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²éѯ½á¹û£º¹²²éµ½2972¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ergosta-4,6,8(14),22-tetraen-3¦Â-ol C28H42O ÏàËÆ¶È:65.6% Natural Product Research 1993 3 193-196 The Isolation of Ergosta-4, 6, 8 (14), 22-tetraen-3¦Â-ol from Injured Fruit Bodies of Marasmius oreades Zijie Pang; Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 21-acetoxy-3-oxo-cycloart-1,11,24-triene ÏàËÆ¶È:65.6% Phytochemistry 1998 49 2069-2076 Cycloartenoid dienone acids and lactones from Combretum erythrophyllum Colin B. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (24R)-3¦Â,5-dihydroxy-5¦Á-stigmastan-6-one 3-(6-chloronicotinate) ÏàËÆ¶È:62.8% Chemistry of Natural Compounds 2009 45 200-204 SYNTHESIS OF 6-CHLORONICOTINATES OF STEROIDAL3¦Â,5¦Á,6¦Â-TRIOLS AND 3¦Â,5-DIHYDROXY-6-KETONES N. V. Kovganko, Yu. G. Chernov, S. N. Sokolov, Zh. N. Kashkan, and V. L. Survilo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cycloart-23-ene-3¦Â,25,28-triol ÏàËÆ¶È:62.5% Journal of Natural Products 2000 63 636-642 Phytochemical Investigation of Aglaia rubiginosa S. Weber, J. Puripattanavong, V. Brecht, and A. W. Frahm Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (24R)24-ethyl-7¦Á-hydroperoxy-cholest-5-en-3¦Â-ol ÏàËÆ¶È:62.5% Natural Product Research 1994 5 7-14 Hydroperoxysterols in Arum italicum Marina Della Greca; Antonio Fiorentino; Antonio Molinaro; Pietro Monaco; Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . stigmasta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2008 33 909-911 Studies on chemical constituents of Ranunculus ternatus XIONG Ying, DENG Kezhong, GAO Wenyuan, GUO Yuanqiang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 16¦Â-hydroxylanosta-2,8,23-triene C30H48O ÏàËÆ¶È:62.5% Zeitschrift f¨¹r Naturforschung C 2002 57 489-495 Microbial Transformation of a Mixture of Argentatin A and Incanilin Key words: Argentatin A, Incanilin, Biotransformation Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Á-Amino-5¦Á-ergosta-7,22-diene ÏàËÆ¶È:62.5% The Journal of Organic Chemistry 1984 49 5157-5160 Two steroidal alkaloids from a marine sponge, Plakina sp Richard M. Rosser, D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ergosta-5,77,22-trien-3-ol ÏàËÆ¶È:62.5% Periodical of Ocean University of China 2011 41 086-090 Chemical Constituents of Sponge Xestospongia testudinaria from the South China sea KONG Wen-Wen, HAN Lei, LI Liang, SHAO Chang-Lun, ZHANG Rong, Nicole J.de Voogd, WANG Chang-Yun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . isoperadione C30H42O4 ÏàËÆ¶È:62.5% Zeitschrift f¨¹r Naturforschung B 1999 54 415-418 Isoperadione: A New Triterpenoid from Salvia bucharica V. U. Ahmad, M. Zahid, M. S. Ali, Z. Ali, N. Alam, R. B. Tareen, M. Z. Iqbal Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ¦Â-sitosterol benzoate ÏàËÆ¶È:60.6% Planta Medica 1988 54 223-224 Antihepatotoxic Principles of Sambucus formosana Chun-Nan Lin and Whey-Pin Tome Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (23S)-23-methoxy-24-methylenelanost-8-en-3-one C32H52O2 ÏàËÆ¶È:59.3% Helvetica Chimica Acta 2003 Vol. 86 2645 A Diterpenoid with a New Skeleton and Cytotoxic Terpenoids Isolated from Amentotaxus formosana Huey-Jen Su, Li-Wen Wang, Chun-Nan Lin, Shiow-Hwa Day, Bai-Luh Wei, Sheng-Zehn Yang, Shen-Jeu Won Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . antiquol B acetate C32H52O2 ÏàËÆ¶È:59.3% Journal of Natural Products 2002 65 158-162 Eupha-7,9(11),24-trien-3a-ol (¡°Antiquol C¡±) and Other Triterpenes from Euphorbia antiquorum Latex and Their Inhibitory Effects on Epstein-Barr Virus Activation Toshihiro Akihisa, E. M. Kithsiri Wijeratne, Harukuni Tokuda, Fumio Enjo, Masakazu Toriumi,Yumiko Kimura, Kazuo Koike, Tamotsu Nikaido, Yasuhiro Tezuka, and Hoyoku Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . camelliol A acetate C32H52O2 ÏàËÆ¶È:59.3% Journal of Natural Products 1999 62 265-268 Camelliols A-C, Three Novel Incompletely Cyclized Triterpene Alcohols from Sasanqua Oil (Camellia sasanqua) Toshihiro Akihisa, Koichi Arai, Yumiko Kimura, Kazuo Koike, Wilhelmus C. M. C. Kokke, Tsuyoshi Shibata, and Tamotsu Nikaido Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . swinhosterol C C31H52O2 ÏàËÆ¶È:59.3% Journal of Natural Products 1997 60 296-298 Swinhosterols A-C, 4-Methylene Secosteroids from the Marine Sponge Theonella swinhoei Akemi Umeyama, Noboru Shoji, Megumi Enoki, and Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (22E,24R)-stigmasta-1,4-dien-3-one C29H46O ÏàËÆ¶È:59.3% Planta Medica 2003 69 757-764 Anti-Platelet Aggregation and Chemical Constituents from the Rhizome of Gynura japonica Wei-Yu Lin,Yueh-Hsiung Kuo,Ya-Ling Chang, Che-Ming Teng,Eng-Chi Wang, Tsutomu Ishikawa,Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . theonellasterone C30H48O ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1992 40 1773-1778 Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . conicasterone C29H46O ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1992 40 1773-1778 Marine Natural Products. XXX. Two New 3-Keto-4-methylene Steroids, Theonellasterone and Conicasterone, and a Diels-Alder Type Dimeric Steroid Bistheonellasterone, from the Okinawan Marine Sponge Theonella swinhoei Motomasa KOBAYASHI,Kazuyoshi KAWAZOE,Taketo KATORI and Isao KITAGAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Â,5¦Á,9¦Á-trihydroxy-(22E,24R)-ergosta-7,22-dien-6-one C28H44O4 ÏàËÆ¶È:59.3% Chemistry of Natural Compounds 2009 45 759-761 STEROIDS AND OTHER CONSTITUENTS FROMTHE MUSHROOM Armillaria lueo-virens Hui-Yan Xiong, Dong-Qing Fei, Jin-Song Zhou,Chun-Jiang Yang,and Guo-Liang Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (24R)-chlorostigmast-5-ene ÏàËÆ¶È:59.3% Chemistry of Natural Compounds 2000 36 595-598 13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:59.3% China Journal of Chinese Materia Medica 2005 30 193-195 Studies on chemical constituents in the mycelia from fermented culture of Flammulian velutipes KANG Jie, CHEN Ruoyun Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ¦Â-sitosterol ÏàËÆ¶È:59.3% China Journal of Chinese Materia Medica 2003 28 278-279 ¼Ô¹ûÞ§¹áÖÚ»¯Ñ§³É·ÖµÄÑо¿ Ñî á°, ÕÔÓñÓ¢, ÍÀßÏßÏ Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 5¦Á-stigmast-9(11)-en-3¦Â-ol C29H50O ÏàËÆ¶È:59.3% China Journal of Chinese Materia Medica 1996 21 666-667 Studies on Chemical Components of Cynomorium songaricum Rupr. Xu Xiuzhi, Zhang Chengzhong and Li Chong Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . dammara-17E,21-diene ÏàËÆ¶È:59.3% Phytochemistry 1998 48 297-299 Triterpenoid constituents of the moss Floribundaria aurea subsp. Nipponica Masao Toyota, Kazuko Masuda, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (24R)-3¦Â-Methoxy-24-methyl-5¦Á-cholest-8-en-7-one C29H48O2 ÏàËÆ¶È:59.3% Journal of Natural Products 1992 Vol 55 311 Unique 3¦Â-O-Methylsterols from the Pacific Sponge Jereicopsis graphidiophora M. Valeria D'Auria, Luigi Gomez Paloma, Luigi Minale, Raffaele Riccio, Cecil Debitus, Claudi L¨¦vi Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . boeticol acetate ÏàËÆ¶È:59.3% Journal of Natural Products 1995 Vol 58 275-279 Boeticol, a New Tetracyclic Triterpene from Euphorbia boetica Maria Jos¨¦ U. Ferreira, Jos¨¦ R. Ascenso, Olga S. Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Natural Product Sciences 2003 9 270-272 Constituents of Euphorbia milii YunChoi, Hye-Sook; Jin, Jing-Ling; Hong, Sung-Won; Lee, Yong-Yook; Lee, Jo-Hyung Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Natural Product Sciences 2004 10 306-309 Triterpenoids from Orostachys japonicus Lee, Sang-Hyun; Paek, Sun-Ha; Kim, Seung-Ki; Kim, Bak-Kwang; Shin, Kuk-Hyun Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . dammara-17,21-diene C30H50 ÏàËÆ¶È:59.3% Phytochemistry 1991 30 3369-3377 Fern constituents: Triterpenoids isolated from Polypodium vulgare, P. fauriei and P. virginianum Y¨ko Arai, Motoko Yamaide, Sachiko Yamazaki, Hiroyuki Ageta Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . Rhabdastin F C32H48O5 ÏàËÆ¶È:59.3% Journal of Natural Products 2010 73 1512-1518 Cytotoxic Isomalabaricane Derivatives and a Monocyclic Triterpene Glycoside from the Sponge Rhabdastrella globostellata Miyabi Hirashima, Kazuomi Tsuda, Toshiyuki Hamada, Hiroaki Okamura, Tatsuhiko Furukawa, Shin-ichi Akiyama, Yusuke Tajitsu, Ryuji Ikeda, Masaharu Komatsu, Matsumi Doe, Yoshiki Morimoto, Motoo Shiro, Rob W. M. van Soest, Kaoru Takemura, and Tetsuo Iwagawa Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . N-Benzyl 3¦Á,7¦Á,24-trimethoxy-12-az¦Á-5¦Â-cholane C33H53NO3 ÏàËÆ¶È:59.3% Steroids 2011 76 324-330 Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols Malika Ibrahim-Ouali, Khalil Hamze, Luc Rocheblave Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ºúÂܲ·ÜÕ ÏàËÆ¶È:59.3% Chinese Journal of Marine Drugs 2002 21(1) 1-4 Sterol con stituents from marine brown alga ishige okamurai TANG Hai-feng, YI Yang-hua, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . stigmast-5-en-3¦Â,7¦Á-ol ÏàËÆ¶È:59.3% China Journal of Chinese Materia Medica 2010 35 2420-2423 Chemical constituents of Desmodium sambuense LI Chuankuan; ZHANG Qianjun; HUANG Zhongbi; CHEN Qing; YAO Rongjun Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ¦Â-¹ÈçÞ´¼ ÏàËÆ¶È:59.3% Chinese Traditional and Herbal Drugs 2010 41 704-707 Âúɽºì»¯Ñ§³É·ÖµÄÑо¿ ¸¶ÏþÀö;ÕÅÁ¢Î°;ÁÖÎĺ²;ÀîÇàɽ Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . ergosteryl palmitate ÏàËÆ¶È:59.3% Chinese Traditional and Herbal Drugs 2005 36 1601-1603 Chemical constituents from fruiting bodies of Ganoderma lucidum ZHANG Xiao-qi; YIN Zhi-qi; YE Wen-cai; ZHAO Shou-xun Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Archives of Pharmacal Research 2003 26 902-905 Constituents from the non-polar fraction of Artemisia apiacea Sanghyun Lee, Kyoung Soon Kim, Sang Hee Shim, You Mie Park and Bak-Kwang Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Chinese Pharmaceutical Journal 2009 44 1372-1374 Chemical Constituents of the Roots of Uritca fissa E.Pritz. JI Bao-quan, FENG Bao-min, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . (3¦Â,5¦Á,8¦Á,22E,24R)-5,8-epidioxyergosta-6,9(11),22-trien-3-ol ÏàËÆ¶È:59.3% Chinese Journal of Medicinal Chemistry 2007 17 104-107 Isolation and identification of the chemical constituents from Lentinus giganteus Berk GAN Yu-juan, ZENG Yan-bo, MEI Wen-li, DAI Hao-fu Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . (3¦Â,5¦Á,8¦Á,22E,24R)-5,8-epidioxyergosta-6,9(11),22-trien-3-ol ÏàËÆ¶È:59.3% Chinese Journal of Medicinal Chemistry 2008 18 279-283 Chemical constituents from endophytic fungus S26 of Cephalotaxus hainanensis CHEN Ping, WU Jiao, DAI Hao-fu, XIE Xiu-chao, MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Journal of Shenyang Pharmaceutical University 2011 28 364-367 Isolation and identification of chemical constituents of root of Girardinia suborbiculata C. J. Chen subsp. Triloba FENG Bao-min, LIU Jing-yan, WANG Hui-guo, SHI Li-ying, TANG Ling, WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Journal of Shenyang Pharmaceutical University 2010 27 116-119 Isolation and identification of chemical constituents from stems of Smilax glabra Roxb. WU Bo, MA Yue-ping, YUAN Jiu-zhi, SUN Qi-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . (3¦Â,5¦Á,8¦Á,22E,24R)-5,8-epidioxyergosta-6,9(11),22-trien-3-ol ÏàËÆ¶È:59.3% Natural Product Research and Development 2009 21 424-427 Chemical Constituents from the Endophytic Fungus Rhizoctonia sp. J5 of Antiaris toxicaria QUE Dong-mei; DAI Hao-fu; HUANG Gui-xiu; DAI Wen-jun; MEI Wen-li Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:59.3% Natural Product Research and Development 2000 12(6) 33-36 STUDIES ON THE CHEMICAL CONSTITUENTS OF PHELLINUS YAMANOI He Jian; Feng Xiaozhang Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 5-stigmasten-3¦Â,7¦Â-diol ÏàËÆ¶È:59.3% Journal of the Chinese Chemical Society 2004 51 437-441 New Prenylated Flavones from the Roots of Ficus beecheyana Ching-kuo Lee*, Chung-kuang Lu, Yuen-Hsiung Kuo,Jian-Zhi Chen and Guang-Zhong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . acetyltheonellasterol C32H52O2 ÏàËÆ¶È:59.3% Marine Drugs 2012 10 1536-1544 4-Methylenesterols from a Sponge Theonella swinhoei Jheng-Kun Guo, Ching-Ying Chiang, Mei-Chin Lu, Wen-Been Chang and Jui-Hsin Su Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . ergosta-4,6,8,22-tetraene-3-one ÏàËÆ¶È:59.3% Journal of Ethnopharmacology 2012 142 456¨C461 Antiparasitic compounds from Cornus florida L. with activities against Plasmodium falciparum and Leishmania tarentolae Rocky Graziose, Patricio Rojas-Silva, Thirumurugan Rathinasabapathy, Carmen Dekock, Mary H. Grace, Alexander Poulev, Mary Ann Lila, Peter Smith, Ilya Raskin Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . ergosta-4,6,8(14),22-tetraen-3-ona ÏàËÆ¶È:59.3% Qu¨ªmica Nova 2009 32 1710-1712 Steroids produced by Penicillium herquei, an endophytic fungus isolated from the fruits of Melia azedarach (Meliaceae) Marinho, Andrey Moacir do Rosario; Marinho, Patr¨ªcia Santana Barbosa; Rodrigues Filho, Edson Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Academic Journal of Second Military Medical University 2009 30 1199-1202 Study on chemical constituents of methylene chloride extract of Rubus chingii YOU Meng-tao, LI Ya-kui, GUO Mei-li Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Journal of Guangdong Phamaceutical University 2006 22 594-595 Studies on the chemical constituents from Hovenia acerba Lindl.extracted with petroleum ether SHEN Xiang-rong, ZHANG De-zhi Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 8,14-13,17-diseco-stigmast-5,22-diene-3-¦Á-ol C29H52O ÏàËÆ¶È:59.3% Pharmaceutical Biology 2007 45 140-144 New Phytoconstituents from the Aerial Parts of Uraria lagopoides. Hinna Hamid, S. Tarique Abdullah, Mohammed Ali, M. Sarwar Alam Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Journal of Chinese Medicinal Materials 2012 35 404-406 Study on the Chemical Constituent from the Dichloromethane Extract. of the Pine Needles of Cedrus deodara Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Journal of Chinese Medicinal Materials 2012 35 1257-1259 Study on the Chemical Constituents from Patrinia scabra MA Qu-huan, SHI Xiao-feng, FAN Bin, LIU Dong-yan Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . 18-(5-(1-(4-toluenesulfonyl)-1H-1,2,3-triazol-4-yl)pentanoyloxy)-8,11,13-abietatriene C34H45N3O4S ÏàËÆ¶È:59.3% Molecules 2014 19 2523-2535 Synthesis and Antiproliferative Activity of Some Novel Triazole Derivatives from Dehydroabietic Acid Mariano Walter Pertino, Valery Verdugo, Cristina Theoduloz and Guillermo Schmeda-Hirschmann Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Chemistry and Industry of Forest Products 2013 33 121-124 Chemical Components of Alpinia sichuanensis Z. Y. Zhu WU Qiu-yan, WANG Ping-ping, WANG Kui-wu, JIN Zhi-min Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:59.3% Natural Product Research and Development 2013 25 1653-1657 Chemical Constituents of Xylaria euglossa Fr. WANG Xing-na*, LIU Ji-kai, TAN Ren-xiang Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:59.3% Natural Product Research and Development 2014 26 1537-1601 Chemical Constituents Produced by Fusarium sp. S13 Isolated from Pleioblastus amarus WANG Yong, KUANG Yi, YANG Sheng-xiang, LIU Li Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . lappasterol C29H46O ÏàËÆ¶È:59.3% Indian Journal of Chemistry Section B 2004 43B 655-659 phytoconstituents from saussurea lappa roots Vijender Singh & Mohd Ali Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . bengalensinone C30H46O2 ÏàËÆ¶È:59.3% Journal of Asian Natural Products Research 2012 14 1149-1155 Cholinesterase inhibitory constituents from Ficus bengalensis Naheed Riaz, Muhammad Akram Naveed, Muhammad Saleem, Bushra Jabeen, Muhammad Ashraf, Syeda Abida Ejaz, Abdul Jabbar & Ishtiaq Ahmed Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . Nymphasterol C29H48O ÏàËÆ¶È:59.3% Medicinal Chemistry Research 2012 21 783-787 Nymphasterol, a new steroid from Nymphaea stellata Amita Verma , Bahar Ahmed ,Rucha Upadhyay,Neetu Soni Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:59.3% Lishizhen Medicine and Materia Medica Research 2011 22 2868-2870 The Chemical Constituents of N-butanol Fraction from the Seed Cake of Camellia Oleifera Abel MA Li-yuan; LI Lin; TANG Ling; CHEN Yue-long; FENG Bao-min; SHI Li-ying; WANG Yong-qi Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . ¦Â-sitosterol C29H50O ÏàËÆ¶È:59.3% Chinese Traditional and Herbal Drugs 2012 43 2356-2360 Chemical constituents from sporophore of Hericium coralloides (¢ñ) ZHANG Peng; BAO Hai-ying; Tolgor Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . ¦Â-sitosterol ÏàËÆ¶È:59.3% Lishizhen Medicine and Materia Medica Research 2011 22 1701-1703 Research on the Chemical Constituents of Flowers of Camellia pitardii Coh. 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(24R)-3¦Â,5-Dihydroxy-5¦Á-stigmastan-6-one ÏàËÆ¶È:58.8% Chemistry of Natural Compounds 2010 46 750-755 Synthesis of ¦Á-chloropyridine-containing oximes of 3¦Â,5-dihydroxy-6-ketosteroids N. V. Kovganko, S. N. Sokolov, Yu. G. Chernov, Zh. N. Kashkan and V. L. Survilo Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . 2'-Benzoyl-3¦Â-chloro-5¦Á-cholestano-[5,7-c d]-pyrazoline C34H49ClN2 ÏàËÆ¶È:58.8% Steroids 2013 78 1263-1272 Synthesis and anti-tumor evaluation of B-ring substituted steroidal pyrazoline derivatives Shamsuzzaman, Hena Khanam, Ashraf Mashrai, Asif Sherwani, Mohammad Owais, Nazish Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 78 . N,N,N',N',N''-pentamethyl-1,4,7-triazaheptane-1,7-bis(N,N'-3¦Â-acetate-ergosta-5,7,22-triene)ammonium dibromide C69H113N3O4 ÏàËÆ¶È:58.8% Molecules 2014 19 9419-9434 Synthesis, Spectroscopic and Theoretical Studies of New Dimeric Quaternary Alkylammonium Conjugates of Sterols Bogumił Brycki, Hanna Koenig, Iwona Kowalczyk and Tomasz Pospieszny Structure 13C NMR ̼Æ×Ä£Äâͼ 79 . dihydro-20-epi-isoiguesterinol triacetate ÏàËÆ¶È:57.5% Journal of Natural Products 2005 68 251-254 Bisnortriterpenes from Salacia madagascariensis Deborah A. Thiem, Albert T. Sneden, Shabana I. Khan, and Babu L. Tekwani Structure 13C NMR ̼Æ×Ä£Äâͼ 80 . preunusol A C37H54O4 ÏàËÆ¶È:57.5% Agricultural and Biological Chemistry 1991 55 1727-1731 Prunusols A and B, Novel Antioxidative Tocopherol Derivatives Isolated from the Leaf Wax of Prunus grayana Maxim. Toshihiko OSAWA, Shigenori KUMAZAWA, Shunro KAWAKISHI Structure 13C NMR ̼Æ×Ä£Äâͼ 81 . 3-oxo-2-(pyridin-3-ylmethylideno)-lup-20(29)-en-28-oic acid C36H49O3N ÏàËÆ¶È:57.1% Chemistry of Natural Compounds 2011 47 752-758 Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes O. B. Kazakova, N. I. Medvedeva, I. A. Samoilova, I. P. Baikova and G. A. Tolstikov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 82 . ZL-5 C28H40O ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2004 52(8) 1005-1008 Six Immunosuppressive Features from an Ascomycete, Zopfiella longicaudata, Found in a Screening Study Monitored by Immunomodulatory Activity Haruhiro FUJIMOTO,Etsuko NAKAMURA, Emi OKUYAMA, and Masami ISHIBASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 83 . 9(11)-dehydroaxinysterol C28H40O3 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2002 50(9) 1286-1289 New Biologically Active Marine Sesquiterpenoid and Steroid from the Okinawan Sponge of the Genus Axinyssa Makoto IWASHIMA,Ikuo TERADA,Kazuo IGUCHI,and Takao YAMORI Structure 13C NMR ̼Æ×Ä£Äâͼ 84 . 24(E)-ethylidenecycloarta-3¦Á-ol C32H54O ÏàËÆ¶È:56.2% Phytochemistry 2005 66 2304-2308 Cycloartane type triterpenoids from the rhizomes of Polygonum bistorta Karuppiah Pillai Manoharan, Tan Kwong Huat Benny, Daiwen Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 85 . 22,25-dihydroxycycloart-23E-en-3-one C30H48O3 ÏàËÆ¶È:56.2% Phytochemistry 2002 60 329-332 Cycloartane triterpenoids from Guarea macrophylla João Henrique G. Lago, N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ 86 . (23S*)-cycloarta-24-en-3¦Â,23-diol ÏàËÆ¶È:56.2% Phytochemistry 2002 60 333-338 Terpenoids from Guarea guidonia João Henrique G. Lago, Cl¨¢udia B. Brochini, N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ 87 . cycloartan-23E-ene-1¦Á,2¦Á,3¦Â,25-tetrol C30H50O4 ÏàËÆ¶È:56.2% Journal of Natural Products 2008 71(1) 81-86 Cycloartane-Type Triterpenoids from the Resinous Exudates of Commiphora opobalsamum Tao Shen, Hui-Qing Yuan, Wen-Zhu Wan, Xiao-Ling Wang, Xiao-Ning Wang, Mei Ji, and Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 88 . (17¦Â,20R,22E,24R)-1-methyl-19-norergosta-1,3,5,7,9,14,22-heptaene C28H36 ÏàËÆ¶È:56.2% Journal of Natural Products 2004 67 2133-2135 Natural Aromatic Steroids as Potential Molecular Fossils from the Fruiting Bodies of the Ascomycete Daldinia concentrica Xiang-Dong Qin, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 89 . (23E)-23-dehydro-25-hydroxysunpollenol C30H52O3 ÏàËÆ¶È:56.2% Journal of Natural Products 2003 66 1476-1479 Sunpollenol and Five Other Rearranged 3,4-seco-Tirucallane-Type Triterpenoids from Sunflower Pollen and Their Inhibitory Effects on Epstein-Barr Virus Activation Motohiko Ukiya, Toshihiro Akihisa, Harukuni Tokuda, Kazuo Koike,Yumiko Kimura,Takeshi Asano,Shigeyasu Motohashi,Tamotsu Nikaido, and Hoyoku Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 90 . 29-O-acetyl-3-oxotirucalla-7,24-dien-21-oic acid ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 238-242 Inhibitory Effects on HIV-1 Protease of Constituents from the Wood of Xanthoceras sorbifolia Chao-mei Ma, Norio Nakamura,Masao Hattori, Hiroko Kakuda,Jun-chan Qiao, and Hai-lan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 91 . schleicheol 2 C30H52O2 ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 72-78 Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1 George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami Structure 13C NMR ̼Æ×Ä£Äâͼ 92 . 7¦Á-hydroxytheonellasterol C30H50O2 ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 841-842 7¦Á-Hydroxytheonellasterol, a Cytotoxic 4-Methylene Sterol from the Philippines Sponge Theonella swinhoei Asfia Qureshi and D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . cycloart-23-ene-3¦Â,25-diol ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 636-642 Phytochemical Investigation of Aglaia rubiginosa S. Weber, J. Puripattanavong, V. Brecht, and A. W. Frahm Structure 13C NMR ̼Æ×Ä£Äâͼ 94 . cycloarta-23,25-diene-3¦Â,28-diol ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 636-642 Phytochemical Investigation of Aglaia rubiginosa S. Weber, J. Puripattanavong, V. Brecht, and A. W. Frahm Structure 13C NMR ̼Æ×Ä£Äâͼ 95 . 12¦Â-hydroxykulactone C30H44O4 ÏàËÆ¶È:56.2% Journal of Natural Products 1999 62 546-548 Antimycobacterial Triterpenes from Melia volkensii Charles L. Cantrell, Mohamed S. Rajab, Scott G. Franzblau, and Nikolaus H. Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ 96 . calicoferol F C28H44O2 ÏàËÆ¶È:56.2% Journal of Natural Products 1998 61 1441-1443 New Secosteroids from a Gorgonian of the Genus Muricella Youngwan Seo, Ki Woong Cho, Hosung Chung, Hyi-Seung Lee, and Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . ergosta-7,22-dien-3¦Â-ol C28H46O ÏàËÆ¶È:56.2% Journal of Natural Products 1998 61 1491-1496 Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver Structure 13C NMR ̼Æ×Ä£Äâͼ 98 . ergosta-5,8(14),22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:56.2% Journal of Natural Products 1998 61 1491-1496 Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . cycloart-23-ene-3¦Â,-25-diol ÏàËÆ¶È:56.2% Journal of Natural Products 1996 59 343-347 Cycloartane Derivatives from Tillandsia usneoides Gabriela M. Cabrera, Mariana Gallo, and Alicia M. Seldes Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . (23E)-25-methoxycycloart-23-en-3¦Â-ol ÏàËÆ¶È:56.2% Journal of Natural Products 1996 59 343-347 Cycloartane Derivatives from Tillandsia usneoides Gabriela M. Cabrera, Mariana Gallo, and Alicia M. Seldes Structure 13C NMR ̼Æ×Ä£Äâͼ |
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