1    Xue, Y.2    Cuo, Z.3    Zou, K.4    Li, X.5
  • 20
    • 85038255931 scopus 로고    scopus 로고
    • Research on chemical constituents and pharmacological activities of steroidal saponins from plants of Ophiopogon Ker-Gawl
    • Mei Z, Peng Z, Sun Z, Meng Q, Shi Y, Tao L et al (2008) Research on chemical constituents and pharmacological activities of steroidal saponins from plants of Ophiopogon Ker-Gawl. Xiandai Shengwuyixue Jinzhan 8:1511-1514
    • (2008) Xiandai Shengwuyixue Jinzhan , vol.8 , pp. 1511-1514
    • Mei, Z.1    Peng, Z.2    Sun, Z.3    Meng, Q.4    Shi, Y.5    Tao, L.6
  • 21
    • 28644440014 scopus 로고    scopus 로고
    • Saponins in Tribulus terrestris-chemistry and bioactivity
    • Kostova I, Dinchev D (2005) Saponins in Tribulus terrestris-chemistry and bioactivity. Phytochem Rev 4:111-137
    • (2005) Phytochem Rev , vol.4 , pp. 111-137
    • Kostova, I.1    Dinchev, D.2
  • 22
    • 85038240642 scopus 로고    scopus 로고
    • Research advances on chemical constituents and pharmacological activities of steroidal saponins in Tribulus terrestris
    • Sun G, Zhang J, Ma B (2007) Research advances on chemical constituents and pharmacological activities of steroidal saponins in Tribulus terrestris. Zhongcaoyao 38:1111-1115
    • (2007) Zhongcaoyao , vol.38 , pp. 1111-1115
    • Sun, G.1    Zhang, J.2    Ma, B.3
  • 23
    • 33947193500 scopus 로고    scopus 로고
    • Progress in study on the chemical constituents about sesquiterpene lactones and steroidal saponins from genus Vernonia and their pharmacological activities
    • Liu Q, Yang J, Suo M (2007) Progress in study on the chemical constituents about sesquiterpene lactones and steroidal saponins from genus Vernonia and their pharmacological activities. Zhongguo Zhongyao Zazhi 32:10-17
    • (2007) Zhongguo Zhongyao Zazhi , vol.32 , pp. 10-17
    • Liu, Q.1    Yang, J.2    Suo, M.3
  • 24
    • 79953162219 scopus 로고    scopus 로고
    • Steroidal saponins and sapogenins from the Agavaceae family
    • Simmons-Boyce JL, Tinto WF (2007) Steroidal saponins and sapogenins from the Agavaceae family. Nat Prod Commun 2:99-114
    • (2007) Nat Prod Commun , vol.2 , pp. 99-114
    • Simmons-Boyce, J.L.1    Tinto, W.F.2
  • 25
    • 80053295344 scopus 로고    scopus 로고
    • Bioactive steroidal saponins from Brazilian medicinal plants
    • Parente JP, Pereira da Silva B (2008) Bioactive steroidal saponins from Brazilian medicinal plants. Curr Trends Med Chem 5:45-57
    • (2008) Curr Trends Med Chem , vol.5 , pp. 45-57
    • Parente, J.P.1    Pereira Da Silva, B.2
  • 26
  • 27
    • 0035172123 scopus 로고    scopus 로고
    • Steroidal oligoglycosides from the Asteroidea
    • Iorizzi M, De Marino S, Zollo F (2001) Steroidal oligoglycosides from the Asteroidea. Curr Org Chem 5:951-973
    • (2001) Curr Org Chem , vol.5 , pp. 951-973
    • Iorizzi, M.1    De Marino, S.2    Zollo, F.3
  • 28
    • 57249093635 scopus 로고    scopus 로고
    • Marine polar steroids
    • Stonik VA (2001) Marine polar steroids. Russ Chem Rev 70:673-715
    • (2001) Russ Chem Rev , vol.70 , pp. 673-715
    • Stonik, V.A.1
  • 30
    • 79952573815 scopus 로고    scopus 로고
    • Steroid glycosides from marine organisms
    • Ivanchina NV, Kicha AA, Stonik VA (2011) Steroid glycosides from marine organisms. Steroids 76:425-454
    • (2011) Steroids , vol.76 , pp. 425-454
    • Ivanchina, N.V.1    Kicha, A.A.2    Stonik, V.A.3
  • 31
    • 34249929299 scopus 로고
    • Steroids of the spirostane and furostane series from plants of the genus Allium. XXVII. Alliosterol and allosides A and B from Allium suvorovii and Allium stipitatum, structural analogs of furostanols
    • Vollerner YS, Kravets SD, Shashkov AS, Tashkhodzhaev B, Gorovits MB, Yagudaev MR, et al (1991) Steroids of the spirostane and furostane series from plants of the genus Allium. XXVII. Alliosterol and allosides A and B from Allium suvorovii and Allium stipitatum, structural analogs of furostanols. Chem Nat Compd 27:198-207
    • (1991) Chem Nat Compd , vol.27 , pp. 198-207
    • Vollerner, Y.S.1    Kravets, S.D.2    Shashkov, A.S.3    Tashkhodzhaev, B.4    Gorovits, M.B.5    Yagudaev, M.R.6
  • 32
    • 0029360648 scopus 로고
    • Steroidal glycosides from Allium macleanii and A. Senescens, and their inhibitory activity on tumor promoter-induced phospholipid metabolism of HeLa cells
    • Inoue T, Mimaki Y, Sashida Y, Nishino A, Satomi Y, Nishino H (1995) Steroidal glycosides from Allium macleanii and A. senescens, and their inhibitory activity on tumor promoter-induced phospholipid metabolism of HeLa cells. Phytochemistry 40:521-525
    • (1995) Phytochemistry , vol.40 , pp. 521-525
    • Inoue, T.1    Mimaki, Y.2    Sashida, Y.3    Nishino, A.4    Satomi, Y.5    Nishino, H.6
  • 33
    • 0001130669 scopus 로고
    • New cholestane bisdesmosides from the bulbs of Ornithogalum thyrsoides
    • Kubo S, Mimaki Y, Sashida Y, Nikaido T, Ohmoto T (1992) New cholestane bisdesmosides from the bulbs of Ornithogalum thyrsoides. Bull Chem Soc Jpn 65:1120-1124
    • (1992) Bull Chem Soc Jpn , vol.65 , pp. 1120-1124
    • Kubo, S.1    Mimaki, Y.2    Sashida, Y.3    Nikaido, T.4    Ohmoto, T.5
  • 34
    • 7044231166 scopus 로고    scopus 로고
    • Steroidal glycosides from the bulbs of Ornithogalum thyrsoides
    • Kuroda M, Mimaki Y, Ori K, Sakagami H, Sashida Y (2004) Steroidal glycosides from the bulbs of Ornithogalum thyrsoides. J Nat Prod 67:1690-1696
    • (2004) J Nat Prod , vol.67 , pp. 1690-1696
    • Kuroda, M.1    Mimaki, Y.2    Ori, K.3    Sakagami, H.4    Sashida, Y.5
  • 35
    • 0034897297 scopus 로고    scopus 로고
    • Cholestane glycosides from the bulbs of Galtonia candicans and their cytotoxicity
    • Kuroda M, Mimaki Y, Yokosuka A, Sashida Y (2001) Cholestane glycosides from the bulbs of Galtonia candicans and their cytotoxicity. Chem Pharm Bull 49:1042-1046
    • (2001) Chem Pharm Bull , vol.49 , pp. 1042-1046
    • Kuroda, M.1    Mimaki, Y.2    Yokosuka, A.3    Sashida, Y.4
  • 36
    • 0027674864 scopus 로고
    • Steroidal glycosides from Allium albopilosum and A. Ostrowskianum
    • Mimaki Y, Kawashima K, Kanmoto T, Sashida Y (1993) Steroidal glycosides from Allium albopilosum and A. ostrowskianum. Phytochemistry 34:799-805
    • (1993) Phytochemistry , vol.34 , pp. 799-805
    • Mimaki, Y.1    Kawashima, K.2    Kanmoto, T.3    Sashida, Y.4
  • 37
    • 0016693075 scopus 로고
    • Steroid saponins and sapogenins of underground parts of Trillium kamtschaticum II. Pennogenin-and kryptogenin 3-O-glycosides, and related compounds
    • Nohara T, Miyahara K, Kawasaki T (1975) Steroid saponins and sapogenins of underground parts of Trillium kamtschaticum II. Pennogenin-and kryptogenin 3-O-glycosides, and related compounds. Chem Pharm Bull 23:872-885
    • (1975) Chem Pharm Bull , vol.23 , pp. 872-885
    • Nohara, T.1    Miyahara, K.2    Kawasaki, T.3
  • 40
    • 84865504622 scopus 로고    scopus 로고
    • Structure and bioactivity of steroidal saponins isolated from the roots of Chamaelirium luteum (False unicorn)
    • (in press)
    • Challinor VL, Stuthe JMU, Parsons PG, Lambert LK, Lehmann RP, Kitching W, et al (2012) Structure and bioactivity of steroidal saponins isolated from the roots of Chamaelirium luteum (false unicorn). J Nat Prod (in press). doi:10.1021/np300393y
    • (2012) J Nat Prod
    • Challinor, V.L.1    Stuthe, J.2    Parsons, P.G.3    Lambert, L.K.4    Lehmann, R.P.5    Kitching, W.6
  • 41
    • 77049122784 scopus 로고    scopus 로고
    • Cholestane glycosides and trihydroxy fatty acids from the rhizomes of Dioscorea septemloba
    • Liu X-T, Wang Z-Z, Xiao W, Zhao H-W, Yu B (2010) Cholestane glycosides and trihydroxy fatty acids from the rhizomes of Dioscorea septemloba. Planta Med 76:291-294
    • (2010) Planta Med , vol.76 , pp. 291-294
    • Liu, X.-T.1    Wang, Z.-Z.2    Xiao, W.3    Zhao, H.-W.4    Yu, B.5
  • 42
    • 31344476513 scopus 로고    scopus 로고
    • Two new steroid saponins from Paris polyphylla
    • Zhang Y, Yin F, Hu L (2005) Two new steroid saponins from Paris polyphylla. Heterocycles 65:1197-1203
    • (2005) Heterocycles , vol.65 , pp. 1197-1203
    • Zhang, Y.1    Yin, F.2    Hu, L.3
  • 43
    • 14344259068 scopus 로고    scopus 로고
    • Steroidal saponins from the aerial parts of Tribuluspentandrus Forssk
    • Hamed AI, Oleszek W, Stochmal A, Pizza C, Piacente S (2004) Steroidal saponins from the aerial parts of Tribuluspentandrus Forssk. Phytochemistry 65:2935-2945
    • (2004) Phytochemistry , vol.65 , pp. 2935-2945
    • Hamed, A.I.1    Oleszek, W.2    Stochmal, A.3    Pizza, C.4    Piacente, S.5
  • 45
    • 0034056558 scopus 로고    scopus 로고
    • Cholestane glycosides from Solanum abutiloides. III
    • Yoshimitsu H, Nishida M, Nohara T (2000) Cholestane glycosides from Solanum abutiloides. III. Chem Pharm Bull 48:556-558
    • (2000) Chem Pharm Bull , vol.48 , pp. 556-558
    • Yoshimitsu, H.1    Nishida, M.2    Nohara, T.3
  • 46
  • 47
    • 0031552155 scopus 로고    scopus 로고
    • Cholestane glycosides with potent cytostatic activities on various tumor cells from Ornithogalum saundersiae bulbs
    • Mimaki Y, Kuroda M, Kameyama A, Sashida Y, Hirano T, Oka K et al (1997) Cholestane glycosides with potent cytostatic activities on various tumor cells from Ornithogalum saundersiae bulbs. Bioorg Med Chem Lett 7:633-636
    • (1997) Bioorg Med Chem Lett , vol.7 , pp. 633-636
    • Mimaki, Y.1    Kuroda, M.2    Kameyama, A.3    Sashida, Y.4    Hirano, T.5    Oka, K.6
  • 48
    • 0035142056 scopus 로고    scopus 로고
    • Cytotoxic cholestane glycosides from the bulbs of Ornithogalum saundersiae
    • Kuroda M, Mimaki Y, Yokosuka A, Sashida Y, Beutler JA (2001) Cytotoxic cholestane glycosides from the bulbs of Ornithogalum saundersiae. J Nat Prod 64:88-91
    • (2001) J Nat Prod , vol.64 , pp. 88-91
    • Kuroda, M.1    Mimaki, Y.2    Yokosuka, A.3    Sashida, Y.4    Beutler, J.A.5
  • 49
    • 0036772680 scopus 로고    scopus 로고
    • Cholestane glycosides from the bulbs of Ornithogalum thyrsoides and their cytotoxic activity against HL-60 leukemia cells
    • Kuroda M, Mimaki Y, Yokosuka A, Hasegawa F, Sashida Y (2002) Cholestane glycosides from the bulbs of Ornithogalum thyrsoides and their cytotoxic activity against HL-60 leukemia cells. J Nat Prod 65:1417-1423
    • (2002) J Nat Prod , vol.65 , pp. 1417-1423
    • Kuroda, M.1    Mimaki, Y.2    Yokosuka, A.3    Hasegawa, F.4    Sashida, Y.5
  • 50
    • 0032485307 scopus 로고    scopus 로고
    • Cephalostatin support studies. 12. The first synthesis of the aglycon of the potent anti-tumor steroidal saponin OSW-1
    • Guo C, Fuchs PL (1998) Cephalostatin support studies. 12. The first synthesis of the aglycon of the potent anti-tumor steroidal saponin OSW-1. Tetrahedron Lett 39:1099-1102
    • (1998) Tetrahedron Lett , vol.39 , pp. 1099-1102
    • Guo, C.1    Fuchs, P.L.2
  • 51
    • 0033534604 scopus 로고    scopus 로고
    • First total synthesis of an exceptionally potent antitumor saponin, OSW-1
    • Deng S, Yu B, Lou Y, Hui Y (1999) First total synthesis of an exceptionally potent antitumor saponin, OSW-1. J Org Chem 64:202-208
    • (1999) J Org Chem , vol.64 , pp. 202-208
    • Deng, S.1    Yu, B.2    Lou, Y.3    Hui, Y.4
  • 52
    • 84874068678 scopus 로고    scopus 로고
    • Total synthesis of antitumor saponin OSW-1 based on a new synthetic strategy
    • Yamada Y (2001) Total synthesis of antitumor saponin OSW-1 based on a new synthetic strategy. Farumashia 37:1044-1045
    • (2001) Farumashia , vol.37 , pp. 1044-1045
    • Yamada, Y.1
  • 53
    • 0034829735 scopus 로고    scopus 로고
    • A new strategy for the stereoselective introduction of steroid side chain via a-alkoxy vinyl cuprates: Total synthesis of a highly potent antitumor natural product OSW-1
    • Yu W, Jin Z (2001) A new strategy for the stereoselective introduction of steroid side chain via a-alkoxy vinyl cuprates: Total synthesis of a highly potent antitumor natural product OSW-1. J Am Chem Soc 123:3369-3370
    • (2001) J am Chem Soc , vol.123 , pp. 3369-3370
    • Yu, W.1    Jin, Z.2
  • 54
    • 0037067056 scopus 로고    scopus 로고
    • Total synthesis of the anticancer natural product OSW-1
    • Yu W, Jin Z (2002) Total synthesis of the anticancer natural product OSW-1. J Am Chem Soc 124:6576-6583
    • (2002) J am Chem Soc , vol.124 , pp. 6576-6583
    • Yu, W.1    Jin, Z.2
  • 55
    • 36849020952 scopus 로고    scopus 로고
    • A new synthesis of potent antitumor saponin OSW-1 via Wittig rearrangement
    • Tsubuki M, Matsuo S, Honda T (2008) A new synthesis of potent antitumor saponin OSW-1 via Wittig rearrangement. Tetrahedron Lett 49:229-232
    • (2008) Tetrahedron Lett , vol.49 , pp. 229-232
    • Tsubuki, M.1    Matsuo, S.2    Honda, T.3
  • 56
    • 37549028745 scopus 로고    scopus 로고
    • A total synthesis of OSW-1
    • Xue J, Liu P, Pan Y, Guo Z (2008) A total synthesis of OSW-1. J Org Chem 73:157-161
    • (2008) J Org Chem , vol.73 , pp. 157-161
    • Xue, J.1    Liu, P.2    Pan, Y.3    Guo, Z.4
  • 57
    • 0026759808 scopus 로고
    • New polyhydroxylated cholestane glycosides from the bulbs of Ornithogalum saundersiae
    • Kubo S, Mimaki Y, Sashida Y, Nikaido T, Ohmoto T (1992) New polyhydroxylated cholestane glycosides from the bulbs of Ornithogalum saundersiae. Chem Pharm Bull 40:2469-2472
    • (1992) Chem Pharm Bull , vol.40 , pp. 2469-2472
    • Kubo, S.1    Mimaki, Y.2    Sashida, Y.3    Nikaido, T.4    Ohmoto, T.5
  • 58
    • 79960734976 scopus 로고    scopus 로고
    • Structure and absolute configuration of helosides A and B. New saponins from Chamaelirium luteum
    • Challinor VL, Stuthe JMU, Bernhardt PV, Lehmann RP, Kitching W, De Voss JJ (2011) Structure and absolute configuration of helosides A and B. New saponins from Chamaelirium luteum. J Nat Prod 74:1557-1560. doi:10.1021/np200100a
    • (2011) J Nat Prod , vol.74 , pp. 1557-1560
    • Challinor, V.L.1    Stuthe, J.2    Bernhardt, P.V.3    Lehmann, R.P.4    Kitching, W.5    De Voss, J.J.6
  • 60
    • 0344873728 scopus 로고    scopus 로고
    • Lanosterol and tetranorla-nosterol glycosides from the bulbs of Muscari paradoxum
    • Ori K, Koroda M, Mimaki Y, Sakagami H, Sashida Y (2003) Lanosterol and tetranorla-nosterol glycosides from the bulbs of Muscari paradoxum. Phytochemistry 64:1351-1359
    • (2003) Phytochemistry , vol.64 , pp. 1351-1359
    • Ori, K.1    Koroda, M.2    Mimaki, Y.3    Sakagami, H.4    Sashida, Y.5
  • 61
    • 84943006707 scopus 로고    scopus 로고
    • A new lanostanyl diglucuronoside from the flowers of Punica granatum L
    • Jabbar Z, Ali M (2011) A new lanostanyl diglucuronoside from the flowers of Punica granatum L. Int Res J Pharm 2:141-144
    • (2011) Int Res J Pharm , vol.2 , pp. 141-144
    • Jabbar, Z.1    Ali, M.2
  • 62
    • 0037123283 scopus 로고    scopus 로고
    • A chlorinated monoterpene ketone, acylated b-sitosterol glycosides and a flavanone glycoside from Mentha longifolia (Lamiaceae)
    • Shaiq Ali M, Saleem M, Ahmad W, Parvez M, Yamdagni R (2002) A chlorinated monoterpene ketone, acylated b-sitosterol glycosides and a flavanone glycoside from Mentha longifolia (Lamiaceae). Phytochemistry 59:889-895
    • (2002) Phytochemistry , vol.59 , pp. 889-895
    • Shaiq Ali, M.1    Saleem, M.2    Ahmad, W.3    Parvez, M.4    Yamdagni, R.5
  • 63
    • 0006020208 scopus 로고
    • Studies on the constituents of Paris formosana Hayata. Part II
    • Yeh PH, Chiang HC (1982) Studies on the constituents of Paris formosana Hayata. Part II. J Chin Chem Soc 29:39-46
    • (1982) J Chin Chem Soc , vol.29 , pp. 39-46
    • Yeh, P.H.1    Chiang, H.C.2
  • 64
    • 33745702494 scopus 로고
    • B-Sitosterol-3-O-b-D-arabinofuranosyl-O-a-L-rhamnopyranosyl-O-b-D-glucopyranoside from roots of Streblus asper Lour
    • Chaturvedi SK, Saxena VK (1984) b-Sitosterol-3-O-b-D-arabinofuranosyl-O-a-L-rhamnopyranosyl-O-b-D-glucopyranoside from roots of Streblus asper Lour. Acta Ciencia Indica Chem 10:122-123
    • (1984) Acta Ciencia Indica Chem , vol.10 , pp. 122-123
    • Chaturvedi, S.K.1    Saxena, V.K.2
  • 65
    • 79958817541 scopus 로고
    • A new steroidal saponin from Trichosanthes dioica (Roxb.)
    • Saxena VK, Dave RK (1995) A new steroidal saponin from Trichosanthes dioica (Roxb.). Asian J Chem 7:490-494
    • (1995) Asian J Chem , vol.7 , pp. 490-494
    • Saxena, V.K.1    Dave, R.K.2
  • 66
    • 0003051601 scopus 로고
    • Steroid glycosides from Asparagus adscendens
    • Tandon M, Shukla YN, Thakur RS (1990) Steroid glycosides from Asparagus adscendens. Phytochemistry 29:2957-2959
    • (1990) Phytochemistry , vol.29 , pp. 2957-2959
    • Tandon, M.1    Shukla, Y.N.2    Thakur, R.S.3
  • 67
    • 0030055231 scopus 로고    scopus 로고
    • Oleanene and stigmasterol derivatives from Ambroma augusta
    • Alam MS, Chopra N, Ali M, Niwa M (1996) Oleanene and stigmasterol derivatives from Ambroma augusta. Phytochemistry 41:1197-1200
    • (1996) Phytochemistry , vol.41 , pp. 1197-1200
    • Alam, M.S.1    Chopra, N.2    Ali, M.3    Niwa, M.4
  • 68
    • 0028883678 scopus 로고
    • 26-Aminocholestanol derivative, a novel key intermediate of steroidal alkaloids, from Solanum abutiloides
    • Ohmura E, Nakamura T, Tian RH, Yahara S, Yoshimitsu H, Nohara T (1995) 26-Aminocholestanol derivative, a novel key intermediate of steroidal alkaloids, from Solanum abutiloides. Tetrahedron Lett 36:8443-8444
    • (1995) Tetrahedron Lett , vol.36 , pp. 8443-8444
    • Ohmura, E.1    Nakamura, T.2    Tian, R.H.3    Yahara, S.4    Yoshimitsu, H.5    Nohara, T.6
  • 69
    • 0030015315 scopus 로고    scopus 로고
    • Solanaceous plants. XXXIV. Cholestane glycosides from Solatium abutiloides
    • Tian R-H, Ohmura E, Yoshimitsu H, Nohara T, Matsui M (1996) Solanaceous plants. XXXIV. Cholestane glycosides from Solatium abutiloides. Chem Pharm Bull 44:1119-1121
    • (1996) Chem Pharm Bull , vol.44 , pp. 1119-1121
    • Tian, R.-H.1    Ohmura, E.2    Yoshimitsu, H.3    Nohara, T.4    Matsui, M.5
  • 70
    • 0031081120 scopus 로고    scopus 로고
    • Abutiloside A, a 26-acylamino-3b,16a-dihydroxy-5a-cholesta-22-one glycoside from Solatium abutiloides
    • Tian R-H, Ohmura E, Matsui M, Noharas T (1997) Abutiloside A, a 26-acylamino-3b,16a-dihydroxy-5a-cholesta-22-one glycoside from Solatium abutiloides. Phytochemistry 44:723-726
    • (1997) Phytochemistry , vol.44 , pp. 723-726
    • Tian, R.-H.1    Ohmura, E.2    Matsui, M.3    Noharas, T.4
  • 72
    • 2342564917 scopus 로고    scopus 로고
    • Tomato steroidal alkaloid glycosides, esculeosides A and B, from ripe fruits
    • Fujiwara Y, Takaki A, Uehara Y, Ikeda T, Okawa M, Yamauchi K et al (2004) Tomato steroidal alkaloid glycosides, esculeosides A and B, from ripe fruits. Tetrahedron 60:4915-4920
    • (2004) Tetrahedron , vol.60 , pp. 4915-4920
    • Fujiwara, Y.1    Takaki, A.2    Uehara, Y.3    Ikeda, T.4    Okawa, M.5    Yamauchi, K.6
  • 73
    • 54349108836 scopus 로고    scopus 로고
    • A new steroidal glycoside and a new phenyl glycoside from a ripe cherry tomato
    • Ono M, Shiono Y, Yanai Y, Fujiwara Y, Ikeda T, Nohara T (2008) A new steroidal glycoside and a new phenyl glycoside from a ripe cherry tomato. Chem Pharm Bull 56:1499-1501
    • (2008) Chem Pharm Bull , vol.56 , pp. 1499-1501
    • Ono, M.1    Shiono, Y.2    Yanai, Y.3    Fujiwara, Y.4    Ikeda, T.5    Nohara, T.6
  • 74
    • 0001046334 scopus 로고
    • Two steroidal alkaloids, hapepunine and anrakorinine, from the mature Fritillaria camtschatcensis
    • Kaneko K, Nakaoka U, Tanaka M, Yoshida N, Mitsuhashi H (1981) Two steroidal alkaloids, hapepunine and anrakorinine, from the mature Fritillaria camtschatcensis. Phytochemistry 20:157-160
    • (1981) Phytochemistry , vol.20 , pp. 157-160
    • Kaneko, K.1    Nakaoka, U.2    Tanaka, M.3    Yoshida, N.4    Mitsuhashi, H.5
  • 75
    • 0025078992 scopus 로고
    • Two new steroidal alkaloids from Fritillaria ussuriensis
    • Xu D, Xu M, Wang S, Hung E, Wen X, Arihara S et al (1990) Two new steroidal alkaloids from Fritillaria ussuriensis. J Nat Prod 53:549-552
    • (1990) J Nat Prod , vol.53 , pp. 549-552
    • Xu, D.1    Xu, M.2    Wang, S.3    Hung, E.4    Wen, X.5    Arihara, S.6
  • 76
    • 0029379577 scopus 로고
    • Steroidal alkaloids of Fritillaria maximowiczii
    • Qian Z-Z, Nohara T (1995) Steroidal alkaloids of Fritillaria maximowiczii. Phytochemistry 40:979-981
    • (1995) Phytochemistry , vol.40 , pp. 979-981
    • Qian, Z.-Z.1    Nohara, T.2
  • 78
    • 77954050076 scopus 로고    scopus 로고
    • Anti-ischemia steroidal saponins from the seeds of Allium fistulosum
    • Lai W, Wu Z, Lin H, Li T, Sun L, Chai Y et al (2010) Anti-ischemia steroidal saponins from the seeds of Allium fistulosum. J Nat Prod 73:1053-1057
    • (2010) J Nat Prod , vol.73 , pp. 1053-1057
    • Lai, W.1    Wu, Z.2    Lin, H.3    Li, T.4    Sun, L.5    Chai, Y.6
  • 81
    • 78650680733 scopus 로고    scopus 로고
    • Steroidal saponins from Yucca gloriosa L. Rhizomes: LC-MS profiling, isolation and quantitative determination
    • Skhirtladze A, Perrone A, Montoro P, Benidze M, Kemertelidze E, Pizza C et al (2011) Steroidal saponins from Yucca gloriosa L. rhizomes: LC-MS profiling, isolation and quantitative determination. Phytochemistry 72:126-135
    • (2011) Phytochemistry , vol.72 , pp. 126-135
    • Skhirtladze, A.1    Perrone, A.2    Montoro, P.3    Benidze, M.4    Kemertelidze, E.5    Pizza, C.6
  • 82
    • 30144444641 scopus 로고    scopus 로고
    • Twenty years of evaporative light scattering detection
    • Megoulas NC, Koupparis MA (2005) Twenty years of evaporative light scattering detection. Crit Rev Anal Chem 35:301-316
    • (2005) Crit Rev Anal Chem , vol.35 , pp. 301-316
    • Megoulas, N.C.1    Koupparis, M.A.2
  • 83
    • 34547266523 scopus 로고    scopus 로고
    • Evaporative light scattering detection (ELSD) for the analysis of natural products
    • Ganzera M, Stuppner H (2005) Evaporative light scattering detection (ELSD) for the analysis of natural products. Curr Pharm Anal 1:135-144
    • (2005) Curr Pharm Anal , vol.1 , pp. 135-144
    • Ganzera, M.1    Stuppner, H.2
  • 84
    • 33645830693 scopus 로고    scopus 로고
    • Chromatographic determination of plant saponins-an update (2002-2005)
    • Oleszek W, Bialy Z (2006) Chromatographic determination of plant saponins-an update (2002-2005). J Chromatogr A 1112:78-91. doi:10.1016/j.chroma.2006.01.037
    • (2006) J Chromatogr A , vol.1112 , pp. 78-91
    • Oleszek, W.1    Bialy, Z.2
  • 88
    • 79959485788 scopus 로고    scopus 로고
    • The truth about false unicorn (Chamaelirium luteum): Total synthesis of 23R,24 S-chiograsterol B defines the structure and stereochemistry of the major saponins from this medicinal herb
    • Matovic NJ, Stuthe JMU, Challinor VL, Bernhardt PV, Lehmann RP, Kitching W et al (2011) The truth about false unicorn (Chamaelirium luteum): Total synthesis of 23R,24 S-chiograsterol B defines the structure and stereochemistry of the major saponins from this medicinal herb. Chem-Eur J 17:7578-7591. doi:10.1002/chem.201100503
    • (2011) Chem-Eur J , vol.17 , pp. 7578-7591
    • Matovic, N.J.1    Stuthe, J.2    Challinor, V.L.3    Bernhardt, P.V.4    Lehmann, R.P.5    Kitching, W.6
  • 89
    • 15944377716 scopus 로고    scopus 로고
    • A new steroidal saponin from Dioscorea deltoidea Wall var. Orbiculata
    • Shen P, Wang SL, Liu XK, Yang CR, Cai B, Yao XS (2002) A new steroidal saponin from Dioscorea deltoidea Wall var. orbiculata. Chin Chem Lett 13:851-854
    • (2002) Chin Chem Lett , vol.13 , pp. 851-854
    • Shen, P.1    Wang, S.L.2    Liu, X.K.3    Yang, C.R.4    Cai, B.5    Yao, X.S.6
  • 90
    • 0035983390 scopus 로고    scopus 로고
    • Structural characterization of steroidal saponins by electrospray ionization and fast-atom bombardment tandem mass spectrometry
    • Liang F, Li LJ, Abliz Z, Yang YC, Shi JG (2002) Structural characterization of steroidal saponins by electrospray ionization and fast-atom bombardment tandem mass spectrometry. Rapid Commun Mass Spectrom 16:1168-1173
    • (2002) Rapid Commun Mass Spectrom , vol.16 , pp. 1168-1173
    • Liang, F.1    Li, L.J.2    Abliz, Z.3    Yang, Y.C.4    Shi, J.G.5
  • 92
    • 4644250833 scopus 로고    scopus 로고
    • Multiple-stage tandem mass spectrometry for differentiation of isomeric saponins
    • Song F, Cui M, Liu Z, Yu B, Liu S (2004) Multiple-stage tandem mass spectrometry for differentiation of isomeric saponins. Rapid Commun Mass Spectrom 18:2241-2248
    • (2004) Rapid Commun Mass Spectrom , vol.18 , pp. 2241-2248
    • Song, F.1    Cui, M.2    Liu, Z.3    Yu, B.4    Liu, S.5
  • 93
    • 35848930591 scopus 로고    scopus 로고
    • Multistage and tandem mass spectrometry of glycosylated triterpenoid saponins isolated from bacopa monnieri: Comparison of the information content provided by different techniques
    • Zehl M, Pittenauer E, Jirovetz L, Bandhari P, Singh B, Kaul VK et al (2007) Multistage and tandem mass spectrometry of glycosylated triterpenoid saponins isolated from bacopa monnieri: comparison of the information content provided by different techniques. Anal Chem 79:8214-8221
    • (2007) Anal Chem , vol.79 , pp. 8214-8221
    • Zehl, M.1    Pittenauer, E.2    Jirovetz, L.3    Bandhari, P.4    Singh, B.5    Kaul, V.K.6
  • 94
    • 68949212841 scopus 로고    scopus 로고
    • Characterization of steroidal saponins in saponin extract from Paris polyphylla by liquid chromatography tandem multistage mass spectrometry
    • Man S, Gao W, Zhang Y, Jin X, Ma C, Huang X et al (2009) Characterization of steroidal saponins in saponin extract from Paris polyphylla by liquid chromatography tandem multistage mass spectrometry. Anal Bioanal Chem 395:495-505
    • (2009) Anal Bioanal Chem , vol.395 , pp. 495-505
    • Man, S.1    Gao, W.2    Zhang, Y.3    Jin, X.4    Ma, C.5    Huang, X.6
  • 95
    • 84994936401 scopus 로고
    • NMR spectroscopy of steroidal sapogenins and steroidal saponins: An update
    • Agrawal PK, Jain DC, Pathak AK (1995) NMR spectroscopy of steroidal sapogenins and steroidal saponins: An update. Magn Reson Chem 33:923-953
    • (1995) Magn Reson Chem , vol.33 , pp. 923-953
    • Agrawal, P.K.1    Jain, D.C.2    Pathak, A.K.3
  • 96
    • 0036180639 scopus 로고    scopus 로고
    • Choosing the best pulse sequences, acquisition parameters, postacquisition processing strategies, and probes for natural product structure elucidation by NMR spectroscopy
    • Reynolds WF, Enriquez RG (2002) Choosing the best pulse sequences, acquisition parameters, postacquisition processing strategies, and probes for natural product structure elucidation by NMR spectroscopy. J Nat Prod 65:221-244. doi:10.1021/np010444o
    • (2002) J Nat Prod , vol.65 , pp. 221-244
    • Reynolds, W.F.1    Enriquez, R.G.2
  • 97
    • 16844369270 scopus 로고    scopus 로고
    • Strategies and tools for structure determination of natural products using modern methods of NMR spectroscopy
    • Bross-Walch N, Kuhn T, Moskau D, Zerbe O (2005) Strategies and tools for structure determination of natural products using modern methods of NMR spectroscopy. Chem Biodiversity 2:147-177
    • (2005) Chem Biodiversity , vol.2 , pp. 147-177
    • Bross-Walch, N.1    Kuhn, T.2    Moskau, D.3    Zerbe, O.4
  • 98
    • 53749084936 scopus 로고    scopus 로고
    • Structural elucidation with NMR spectroscopy: Practical strategies for organic chemists
    • Kwan EE, Huang SG (2008) Structural elucidation with NMR spectroscopy: practical strategies for organic chemists. Eur J Org Chem 2008:2671-2688. doi:10.1002/ejoc.200700966
    • (2008) Eur J Org Chem , vol.2008 , pp. 2671-2688
    • Kwan, E.E.1    Huang, S.G.2
  • 99
    • 0031594622 scopus 로고    scopus 로고
    • Dependence of the H-1 NMR chemical shifts of ring F resonances on the orientation of the 27-methyl group of spirostane-type steroidal sapogenins
    • Agrawal PK, Bunsawansong P, Morris GA (1998) Dependence of the H-1 NMR chemical shifts of ring F resonances on the orientation of the 27-methyl group of spirostane-type steroidal sapogenins. Phytochemistry 47:255-257
    • (1998) Phytochemistry , vol.47 , pp. 255-257
    • Agrawal, P.K.1    Bunsawansong, P.2    Morris, G.A.3
  • 100
    • 0242522145 scopus 로고    scopus 로고
    • 25R/25 S stereochemistry of spirostane-type steroidal sapogenins and steroidal saponins via chemical shift of geminal protons of ring F
    • Agrawal PK (2003) 25R/25 S stereochemistry of spirostane-type steroidal sapogenins and steroidal saponins via chemical shift of geminal protons of ring F. Magn Reson Chem 41:965-968. doi:10.1002/mrc.1278
    • (2003) Magn Reson Chem , vol.41 , pp. 965-968
    • Agrawal, P.K.1
  • 101
    • 0030019309 scopus 로고    scopus 로고
    • Conversion of furostanol glycoside to spirostanol glycoside by b-glucosidase in Costus speciosus
    • Inoue K, Shimomura K, Kobayashi S, Sankawa U, Ebizuka Y (1996) Conversion of furostanol glycoside to spirostanol glycoside by b-glucosidase in Costus speciosus. Phytochemistry 41:725-727
    • (1996) Phytochemistry , vol.41 , pp. 725-727
    • Inoue, K.1    Shimomura, K.2    Kobayashi, S.3    Sankawa, U.4    Ebizuka, Y.5
  • 102
    • 10944242237 scopus 로고    scopus 로고
    • Dependence of H-1 NMR chemical shifts of geminal protons of glycosyloxy methylene (H2-26) on the orientation of the 27-methyl group of furostane-type steroidal saponins
    • Agrawal PK (2004) Dependence of H-1 NMR chemical shifts of geminal protons of glycosyloxy methylene (H2-26) on the orientation of the 27-methyl group of furostane-type steroidal saponins. Magn Reson Chem 42:990-993
    • (2004) Magn Reson Chem , vol.42 , pp. 990-993
    • Agrawal, P.K.1
  • 103
    • 21844463055 scopus 로고    scopus 로고
    • Assigning stereodiversity of the 27-Me group of furostane-type steroidal saponins via NMR chemical shifts
    • Agrawal PK (2005) Assigning stereodiversity of the 27-Me group of furostane-type steroidal saponins via NMR chemical shifts. Steroids 70:715-724
    • (2005) Steroids , vol.70 , pp. 715-724
    • Agrawal, P.K.1
  • 104
    • 84859850134 scopus 로고    scopus 로고
    • NMR assignment of the absolute configuration of C-25 in furostanol steroidal saponins
    • Challinor VL, Piacente S, De Voss JJ (2012) NMR assignment of the absolute configuration of C-25 in furostanol steroidal saponins. Steroids 77:602-608
    • (2012) Steroids , vol.77 , pp. 602-608
    • Challinor, V.L.1    Piacente, S.2    De Voss, J.J.3
  • 105
    • 34147172681 scopus 로고    scopus 로고
    • Pancreatic lipase-inhibiting triterpenoid saponins from Gypsophila oldhamiana
    • Zheng Q, Li W, Han LK, Koike K (2007) Pancreatic lipase-inhibiting triterpenoid saponins from Gypsophila oldhamiana. Chem Pharm Bull 55:646-650
    • (2007) Chem Pharm Bull , vol.55 , pp. 646-650
    • Zheng, Q.1    Li, W.2    Han, L.K.3    Koike, K.4
  • 106
    • 84985571876 scopus 로고
    • Gas-chromatographic separation of carbohydrate enantiomers on a new chiral stationary phase
    • Konig WA, Benecke I, Bretting H (1981) Gas-chromatographic separation of carbohydrate enantiomers on a new chiral stationary phase. Angew Chem Int Ed Engl 20:693-694
    • (1981) Angew Chem Int Ed Engl , vol.20 , pp. 693-694
    • Konig, W.A.1    Benecke, I.2    Bretting, H.3
  • 109
    • 3242670779 scopus 로고    scopus 로고
    • Biosynthesis and accumulation of sterols
    • 421 plate C421
    • Benveniste P (2004) Biosynthesis and accumulation of sterols. Annu Rev Plant Biol 55:429-457, 421 plate C421
    • (2004) Annu Rev Plant Biol , vol.55 , pp. 429-457
    • Benveniste, P.1
  • 110
    • 84948971366 scopus 로고    scopus 로고
    • Biochemistry of sterols, cardiac glycosides, brassinosteroids, phytoecdysteroids and steroid saponins
    • Kreis W, Muller-Uri F (2010) Biochemistry of sterols, cardiac glycosides, brassinosteroids, phytoecdysteroids and steroid saponins. Annu Plant Rev 40:304-363
    • (2010) Annu Plant Rev , vol.40 , pp. 304-363
    • Kreis, W.1    Muller-Uri, F.2
  • 111
    • 80052059686 scopus 로고    scopus 로고
    • The saponins-polar isoprenoids with important and diverse biological activities
    • Osbourn A, Goss RJM, Field RA (2011) The saponins-polar isoprenoids with important and diverse biological activities. Nat Prod Rep 28:1261-1268
    • (2011) Nat Prod Rep , vol.28 , pp. 1261-1268
    • Osbourn, A.1    Goss, R.2    Field, R.A.3
  • 114
    • 77952953046 scopus 로고    scopus 로고
    • Identification and characterization of glycosyltransferases involved in the biosynthesis of soyasaponin I in Glycine max
    • Shibuya M, Nishimura K, Yasuyama N, Ebizuka Y (2010) Identification and characterization of glycosyltransferases involved in the biosynthesis of soyasaponin I in Glycine max. FEBS Lett 584:2258-2264
    • (2010) FEBS Lett , vol.584 , pp. 2258-2264
    • Shibuya, M.1    Nishimura, K.2    Yasuyama, N.3    Ebizuka, Y.4
  • 115
    • 33646153986 scopus 로고    scopus 로고
    • Acyltransferases in plants: A good time to be BAHD
    • D’Auria JC (2006) Acyltransferases in plants: A good time to be BAHD. Curr Opin Plant Biol 9:331-340
    • (2006) Curr Opin Plant Biol , vol.9 , pp. 331-340
    • D’auria, J.C.1
  • 116
    • 0034521898 scopus 로고    scopus 로고
    • The bioactivity of saponins: Triterpenoid and steroidal glycosides
    • Rao AV, Gurfinkel DM (2000) The bioactivity of saponins: Triterpenoid and steroidal glycosides. Drug Metab Drug Interact 17:211-235
    • (2000) Drug Metab Drug Interact , vol.17 , pp. 211-235
    • Rao, A.V.1    Gurfinkel, D.M.2
  • 118
    • 77956655047 scopus 로고    scopus 로고
    • Chemical study and medical application of saponins as anti-cancer agents
    • Man SL, Gao WY, Zhang YJ, Huang LQ, Liu CX (2010) Chemical study and medical application of saponins as anti-cancer agents. Fitoterapia 81:703-714. doi:10.1016/j.fitote.2010.06.004
    • (2010) Fitoterapia , vol.81 , pp. 703-714
    • Man, S.L.1    Gao, W.Y.2    Zhang, Y.J.3    Huang, L.Q.4    Liu, C.X.5
  • 122
    • 0035172063 scopus 로고    scopus 로고
    • Cytotoxic activities and structure-cytotoxic relationships of steroidal saponins
    • Mimaki Y, Yokosuka A, Kuroda M, Sashida Y (2001) Cytotoxic activities and structure-cytotoxic relationships of steroidal saponins. Biol Pharm Bull 24:1286-1289
    • (2001) Biol Pharm Bull , vol.24 , pp. 1286-1289
    • Mimaki, Y.1    Yokosuka, A.2    Kuroda, M.3    Sashida, Y.4
  • 123
    • 0036257506 scopus 로고    scopus 로고
    • Protodioscin (NSC-698 796): Its spectrum of cytotoxicity against sixty human cancer cell lines in an anticancer drug screen panel
    • Hu K, Yao X (2002) Protodioscin (NSC-698 796): its spectrum of cytotoxicity against sixty human cancer cell lines in an anticancer drug screen panel. Planta Med 68:297-301
    • (2002) Planta Med , vol.68 , pp. 297-301
    • Hu, K.1    Yao, X.2
  • 124
    • 0041857788 scopus 로고    scopus 로고
    • The cytotoxicity of methyl protodioscin against human cancer cell lines in vitro
    • Hu K, Yao X (2003) The cytotoxicity of methyl protodioscin against human cancer cell lines in vitro. Cancer Invest 21:389-393
    • (2003) Cancer Invest , vol.21 , pp. 389-393
    • Hu, K.1    Yao, X.2
  • 125
    • 0038802394 scopus 로고    scopus 로고
    • The cytotoxicity of methyl protoneogracillin (NSC-698793) and gracillin (NSC-698787), two steroidal saponins from the rhizomes of Dioscorea colletta var. Hypoglauca, against human cancer cells in vitro
    • Hu K, Yao X (2003) The cytotoxicity of methyl protoneogracillin (NSC-698793) and gracillin (NSC-698787), two steroidal saponins from the rhizomes of Dioscorea colletta var. hypoglauca, against human cancer cells in vitro. Phytother Res 17:620-626
    • (2003) Phytother Res , vol.17 , pp. 620-626
    • Hu, K.1    Yao, X.2
  • 126
    • 0034915870 scopus 로고    scopus 로고
    • Methyl protogracillin (NSC-698792): The spectrum of cytotoxicity against 60 human cancer cell lines in the National Cancer Institute’s anticancer drug screen panel
    • Hu K, Yao X (2001) Methyl protogracillin (NSC-698792): The spectrum of cytotoxicity against 60 human cancer cell lines in the National Cancer Institute’s anticancer drug screen panel. Anticancer Drugs 12:541-547
    • (2001) Anticancer Drugs , vol.12 , pp. 541-547
    • Hu, K.1    Yao, X.2
  • 127
    • 0036746180 scopus 로고    scopus 로고
    • The cytotoxicity of protoneodioscin (NSC-698789), a furostanol saponin from the rhizomes of Dioscorea collettii var. Hypoglauca, against human cancer cells in vitro
    • Hu K, Yao X (2002) The cytotoxicity of protoneodioscin (NSC-698789), a furostanol saponin from the rhizomes of Dioscorea collettii var. hypoglauca, against human cancer cells in vitro. Phytomedicine 9:560-565
    • (2002) Phytomedicine , vol.9 , pp. 560-565
    • Hu, K.1    Yao, X.2
  • 128
    • 0036244470 scopus 로고    scopus 로고
    • The cytotoxicity of methyl protoneodioscin (NSC-698791) against human cancer cell lines in vitro
    • Hu K, Yao XS (2002) The cytotoxicity of methyl protoneodioscin (NSC-698791) against human cancer cell lines in vitro. Anticancer Res 22:1001-1005
    • (2002) Anticancer Res , vol.22 , pp. 1001-1005
    • Hu, K.1    Yao, X.S.2
  • 129
    • 34547611529 scopus 로고    scopus 로고
    • Structures and biological activities of plant glycosides: Cholestane glycosides from Ornithogalum saundersiae, O. Thyrsoides and Galtonia candicans, and their cytotoxic and antitumor activities
    • Mimaki Y (2006) Structures and biological activities of plant glycosides: cholestane glycosides from Ornithogalum saundersiae, O. thyrsoides and Galtonia candicans, and their cytotoxic and antitumor activities. Nat Prod Commun 1:247-253
    • (2006) Nat Prod Commun , vol.1 , pp. 247-253
    • Mimaki, Y.1


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