Yoshikawa M, Uchida E, Chatani N, et al. Thunberginols A, B, and F, new antiallergic and antimicrobial principles from Hydrangeae Dulcis Folium[J]. Chem Pharm Bull, 1992, 40(11): 3121.
[2]
Inouye H, Takeda Y, Uesato S, et al. A novel type secoiridoid glucoside, hydrangenoside A from Hydrangea macrophylla[J]. Tetrahedron Lett, 1980, 21(11): 1059.
[3]
Uesato S, Toshihiro H, Yoshio T, et al. Novel type secoiridoid glucosides, hydrangenosides B, C and D from Hydrangea macrophylla[J]. Chem Pharm Bull, 1981, 29(11): 3421.
[4]
Uesato S, Takeda Y, Hashimoto T, et al. Studies on monoterpene glucosides and related natural products-absolute structures of hydrangenosides A, B, C, D, E, F, and G. Novel type secoiridoid glucosides from two Hydrangea plants[J]. Helv Chim Acta, 1984, 67(8): 2111.
[5]
Yoshikawa M, Ueda T, Matsuda H, et al. Absolute stereostructures of hydramacrosides A and B, new bioactive secoiridoid glucoside complexes from the leaves of Hydrangea macrophylla Seringe var. thunbergii Makino[J]. Chem Pharm Bull, 1994, 42(8), 691.
[6]
Matsuda H, Shimoda H, Uemura T, et al. Chemical constituents from the leaves of Hydrangea macrophylla var. thunbergii(III): absolute stereostructures of hydramacrosides A and B, secoiridoid glucoside complexes with inhibitory activity on histamine release[J]. Chem Pharm Bull, 1999, 47(12): 1753.
[7]
Kikuchi M, Kakuda R and Yaotita T. Macrophyllanosides A-D, secoiridoid glycosides from Hydrangea macrophylla subsp. serrata[J]. Heterocycles, 2008, 76(1): 313.
Johji Y, Hisashi M, Hiroshi S, et al. Development of bioactive functions in Hydrangeae Dulcis Folium. Ⅱ. Antiulcer, antiallergy, and cholagoic effects of the extract from Hydrangeae Dulcis Folium[J]. Yakugaku Zasshi, 1994, 114(6): 401.
[10]
Matsuda H, Shimoda H, Yamahara J, et al. Effects of phylloducin, hydrangenol, and their 8-O-glucosides, and thunberginols A and F from Hydrangea macrophylla Seringe var. thunbergii Makino on passive cutaneous anaphylaxis reaction in rats[J]. Biol Pharm Bull, 1999, 22(8): 870.
[11]
Kim H, Kim M, Lyu E, et al. Improvement of diabetic complication by Hydrangeae Dulcis Folium in streptozotocin-induced diabetic rats[J]. Biol Pharm Bull, 2009, 32(1): 153.
[12]
Zhang H, Hisashi M, Akria K, et al. New type of antidiabetic compounds from the processed leaves of Hydrangea macrophylla var. thunbergii(Hydrangeae Dulcis Folium)[J]. Bioorg Med Chem Lett, 2007, 17(17): 4972.
[13]
Elix J, Whitton A, Jones A. Triterpenes from the lichen genus Physcia[J]. Aust J Chem, 1982, 35(3): 641.
[14]
Mochammad S, Kazuo Y, Ryoji K, et al. 13C nuclear magnetic resonance of lupane-type triterpenes, lupeol, betulin and berulinic acid[J]. Chem Pharm Bull, 1980, 28(3): 1006.
[15]
Hu X, Dou D, Pei Y, et al. Chemical constituents of roots of Ranunculus ternatus Thunb.[J]. J Chin Pharm Sci, 2006, 15(2): 127.
[16]
Baderschneider B, Messerer M, Winterhalter P. Isolation of 2-ethli-3-methylmaleimide-N-β-D-glucopyranoside from Riesling wine[J]. Vitis, 1997, 36(3): 159.
[17]
Ciuffreda P, Casati S, Manzocchi A. Complete 1H and 13C-NMR spectral assignment of α- and β-adenosine, 2\'-deoxyadenosine and their acetate derivatives[J]. Magn Reson Chem, 2007, 45(9): 781.
[18]
江苏新医学院. 中药大辞典[M]. 上海科学技术出版社, 1985: 21.
[19]
Hashimoto T, Tori M, Asakawa Y. Three dihydroisocoumarin glucosides from Hydrangea macrophylla subsp. serrata[J]. Phytochemistry, 1987, 26(12): 3323.
[20]
Yoshikawa M, Uchida E, Chatani N, et al. Thunberginols C, D, and E, new antiallergic and antimicrobial dihydroisocoumarins, and thunberginol G 3\'-O-glucoside and(-)-hydrangenol 4\'-O-glucoside, new dihydroisocoumarin glycosides, from Hydrangeae Dulcis Folium[J]. Chem Pharm Bull, 1992, 40(12): 3352.
[21]
Yoshikawa M, Matsuda H, Shimoda H, et al. Development of bioactive functions in hydrangeae dulcis folium. V. On the antiallergic and antimicrobial principles of hydrangeae dulcis folium.(2). Thunberginols C, D, and E, thunberginol G 3\'-O-glucoside,(-)-hydrangenol 4\'-O-glucoside, and(+)-hydrangenol 4\'-O-glucoside[J]. Chem Pharm Bull, 1996, 44(8): 1440.
[22]
Yoshikawa M, Ueda T, Shimoda H, et al. Dihydroisocoumarin constituents from the leaves of Hydrangea macrophylla var. thunbergii(2). Absolute stereostructures of hydrangenol, thunberginol I, and phyllodulcin glycosides and isomerization reaction at the 3-positions of phyllodulcin and its glycosides[J]. Chem Pharm Bull, 1999, 47(3), 383.
[23]
Kikuchi M, Kakuda R, Kikuchi M, et al. Constituents of the genus Hydrangea plants. III. Three new glycosides from the leaves of Hydrangea macrophylla subsp. serrata(THUNB.) MAKINO[J]. Chem Pharm Bull, 2008, 56(4), 610.
[24]
Yoshikawa M, Murakami T, Ueda T, et al. 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[J]. Heterocycles, 1999, 50(1): 411.
[25]
Yoshikawa M, Harada E, Naitoh Y, et al. Development of bioactive functions in Hydrangeae Dulcis Folium. III. On the antiallergic and antimicrobial principles of Hydrangeae Dulcis Folium.(1). Thunberginols A, B, and F[J]. Chem Pharm Bull, 1994, 42(11): 2225.
[26]
Jones A, Grant D, Winkley M, et al. Carbon-13 magnetic resonance. ⅩⅦ. Pyrimidine and purine nucleosides[J]. J Am Chem Soc, 1970, 92(13): 4079.
[27]
Roger D, Eddy F, Eddy E, et al. 13C-NMR shift increments for 3-substituted pyridines[J]. Heterocycles, 1981, 16(11): 1893.
[28]
Yang Y, Tan N, Zhang F, et al. Cyclopeptides and amides from Pseudostellaria heterophylla[J]. Helv Chim Acta, 2003, 86(10): 3376.
