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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-04-23 08:27:41
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