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1 . hydrangenol ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1996 44 1440-1447 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 (+)-Hydran Masayuki YOSHIKAWA,Hisashi MATSUDA,Hiroshi SHIMODA,Hiromi SHIMADA,Emiko HARADA,Yoshikazu NAITOH,Akiko MIKI,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . hydrangenol ÏàËÆ¶È:100% Phytochemistry 1987 26 3323-3330 Three dihydroisocoumarin glucosides from Hydrangea macrophylla subsp. serrata Toshihiro Hashimoto,Motoo Tori,Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Scorzoveratrin C15H12O4 ÏàËÆ¶È:100% Natural Product Research 2010 24 56-62 Two new 3-benzylphthalides from Scorzonera veratrifolia Fenzl Aynur Sarı Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (-)-hydrangenol 4'-O-glucoside C21H22O9 ÏàËÆ¶È:93.3% Chemical & Pharmaceutical Bulletin 1992 40 3352-3354 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 Masayuki TOSHIKAWA,Emiko UCHIDA,Nobuyasu CHATANI,Hiromi KOBAYASHI,Yoshikazu NAITOH,Yasuhiro OKUNO,Hisashi MATSUDA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-3,4-dihydro-3-(4-methoxyphenyl)-isocoumarin-8-ol ÏàËÆ¶È:87.5% Phytochemistry 1997 44 89-99 Plagiochilines and other sesquiterpenoids from Plagiochila (Hepaticae) Susanne Valcic, Josef Zapp, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . hydrangenol ÏàËÆ¶È:86.6% Natural Product Research 2006 20 860-865 A new dihydroisocoumarin from the rhizomes of Notopterygium forbesii Yan-Hui Li; Fan Luo; Shu-Lin Peng; Jian Liang; Li-Sheng Ding Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . typharin C17H14O3 ÏàËÆ¶È:80% Phytochemistry 2002 61 955-957 Typhaphthalide and typharin, two phenolic compounds from Typha capensis Francis O. Shode, Abdul S. Mahomed, Colin B. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . hydrangenol C15H12O4 ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 1994 19 293-295 Studies on Chemcial Constituents of Hydrangea macrophylla (Thunb.) Ser Yang Dajian, Zhongchang and Liu Hongya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . thunberginol C C15H12O5 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 1996 44 1440-1447 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 6'-O-Glucoside, and (+)-Hydran Masayuki YOSHIKAWA,Hisashi MATSUDA,Hiroshi SHIMODA,Hiromi SHIMADA,Emiko HARADA,Yoshikazu NAITOH,Akiko MIKI,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . thunberginol C C15H12O5 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 1992 40 3352-3354 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 Masayuki TOSHIKAWA,Emiko UCHIDA,Nobuyasu CHATANI,Hiromi KOBAYASHI,Yoshikazu NAITOH,Yasuhiro OKUNO,Hisashi MATSUDA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . yangonin ÏàËÆ¶È:73.3% Phytochemistry 1997 45 701-703 Antifungal stress compounds from Vicia cracca Mustafa M. Saleh, Karl-Werner Glombitza Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 10 C16H14O4 ÏàËÆ¶È:73.3% Phytochemistry 1988 27 109-113 A Highly efficient preparation of lunularic acid and some biological activities of stilbene and dihydrostilbene derivatives Toshihiro Hashimoto,Motoo Tori,Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 8h C14H12FNO2 ÏàËÆ¶È:73.3% Archiv der Pharmazie 2003 336 53-71 Relationship between the Structure and Antimycobacterial Activity of Substituted Salicylanilides Karel Waisser, Otakar Bureš, Pavel Holý, Jiř¨ª Kuneš, Radek Oswald, Lucie Jir¨¢skov¨¢, Milan Pour, V¨§ra Klimešov¨¢, Lenka Kubicov¨¢ and Jarmila Kaustov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . prunolide C C34H22O9 ÏàËÆ¶È:73.3% The Journal of Organic Chemistry 1999 64 2680-2682 Prunolides A, B, and C: Novel Tetraphenolic Bis-Spiroketals from the Australian Ascidian Synoicum prunum Anthony R. Carroll, Peter C. Healy, Ronald J. Quinn, and Carolyn J. Tranter Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 1-(4-hydroxyphenyl)-12-(3-methoxyphenyl)-1,12-dicarba-closo-dodecaborane C15H22B10O2 ÏàËÆ¶È:73.3% Bioorganic & Medicinal Chemistry 2009 17 1109-1117 Synthesis and biological evaluation of p-carborane bisphenols and their derivatives: Structure¨Cactivity relationship for estrogenic activity Takumi Ogawa, Kiminori Ohta, Toru Iijima, Tomoharu Suzuki, Shigeru Ohta, Yasuyuki Endo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (¡À)-scorzophthalide C16H14O5 ÏàËÆ¶È:68.7% Helvetica Chimica Acta 2007 Vol. 90 311 Phenolic Compounds from Scorzonera tomentosa L. Aynur Sarı, Christian Zidorn, Ernst P. Ellmerer, Fevzi Özgökçe, Karl-Hans Ongania, and Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . scorzocreticin C16H14O5 ÏàËÆ¶È:68.7% Journal of Natural Products 2001 64 1585-1587 Three New Dihydroisocoumarins from the Greek Endemic Species Scorzonera cretica1 Sotiris Paraschos, Prokopios Magiatis, Eleftherios Kalpoutzakis, Catherine Harvala,and Alexios-Leandros Skaltsounis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (E)-Methyl 3-(3-(benzyloxy)phenyl)but-2-enoate ÏàËÆ¶È:68.7% Molecules 2010 15 5928-5942 An Efficient Procedure Based on a MW-Assisted Horner¨CWadsworth-Emmons Reaction for the Synthesis of (Z)-3,3-Trisubstituted-a,b-unsaturated Esters Daniela Rossi, Anna Carnevale Baraglia, Massimo Serra, Ornella Azzolina and Simona Collina Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 2-(3-Hydroxyphenyl)-3-[(2-propynylamino)methyl]-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide hydro-chloride C16H15N3O5S3 ÏàËÆ¶È:68.7% Bioorganic & Medicinal Chemistry 2000 8 957-975 2H-Thieno[3,2-e]- and [2,3-e]-1,2-thiazine-6-sulfonamide 1,1-dioxides as ocular hypotensive agents: synthesis, carbonic anhydrase inhibition and evaluation in the rabbit Hwang-Hsing Chen, Sharon Gross, John Liao, Marsha McLaughlin, Tom Dean, William S. Sly, Jesse A. May Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 5-(3'-hydroxybiphenyl-4-yl)pyridin-2(1H)-one ÏàËÆ¶È:68.7% Bioorganic & Medicinal Chemistry 2010 18 3494-3505 Novel estrone mimetics with high 17¦Â-HSD1 inhibitory activity Alexander Oster, Tobias Klein, Ruth Werth, Patricia Kruchten, Emmanuel Bey, Matthias Negri, Sandrine Marchais-Oberwinkler, Martin Frotscher, Rolf W. Hartmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 1-p-methoxyphenyl-3-methyl-1H-isochromeno[3,4-d]imidazol-5-onium iodide ÏàËÆ¶È:68.7% Heterocycles 2012 84 537-554 Synthesis and Reactivity of Novel 1H-Isochromeno[3,4-d]imidazol-1-onium Salts Bart I. Roman, Marie Gu¨¦gan, Nils De Vos, Cedric Maton, and Christian V. Stevens Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 1-(1-(4-(Thiophen-2-yl)phenyl)-1H-pyrrol-2-yl)ethene-1,2,2-tricarbonitrile C19H10N4S ÏàËÆ¶È:68.7% Tetrahedron 2012 68 8147-8155 Synthesis and characterization of novel second-order NLO-chromophores bearing pyrrole as an electron donor group M. Cid¨¢lia R. Castro, M. Belsley, A. Maur¨ªcio C. Fonseca, M. Manuela M. Raposo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 5-hydroxy-2-(2-phenylethyl)chromone C17H14O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69(2) 290-291 Neuroprotective 2-(2-Phenylethyl)chromones of Imperata cylindrica Jeong Seon Yoon, Mi Kyeong Lee, Sang Hyun Sung, and Young Choong Kim Structure 13C NMR ̼Æ×Ä£Äâͼ |
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