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Volumn 67, Issue 4, 2013, Pages 799-806

Structures of acylated sucroses and an acylated flavonol glycoside and inhibitory effects of constituents on aldose reductase from the flower buds of Prunus mume

Author keywords

Acylated sucrose; Aldose reductase; Medicinal flower; Mumeflavonoside; Mumeose; Prunus mume

Indexed keywords

ALDEHYDE REDUCTASE; FLAVONOID GLYCOSIDE; MUMEOSE A; MUMEOSE K; MUMEOSE L; MUMEOSE M; MUMEOSE N; MUMEOSE O; SUCROSE; UNCLASSIFIED DRUG;

EID: 84884211147     PISSN: 13403443     EISSN: 18610293     Source Type: Journal    
DOI: 10.1007/s11418-013-0750-7     Document Type: Article
Times cited : (31)

References (21)
  • 1
    • 84876482882 scopus 로고    scopus 로고
    • Medicinal flowers. XXXVIII. Structures of acylated sucroses and inhibitory effects of constituents on aldose reducatase from the flower buds of Prunus mume
    • in press
    • Fujimoto K, Nakamura S, Matsumoto T, Ohta T, Ogawa K, Tamura H, Matsuda H, Yoshikawa M (2013) Medicinal flowers. XXXVIII. Structures of acylated sucroses and inhibitory effects of constituents on aldose reducatase from the flower buds of Prunus mume. Chem Pharm Bull (in press)
    • (2013) Chem Pharm Bull
    • Fujimoto, K.1    Nakamura, S.2    Matsumoto, T.3    Ohta, T.4    Ogawa, K.5    Tamura, H.6    Matsuda, H.7    Yoshikawa, M.8
  • 2
    • 84884909502 scopus 로고    scopus 로고
    • Acylated sucroses and acylated quinic acids analogs from the flower buds of Prunus mume and their inhibitory effects on melanogenesis
    • submitted
    • Nakamura S, Fujimoto K, Matsumoto T, Nakashima S, Ohta T, Ogawa K, Matsuda H, Yoshikawa M (2013) Acylated sucroses and acylated quinic acids analogs from the flower buds of Prunus mume and their inhibitory effects on melanogenesis. Phytochemistry (submitted)
    • (2013) Phytochemistry
    • Nakamura, S.1    Fujimoto, K.2    Matsumoto, T.3    Nakashima, S.4    Ohta, T.5    Ogawa, K.6    Matsuda, H.7    Yoshikawa, M.8
  • 4
    • 84862338901 scopus 로고    scopus 로고
    • Medicinal Flowers. XXXVI. Acylated oleanane-type triterpene saponins with inhibitory effects on melanogenesis from the flower buds of Chinese Camellia japonica
    • 22689427 10.1248/cpb.60.752 1:CAS:528:DC%2BC38Xht1egurzL
    • Nakamura S, Fujimoto K, Nakashima S, Matsumoto T, Miura T, Uno K, Matsuda H, Yoshikawa M (2012) Medicinal Flowers. XXXVI. Acylated oleanane-type triterpene saponins with inhibitory effects on melanogenesis from the flower buds of Chinese Camellia japonica. Chem Pharm Bull 60:752-758
    • (2012) Chem Pharm Bull , vol.60 , pp. 752-758
    • Nakamura, S.1    Fujimoto, K.2    Nakashima, S.3    Matsumoto, T.4    Miura, T.5    Uno, K.6    Matsuda, H.7    Yoshikawa, M.8
  • 5
    • 84865961092 scopus 로고    scopus 로고
    • Medicinal flowers. XXXV. Nor-oleanane-type and acylated oleanane-type triterpene saponins from the flower buds of Chinese Camellia japonica and their inhibitory effects on melanogenesis
    • 22976329 10.1248/cpb.c12-00473 1:CAS:528:DC%2BC38XhslSmsb7I
    • Fujimoto K, Nakamura S, Nakashima S, Matsumoto T, Uno K, Ohta T, Miura T, Matsuda H, Yoshikawa M (2012) Medicinal flowers. XXXV. Nor-oleanane-type and acylated oleanane-type triterpene saponins from the flower buds of Chinese Camellia japonica and their inhibitory effects on melanogenesis. Chem Pharm Bull 60:1188-1194
    • (2012) Chem Pharm Bull , vol.60 , pp. 1188-1194
    • Fujimoto, K.1    Nakamura, S.2    Nakashima, S.3    Matsumoto, T.4    Uno, K.5    Ohta, T.6    Miura, T.7    Matsuda, H.8    Yoshikawa, M.9
  • 6
    • 84865504762 scopus 로고    scopus 로고
    • Melanogenesis inhibitory and fibroblast proliferation accelerating effects of noroleanane- and oleanane-type triterpene oligoglycosides from the flower buds of Camellia japonica
    • 22834923 10.1021/np3001078 1:CAS:528:DC%2BC38XhtFSju77E
    • Nakamura S, Moriura T, Park S, Fujimoto K, Matsumoto T, Ohta T, Matsuda H, Yoshikawa M (2012) Melanogenesis inhibitory and fibroblast proliferation accelerating effects of noroleanane- and oleanane-type triterpene oligoglycosides from the flower buds of Camellia japonica. J Nat Prod 75:1425-1430
    • (2012) J Nat Prod , vol.75 , pp. 1425-1430
    • Nakamura, S.1    Moriura, T.2    Park, S.3    Fujimoto, K.4    Matsumoto, T.5    Ohta, T.6    Matsuda, H.7    Yoshikawa, M.8
  • 7
    • 84860776495 scopus 로고    scopus 로고
    • Medicinal flowers. XXXIII. Anti-hyperlipidemic and Anti-hyperglycemic effects of chakasaponins I-III and structure of chakasaponin IV from flower buds of Chinese tea plant (Camellia sinensis)
    • 22689407 1:CAS:528:DC%2BC38XhtVWht7rM
    • Matsuda H, Hamao M, Nakamura S, Kon'i H, Murata M, Yoshikawa M (2012) Medicinal flowers. XXXIII. Anti-hyperlipidemic and Anti-hyperglycemic effects of chakasaponins I-III and structure of chakasaponin IV from flower buds of Chinese tea plant (Camellia sinensis). Chem Pharm Bull 60:674-680
    • (2012) Chem Pharm Bull , vol.60 , pp. 674-680
    • Matsuda, H.1    Hamao, M.2    Nakamura, S.3    Kon'I, H.4    Murata, M.5    Yoshikawa, M.6
  • 8
    • 0242317711 scopus 로고    scopus 로고
    • Medicinal flowers. VIII. Radical scavenging constituents from the flowers of Prunus mume: Structure of prunose III
    • 12673002 10.1248/cpb.51.440 1:CAS:528:DC%2BD3sXltVejt70%3D
    • Matsuda H, Morikawa T, Ishiwada T, Managi H, Kagawa M, Higashi Y, Yoshikawa M (2003) Medicinal flowers. VIII. Radical scavenging constituents from the flowers of Prunus mume: structure of prunose III. Chem Pharm Bull 51:440-443
    • (2003) Chem Pharm Bull , vol.51 , pp. 440-443
    • Matsuda, H.1    Morikawa, T.2    Ishiwada, T.3    Managi, H.4    Kagawa, M.5    Higashi, Y.6    Yoshikawa, M.7
  • 9
    • 0036691566 scopus 로고    scopus 로고
    • New flavonol oligoglycosides and polyacylated sucroses with inhibitory effects on aldose reductase and platelet aggregation from the flowers of Prunus mume
    • 12193020 10.1021/np020058m 1:CAS:528:DC%2BD38Xlt1Cjurs%3D
    • Yoshikawa M, Murakami T, Ishikawa T, Morikawa T, Kagawa M, Higashi Y, Matsuda H (2002) New flavonol oligoglycosides and polyacylated sucroses with inhibitory effects on aldose reductase and platelet aggregation from the flowers of Prunus mume. J Nat Prod 65:1151-1155
    • (2002) J Nat Prod , vol.65 , pp. 1151-1155
    • Yoshikawa, M.1    Murakami, T.2    Ishikawa, T.3    Morikawa, T.4    Kagawa, M.5    Higashi, Y.6    Matsuda, H.7
  • 10
    • 60849094445 scopus 로고    scopus 로고
    • Five new glycosides from Hypericum erectum Thunb
    • 19184276 10.1007/s11418-009-0313-0 1:CAS:528:DC%2BD1MXit1eqtb4%3D
    • Machida K, Matsuoka E, Kikuchi M (2009) Five new glycosides from Hypericum erectum Thunb. J Nat Med 63:223-226
    • (2009) J Nat Med , vol.63 , pp. 223-226
    • Machida, K.1    Matsuoka, E.2    Kikuchi, M.3
  • 11
    • 46749127109 scopus 로고    scopus 로고
    • Two new flavonol glycosides from Sarcopyramis bodinieri var. Delicate
    • 18596665 10.3390/molecules13061399 1:CAS:528:DC%2BD1cXotlOlurs%3D
    • Wang XM, Wan CP, Zhou SR, Qiu Y (2008) Two new flavonol glycosides from Sarcopyramis bodinieri var. delicate. Molecules 13:1399-1405
    • (2008) Molecules , vol.13 , pp. 1399-1405
    • Wang, X.M.1    Wan, C.P.2    Zhou, S.R.3    Qiu, Y.4
  • 12
    • 0345320139 scopus 로고    scopus 로고
    • Flavonol glycosides from Eschscholtzia californica
    • 9933948 10.1016/S0031-9422(98)00503-2 1:CAS:528:DyaK1MXns1yqsA%3D%3D
    • Beck MA, Häberlein H (1999) Flavonol glycosides from Eschscholtzia californica. Phytochemistry 50:329-332
    • (1999) Phytochemistry , vol.50 , pp. 329-332
    • Beck, M.A.1    Häberlein, H.2
  • 13
    • 67349085090 scopus 로고    scopus 로고
    • Isolation of specific cranberry flavonoids for biological activity assessment
    • 20161027 10.1016/j.foodchem.2009.03.062 1:CAS:528:DC%2BD1MXmsFKhu78%3D
    • Singh AP, Wilson T, Kalk AJ, Cheong J, Vorsa N (2009) Isolation of specific cranberry flavonoids for biological activity assessment. Food Chem 116:963-968
    • (2009) Food Chem , vol.116 , pp. 963-968
    • Singh, A.P.1    Wilson, T.2    Kalk, A.J.3    Cheong, J.4    Vorsa, N.5
  • 14
    • 11144303566 scopus 로고    scopus 로고
    • Chemical constituents from the leaves of Mahonia japonica
    • 1:CAS:528:DC%2BD2MXpsFansw%3D%3D
    • Hsich TJ, Wu YC, Lo WL, Chen SC, Kuo SH, Chen CY (2004) Chemical constituents from the leaves of Mahonia japonica. Chin Pharm J 56:17-24
    • (2004) Chin Pharm J , vol.56 , pp. 17-24
    • Hsich, T.J.1    Wu, Y.C.2    Lo, W.L.3    Chen, S.C.4    Kuo, S.H.5    Chen, C.Y.6
  • 15
    • 34250005675 scopus 로고    scopus 로고
    • Facile discrimination of aldose enantiomers by reversed-phase HPLC
    • 17541189 10.1248/cpb.55.899 1:CAS:528:DC%2BD2sXotFaku74%3D
    • Tanaka T, Nakashima T, Ueda T, Tomii K, Kouno I (2007) Facile discrimination of aldose enantiomers by reversed-phase HPLC. Chem Pharm Bull 55:899-901
    • (2007) Chem Pharm Bull , vol.55 , pp. 899-901
    • Tanaka, T.1    Nakashima, T.2    Ueda, T.3    Tomii, K.4    Kouno, I.5
  • 18
    • 27744479680 scopus 로고    scopus 로고
    • Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of saussureosides A and B from Saussurea medusa
    • 16272724 10.1248/cpb.53.1416 1:CAS:528:DC%2BD2MXhtlWru7jE
    • Xie H, Wang T, Matsuda H, Morikawa T, Yoshikawa M, Tani T (2005) Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of saussureosides A and B from Saussurea medusa. Chem Pharm Bull 53:1416-1422
    • (2005) Chem Pharm Bull , vol.53 , pp. 1416-1422
    • Xie, H.1    Wang, T.2    Matsuda, H.3    Morikawa, T.4    Yoshikawa, M.5    Tani, T.6
  • 19
    • 0141677814 scopus 로고    scopus 로고
    • Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis
    • 14510595 10.1021/np0301543 1:CAS:528:DC%2BD3sXmsl2nsrc%3D
    • Morikawa T, Kishi A, Pongpiriyadacha Y, Matsuda H, Yoshikawa M (2003) Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis. J Nat Prod 66:1191-1196
    • (2003) J Nat Prod , vol.66 , pp. 1191-1196
    • Morikawa, T.1    Kishi, A.2    Pongpiriyadacha, Y.3    Matsuda, H.4    Yoshikawa, M.5
  • 20
    • 0036635201 scopus 로고    scopus 로고
    • Medicinal flowers. VI. Absolute stereostructures of two new flavanone glycosides and a phenylbutanoid glycoside from the flowers of Chrysanthemum indicum L.: Their inhibitory activities for rat lens aldose reductase
    • 12130858 10.1248/cpb.50.972 1:CAS:528:DC%2BD38XlvVChtL0%3D
    • Matsuda H, Morikawa T, Toguchida I, Harima S, Yoshikawa M (2002) Medicinal flowers. VI. Absolute stereostructures of two new flavanone glycosides and a phenylbutanoid glycoside from the flowers of Chrysanthemum indicum L.: their inhibitory activities for rat lens aldose reductase. Chem Pharm Bull 50:972-975
    • (2002) Chem Pharm Bull , vol.50 , pp. 972-975
    • Matsuda, H.1    Morikawa, T.2    Toguchida, I.3    Harima, S.4    Yoshikawa, M.5
  • 21
    • 0036594601 scopus 로고    scopus 로고
    • Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity
    • 12045333 10.1248/cpb.50.788 1:CAS:528:DC%2BD38XkvFOlt7s%3D
    • Matsuda H, Morikawa T, Toguchida I, Yoshikawa M (2002) Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity. Chem Pharm Bull 50:788-795
    • (2002) Chem Pharm Bull , vol.50 , pp. 788-795
    • Matsuda, H.1    Morikawa, T.2    Toguchida, I.3    Yoshikawa, M.4


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