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huadong1227: ½ð±Ò+5, ¡ïÓаïÖú 2014-11-13 19:45:19
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1 .     29¦Á-I-butyl-29¦Â-methyl-20,22-O-methylidene-20-hydroxyecdysone
    ÏàËÆ¶È:68.4%
Molecules          2013          18          15255-15275
Synthesis and Structure-Activity Relationships of Novel Ecdysteroid Dioxolanes as MDR Modulators in Cancer
Ana Martins, J¨®zsef Cs¨¢bi, Attila Bal¨¢zs, Di¨¢na Kitka, Leonard Amaral, J¨®zsef Moln¨¢r, Andr¨¢s Simon, G¨¢bor T¨®th and Attila Hunyadi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (20R,22R)-6¦Á,14¦Á-dihydroxy-2¦Â,3¦Â:20,22-bis-(isopropylidenedioxy)-5¦Â,8¦Á-cholestane
    ÏàËÆ¶È:65.7%
Russian Journal of Organic Chemistry          2009          45          1149-1153
Regio and stereo directional oxidation of ecdysteroids and their 7,8-dihydroanalogs with ozone in pyridine
R. G. Savchenko, Ya. R. Urazaeva, R. V. Shafikov and V. N. Odinokov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid
C36H56O9     ÏàËÆ¶È:65.7%
Journal of Ethnopharmacology          2011          135          78-87
Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities
Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     20-hydroxyecdysone 25-O-¦Â-D-glucopyranoside
C33H54O12     ÏàËÆ¶È:65.7%
Chinese Traditional and Herbal Drugs          2014          45          906-912
Chemical constituents from roots tubers of Serratula chinensis
TANG Hai-jiao, FAN Chun-lin, WANG Gui-yang, WEI Wei, WANG Ying, YE Wen-cai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     momordicoside Q
C36H60O10     ÏàËÆ¶È:65.7%
Chemistry & Biology          2008          15          263-273
Antidiabetic Activities of Triterpenoids Isolated from Bitter Melon Associated with Activation of the AMPK Pathway
Min-Jia Tan, Ji-Ming Ye, Nigel Turner, Cordula Hohnen-Behrens, Chang-Qiang Ke, Chun-Ping Tang, Tong Chen, Hans-Christoph Weiss, Ernst-Rudolf Gesing, Alex Rowland, David E. James, and Yang Ye
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (20R,22R)-6¦Á,14¦Á-dihydroxy-2,3:20,22-bis(isopropylidenedioxy)-5¦Á-cholesta-7,24-diene
    ÏàËÆ¶È:63.4%
Russian Journal of Organic Chemistry          2005          41          1296-1305
Stereochemistry of Hydride Reduction of 20-Hydroxyecdysone Derivatives
V. N. Odinokov, R. G. Savchenko, R. V. Shafikov, S. R. Afon'kina and L. M. Khalilov, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     1,3-diacetyl-24-epi-polacandrin
C34H56O7     ÏàËÆ¶È:63.1%
Journal of Natural Products          2003          66          1586-1592
New Dammarane Triterpenes from the Aerial Parts of Ibicella lutea Grown in Argentina
Mario J. Simirgiotis,Carlos Jim¨¦nez,Jaime Rodr¨ªguez,Oscar S. Giordano, and Carlos E. Tonn
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     digitoxigenin 3-O-¦Â-D-glucopyranosyl-(1¡ú4)-¦Á-L-acofriopyranoside
C36H56O13     ÏàËÆ¶È:63.1%
Chemical & Pharmaceutical Bulletin          1997          45          1536-1538
Cardenolide Glycosides from Thevetia ahouai (LINN.) A.DC.
Hirokatsu ENDO,Tsutomu WARASHINA,Tadataka NORO,Victor H. CASTRO,Gerardo A. MORA,Luis J. POVEDA and Pablo E. SANCHEZ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     cumingianoside H
C38H64O11     ÏàËÆ¶È:63.1%
Chemical & Pharmaceutical Bulletin          1997          45          68-74
Antitumor Agents. 168. Dysoxylum cumingianum. IV. The Structures of Cumingianosides G-O, New Triterpene Glucosides with a 14, 18-Cycloapotirucallane-Type Skeleton from Dysoxylum cumingianum, and Their Cytotoxicity against Human Cancer Cell Lines
Toshihiro FUJIOKA,Akio SAKURAI,Kunihide MIHASHI,Yoshiki KASHIWADA,Ih-Sheng CHEN and Kuo-Hsiung LEE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (24R)-and (24S)-9,19-cyclolanost-3-one-24,25-diol
C30H50O3     ÏàËÆ¶È:63.1%
Phytochemistry          1994          35          1001-1004
triterpenoids from Artocarpus heterophyllus
B.R.Barik, T. Bhaumik, A.K.Dey and A.B.Kundu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     glucosyl divaricoside
    ÏàËÆ¶È:63.1%
Phytochemistry          1993          34          1317-1321
Cardenolides in the regenerated plants obtained from Strophanthus divaricatus calli
Kiichiro Kawaguchi, Isao Asaka, Masao Hirotani, Tsutomu Furuya, Shigeki Katsuki
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     pfaffiaglycoside C
C33H54O11     ÏàËÆ¶È:63.1%
Chemical & Pharmaceutical Bulletin          2010          58          690-695
Brazilian Natural Medicines. IV. New Noroleanane-Type Triterpene and Ecdysterone-Type Sterol Glycosides and Melanogenesis Inhibitors from the Roots of Pfaffia glomerata
Seikou Nakamura, Gang Chen, Souichi Nakashima, Hisashi Matsuda, Yuehu Pei and Masayuki Yoshikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     3-O-(2-propyl)malonyl-12¦Â-acetoxy-3¦Á,25-dihydroxy-(20S,24R)-epoxydammarane
C38H62O8     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     3-O-(N-ethyl)malonamoyl-12¦Â-acetoxy-3¦Á,25-dihy-droxy-(20S,24R)-epoxydammarane
C37H61NO7     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2010          18          2964-2975
Papyriferic acid derivatives as reversal agents of multidrug resistance in cancer cells
Juan Xiong, Masatoshi Taniguchi, Yoshiki Kashiwada, Michiko Sekiya, Takashi Yamagishi, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     ecdysterone 22-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:63.1%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     compound 12
    ÏàËÆ¶È:63.1%
Magnetic Resonance in Chemistry          2013          15          830-836
1H and 13C NMR investigation of 20-hydroxyecdysone dioxolane derivatives, a novel group of MDR modulator agents
Attila Bal¨¢zs, Attila Hunyadi, J¨®zsef Cs¨¢bi, Nikoletta Jedlinszki, Ana Martins, Andr¨¢s Simon and G¨¢bor T¨®th
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     compound 13
    ÏàËÆ¶È:63.1%
Magnetic Resonance in Chemistry          2013          15          830-836
1H and 13C NMR investigation of 20-hydroxyecdysone dioxolane derivatives, a novel group of MDR modulator agents
Attila Bal¨¢zs, Attila Hunyadi, J¨®zsef Cs¨¢bi, Nikoletta Jedlinszki, Ana Martins, Andr¨¢s Simon and G¨¢bor T¨®th
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3'-O-acetylglucoevatromonoside
C37H56O13     ÏàËÆ¶È:63.1%
Bioscience, Biotechnology, and Biochemistry          2013          77          1186-1192
New Cardenolide Glycosides from the Seeds of Digitalis purpurea and Their Cytotoxic Activity
Minpei KURODA, Satoshi KUBO, Yukiko MATSUO, Tomomi ATOU, Junichi SATOH, Tomofumi FUJINO, Makio HAYAKAWA, Yoshihiro MIMAKI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-11-13 18:35:15
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