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mingax: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-07-07 11:03:53
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²éѯ½á¹û£º¹²²éµ½2248¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 32,33,34-trimethyl-bacteriohopan-16-ene 3-O-¦Â-D-glucopyranoside C44H76O6 ÏàËÆ¶È:71.7% 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 ̼Æ×Ä£Äâͼ 2 . 24-Ethylcholesterol-acetate ÏàËÆ¶È:69.5% Steroids 1989 53 625-638 Sterols of some Clerodendrum species(verbenaceae): Occurrence of the 24¦Á- and 24¦Â-epimers of 24-ethylsterols lacking a ¦¤25-bond Toshihiro Akihisa, Yuzuru Matsubara, Parthasarathi Ghosh, Swapnadip Thakur, Toshitake Tamura, Taro Matsumoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Pariposide F C47H80O16 ÏàËÆ¶È:68.0% Planta Medica 2012 78 1667-1675 New Steroidal Saponins and Sterol Glycosides from Paris polyphylla var. yunnanensis Wu, Xia; Wang, Lei; Wang, Guo-Cai; Wang, Hui; Dai, Yi; Ye, Wen-Cai; Li, Yao-Lan: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . glucoraphenin ÏàËÆ¶È:67.3% Natural Product Research and Development 2010 22 58-59 Studies on the Chemical Constituents of Cirsium henryi ZHANG Yue; RUAN Han-li; ZHANG Yong-hui; PI Hui-fang; WU Ji-zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-O-¦Â-[{2-L-rhamnopyranosyl(1¡ú2)-¦Â-D-apiofuranosyl(1¡ú6)-¦Â-D-glucopyranosyl]rosaterol C46H78O14 ÏàËÆ¶È:67.3% Indian Journal of Chemistry Section B 1998 37B 825-827 Studies on the two new stereo-saponins from Morchella conica Shangzhen Zheng, Liming Gao, Shuhe Kang & Xuwei Shen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:67.3% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosteryl-3'-glucopyranoside-6'-O-palmitate ÏàËÆ¶È:67.3% Chinese Herbal Medicines 2014 6 65-69 Chemical Constituents from Barks of Lannea coromandelica Xiao-juan Yun, Huo-ming Shu, Guang-ying Chen, Ming-hui Ji, Jin-yue Ding Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound A ÏàËÆ¶È:67.3% Yakugaku Zasshi 1983 103 43-48 The Principles of Tetragonia tetragonoides Having an Antiulcerogenic Activity. I. Isolation and Identification of Sterylglucoside Mixture (Compound A) EMI OKUYAMA, MIKIO YAMAZAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . lanoscopariol C46H80O3 ÏàËÆ¶È:65.2% Journal of Natural Products 1996 59 181-184 New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia Surendra Kumar Sharma and Mohammad Ali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . cumingianoside P C41H68O12 ÏàËÆ¶È:65.2% Chemical & Pharmaceutical Bulletin 1997 45 202-206 Antitumor Agents. 169. Dysoxylum cumingianum. V. Cumingianosides P and Q, New Cytotoxic Triterpene Glucosides with an Apotirucallane-Type Skeleton from Dysoxylum cumingianum Toshihiro FUJIOKA,Akio SAKURAI,Kunihide MIHASHI,Yoshiki KASHIWADA,Ih-Sheng CHEN and Kuo-Hsiung LEE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . stigmast-5-en-3-O-¦Â-D-glucopyranoside tetraacetate C43H68O10 ÏàËÆ¶È:65.2% Natural Product Sciences 1999 5 124-126 Sterols and Sterol Glycosides from Cuscuta Reflexa Anis, E.; Mustafa, G.; Ahmed, S.; Nisarullah, Nisarullah; Malik, A.; Afza, N.; Badar, Y. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . stigmast-5-en-3¦Â-ol-3-O-¦Â-D-(2'-n-triacontanoyl) glucopyranoside C65H118O7 ÏàËÆ¶È:65.2% Journal of Asian Natural Products Research 2012 14 301-307 New steroidal glycoside ester and aliphatic acid from the fruits of Lycium chinense Woo-Suk Jung,Ill-Min Chung,Mohd Ali and Ateeque Ahmad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 1 C61H110O7 ÏàËÆ¶È:65.2% Archives of Pharmacal Research 2007 30 172-176 Isolation of constituents and anti-complement activity from Acer okamotoanum WenYi Jin, Byung-Sun Min, JongPill Lee, Phuong Thien Thuong and Hyeong-Kyu Lee, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ºúÂܲ·ÜÕרéµËáõ¥ ÏàËÆ¶È:65.2% Chinese Pharmaceutical Journal 2008 43 971-973 Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Â-sitosteryl glucoside-3'-O-heptadecoicate ÏàËÆ¶È:65.2% Natural Product Research and Development 1997 9(2) 7-10 STUDIES ON THE CHEMICAL CONSTITUENTS OF THE CULTIVATED DESERTLIVING CISTANCHE (CISTANCHE DESERTICOLA) Tu Pengfei; He Yanping and Lou Zhicen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-O-¦Â-[{2-L-rhamnopyranosyl(1¡ú2)-¦Â-D-xylopyranosyl}-¦Â-D-glucopyranosyl]rosaterol C46H78O14 ÏàËÆ¶È:65.2% Indian Journal of Chemistry Section B 1998 37B 825-827 Studies on the two new stereo-saponins from Morchella conica Shangzhen Zheng, Liming Gao, Shuhe Kang & Xuwei Shen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-Sitosteryl linoleate ÏàËÆ¶È:65.2% Zeitschrift f¨¹r Naturforschung C 2012 67 172-180 Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . daucosterol+stigmasterol-3-O-glucopyranoside ÏàËÆ¶È:64.7% Chinese Traditional and Herbal Drugs 2004 35 608-611 Studies on chemical constituents of Indigofera carlesii SU Yan-fang; ZHANG Xin-xin; YANG Jing; GUO Zeng-jun; L¨¹ Ju-xian; GUO De-an Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . sitosteryl 9,10-dihydroxystearate C50H88O4 ÏàËÆ¶È:63.8% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide C47H75NO2 ÏàËÆ¶È:63.8% Steroids 2009 74 88-94 Steroids linked with amide bond¡ªExtended cholesterol Ivan Černy, Miloš Bud¨§š¨ªnsky, Vladim¨ªr Pouzar, Pavel Drašar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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