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shaoyan415гæ (СÓÐÃûÆø)
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[ÇóÖú]
GS8---CÆ×ÇóÖú--2 ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (125 MHz, Pyr) ¦Ä 14.04,16.33,17.36,19.25,19.42,20.01,20.10,22.30,23.35,27.54,28.44,29.66,35.07,35.30,38.66,38.96,46.68,47.17,48.11,48.55,49.31,49.79,54.35,56.64,69.07,72.00,76.83,77.34,125.53,141.38,154.18,161.38,178.46,199.97,208.16 |
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shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú 2015-04-26 17:24:48
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shaoyan415: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ллÄú 2015-04-26 17:24:48
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²éѯ½á¹û£º¹²²éµ½6450¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3¦Â,7¦Â,15¦Â-Trihydroxy-11,23-dioxo-lanost-8,16-dien-26-oic acid C30H44O7 ÏàËÆ¶È:82.8% Journal of Asian Natural Products Research 2013 15 357-362 Three new lanostanoid triterpenes from the fruiting bodies of Ganoderma tropicum Li-Li Hu, Qing-Yun Ma, Sheng-Zhuo Huang, Zhi-Kai Guo, Hai-Xia Ma, Jian-Chun Guo, Hao-Fu Dai & You-Xing Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ganoderic acid C30H46O7 ÏàËÆ¶È:77.1% Chemical & Pharmaceutical Bulletin 1985 33 1367-1374 The Biologically Active Constituents of Ganoderma lucidum (FR.) KARST. Histamine Release-Inhibitory Triterpenes HIROSHI KOHDA,WAKAKO TOKUMOTO,KIYOE SAKAMOTO,MICHIKO FUJII,YUKO HIRAI,KAZUO YAMASAKI,YASUO KOMODA,HIDEO NAKAMURA,SHIGEMASA ISHIHARA and MASARU UCHIDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ganoderic acid C ÏàËÆ¶È:77.1% Chemical & Pharmaceutical Bulletin 1985 33 4829-4835 Structures of New Terpenoid Constituents of Ganoderma lucidum (Fr.) KARST (Polyporaceae) YASUO KOMODA,HIDEO NAKAMURA,SHIGEMASA ISHIHARA,MASARU UCHIDA,HIROSHI KOHDA and KAZUO YAMASAKI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ganoderic acid C C30H46O7 ÏàËÆ¶È:77.1% Acta Pharmaceutica Sinica 1997 32 447-450 STUDIES ON THE GANODERIC ACID, A NEW CONSTITUENTS FROM THE FRUITING BODY OF GANODERMA LUCIDUM (FR.) KARST FS Wang; H Cai; JS Yang; YM Zhang; CY Hou; JQ Liu and MJ Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . butyl ganoderate A C34H52O7 ÏàËÆ¶È:77.1% Journal of Natural Products 2010 73 172-176 Lanostane Triterpenes from the Fruiting Bodies of Ganoderma lucidum and Their Inhibitory Effects on Adipocyte Differentiation in 3T3-L1 Cells IkSoo Lee, JungJu Seo, JinPyo Kim, HongJin Kim, UiJung Youn, JoonSeok Lee, HyunJu Jung, MinKyun Na, Masao Hattori, ByungSun Min and KiHwan Bae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 2¦Á,3¦Â,23-Triacetoxy-11¦Â-methoxy-urs-12-en-28-oate C38H58O9 ÏàËÆ¶È:77.1% Phytochemistry 1993 32 466-468 Triterpenoids from the resin of Shorea robusta Rai K. Hota, Maringanti Bapuji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ganoderic acid A ÏàËÆ¶È:77.1% Chinese Traditional and Herbal Drugs 2007 38 1610-1612 Chemical constituents from fruiting bodies of Ganoderma tsugae (¢ò) LIU Chao; PU Qiong-hui; WANG Hong-qing; CHEN Ruo-yun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Butyl ganoderate A ÏàËÆ¶È:77.1% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Ganoderic acid C ÏàËÆ¶È:77.1% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3¦Â,7¦Â,15¦Á,28-tetrahydroxy-11,23-dioxo-lanost-8,16-dien-26-oic acid C30H44O8 ÏàËÆ¶È:77.1% Molecules 2015 20 3281−3289 Three New Lanostanoids from the Mushroom Ganoderma tropicum Shuang-Shuang Zhang, Yu-Guang Wang, Qing-Yun Ma, Sheng-Zhuo Huang, Li-Li Hu, Hao-Fu Dai, Zhi-Fang Yu and You-Xing Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Ganoderic acid A C30H42O8 ÏàËÆ¶È:74.2% Molecules 2007 12 2038-2046 Two Novel Lanostane Triterpenoids from Ganoderma Sinense Yin Qiao, Xian-min Zhang and Ming-hua Qiu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . butyl ganoderate B C34H52O7 ÏàËÆ¶È:74.2% Journal of Natural Products 2010 73 172-176 Lanostane Triterpenes from the Fruiting Bodies of Ganoderma lucidum and Their Inhibitory Effects on Adipocyte Differentiation in 3T3-L1 Cells IkSoo Lee, JungJu Seo, JinPyo Kim, HongJin Kim, UiJung Youn, JoonSeok Lee, HyunJu Jung, MinKyun Na, Masao Hattori, ByungSun Min and KiHwan Bae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ganoderic acid C2 ÏàËÆ¶È:74.2% Journal of Shenyang Pharmaceutical University 2008 25 183-193 Chemical constituents of Ganoderma lucidum (Leys. ex Fr.) Karst LIU Si-yu, WANG Yan, HE Rong-rong, QU Ge-xia, QIU Feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . Ganoderic acid C2 ÏàËÆ¶È:74.2% Journal of Natural Products 2012 75 876-882 Direct 13C NMR Detection in HPLC Hyphenation Mode: Analysis of Ganoderma lucidum Terpenoids Sileshi G. Wubshet, Kenneth T. Johansen, Nils T. Nyberg, and Jerzy W. Jaroszewski Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â-angeloyloyl-2¦Â,23-dihydroxyolean-12-en-28-oic acid C35H54O6 ÏàËÆ¶È:74.2% Indian Journal of Chemistry Section B 2000 39B 875-878 Triterpenoids from Mosla chinensis Shangzhen Zheng, Shuhe Kang, Tong Shen, Liping Sun, Xuwei Shen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â,7¦Â,21¦Â-trihydroxy-urs-12-en-28-oic acid C30H48O5 ÏàËÆ¶È:74.2% Fitoterapia 2013 86 123-128 Biotransformation of ursolic acid by Syncephalastrum racemosum CGMCC 3.2500 and anti-HCV activity Shao-bin Fu, Jun-shan Yang, Jin-long Cui, Di-An Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3¦Â,7¦Â,15¦Â-Trihydroxy-11,23-dioxo-lanost-8,16-dien-26-oic acid methyl ester C31H46O7 ÏàËÆ¶È:74.2% Journal of Asian Natural Products Research 2013 15 357-362 Three new lanostanoid triterpenes from the fruiting bodies of Ganoderma tropicum Li-Li Hu, Qing-Yun Ma, Sheng-Zhuo Huang, Zhi-Kai Guo, Hai-Xia Ma, Jian-Chun Guo, Hao-Fu Dai & You-Xing Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Butyl ganoderate B ÏàËÆ¶È:74.2% Molecules 2014 19 17478-17535 A Comprehensive Review of the Structure Elucidation and Biological Activity of Triterpenoids from Ganoderma spp. Qing Xia, Huazheng Zhang, Xuefei Sun, Haijuan Zhao, Lingfang Wu, Dan Zhu, Guanghui Yang, Yanyan Shao, Xiaoxue Zhang, Xin Mao, Lanzhen Zhang and Gaimei She Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . Taccalonolide AY 36H46O15 ÏàËÆ¶È:74.2% Planta Medica 2015 81 247−256 Cytotoxic Taccalonolides and Withanolides from Tacca chantrieri Ni, Gang; Yang, Han-Ze; Fu, Nai-Jie; Zhang, Lei-Lei; Wang, Ming-Chun; Chen, Jing; Zhang, Chun-Lei; Li, Yan; Chen, Xiao-Guang; Chen, Ruo-Yun; Yu, De-Quan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 35-methoxyhop-6-ene-32,33,34-triol ÏàËÆ¶È:74.2% Chemistry of Natural Compounds 1992 28 321-325 Hopanoids of methylotropic acetobacteria L. M. Kogan, I. V. Kozlova, T. M. Filippova, E. A. Obol'nikova Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . Racemosol A C30H60O8 ÏàËÆ¶È:72.9% Journal of Natural Products 2009 72 791-795 Oleanane-Type Isomeric Triterpenoids from Barringtonia racemosa P. Mangala Gowri, S. V. S. Radhakrishnan, S. Jeelani Basha, A. V. S. Sarma, and J. Madhusudana Rao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . taikuguasin A C37H58O9 ÏàËÆ¶È:72.9% Planta Medica 2015 81 62-70 5¦Â,19-Epoxycucurbitane Triterpenoids from Momordica charantia and Their Anti-Inflammatory and Cytotoxic Activity Liaw, Chia-Ching; Huang, Hui-Chi; Hsiao, Ping-Chun; Zhang, Li-Jie; Lin, Zhi-Hu; Hwang, Syh-Yuan; Hsu, Feng-Lin; Kuo, Yao-Haur |

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