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Volumn 25, Issue 6, 2002, Pages 725-746

Highly sweet compounds of plant origin

Author keywords

Flavonoids; Glycyrrhizin; Low Calorie Natural Sweeteners; Mogroside V; Plants; Proteins; Rebaudioside A; Steroids; Stevioside; Terpenoids; Thaumatin

Indexed keywords

SWEETENING AGENT;

EID: 0038341853     PISSN: 02536269     EISSN: 02536269     Source Type: Journal    
DOI: 10.1007/BF02976987     Document Type: Review
Times cited : (77)

References (125)
  • 1
    • 11244329407 scopus 로고    scopus 로고
    • FDA approves new sweetener
    • Anonymous, FDA approves new sweetener. Chem. Eng. News, July 15, 30 (2002).
    • (2002) Chem. Eng. News , vol.JULY 15 , pp. 30
  • 2
    • 37049089391 scopus 로고
    • Synthesis and sweet taste of optically active (-)-haematoxylin and of some (±)-haematoxylin derivatives
    • Arnoldi, A., Bassoli, A., Borgonovo, G. and Merlini, L., Synthesis and sweet taste of optically active (-)-haematoxylin and of some (±)-haematoxylin derivatives. J. Chem. Soc., Perkin Trans. 1, 2447-2453 (1995).
    • (1995) J. Chem. Soc., Perkin Trans. 1 , pp. 2447-2453
    • Arnoldi, A.1    Bassoli, A.2    Borgonovo, G.3    Merlini, L.4
  • 4
    • 37049091674 scopus 로고
    • 2R,3R-(+)-Acetoxy-4′,5-dihydroxy-7-methoxyflavanone and 2 R,3R-(+)-acetoxy-4′,5,7-trihydroxyflavonone: Two new 3-acetylated dihydroflavonols from Aframomum pruinosum Gagnepain (Zingiberaceae)
    • Ayafor, J. F. and Connolly, J. D., 2R,3R-(+)-Acetoxy-4′,5- dihydroxy-7-methoxyflavanone and 2 R,3R-(+)-acetoxy-4′,5,7- trihydroxyflavonone: two new 3-acetylated dihydroflavonols from Aframomum pruinosum Gagnepain (Zingiberaceae). J. Chem. Soc., Perkin Trans. 1, 1750-1754 (1981).
    • (1981) J. Chem. Soc., Perkin Trans. 1 , pp. 1750-1754
    • Ayafor, J.F.1    Connolly, J.D.2
  • 8
    • 0036664904 scopus 로고    scopus 로고
    • Isovanillyl sweeteners. From molecules to receptors
    • Bassoli, A., Merlini, L. and Morini, G., Isovanillyl sweeteners. From molecules to receptors. Pure Appl. Chem., 74, 1181-1187 (2002).
    • (2002) Pure Appl. Chem. , vol.74 , pp. 1181-1187
    • Bassoli, A.1    Merlini, L.2    Morini, G.3
  • 12
    • 0024415554 scopus 로고
    • Abrusosides A-D, four novel sweet-tasting triterpene glycosides from the leaves of Abrus precatorius
    • Choi, Y.-H., Hussain, R. A., Pezzuto, J. M., Kinghorn, A. D. and Morton, J. F., Abrusosides A-D, four novel sweet-tasting triterpene glycosides from the leaves of Abrus precatorius. J. Nat. Prod., 52, 1118-1127 (1989a).
    • (1989) J. Nat. Prod. , vol.52 , pp. 1118-1127
    • Choi, Y.-H.1    Hussain, R.A.2    Pezzuto, J.M.3    Kinghorn, A.D.4    Morton, J.F.5
  • 14
  • 15
    • 11244287655 scopus 로고    scopus 로고
    • Licorice. Root is used worldwide as a flavor and a medicine
    • Dalton, L., Licorice. Root is used worldwide as a flavor and a medicine. Chem. Eng. News, August 12, 37 (2002).
    • (2002) Chem. Eng. News , vol.AUGUST 12 , pp. 37
    • Dalton, L.1
  • 16
    • 0031559185 scopus 로고    scopus 로고
    • Lesson of the week: Hypokalaemia and hypertension associated with use of liquorice flavoured chewing gum
    • de Klerk, G. J., Nieuwenhuis, M. G. and Beutler, J. J., Lesson of the week: hypokalaemia and hypertension associated with use of liquorice flavoured chewing gum. BMJ, 314, 731-732 (1997).
    • (1997) BMJ , vol.314 , pp. 731-732
    • De Klerk, G.J.1    Nieuwenhuis, M.G.2    Beutler, J.J.3
  • 17
    • 11244292764 scopus 로고    scopus 로고
    • Brazzein, a potential low-calorie protein sweetener: High-resolution solution structure of the protein determined from multi-dimensional, multi-nuclear magnetic resonance spectroscopy
    • Hiroshima, Japan, November 13-17, Abstract PL-08
    • DeRider, M. L., Kuloglu, E. S., Abildgaard, F., Aceti, D. J., Assadi-Porter, F. B., West-Nielsen, M. and Markley, J. L. Brazzein, a potential low-calorie protein sweetener: high-resolution solution structure of the protein determined from multi-dimensional, multi-nuclear magnetic resonance spectroscopy. 2nd IUPAC-International Symposium on Sweeteners, Hiroshima, Japan, November 13-17, 2001, Abstract PL-08.
    • (2001) 2nd IUPAC-International Symposium on Sweeteners
    • DeRider, M.L.1    Kuloglu, E.S.2    Abildgaard, F.3    Aceti, D.J.4    Assadi-Porter, F.B.5    West-Nielsen, M.6    Markley, J.L.7
  • 18
    • 11244342341 scopus 로고
    • Nonnutritive sweeteners
    • DuBois, G. E., Nonnutritive sweeteners. Annu. Rep. Med. Chem., 17, 323-332 (1982).
    • (1982) Annu. Rep. Med. Chem. , vol.17 , pp. 323-332
    • DuBois, G.E.1
  • 19
    • 11244320828 scopus 로고
    • Diterpenoid sweeteners. Synthesis and sensory evaluation of biologically stable analogues of stevioside
    • DuBois, G. E., Bunes, L. A., Dietrich, P. S. and Stephenson, R. A., Diterpenoid sweeteners. Synthesis and sensory evaluation of biologically stable analogues of stevioside. J. Agric. Food Chem., 32, 1321-1325 (1984).
    • (1984) J. Agric. Food Chem. , vol.32 , pp. 1321-1325
    • DuBois, G.E.1    Bunes, L.A.2    Dietrich, P.S.3    Stephenson, R.A.4
  • 20
    • 0031923157 scopus 로고    scopus 로고
    • Position of the American Dietetic Association: Use of nutritive and nonnutritive sweeteners
    • Duffy, V. B. and Anderson, G. H., Position of the American Dietetic Association: use of nutritive and nonnutritive sweeteners. J. Am. Diet. Assoc., 98, 580-587 (1998).
    • (1998) J. Am. Diet. Assoc. , vol.98 , pp. 580-587
    • Duffy, V.B.1    Anderson, G.H.2
  • 21
    • 0004029525 scopus 로고
    • Synthesis and taste of certain steviol glycosides
    • Esaki, S., Tanaka, R. and Kamiya, S., Synthesis and taste of certain steviol glycosides. Agric. Biol. Chem., 48, 1831-1834 (1984).
    • (1984) Agric. Biol. Chem. , vol.48 , pp. 1831-1834
    • Esaki, S.1    Tanaka, R.2    Kamiya, S.3
  • 22
    • 0025050487 scopus 로고
    • Liquorice, Glycyrrhiza glabra L. - Composition, uses, and analysis
    • Fenwick, G. R., Lutomski, J. and Nieman, C., Liquorice, Glycyrrhiza glabra L. - composition, uses, and analysis. Food Chem., 38, 119-143 (1990).
    • (1990) Food Chem. , vol.38 , pp. 119-143
    • Fenwick, G.R.1    Lutomski, J.2    Nieman, C.3
  • 24
    • 84938498906 scopus 로고
    • Enzymatic transglucosylation products of stevioside: Separation and sweetness evaluation
    • Fukunaga, Y., Miyata, T., Nakayasu, N., Mizutani, K., Kasai, R. and Tanaka, O., Enzymatic transglucosylation products of stevioside: separation and sweetness evaluation. Agric. Biol. Chem., 53, 1603-1607 (1989).
    • (1989) Agric. Biol. Chem. , vol.53 , pp. 1603-1607
    • Fukunaga, Y.1    Miyata, T.2    Nakayasu, N.3    Mizutani, K.4    Kasai, R.5    Tanaka, O.6
  • 25
    • 0025363217 scopus 로고
    • Sweet-tasting triterpene glycoside constituents of Abrus fruticulosus
    • Fullas, F., Choi, Y.-H., Kinghorn, A. D. and Bunyapraphatsara, N., Sweet-tasting triterpene glycoside constituents of Abrus fruticulosus. Planta Med., 56, 332-333 (1990).
    • (1990) Planta Med. , vol.56 , pp. 332-333
    • Fullas, F.1    Choi, Y.-H.2    Kinghorn, A.D.3    Bunyapraphatsara, N.4
  • 26
    • 0026005050 scopus 로고
    • Gaudichaudiosides A-E, five novel diterpene glycoside constituents from the sweet-tasting plant, Baccharis gaudichaudiana
    • Fullas, F., Hussain, R. A., Bordas, E., Pezzuto, J. M., Soejarto, D. D. and Kinghorn, A. D., Gaudichaudiosides A-E, five novel diterpene glycoside constituents from the sweet-tasting plant, Baccharis gaudichaudiana. Tetrahedron, 47, 8515-8522 (1991).
    • (1991) Tetrahedron , vol.47 , pp. 8515-8522
    • Fullas, F.1    Hussain, R.A.2    Bordas, E.3    Pezzuto, J.M.4    Soejarto, D.D.5    Kinghorn, A.D.6
  • 27
    • 0001583429 scopus 로고
    • Dihydroflavonol sweeteners and other constituents from Hymenoxys turneri
    • Gao, F., Wang, H., Mabry, T. J. and Kinghorn, A. D., Dihydroflavonol sweeteners and other constituents from Hymenoxys turneri. Phytochemistry, 29, 2865-2869 (1990).
    • (1990) Phytochemistry , vol.29 , pp. 2865-2869
    • Gao, F.1    Wang, H.2    Mabry, T.J.3    Kinghorn, A.D.4
  • 28
    • 0030248921 scopus 로고    scopus 로고
    • Sweet and taste-modifying proteins: A review
    • Gibbs, B. F., Alli, I. and Mulligan, C., Sweet and taste-modifying proteins: a review. Nutr. Res. (N. Y.), 16, 1619-1630 (1996).
    • (1996) Nutr. Res. (N. Y.) , vol.16 , pp. 1619-1630
    • Gibbs, B.F.1    Alli, I.2    Mulligan, C.3
  • 30
    • 0026141057 scopus 로고
    • Prospects for sugar substitutes
    • Grenby, T. H., Prospects for sugar substitutes. Chem. Br., 27, 342-345 (1991).
    • (1991) Chem. Br. , vol.27 , pp. 342-345
    • Grenby, T.H.1
  • 31
    • 0024992102 scopus 로고
    • Sweet and bitter diterpene-glucosides from leaves of Rubus suavissimus
    • Hirono, S., Chou, W.-H., Kasai, R., Tanaka, O. and Tada, T., Sweet and bitter diterpene-glucosides from leaves of Rubus suavissimus. Chem. Pharm. Bull., 38, 1743-1744 (1990).
    • (1990) Chem. Pharm. Bull. , vol.38 , pp. 1743-1744
    • Hirono, S.1    Chou, W.-H.2    Kasai, R.3    Tanaka, O.4    Tada, T.5
  • 32
    • 0012470990 scopus 로고
    • Studies on mabinlin, a sweet protein from the seeds of Capparis masaikai Levl. I. Extraction, purification and some characteristics
    • Hu, Z. and He, M., Studies on mabinlin, a sweet protein from the seeds of Capparis masaikai Levl. I. Extraction, purification and some characteristics. Yunnan Zhiwu Yanjiu, 5, 207-212 (1991).
    • (1991) Yunnan Zhiwu Yanjiu , vol.5 , pp. 207-212
    • Hu, Z.1    He, M.2
  • 35
    • 0001711813 scopus 로고
    • Sweetening agents of plant origin: Phenylpropanoid constituents of seven sweet-tasting plants
    • Hussain, R. A., Poveda, L. J., Pezzuto, J. M., Soejarto, D. D. and Kinghorn, A. D., Sweetening agents of plant origin: phenylpropanoid constituents of seven sweet-tasting plants. Econ. Bot., 44, 174-182 (1990b).
    • (1990) Econ. Bot. , vol.44 , pp. 174-182
    • Hussain, R.A.1    Poveda, L.J.2    Pezzuto, J.M.3    Soejarto, D.D.4    Kinghorn, A.D.5
  • 36
    • 0142097536 scopus 로고    scopus 로고
    • Pharmacology and toxicology of stevioside, rebaudioside A, and steviol
    • Kinghorn, A. D. (Ed.). Taylor & Francis, London
    • Huxtable, R. J., Pharmacology and toxicology of stevioside, rebaudioside A, and steviol. In Kinghorn, A. D. (Ed.). Stevia: the Genus Stevia. Taylor & Francis, London, pp. 161-177 (2002).
    • (2002) Stevia: The Genus Stevia , pp. 161-177
    • Huxtable, R.J.1
  • 37
    • 84942706959 scopus 로고
    • Production of stevioside and rubusoside derivatives by transfructosylation of β-fructofuranosidase
    • Ishikawa, H., Kitahata, S., Ohtani, K., Ikuhara, C. and Tanaka, O., Production of stevioside and rubusoside derivatives by transfructosylation of β-fructofuranosidase. Agric. Biol. Chem., 54, 3137-3143 (1990).
    • (1990) Agric. Biol. Chem. , vol.54 , pp. 3137-3143
    • Ishikawa, H.1    Kitahata, S.2    Ohtani, K.3    Ikuhara, C.4    Tanaka, O.5
  • 38
    • 0642355562 scopus 로고
    • Synthesis and taste of some analogs of stevioside
    • Kamiya, S., Konishi, F. and Esaki, S., Synthesis and taste of some analogs of stevioside. Agric. Biol. Chem., 43, 3553-3557 (1979).
    • (1979) Agric. Biol. Chem. , vol.43 , pp. 3553-3557
    • Kamiya, S.1    Konishi, F.2    Esaki, S.3
  • 39
    • 0017692860 scopus 로고
    • Chemical studies on sweet diterpene-glycosides of Stevia rebaudiana: Conversion of stevioside into rebaudioside A
    • Kaneda, N., Kasai, R., Yamasaki, K. and Tanaka, O., Chemical studies on sweet diterpene-glycosides of Stevia rebaudiana: conversion of stevioside into rebaudioside A. Chem. Pharm. Bull., 25, 2466-2467 (1977).
    • (1977) Chem. Pharm. Bull. , vol.25 , pp. 2466-2467
    • Kaneda, N.1    Kasai, R.2    Yamasaki, K.3    Tanaka, O.4
  • 40
    • 0026655567 scopus 로고
    • (+)-4β-Hydroxyhernandulcin, a new sweet sesquiterpene from the leaves and flowers of Lippia dulcis
    • Kaneda, N., Lee, I.-S., Gupta, M. P., Soejarto, D. D. and Kinghorn, A. D., (+)-4β-Hydroxyhernandulcin, a new sweet sesquiterpene from the leaves and flowers of Lippia dulcis. J. Nat. Prod., 55, 1136-1141 (1992).
    • (1992) J. Nat. Prod. , vol.55 , pp. 1136-1141
    • Kaneda, N.1    Lee, I.-S.2    Gupta, M.P.3    Soejarto, D.D.4    Kinghorn, A.D.5
  • 42
    • 0023691120 scopus 로고
    • Sweet dihydroflavonol rhamnoside from leaves of Engelhardtia chrysolepis, a Chinese folk medicine, Huang-qi
    • Kasai, R., Hirono, S., Chou, W.-H., Tanaka, O. and Chen, F.-H., Sweet dihydroflavonol rhamnoside from leaves of Engelhardtia chrysolepis, a Chinese folk medicine, Huang-qi. Chem. Pharm. Bull., 36, 4167-4170 (1988a).
    • (1988) Chem. Pharm. Bull. , vol.36 , pp. 4167-4170
    • Kasai, R.1    Hirono, S.2    Chou, W.-H.3    Tanaka, O.4    Chen, F.-H.5
  • 43
    • 0025883531 scopus 로고
    • An additional sweet dihydroflavonol glycoside from leaves of Engelhardtia chrysolepis, a Chinese folk medicine, Huang-qi
    • Kasai, R., Hirono, S., Chou, W.-H., Tanaka, O. and Chen, F.-H., An additional sweet dihydroflavonol glycoside from leaves of Engelhardtia chrysolepis, a Chinese folk medicine, Huang-qi. Chem. Pharm. Bull., 39, 1871-1872 (1991).
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 1871-1872
    • Kasai, R.1    Hirono, S.2    Chou, W.-H.3    Tanaka, O.4    Chen, F.-H.5
  • 44
    • 0023845927 scopus 로고
    • Glycosides from Chinese medicinal plants, Hemsleya panacisscandens, and structure-taste relationship of cucurbitane glycosides
    • Kasai, R., Matsumoto, K., Nie, R. L., Zhou, J. and Tanaka, O., Glycosides from Chinese medicinal plants, Hemsleya panacisscandens, and structure-taste relationship of cucurbitane glycosides. Chem. Pharm. Bull., 36, 234-243 (1988b).
    • (1988) Chem. Pharm. Bull. , vol.36 , pp. 234-243
    • Kasai, R.1    Matsumoto, K.2    Nie, R.L.3    Zhou, J.4    Tanaka, O.5
  • 45
    • 0001702549 scopus 로고
    • Sweet cucurbitane glycosides from fruits of Siraitia siamensis ("hi-zi lou-han-kuo")
    • Kasai, R., Nie, R.-L., Nashi, K., Ohtani, K., Zhou, J., Tao, G.-D. and Tanaka, O., Sweet cucurbitane glycosides from fruits of Siraitia siamensis ("hi-zi lou-han-kuo"). Agric. Biol. Chem., 53, 3347-3349 (1989).
    • (1989) Agric. Biol. Chem. , vol.53 , pp. 3347-3349
    • Kasai, R.1    Nie, R.-L.2    Nashi, K.3    Ohtani, K.4    Zhou, J.5    Tao, G.-D.6    Tanaka, O.7
  • 46
    • 0030064481 scopus 로고    scopus 로고
    • Abrusoside E, a further sweet-tasting cycloartane glycoside from the leaves of Abrus precatorius
    • Kennelly, E. J., Cai, L., Kim, N.-C. and Kinghorn, A. D., Abrusoside E, a further sweet-tasting cycloartane glycoside from the leaves of Abrus precatorius. Phytochemistry, 41, 1381-1383 (1996a).
    • (1996) Phytochemistry , vol.41 , pp. 1381-1383
    • Kennelly, E.J.1    Cai, L.2    Kim, N.-C.3    Kinghorn, A.D.4
  • 48
    • 0029807215 scopus 로고    scopus 로고
    • Novel sweet-tasting saponins of the cycloartane, oleanane, secodammarane, and steroidal types
    • Waller, G. R. and Yamasaki, K. (Eds.). Plenum Press, New York
    • Kennelly, E. J., Suttisri, R. and Kinghorn, A. D., Novel sweettasting saponins of the cycloartane, oleanane, secodammarane, and steroidal types. In Waller, G. R. and Yamasaki, K. (Eds.). Saponins Used in Food and Agriculture. Plenum Press, New York, pp. 13-24 (1996b).
    • (1996) Saponins Used in Food and Agriculture , pp. 13-24
    • Kennelly, E.J.1    Suttisri, R.2    Kinghorn, A.D.3
  • 49
    • 0142033929 scopus 로고    scopus 로고
    • Use of stevioside and cultivation of Stevia rebaudiana in Korea
    • Kinghorn, A. D. (Ed.). Taylor & Francis, London
    • Kim, J., Choi, Y. H. and Choi, Y.-H., Use of stevioside and cultivation of Stevia rebaudiana in Korea. In Kinghorn, A. D. (Ed.). Stevia: the Genus Stevia. Taylor & Francis, London, pp. 196-202 (2002).
    • (2002) Stevia: The Genus Stevia , pp. 196-202
    • Kim, J.1    Choi, Y.H.2    Choi, Y.-H.3
  • 50
    • 0346773644 scopus 로고
    • Further steroidal and flavonoid constituents of the sweet plant, Polypodium glycyrrhiza
    • Kim, J. and Kinghorn, A. D., Further steroidal and flavonoid constituents of the sweet plant, Polypodium glycyrrhiza. Phytochemistry, 28, 4, 1225-1228 (1989).
    • (1989) Phytochemistry , vol.28 , Issue.4 , pp. 1225-1228
    • Kim, J.1    Kinghorn, A.D.2
  • 51
    • 0024211706 scopus 로고
    • Polypodoside A, an intensely sweet constituent of the rhizomes of Polypodium glycyrrhiza
    • Kim, J., Pezzuto, J. M., Soejarto, D. D., Lang, F. A. and Kinghorn, A. D., Polypodoside A, an intensely sweet constituent of the rhizomes of Polypodium glycyrrhiza. J. Nat. Prod., 51, 1166-1172 (1988).
    • (1988) J. Nat. Prod. , vol.51 , pp. 1166-1172
    • Kim, J.1    Pezzuto, J.M.2    Soejarto, D.D.3    Lang, F.A.4    Kinghorn, A.D.5
  • 52
    • 0036644112 scopus 로고    scopus 로고
    • Synthesis of (-)-hernandulcin and (+)-hernandulcin
    • Kim, J. H., Lim, H. J. and Cheon, S. H., Synthesis of (-)-hernandulcin and (+)-hernandulcin. Tetrahedron Lett., 43, 4721-4722 (2002).
    • (2002) Tetrahedron Lett. , vol.43 , pp. 4721-4722
    • Kim, J.H.1    Lim, H.J.2    Cheon, S.H.3
  • 53
    • 0035988167 scopus 로고    scopus 로고
    • New triterpenoids from the leaves of Abrus precatorius
    • Kim, N.-C., Kim, D. S. H. L. and Kinghorn, A. D., New triterpenoids from the leaves of Abrus precatorius. Nat. Prod. Lett., 16, 261-266 (2002).
    • (2002) Nat. Prod. Lett. , vol.16 , pp. 261-266
    • Kim, N.-C.1    Kim, D.S.H.L.2    Kinghorn, A.D.3
  • 54
    • 0033614880 scopus 로고    scopus 로고
    • Semisynthesis of abrusoside a methyl ester
    • Kim, N.-C., Kinghorn, A. D. and Kim, D. S. H. L., Semisynthesis of abrusoside A methyl ester. Org. Lett., 1, 223-224 (1999).
    • (1999) Org. Lett. , vol.1 , pp. 223-224
    • Kim, N.-C.1    Kinghorn, A.D.2    Kim, D.S.H.L.3
  • 55
    • 0013160940 scopus 로고    scopus 로고
    • Overview
    • Kinghorn, A. D. (Ed.). Taylor & Francis, London
    • Kinghorn, A. D., Overview. In Kinghorn, A. D. (Ed.). Stevia: the Genus Stevia. Taylor & Francis, London, pp. 1-17 (2002).
    • (2002) Stevia: The Genus Stevia , pp. 1-17
    • Kinghorn, A.D.1
  • 57
    • 77957069535 scopus 로고
    • Structure-activity relationships of highly sweet natural products
    • Atta-ur-Rahman (Ed.). Elsevier Science Publishers, Amsterdam
    • Kinghorn, A. D., Fullas, F. and Hussain, R. A., Structure-activity relationships of highly sweet natural products. In Atta-ur-Rahman (Ed.). Studies in Natural Product Chemistry. Elsevier Science Publishers, Amsterdam, pp. 3-41 (1995).
    • (1995) Studies in Natural Product Chemistry , pp. 3-41
    • Kinghorn, A.D.1    Fullas, F.2    Hussain, R.A.3
  • 59
    • 33751154424 scopus 로고
    • Discovery of highly sweet compounds from natural sources
    • Kinghorn, A. D. and Kennelly, E. J., Discovery of highly sweet compounds from natural sources. J. Chem. Educ., 72, 676-680 (1995).
    • (1995) J. Chem. Educ. , vol.72 , pp. 676-680
    • Kinghorn, A.D.1    Kennelly, E.J.2
  • 62
    • 0024592103 scopus 로고
    • Intensely sweet compounds of natural origin
    • Kinghorn, A. D. and Soejarto, D. D., Intensely sweet compounds of natural origin. Med. Res. Rev., 9, 91-115 (1989).
    • (1989) Med. Res. Rev. , vol.9 , pp. 91-115
    • Kinghorn, A.D.1    Soejarto, D.D.2
  • 63
    • 0036664503 scopus 로고    scopus 로고
    • Discovery of terpenoid and phenolic sweeteners from plants
    • Kinghorn, A. D. and Soejarto, D. D., Discovery of terpenoid and phenolic sweeteners from plants. Pure Appl. Chem., 74, 1169-1179 (2002).
    • (2002) Pure Appl. Chem. , vol.74 , pp. 1169-1179
    • Kinghorn, A.D.1    Soejarto, D.D.2
  • 65
    • 0342887230 scopus 로고    scopus 로고
    • Hepatoprotective oleanane glucuronides in Fabaceae
    • Ageta, H., Aimi, N., Ebizuka, Y., Fujita, T. and Honda, G. (Eds.). Elsevier, Amsterdam
    • Kinjo, J. and Nohara, T., Hepatoprotective oleanane glucuronides in Fabaceae. In Ageta, H., Aimi, N., Ebizuka, Y., Fujita, T. and Honda, G. (Eds.). Towards Natural Medicine Research in the 21st Century. Elsevier, Amsterdam, pp. 237-248 (1998).
    • (1998) Towards Natural Medicine Research in the 21st Century , pp. 237-248
    • Kinjo, J.1    Nohara, T.2
  • 66
    • 0036664733 scopus 로고    scopus 로고
    • Licorice root. A natural sweetener and an important ingredient in Chinese medicine
    • Kitagawa, I., Licorice root. A natural sweetener and an important ingredient in Chinese medicine. Pure Appl. Chem., 74, 1189-1198 (2002).
    • (2002) Pure Appl. Chem. , vol.74 , pp. 1189-1198
    • Kitagawa, I.1
  • 67
    • 0024557975 scopus 로고
    • Apioglycyrrhizin and araboglycyrrhizin, two new sweet oleanane-type triterpene oligoglycosides from the root of Glycyrrhiza inflata
    • Kitagawa, I., Sakagami, M., Hashiuchi, F., Zhou, J. L., Yoshikawa, M. and Ren, J., Apioglycyrrhizin and araboglycyrrhizin, two new sweet oleanane-type triterpene oligoglycosides from the root of Glycyrrhiza inflata. Chem. Pharm. Bull., 37, 551-553 (1989).
    • (1989) Chem. Pharm. Bull. , vol.37 , pp. 551-553
    • Kitagawa, I.1    Sakagami, M.2    Hashiuchi, F.3    Zhou, J.L.4    Yoshikawa, M.5    Ren, J.6
  • 70
    • 0032487613 scopus 로고    scopus 로고
    • Chemical synthesis and characterization of the sweet protein mabinlin II
    • Kohmura, M. and Ariyoshi, Y., Chemical synthesis and characterization of the sweet protein mabinlin II. Biopolymers, 46, 215-223 (1998).
    • (1998) Biopolymers , vol.46 , pp. 215-223
    • Kohmura, M.1    Ariyoshi, Y.2
  • 72
  • 73
    • 0036664745 scopus 로고    scopus 로고
    • Cancer-chemopreventive effects of natural sweeteners and related compounds
    • Konoshima, T. and Takasaki, M., Cancer-chemopreventive effects of natural sweeteners and related compounds. Pure Appl. Chem., 74, 1309-1316 (2002).
    • (2002) Pure Appl. Chem. , vol.74 , pp. 1309-1316
    • Konoshima, T.1    Takasaki, M.2
  • 76
    • 0026619450 scopus 로고
    • Characterization of antisweet substance, sweet proteins, and sweetness-inducing proteins
    • Kurihara, Y., Characterization of antisweet substance, sweet proteins, and sweetness-inducing proteins. Crit. Rev. Food Sci. Nutr., 32, 231-252 (1992).
    • (1992) Crit. Rev. Food Sci. Nutr. , vol.32 , pp. 231-252
    • Kurihara, Y.1
  • 77
    • 0025909268 scopus 로고
    • Chemical study on Haematoxylon campechianum: A sweet principle and new dibenz[b,d]oxocin derivatives
    • Masuda, H., Ohtani, K., Mizutani, K., Ogawa, S., Kasai, R. and Tanaka, O., Chemical study on Haematoxylon campechianum: a sweet principle and new dibenz[b,d]oxocin derivatives. Chem. Pharm. Bull., 39, 1382-1384 (1991).
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 1382-1384
    • Masuda, H.1    Ohtani, K.2    Mizutani, K.3    Ogawa, S.4    Kasai, R.5    Tanaka, O.6
  • 78
    • 10544252280 scopus 로고    scopus 로고
    • Regionally targeted mutagenesis by metabolically-activated steviol; DNA sequence analysis of steviol-induced mutants of guanine phosphoribosyltransferase (gpt) gene of Salmonella typhimurium TM677
    • Matsui, M., Sofuni, T. and Nohmi, T., Regionally targeted mutagenesis by metabolically-activated steviol; DNA sequence analysis of steviol-induced mutants of guanine phosphoribosyltransferase (gpt) gene of Salmonella typhimurium TM677. Mutagenesis, 11, 565-572 (1996).
    • (1996) Mutagenesis , vol.11 , pp. 565-572
    • Matsui, M.1    Sofuni, T.2    Nohmi, T.3
  • 79
    • 0025002549 scopus 로고
    • Minor cucurbitane glycosides from fruits of Siraitia grosvenori (Cucurbitaceae)
    • Matsumoto, K., Kasai, R., Ohtani, K. and Tanaka, O., Minor cucurbitane glycosides from fruits of Siraitia grosvenori (Cucurbitaceae). Chem. Pharm. Bull., 38, 2030-2032 (1990).
    • (1990) Chem. Pharm. Bull. , vol.38 , pp. 2030-2032
    • Matsumoto, K.1    Kasai, R.2    Ohtani, K.3    Tanaka, O.4
  • 80
    • 0027959475 scopus 로고
    • Brazzein, a new high-potency thermostable sweet protein from Pentadiplandra brazzeana B
    • Ming, D. and Hellekant, G., Brazzein, a new high-potency thermostable sweet protein from Pentadiplandra brazzeana B. FEBS Lett., 355, 106-108 (1994).
    • (1994) FEBS Lett. , vol.355 , pp. 106-108
    • Ming, D.1    Hellekant, G.2
  • 83
    • 0007693840 scopus 로고
    • Study on improvement of sweeteners of steviol bisglycosides: Selective enzymatic transglucosylation of the 13-O-glycosyl moiety
    • Mizutani, K., Miyata, T., Kasai, R., Tanaka, O., Ogawa, S. and Doi, S., Study on improvement of sweeteners of steviol bisglycosides: selective enzymatic transglucosylation of the 13-O-glycosyl moiety. Agric. Biol. Chem., 53, 395-398 (1989).
    • (1989) Agric. Biol. Chem. , vol.53 , pp. 395-398
    • Mizutani, K.1    Miyata, T.2    Kasai, R.3    Tanaka, O.4    Ogawa, S.5    Doi, S.6
  • 84
    • 0142097538 scopus 로고    scopus 로고
    • Use of Stevia rebaudiana sweeteners in Japan
    • Kinghorn, A. D. (Ed.). Taylor & Francis, London
    • Mizutani, K. and Tanaka, O., Use of Stevia rebaudiana sweeteners in Japan. In Kinghorn, A. D. (Ed.). Stevia: the Genus Stevia. Taylor & Francis, London, pp. 178-195 (2002).
    • (2002) Stevia: The Genus Stevia , pp. 178-195
    • Mizutani, K.1    Tanaka, O.2
  • 86
    • 0000211760 scopus 로고
    • Synthesis of (6S,1′S)-(+)-hernandulcin, a sweetener, and its stereoisomers
    • Mori, K. and Kato, M., Synthesis of (6S,1′S)-(+)-hernandulcin, a sweetener, and its stereoisomers. Tetrahedron, 42, 5895-5900 (1986).
    • (1986) Tetrahedron , vol.42 , pp. 5895-5900
    • Mori, K.1    Kato, M.2
  • 87
    • 0022389110 scopus 로고
    • Tannins and related compounds. XXXV. Proanthocyanidins with a doubly linked unit from the root bark of Cinnamomum sieboldii Meisner
    • Morimoto, S., Nonaka, G.-I. and Nishioka, I., Tannins and related compounds. XXXV. Proanthocyanidins with a doubly linked unit from the root bark of Cinnamomum sieboldii Meisner. Chem. Pharm. Bull., 33, 4338-4345 (1985).
    • (1985) Chem. Pharm. Bull. , vol.33 , pp. 4338-4345
    • Morimoto, S.1    Nonaka, G.-I.2    Nishioka, I.3
  • 88
    • 0034699283 scopus 로고    scopus 로고
    • The total synthesis of monatin
    • Nakamura, K., Baker, T. J. and Goodman, M., The total synthesis of monatin. Org. Lett., 2, 2967-2970 (2000).
    • (2000) Org. Lett. , vol.2 , pp. 2967-2970
    • Nakamura, K.1    Baker, T.J.2    Goodman, M.3
  • 89
    • 0029851198 scopus 로고    scopus 로고
    • Intensely sweet saponin osladin: Synthetic and structural study
    • Waller, G. R. and Yamasaki, K. (Eds.). Plenum Press, New York
    • Nishizawa, M. and Yamada, H., Intensely sweet saponin osladin: synthetic and structural study. In Waller, G. R. and Yamasaki, K. (Eds.). Saponins Used in Food and Agriculture. Plenum Press, New York, pp. 25-36 (1996).
    • (1996) Saponins Used in Food and Agriculture , pp. 25-36
    • Nishizawa, M.1    Yamada, H.2
  • 92
    • 0027096460 scopus 로고
    • Crystal structure of a sweet-tasting protein, thaumatin, at 1.65 Å resolution
    • Ogata, C. M., Gordon, P. F., De Vos, A. M. and Kim, S.-H., Crystal structure of a sweet-tasting protein, thaumatin, at 1.65 Å resolution. J. Mol. Biol., 228, 893-908 (1992).
    • (1992) J. Mol. Biol. , vol.228 , pp. 893-908
    • Ogata, C.M.1    Gordon, P.F.2    De Vos, A.M.3    Kim, S.-H.4
  • 94
    • 11244336958 scopus 로고    scopus 로고
    • Methods to improve the taste of the sweet principles of Stevia rebaudiana
    • Kinghorn, A. D. (Ed.). Taylor & Francis, London
    • Ohtani, K. and Yamasaki, K., Methods to improve the taste of the sweet principles of Stevia rebaudiana. In Kinghorn, A. D. (Ed.). Stevia: the Genus Stevia. Taylor & Francis, London, pp. 138-159 (2002).
    • (2002) Stevia: The Genus Stevia , pp. 138-159
    • Ohtani, K.1    Yamasaki, K.2
  • 95
    • 0026826173 scopus 로고
    • Structural revision of bryonoside and structure elucidation of minor saponins from Bryonia dioica
    • Oobayashi, K., Yoshikawa, K. and Arihara, S., Structural revision of bryonoside and structure elucidation of minor saponins from Bryonia dioica. Phytochemistry, 31, 943-946 (1992).
    • (1992) Phytochemistry , vol.31 , pp. 943-946
    • Oobayashi, K.1    Yoshikawa, K.2    Arihara, S.3
  • 98
    • 11244344837 scopus 로고    scopus 로고
    • Replacement. A steady diet of growth of sweeteners and fat substitutes
    • Seewald, N., Replacement. A steady diet of growth of sweeteners and fat substitutes. Chem. Week, June 7, 41 (2000).
    • (2000) Chem. Week , vol.JUNE 7 , pp. 41
    • Seewald, N.1
  • 99
    • 11244355191 scopus 로고
    • Current status of Stevia sweeteners and its application
    • Shibasato, M., Current status of Stevia sweeteners and its application. Japan Food Sci., 51-58 (1995).
    • (1995) Japan Food Sci. , pp. 51-58
    • Shibasato, M.1
  • 100
    • 0000045354 scopus 로고
    • Studies on the sweet principles from the leaves of Cyclocarya paliurus (Batal.) Iljinsk
    • Shu, R. G., Xu, C. R. and Li, L. N., Studies on the sweet principles from the leaves of Cyclocarya paliurus (Batal.) Iljinsk. Acta Pharmaceutica Sinica, 30, 757-761 (1995).
    • (1995) Acta Pharmaceutica Sinica , vol.30 , pp. 757-761
    • Shu, R.G.1    Xu, C.R.2    Li, L.N.3
  • 102
    • 0037176729 scopus 로고    scopus 로고
    • Rebaudioside F, a diterpene glycoside from Stevia rebaudiana
    • Starratt, A. N., Kirby, C. W., Pocs, R. and Brandle, J. E., Rebaudioside F, a diterpene glycoside from Stevia rebaudiana. Phytochemistry, 59, 367-370 (2002).
    • (2002) Phytochemistry , vol.59 , pp. 367-370
    • Starratt, A.N.1    Kirby, C.W.2    Pocs, R.3    Brandle, J.E.4
  • 103
    • 0033777091 scopus 로고    scopus 로고
    • Analgesic and anti-inflammatory activity of the proanthocyanidin shelligueain a from Polypodium feei METT
    • Subarnas, A. and Wagner, H., Analgesic and anti-inflammatory activity of the proanthocyanidin shelligueain A from Polypodium feei METT. Phytomedicine, 7, 401-405 (2000).
    • (2000) Phytomedicine , vol.7 , pp. 401-405
    • Subarnas, A.1    Wagner, H.2
  • 104
  • 105
    • 0029000986 scopus 로고
    • Plant-derived triterpenoid sweetness inhibitors
    • Suttisri, R., Lee, I.-S. and Kinghorn, A. D., Plant-derived triterpenoid sweetness inhibitors. J. Ethnopharmacol., 47, 9-26 (1995).
    • (1995) J. Ethnopharmacol. , vol.47 , pp. 9-26
    • Suttisri, R.1    Lee, I.-S.2    Kinghorn, A.D.3
  • 106
    • 0020852449 scopus 로고
    • Studies on the constituents of Fructus Momordicae. I. On the sweet principle
    • Takemoto, T., Arihara, S., Nakajima, T. and Okuhira, M., Studies on the constituents of Fructus Momordicae. I. On the sweet principle. Yakugaku Zasshi, 103, 1151-1154 (1983a).
    • (1983) Yakugaku Zasshi , vol.103 , pp. 1151-1154
    • Takemoto, T.1    Arihara, S.2    Nakajima, T.3    Okuhira, M.4
  • 107
    • 0008131632 scopus 로고
    • Studies on the constituents of Gynostemma pentaphyllum Makino. II. Structures of gypenoside XV-XXI
    • Takemoto, T., Arihara, S., Nakajima, T. and Okuhira, M., Studies on the constituents of Gynostemma pentaphyllum Makino. II. Structures of gypenoside XV-XXI. Yakugaku Zasshi, 103, 1015-1023 (1983b).
    • (1983) Yakugaku Zasshi , vol.103 , pp. 1015-1023
    • Takemoto, T.1    Arihara, S.2    Nakajima, T.3    Okuhira, M.4
  • 108
    • 0026022517 scopus 로고
    • Chemical and chemotaxonomical studies of ferns. LXXX. Proanthocyanidins of Arachniodes sporadosora Nakaike and A. exilis Ching
    • Tanaka, N., Orii, R., Ogasa, K., Wada, H., Murakami, T., Sakai, Y. and Chen, C. M., Chemical and chemotaxonomical studies of ferns. LXXX. Proanthocyanidins of Arachniodes sporadosora Nakaike and A. exilis Ching. Chem. Pharm. Bull., 39, 55-59 (1991).
    • (1991) Chem. Pharm. Bull. , vol.39 , pp. 55-59
    • Tanaka, N.1    Orii, R.2    Ogasa, K.3    Wada, H.4    Murakami, T.5    Sakai, Y.6    Chen, C.M.7
  • 109
    • 0001081954 scopus 로고    scopus 로고
    • Improvement of taste of natural sweeteners
    • Tanaka, O., Improvement of taste of natural sweeteners. Pure Appl. Chem., 69, 675-683 (1997).
    • (1997) Pure Appl. Chem. , vol.69 , pp. 675-683
    • Tanaka, O.1
  • 110
    • 0036634168 scopus 로고    scopus 로고
    • Mutagenicity of steviol and its oxidative derivatives in Salmonella typhimurium TM677
    • Terai, T., Ren, H., Mori, G., Yamaguchi, Y. and Hayashi, T., Mutagenicity of steviol and its oxidative derivatives in Salmonella typhimurium TM677. Chem. Pharm. Bull., 50, 1007-1010 (2002).
    • (2002) Chem. Pharm. Bull. , vol.50 , pp. 1007-1010
    • Terai, T.1    Ren, H.2    Mori, G.3    Yamaguchi, Y.4    Hayashi, T.5
  • 112
    • 0029854143 scopus 로고    scopus 로고
    • 3-Acetoxy-5,7-dihydroxy-4′-methoxyflavanone, a new cytotoxic dihydroflavanol from Aframomum hanburyi K. Schum
    • Tsopmo, A., Tchuendem, M. H., Ayafor, J. F., Tillequin, F., Koch, M. and Anke, H., 3-Acetoxy-5,7-dihydroxy-4′-methoxyflavanone, a new cytotoxic dihydroflavanol from Aframomum hanburyi K. Schum. Nat. Prod. Lett., 9, 33-37 (1996).
    • (1996) Nat. Prod. Lett. , vol.9 , pp. 33-37
    • Tsopmo, A.1    Tchuendem, M.H.2    Ayafor, J.F.3    Tillequin, F.4    Koch, M.5    Anke, H.6
  • 113
    • 0003144348 scopus 로고
    • Isolation and characterization of the sweet principles from Dioscoreophyllum cumminsii
    • Van der Wel, H., Isolation and characterization of the sweet principles from Dioscoreophyllum cumminsii. FEBS Lett., 21, 88-90 (1972).
    • (1972) FEBS Lett. , vol.21 , pp. 88-90
    • Van Der Wel, H.1
  • 114
    • 0000804899 scopus 로고
    • Isolation and characterization of pentadin, the sweet principle of Pentadiplandra brazzeana
    • Van der Wel, H., Larson, G., Hladik, A., Hladik, C. M., Hellekant, G. and Glaser, D., Isolation and characterization of pentadin, the sweet principle of Pentadiplandra brazzeana. Chem. Senses, 14, 75-79 (1989).
    • (1989) Chem. Senses , vol.14 , pp. 75-79
    • Van Der Wel, H.1    Larson, G.2    Hladik, A.3    Hladik, C.M.4    Hellekant, G.5    Glaser, D.6
  • 115
    • 0015494327 scopus 로고
    • Isolation and characterization of thaumatin I and II, the sweet-tasting proteins from Thaumatococcus daniellii
    • Van der Wel, H. and Loeve, K., Isolation and characterization of thaumatin I and II, the sweet-tasting proteins from Thaumatococcus daniellii. Eur. J. Biochem., 31, 221-225 (1972).
    • (1972) Eur. J. Biochem. , vol.31 , pp. 221-225
    • Van Der Wel, H.1    Loeve, K.2
  • 116
  • 117
    • 0031439362 scopus 로고    scopus 로고
    • The flavonoid constituents of two Polypodium species (Calaguala) and their effect on the elastase release in human neutrophils
    • Vasaenge, M., Liu, B., Welch, C. J., Rolfsen, W. and Bohlin, L., The flavonoid constituents of two Polypodium species (Calaguala) and their effect on the elastase release in human neutrophils. Planta Med., 63, 511-517 (1997).
    • (1997) Planta Med. , vol.63 , pp. 511-517
    • Vasaenge, M.1    Liu, B.2    Welch, C.J.3    Rolfsen, W.4    Bohlin, L.5
  • 118
    • 37049073047 scopus 로고
    • Structure elucidation of monatin, a high-intensity sweetener isolated from the plant Schlerochiton ilicifolius
    • Vleggaar, R., Ackerman, L. G. J. and Steyn, P. S., Structure elucidation of monatin, a high-intensity sweetener isolated from the plant Schlerochiton ilicifolius. J. Chem. Soc., Perkin Trans. 1, 3095-3098 (1992).
    • (1992) J. Chem. Soc., Perkin Trans. 1 , pp. 3095-3098
    • Vleggaar, R.1    Ackerman, L.G.J.2    Steyn, P.S.3
  • 120
    • 0034704802 scopus 로고    scopus 로고
    • The active conformations conformations of neotame and other high-potency sweeteners
    • Walters, D. E., Prakash, I. and Desai, N., The active conformations conformations of neotame and other high-potency sweeteners. J. Med. Chem., 43, 1242-1245 (2000).
    • (2000) J. Med. Chem. , vol.43 , pp. 1242-1245
    • Walters, D.E.1    Prakash, I.2    Desai, N.3
  • 121
    • 0026506726 scopus 로고
    • Syntheses of sweet tasting diterpene glycosides, baiyunoside and analogs
    • Yamada, H. and Nishizawa, M., Syntheses of sweet tasting diterpene glycosides, baiyunoside and analogs. Tetrahedron, 48, 3021-3044 (1992).
    • (1992) Tetrahedron , vol.48 , pp. 3021-3044
    • Yamada, H.1    Nishizawa, M.2
  • 122
    • 0025126845 scopus 로고
    • Purification and complete amino acid sequence of a new type of sweet protein with taste-modifying activity, curculin
    • Yamashita, H., Theerasilp, S., Aiuchi, T., Nakaya, K., Nakamura, Y. and Kurihara, Y., Purification and complete amino acid sequence of a new type of sweet protein with taste-modifying activity, curculin. J. Biol. Chem., 265, 15770-15775 (1990).
    • (1990) J. Biol. Chem. , vol.265 , pp. 15770-15775
    • Yamashita, H.1    Theerasilp, S.2    Aiuchi, T.3    Nakaya, K.4    Nakamura, Y.5    Kurihara, Y.6
  • 123
    • 0027026362 scopus 로고
    • Studies on the sweet principles from the leaves of Cyclocarya paliurus (Batal.) Iljinskaya
    • Yang, D. J., Zhong, Z. C. and Xie, Z. M., Studies on the sweet principles from the leaves of Cyclocarya paliurus (Batal.) Iljinskaya. Yao Hsueh Hsueh Pao, 27, 841-844 (1992).
    • (1992) Yao Hsueh Hsueh Pao , vol.27 , pp. 841-844
    • Yang, D.J.1    Zhong, Z.C.2    Xie, Z.M.3
  • 125
    • 0032838119 scopus 로고    scopus 로고
    • Development of bioactive functions in Hydrangea dulcis folium. VII. Absolute stereostructures of 3S-phyllodulcin, 3R- and 3S-phyllodulcin glycosides, and 3R and 3S-thunberginol H glycosides from the leaves of Hydrangea macrophylla Seringe var. thunbergii Makino
    • Yoshikawa, M., Murakami, T., Ueda, T., Shimoda, H., Yamahara, J. and Matsuda, H., Development of bioactive functions in Hydrangea dulcis folium. VII. Absolute stereostructures of 3S-phyllodulcin, 3R- and 3S-phyllodulcin glycosides, and 3R and 3S-thunberginol H glycosides from the leaves of Hydrangea macrophylla Seringe var. thunbergii Makino. Heterocycles, 50, 411-418 (1999).
    • (1999) Heterocycles , vol.50 , pp. 411-418
    • Yoshikawa, M.1    Murakami, T.2    Ueda, T.3    Shimoda, H.4    Yamahara, J.5    Matsuda, H.6


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