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»¯ºÏÎï1 13C NMR (100 MHz, CDCl3) ¦Ä 15.78, 17.88, 19.87, 20.28, 20.70, 21.13, 21.65, 24.31, 25.88, 27.62, 28.18, 29.11, 35.38, 37.4, 38.06, 38.20, 38.63, 38.76, 39.09, 41.87, 43.43, 44.90, 66.36, 66.65, 70.15, 78.30, 78.60, 83.82, 123.36, 123.85, 127.61, 130.23, 135.09, 136.05, 142.79, 152.38, 199.39 »¯ºÏÎï2 13C NMR (100 MHz, CDCl3) ¦Ä 11.98, 12.17, 16.87, 18.74, 19.06, 19.80, 21.20, 23.12, 24.16, 26.24, 28.23, 29.23, 29.70, 30.24, 30.90, 32.41, 33.98, 34.60, 36.18, 38.35, 39.98, 40.80, 42.78, 45.90, 45.94, 55.99, 56.21, 67.64, 76.11, 76.13, 77.20 »¯ºÏÎï3 13C NMR (100 MHz, CDCl3) ¦Ä 11.93, 11.96, 14.07, 17.37, 18.69, 19.03, 19.78, 21.04, 22.66, 23.09, 24.17, 26.14, 28.17, 29.20, 29.34, 29.68, 31.91, 32.06, 32.93, 33.90, 33.95, 35.64, 35.70, 36.10, 38.59, 39.64, 42.39, 45.86, 53.84, 55.89, 56.04, 123.74, 123.75, 171.56, 199.51 »¯ºÏÎï4 13C NMR (101 MHz, CDCl3) ¦Ä 11.84, 11.96, 18.76, 19.03, 19.27, 19.79, 21.02, 23.07, 24.27, 26.10, 27.76, 28.22, 29.16, 29.68, 31.84, 31.88, 33.94, 36.14, 36.56, 36.92, 38.06, 39.70, 42.31, 45.84, 50.02, 56.04, 56.68, 73.96, 122.97, 139.30, 160.61 »¯ºÏÎï5 13C NMR (100 MHz, DMSO) ¦Ä 11.65, 11.76, 18.59, 18.91, 19.07, 19.68, 20.56, 22.58, 23.84, 25.43, 27.76, 28.69, 29.25, 31.35, 31.40, 33.33, 35.45, 36.19, 36.81, 38.29, 41.83, 45.12, 49.58, 55.41, 56.15, 61.07, 70.09, 73.45, 76.73, 76.76, 76.89, 100.77, 121.17, 140.43 |
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»¯ºÏÎï1 ²éѯ½á¹û£º¹²²éµ½572¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . quadranoside V C36H56O11 ÏàËÆ¶È:59.4% Journal of Natural Products 2000 63 496-500 Quadranosides I-V, New Triterpene Glucosides from the Seeds of Combretum quadrangulare I Ketut Adnyana, Yasuhiro Tezuka, Arjun H. Banskota, Quanbo Xiong, Kim Qui Tran, and Shigetoshi Kadota Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . kakisaponin C C36H58O10 ÏàËÆ¶È:59.4% Chemical & Pharmaceutical Bulletin 2009 57 532-535 Three Minor Novel Triterpenoids from the Leaves of Diospyros kaki Guang Chen, Zong-Quan Wang and Ji-Ming Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . adociasulfate 3 C36H54O10S2Na2 ÏàËÆ¶È:59.4% The Journal of Organic Chemistry 1999 64 5565-5570 Adociasulfates 1−6, Inhibitors of Kinesin Motor Proteins from the Sponge Haliclona (aka Adocia) sp. Christine L. Blackburn, Cordula Hopmann, Roman Sakowicz, Michael S. Berdelis, Lawrence S. B. Goldstein, and D. John Faulkner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . adociasulfate 6 C36H53O6SNa ÏàËÆ¶È:59.4% The Journal of Organic Chemistry 1999 64 5565-5570 Adociasulfates 1−6, Inhibitors of Kinesin Motor Proteins from the Sponge Haliclona (aka Adocia) sp. Christine L. Blackburn, Cordula Hopmann, Roman Sakowicz, Michael S. Berdelis, Lawrence S. B. Goldstein, and D. John Faulkner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Feroniellide E C35H56O6 ÏàËÆ¶È:59.4% Natural Product Research 2013 27 753-760 Feroniellides C-E, new apotirucallane triterpenoids from the stem bark of Feroniella lucida Preecha Phuwapraisirisan, Sitthidesch Sombund, Santi Tip-pyang & Pongpun Siripong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . cumingianoside B C38H64O11 ÏàËÆ¶È:57.8% The Journal of Organic Chemistry 1992 57 6946-6953 Anti-tumor agents. 136. Cumingianosides A-F, potent antileukemic new triterpene glucosides, and cumindysosides A and B, trisnor- and tetranortriterpene glucosides with a 14,18-cycloapoeuphane-type skeleton from Dysoxylum cumingianum Yoshiki Kashiwada, Toshihiro Fujioka, Jer Jang Chang, Ih Sheng Chen, Kunihide Mihashi, Kuo Hsiung Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . pittoviridagenin C40H62O8 ÏàËÆ¶È:57.5% Journal of Natural Products 2002 65 65-68 A New Triterpene Saponin from Pittosporum viridiflorum from the Madagascar Rainforest1 Youngwan Seo,John M. Berger, Jeannine Hoch, Kim M. Neddermann, Isia Bursuker,Steven W. Mamber, and David G. I. Kingston Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-epi-29-acetoxystelliferin E C36H52O7 ÏàËÆ¶È:56.7% Journal of Natural Products 2006 69(3) 373-376 Bioactive Isomalabaricane Triterpenoids from Rhabdastrella globostellata that Stabilize the Binding of DNA Polymerase ¦Â to DNA Jason A. Clement, Mei Li, Sidney M. Hecht, and David G. I. Kingston Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . stelliferin G C32H48O5 ÏàËÆ¶È:56.7% Journal of Natural Products 2001 64 389-392 New Cytotoxic Isomalabaricane Triterpenes from the Sponge Jaspis Species Karina M. Meragelman, Tawnya C. McKee, and Michael R. Boyd Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-epi-29-hydroxystelliferin E C34H50O6 ÏàËÆ¶È:56.7% Journal of Natural Products 2000 63 205-209 New Isomalabaricane Triterpenes from the Marine Sponge Stelletta globostellata That Induce Morphological Changes in Rat Fibroblasts1 Naoya Oku, Shigeki Matsunaga, Shun-ichi Wada, Shugo Watabe, and Nobuhiro Fusetani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 1b ÏàËÆ¶È:56.7% Chinese Chemical Letters 2005 16 867-870 Synthesis of Boswellic Acid Derivatives and Primary Research on their Activities Yan Qiu MENG, Lin Xiang ZHAO, Zan WANG, Dan LIU, Yong Kui JING Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-O-¦Â-D-glucopyranosylpyrocincholate C35H56O8 ÏàËÆ¶È:56.7% Journal of Asian Natural Products Research 2007 9 505-510 27-Nor-triterpenoid glycosides from the barks of Zygophyllum fabago L YU-LIN FENG, HE-RAN LI, LI-ZHEN XU and SHI-LIN YANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 22-O-angeloyltheasapogenol B C35H58O6 ÏàËÆ¶È:56.7% China Journal of Chinese Materia Medica 1997 22 228-230 Studies on the Chemical Constituents of Seeds of Camellia sinensis var. Assamica Wei J unxian , Zuo Qunying and Zhu Yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . l¦Á,7¦Á-diacetoxyapotirucall-14-ene-3¦Á,21,22,24,25-pentaol C34H56O9 ÏàËÆ¶È:56.7% Fitoterapia 2000 71 668-672 A new triterpenoid from Azadirachta indica Xiao-Dong Luo, Shao-Hua Wu, Yun-Bao Ma,Da-Gang Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 24-ethyllanosta-8,24(24')-diene-3¦Â,22-diol C32H54O2 ÏàËÆ¶È:56.7% Phytochemistry 1997 45 499-504 Triterpenoids from Pisolithus tinctorius isolates and ectomycorrhizas Alfred Baumert, Brigitte Schumann, Andrea Porzel, J¨¹rgen Schmidt, Dieter Strack Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . sigmoside C C36H60O8 ÏàËÆ¶È:56.7% Phytochemistry 1997 44 1151-1155 Triterpenoid saponins from Erythrina sigmoidea J. Tanyi Mbafor, Jean-Claude Ndom, Z. Tanee Fomum Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . isomultiflorenyl acetate ÏàËÆ¶È:56.7% Journal of Natural Products 1991 Vol 54 1564 Application of Inverse-Detected Two-Dimensional Heteronuclear-Correlated Nmr Spectroscopy to the Complete Carbon- 13 Assignment of Isomultiflorenyl Acetate Robert Faure, Emile M. Gaydou, Eckhard Wollenweber Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Carpesterol C37H54O4 ÏàËÆ¶È:56.7% Phytochemistry 1996 41 935-939 A neolignan and sterols in fruits of Solanum sisymbrifolium Ajit Kumar Chakravarty, Sibabrata Mukhopadhyay, Subrata Saha, Satyesh Chandra Pakrashi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . cis-karenin C39H54O6 ÏàËÆ¶È:56.7% Phytochemistry 1995 39 171-174 Two cytotoxic pentacyclic triterpenoids from Nerium oleander Bina Shaheen Siddiqui, Sabira Begum, Salimuzzaman Siddiqui, Wolf Lichter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . trans-karenin C39H54O6 ÏàËÆ¶È:56.7% Phytochemistry 1995 39 171-174 Two cytotoxic pentacyclic triterpenoids from Nerium oleander Bina Shaheen Siddiqui, Sabira Begum, Salimuzzaman Siddiqui, Wolf Lichter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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»¯ºÏÎï2 ²éѯ½á¹û£º¹²²éµ½15011¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . stigmastane-3¦Â5,6¦Á-triol ÏàËÆ¶È:90.3% Natural Product Research and Development 2000 12(5) 14-16 STEROID CONSTITUENTS FROM EUONYMUS MUPINENSIS Mao Shilong; Sang Shengmin; Lao Aina and Chen Zhongliang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Á-Spinasterol C29H52O3 ÏàËÆ¶È:90.3% Natural Product Research and Development 2011 23 1002-1005 Chemical Constituents from Hypoxis aurea Lour. CHENG, Zhong-quan, YANG, Dan, MA, Qing-yun, LIU, Yu-qing, ZHOU, Jun, ZHAO, You-xing, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 3b ÏàËÆ¶È:87.0% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol ÏàËÆ¶È:87.0% China Journal of Chinese Materia Medica 2008 33 1035-1038 Study on Steroids of Cacalia tangutica LIU Qing, LIU Zhenling, TIAN Xuan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:87.0% Journal of Natural Products 1991 Vol 54 1570 3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 5¦Á,6¦Â-Dihydroxysitosterol ÏàËÆ¶È:87.0% Korean Journal of Pharmacognosy 2008 39(3) 186-193 Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5,6-epoxystigmastan-3-ol C29H50O2 ÏàËÆ¶È:87.0% Chinese Traditional and Herbal Drugs 2005 36 1142-1144 ÇåÏãľ½ª×ӵĻ¯Ñ§³É·ÖÑо¿ ФÓÂ,Öܺ콿,ÑòÏþ¶«,ÕÔ¾²·å,»ÆÈÙ,ÀîÁ¼ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â,5¦Á,6¦Â-ÈýôÇ»ù¶¹çÞÍé ÏàËÆ¶È:87.0% Chinese Traditional and Herbal Drugs 2010 41 1782-1785 ¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿ ÕÅΰ;ËÎÆôʾ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:87.0% Chinese Pharmaceutical Journal 2008 43 897-899 Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook WANG Yuan, ZOU Zhong-mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (24S)-24-ethy lcholesta-3¦Â,5¦Á,6¦Â-triol C29H52O3 ÏàËÆ¶È:87.0% Journal of Northwest A&F University (Natural Science) 2011 39 187-189 Studies on the chemical consitituents in Streptocaulon griffithii Hook XI Peng-zhou, QIN Ya-li, WANG Yue-hu, YAN Yong-ming, ZHANG Yue-jin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 24-methylene-27-methylcholestane-3¦Â,5R,6¦Â-triol C29H50O3 ÏàËÆ¶È:83.8% Journal of Natural Products 2007 70 1114-1117 Stellettins L and M, Cytotoxic Isomalabaricane-Type Triterpenes, and Sterols from the Marine Sponge Stelletta tenuis Hou-wen Lin,Zeng-lei Wang,Jiu-hong Wu, Ning Shi, Hong-jun Zhang,Wan-sheng Chen,Susan L. Morris-Natschke, and An-Shen Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (24R,6E)-24-ethyl-5¦Á-cholestan-6-hydroximino-3¦Â,5-diol ÏàËÆ¶È:83.8% Chemistry of Natural Compounds 2001 37 351-355 13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES N. V. Kovganko and Yu. G. Chernov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (24R,6E)-24-Ethyl-5¦Á-eholestan-6-hydroximino-3¦Â,5-diol ÏàËÆ¶È:83.8% Chemistry of Natural Compounds 2000 36 189-191 NOVEL SYNTHESIS OF (24R,6E)-24-ETHYLCHOLEST-6-HYDROXYIMINO-4-EN-3-ONE, A STEROIDAL OXIME FROM Cinachyrella spp. SPONGES N. B. Kovganko and Yu. G. Chernov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 5¦Á,6¦Â-dihydroxysitosterol C29H52O3 ÏàËÆ¶È:83.8% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . stigmastanol glucoside ÏàËÆ¶È:83.8% Fitoterapia 2000 71 722-724 New constituents from Gliricidia sepium H.M.T.B. Herath, Susila deSilva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 5-hydroxy,6-chloro-sitosterol ÏàËÆ¶È:83.8% Phytochemistry 1998 47 789-797 On the cytotoxity of oxidized phytosterols isolated from photoautotrophic cell cultures of Chenopodium rubrum tested on meal-worms Tenebrio molitor Werner Meyer, Harald Jungnickel, Markus Jandke, Konrad Dettner, Gerhard Spiteller Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (24R)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:83.8% Journal of Natural Products 1991 Vol 54 1570 3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Âó½ÇçÞ-3¦Â,5¦Á,6¦Â-Èý´¼ ÏàËÆ¶È:83.8% Chinese Journal of Marine Drugs 2010 29(2) 6-9 Secondary metabolites from marine actinomycete Strep tomyces sp. ( No. 172221) MA Jing-jing, T ANG Jin-shan, GAO Hao, HONG Kui, ZHOU Guang-xiong, YAO Xin-sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (24S)-stigmast-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:83.8% Chinese Traditional and Herbal Drugs 2010 41 1065-1068 СҶÈ̶¬ÌٵĻ¯Ñ§³É·ÖÑо¿ Áõΰ;°×ËØÆ½;Áº»á¾ê;Ô¬ÓÀÁÁ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . (24R)-stigmastan-3¦Â,5¦Á,6¦Â-triol 3-O-¦Â-D-glucopyranoside C32H62O8 ÏàËÆ¶È:82.8% Journal of China Pharmaceutical University 2006 37 491-493 A new steroidal glycoside from Lygodium japonicum ZHANG Lei-hong; FAN Chun-lin; ZHANG Xian-tao; YIN Zhiqi; YE Wen-cai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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»¯ºÏÎï3 ²éѯ½á¹û£º¹²²éµ½6396¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . stigmastane-3¦Â,6¦Á-diyl C33H56O4 ÏàËÆ¶È:77.1% Chemical & Pharmaceutical Bulletin 1995 43 1813-1817 Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM. Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . poriferastane-3¦Â,6¦Á-diyl diacetates C33H56O4 ÏàËÆ¶È:77.1% Chemical & Pharmaceutical Bulletin 1995 43 1813-1817 Structures of Five Hydroxylated Sterols from the Seeds of Trichosanthes kirilowii MAXIM. Yumiro KIMURA,Toshihiko AKIHISA,Ken YASUKAWA,Michio TAKIDO and Toshitake TAMURA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 24-Hydroxy-5¦Á-cholestan-3-one C29H46O2 ÏàËÆ¶È:75% Steroids 2002 67 291-304 The synthesis of spermine analogs of the shark aminosterol squalamine Youheng Shu, Stephen R. Jones, William A. Kinney, Barry S. Selinsky Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Dispiro[cyclohexan-2'-oxiran-3',3''-(2¦Â,3¦Â-dihydro-cyclopropa[3,4]cholestan)] C34H56O ÏàËÆ¶È:74.2% Helvetica Chimica Acta 1976 59 2821-2829 ¦Ã-Lakton-cis-anellierung an ¦¤2-und ¦¤3-Cholesten Reinhard Dammann, Manfred Braun and Dieter Seebach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ethyl (24R)-24-methylcholestan-3¦Â-ol-26-oate ÏàËÆ¶È:72.2% Chemistry of Natural Compounds 2012 48 606-609 Synthesis of [26-2H3]-campesterin and [26-2H3]-campestanol, deuterated analogs of biosynthetic precursors of 28C-brassinosteroids V. A. Khripach, V. N. Zhabinskii, Yu. V. Ermolovich and O. V. Gulyakevich Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . vignasterol A C38H56O4 ÏàËÆ¶È:72.2% International Journal of Molecular Sciences 2012 13 9754-9768 Constituents from Vigna vexillata and Their Anti-Inflammatory Activity Yann-Lii Leu, Tsong-Long Hwang, Ping-Chung Kuo, Kun-Pei Liou, Bow-Shin Huang and Guo-Feng Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Vignasterol A C38H56O4 ÏàËÆ¶È:72.2% International Journal of Molecular Sciences 2012 13 9754-9768 Constituents from Vigna vexillata and Their Anti-Inflammatory Activity Yann-Lii Leu, Tsong-Long Hwang, Ping-Chung Kuo, Kun-Pei Liou, Bow-Shin Huang and Guo-Feng Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 24-methylenecholesterol palmitate C44H76O2 ÏàËÆ¶È:71.4% Phytochemistry 2008 69 2061-2066 Antioxidant constituents of Nymphaea caerulea flowers Vijai K. Agnihotri, Hala N. ElSohly, Shabana I. Khan, Troy J. Smillie, Ikhlas A. Khan, Larry A. Walker Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . riisein B C36H60O10 ÏàËÆ¶È:71.4% Journal of Natural Products 2000 63 1427-1430 New Cytotoxic Sterol Glycosides from the Octocoral Carijoa (Telesto) riisei Lenize F. Maia, Rosangela de A. Epifanio, and William Fenical Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 24-Amino-5¦Á-cholestan-3-one ÏàËÆ¶È:71.4% Steroids 2002 67 291-304 The synthesis of spermine analogs of the shark aminosterol squalamine Youheng Shu, Stephen R. Jones, William A. Kinney, Barry S. Selinsky Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Di-tert-butyl 4-(2-tert-butoxycarbonylethyl)-4-[3-(5¦Á-cholestan-3¦Á-yl)ureido]heptanedioate C50H88N2O7 ÏàËÆ¶È:71.4% Steroids 2007 72 615-626 Synthesis and antimicrobial evaluation of water-soluble, dendritic derivatives of epimeric 5¦Á-cholestan-3-amines and 5¦Á-cholestan-3-yl aminoethanoates Eko W. Sugandhi, Carla Slebodnick, Joseph O. Falkinham III, Richard D. Gandour Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . ethylpavlovol ÏàËÆ¶È:71.4% Fitoterapia 2005 76 433-438 A new dihydroxysterol from the marine phytoplankton Diacronema sp. Am¨¦lia P. Rauter, Manuela M. Filipe, Carla Prata,João P. Noronha, Maria A.M. Sampayo,Jorge Justino,Jaime Bermejo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 2b C56H62O5 ÏàËÆ¶È:71.4% Phytochemistry 1997 46 729-734 Diterpenes of Bahia glandulosa Ana-L. P¨¦rez-Castorena, Mariano Mart¨ªnez-V¨¢squez, Alfonso Romo de Vivar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (22S,25R)-16¦Â-acetoxy-22,26-N-Cbz-epiminocholest-4-en-3-one C37H51NO5 ÏàËÆ¶È:71.4% Journal of Natural Products 1992 Vol 55 1178 On the Synthesis of 4-Keto-Steroidal Alkaloids Elizabeth Viloria, Gina Meccia, Alfredo N. Usubillaga Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . Dispiro[cyclohexan-2'-oxiran-3',3''-(2¦Â,3¦Â-dihydro-cyclopropa[2,3]cholestan)] C34H56O ÏàËÆ¶È:71.4% Helvetica Chimica Acta 1976 59 2821-2829 ¦Ã-Lakton-cis-anellierung an ¦¤2-und ¦¤3-Cholesten Reinhard Dammann, Manfred Braun and Dieter Seebach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Cordinoic acid C30H44O5 ÏàËÆ¶È:71.4% Chemistry & Biodiversity 2011 Vol.8 850-861 Chemical Constituents of Cordia latifolia and Their Nematicidal Activity Sabira Begum, Sobiya Perwaiz, Bina S. Siddiqui, Shazia Khan, Shahina Fayyaz, and Musarrat Ramzan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 1a C31H32O2 ÏàËÆ¶È:71.4% Phytochemistry 1987 26 753-754 Iridoid glycosides from Penstemon richardsonii Birgit Gering,Peter Junior,Max Wichtl Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . Stigmast-5-en-3-O-¦Â-D-glucoside C35H60O6 ÏàËÆ¶È:71.4% Magnetic Resonance in Chemistry 2001 39 399-405 Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 24 ¦Î-n-propyl-cholestan-3-one ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 2010 41 195-197 ºÚÀÏ»¢¸ù»¯Ñ§³É·ÖµÄÑо¿ Íõéª;ÀîÕ¼ÁÖ;»ª»áÃ÷ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ethylpavlovol ÏàËÆ¶È:71.4% Lipids 1993 28 771-773 Identification of two novel dihydroxysterols fromPavlova Gleen W. Patterson, Patricia K. Gladu, Gary H. Wikfors, Edward J. Parish and Peter D. Livant, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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»¯ºÏÎï4 ½¨Ò飺ÒÔºóÇóÖú ҪÿÌûÇóÖúÒ»¸ö 8¸ö½ð±ÒÒÔÉÏ ÇÒÔÚ Î¢Ì¼Æ×רÀ¸ÇóÖú ²éѯ½á¹û£º¹²²éµ½12891¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Sitost-5-en-3¦Â-ol acetate C31H52O2 ÏàËÆ¶È:93.5% Steroids 2005 70 886-895 Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¡÷5'-3¦Â-OAc (Sitosterol ) ÏàËÆ¶È:93.5% Phytochemistry 1989 28 1721-1724 Acylglucosyl sterols from Momordica charantia Amelia P. Guevara,Clara Y. Lim-Sylianco,Fabian M. Dayrit,Paul Finch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . stigmast-5-ene-3¦Â-yl formate C30H50O2 ÏàËÆ¶È:93.5% Journal of Asian Natural products Research 2010 12 424-428 New cytotoxic steroids from the fruits of Syzygium siamense Parinuch Chumkaew; Shigeru Kato; Kan Chantrapromma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosteryl acetate ÏàËÆ¶È:93.5% Chemical Communications 1978 319-320 Biosynthesis of ¦Â-sitosterol from [4-13C]mevalonic acid and sodium [1, 2-13C]acetate in tissue cultures of Isodon japonicus hara Shujiro Seo, Yutaka Tomita and Kazuo Tori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Â-Sitosteryl acetate ÏàËÆ¶È:93.5% 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 6 . ¦Â-Sitosterol acetate C31H52O2 ÏàËÆ¶È:93.5% Journal of Chinese Pharmaceutical Sciences 2012 21 428-434 Chemical constituents of Pseudolarix kaempferi Gord Tianzhi Cai; Wen Qi; Lianmei Yang; Guangzhong Tu; Rong Yang; Kehui Xie; Hongzheng Fu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â-(acetyloxy)stigmast-5-ene ÏàËÆ¶È:93.5% Yakugaku Zasshi 1991 111 299-305 Studies on the Anticomplementary Activity of Jozann. Antlcomplementary Activity of Steroid Derivatives Tsuyoshi EBIHARA, Tomoko KAWAI, Masanori KUROYANAGI, Seigo FUKUSHIMA, Akira UENO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 2 ÏàËÆ¶È:90.3% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 1a C31H32O2 ÏàËÆ¶È:90.3% Phytochemistry 1987 26 753-754 Iridoid glycosides from Penstemon richardsonii Birgit Gering,Peter Junior,Max Wichtl Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-Sitosterol acetate ÏàËÆ¶È:90.3% Archives of Pharmacal Research 2005 28 1135-1141 Inhibitory effect on TNF-¦Á-induced IL-8 production in the HT29 cell of constituents from the leaf and stem ofWeigela subsessilis Phuong Thien Thuong, WenYi Jin, JongPill Lee, RackSeon Seong and Young-Mi Lee, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 4-methoxy1,2-dihydrocyclobutabenzene C9H10O ÏàËÆ¶È:90.3% Journal of Plant Resources and Environment 2011 20 94-96 ÒæÖÇÈʵĻ¯Ñ§³É·Ö Û¡, ÀÚ, ÍõÖÎÔª, Íõ, Ö¾, Àî, Äþ, Íõ¿ª½ð Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 3 ÏàËÆ¶È:90.3% Chinese Journal of Antibiotics 1998 23 401-463 ¶¾Á¦³æÃ¹EB-82 ÃðÑÁ¾ú·¢½Í²úÎïµÄÓÐЧ³É·ÖÑо¿¢ñ. ÃðÑÁ¾úËØA µÄ·ÖÀëºÍ½á¹¹¼ø¶¨ Íõº£Ñà, ÐíºèÕ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol acetate ÏàËÆ¶È:87.0% Chinese Pharmaceutical Journal 2008 43 897-899 Study on Steroids from the Stem of Croton caudatus Geisel.var.tomentosus Hook WANG Yuan, ZOU Zhong-mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . [(13)C,24,28-(2)H2]clionasteryl acetate ÏàËÆ¶È:87.0% Journal of the Chemical Society, Perkin Transactions 1 1990 105-109 Biosynthesis of isofucosterol from [2-13C2H3]acetate and [1,2-13C2]acetate in tissue cultures of Physalis peruviana−the stereochemistry of the hydride shift from C-24 to C-25 Shujiro Seo, Atsuko Uomori, Yohko Yoshimura, Haruo Seto, Yutaka Ebizuka, Hiroshi Noguchi, Ushio Sankawa and Ken'ichi Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound Ia C29H50O ÏàËÆ¶È:87.0% Journal of Chemical Sciences 2005 117 263-266 ¦Â-Sitosterol-3-O-¦Â-D-xylopyranoside from the flowers of Tridax procumbens Linn. V K SAXENA and SOSANNA ALBERT Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-sitosterol benzoate ÏàËÆ¶È:84.8% Planta Medica 1988 54 223-224 Antihepatotoxic Principles of Sambucus formosana Chun-Nan Lin and Whey-Pin Tome Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ¦Â-sitosterol-3-O-¦Â-D-xylopyranoside C34H58O5 ÏàËÆ¶È:84.8% Chinese Pharmaceutical Journal 1997 32 8-11 Chemical constituents from the seeds of Cuscuta australis Guo Cheng(Guo C), Han Gongyu(Han GY), Su Zhongwu(Su ZW) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . ¦Â-sitosterol ÏàËÆ¶È:83.8% Natural Product Sciences 1996 2 19-23 Sterols and Sterol Glycosides from the Leaves of Gynura procumbens Sadikun, A.; Aminah, I.; Ismail, N.; Ibrahim, P. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . ¦Â-sitosterol ÏàËÆ¶È:83.8% Chinese Traditional and Herbal Drugs 2009 40 1015-1018 Chemical constituents in Tridax procumbens XU Run-sheng; YUAN Ke; YIN Ming-wen; FANG Lei-jie; MAO Nong-nong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-sitosterol ÏàËÆ¶È:83.8% Journal of Shenyang Pharmaceutical University 2010 27 615-617 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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5 ²éѯ½á¹û£º¹²²éµ½6608¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:100% Korean Journal of Pharmacognosy 1996 27(1) 75-79 Phytochemical Constituents from Aconitum pseudolaeve Var. erectum Kim, Dae-Keun; Kwak, Jong-Hwan; Song, Ki-Won; Kwon, Hack-Cheol; Zee, Ok-Pyo; Lee, Kang-Ro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-Sitosterol-3-O-¦Â-D-glycoside ÏàËÆ¶È:100% Archives of Pharmacal Research 2004 27 1016-1019 A new sesquiterpene lactone from Artemisia rubripes nakai Kyu Ha Lee, Yong Deuk Min, Sang Zin Choi, Hak Cheol Kwon and Ock Ryun Cho, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Â-Sitosterol-3-O-glucoside ÏàËÆ¶È:100% Archives of Pharmacal Research 2005 28 39-43 Antitumor and antiinflammatory constituents from celtis sinensis Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Stigmast-5-en-3-O-¦Â-D-glucoside C35H60O6 ÏàËÆ¶È:97.1% Magnetic Resonance in Chemistry 2001 39 399-405 Complete 1H and 13C NMR assignments of stigma-5-en-3-O-¦Â-glucoside and its acetyl derivative Shaheen Faizi, Muhammad Ali, Rubeena Saleem, Irfanullah and Sarah Bibi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . daucosterol C35H60O4 ÏàËÆ¶È:97.1% Chinese Journal of Natural Medicines 2006 4 257-259 Chemical Constituents of Sibiraea angustata TAO Ting-Ting; SEI Yasuo; WANG Tian-Zhi; BAI Chuan; CHANG Yan-Bo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:97.1% Archives of Pharmacal Research 2002 25 628-635 Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-daucosterol ÏàËÆ¶È:97.1% Chinese Pharmaceutical Journal 2011 46 341-343 Chemical Constituents of Lysimachia clethroides Duby YUE Shu-mei, CHEN Bai-quan, YUAN Peng-fei, CUI Wei-heng, KANG Wen-yi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . daucosterol ÏàËÆ¶È:97.1% Chinese Journal of Medicinal Chemistry 2006 16 303-305 The constituents of Veratrum japonicum Loes. f. ZHOU Jian-xia, KANG Lu, SHEN Zheng-wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . daucosterol C35H60O6 ÏàËÆ¶È:97.1% Journal of Shenyang Pharmaceutical University 2008 25 630-632 Chemical constituents from the fruits of Xanthium sibiricum DAI Ying-hui, CUI Zheng, WANG Dong, LI Jian-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . daucosterol ÏàËÆ¶È:97.1% Natural Product Research and Development 2009 21 784-786 Study on the Chemical Constituents of Fruits of Cannabis Sativa L. SHEN Qian;CAI Guang-ming; HE Gui-xia; DU Fang-lu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . daucosterol ÏàËÆ¶È:97.1% Natural Product Research and Development 2008 20 60-62 Chemical Constituents from the Defatted Seeds of Linum usitatissimum L. SHI Gao-feng; SUN Hao-ran;ZHAO Yan-fang; CHEN Xue-fu; QI Zhi-guo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . daucosterol C35H60O6 ÏàËÆ¶È:97.1% Natural Product Research and Development 1998 10(3) 15-19 CHEMICAL STUDY OF RABDOSIA COETSA Wang Jianzhong; Wang Fengpeng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . daucosterol C35H60O6 ÏàËÆ¶È:97.1% Chinese Traditional and Herbal Drugs 2013 44 133-136 Chemical constituents in roots of Phyllanthus emblica ZHAO Qin, LIANG Rui-jun, ZHANG Yu-jie, HONG Ai-hua, WANG Yi-fei, CEN Ying-zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ¦Â-Sitosterol Glucoside ÏàËÆ¶È:97.1% Journal of Agricultural and Food Chemistry 2010 58 180-186 Bioactive Compounds from Sour Orange Inhibit Colon Cancer Cell Proliferation and Induce Cell Cycle Arrest G. K. Jayaprakasha, Y. Jadegoud, G. A. Nagana Gowda and Bhimanagouda S. Patil Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . daucosterol ÏàËÆ¶È:97.1% Chinese Traditional and Herbal Drugs 2012 43 1905-1909 Resource chemical constituents from sarcocarp of Ziziphus jujuba var. spinosa GUO Sheng; DUAN Jin-ao; ZHAO Jin-long; QIAN Ye-fei; TANG Yu-ping; QIAN Da-wei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Â-ºúÂܲ·ÜÕ ÏàËÆ¶È:97.1% China Journal of Chinese Materia Medica 2012 37 1408-1411 ¦Á-glucosidase inhibitory active constituents contained in nutshell of Trapa acornis CHEN Baiquan; ZHANG Qian; WANG Wei; HUANG Huan; KANG Wenyi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 7¦Â-hydroxysitosterol-3-O-¦Â-D-glucoside ÏàËÆ¶È:97.1% Lishizhen Medicine and Materia Medica Research 2012 23 1-2 Chemical Constituents from Angiopteris Fokiensis WEN Xiao-qiong; HU Ying; ZENG Xiao-jun; ZHANG Lei; CEN Ying-zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . daucosterol C35H60O6 ÏàËÆ¶È:97.1% Natural Product Research and Development 2011 23 404-409 Chemical Constituents from Acorus tatarinowii TONG, Xiao-gang, CHENG, Yong-xian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . daucosterol ÏàËÆ¶È:97.1% Marine Sciences 2009 33 81-86 Chemical constituents of EN-22, an endophytic fungus derived from the marine red alga Polysiphonia urceolata ZHAO Ting-ting, LI Xiao-ming, LI Jing-mei, LI Ke, CUI Chuan-ming, LI Chun-shun, WANG Bin-gui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-Sitosterol ¦Â-D-glucopyranoside ÏàËÆ¶È:97.0% Korean Journal of Pharmacognosy 2007 38(4) 354-357 Isolation of Two Steroids and a Triterpenoid from the Roots of Potentilla discolor Park, Hee-Juhn; Lee, Kyung-Tae; Park, Jong-Hee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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