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»¯ºÏÎï34£º13C NMR (151 MHz, MeOD) ¦Ä 212.95, 207.96, 153.11, 152.63, 139.33, 137.26, 135.09, 134.42, 128.48, 128.32, 127.35, 127.02, 118.64, 117.31, 53.51, 49.72, 48.59, 47.80, 40.55, 32.15, 31.53, 28.97, 28.75, 28.19, 27.96, 27.94, 24.09, 23.25, 23.20, 23.16, 21.02, 20.94, 20.65, 20.22 лл´óÏÀ£¡ |
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¹ÈÔÆ·É: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл 2015-04-05 11:14:32
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¹ÈÔÆ·É: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл 2015-04-05 11:14:32
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1 . (1R,3aR,4R,5S,7aR)-5-(N-benzyl-N-pent-4-enylami-no)-1-((R)-1,5-dimethylhexyl)-3a,7a-dimethyloctahydroinden-4-ol ÏàËÆ¶È:55.8% Bioorganic & Medicinal Chemistry 2013 21 1925-1943 Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase Mathias König, Christoph M¨¹ller, Franz Bracher Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3,12-Diacetyl-8-nicotinyl-7-phenylacetyl 19-acetoxyingol C40H46O12N ÏàËÆ¶È:54.2% Bioorganic & Medicinal Chemistry 1996 4 1679-1683 New 19-acetoxyingol diterpenes from the latex of Euphorbia poisonii (Euphorbiaceae) Majekodunmi O. Fatope, Lu Zeng, Joseph E. Ohayagha, Jerry L. McLaughlin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (S)-Methyl 2-((2S,3S,Z)-1-((S)-2-benzamido-6-((Z)-2,3-bis(tert-butoxycarbonyl)guanidino)hexanoyl)-4-ethylidene-3-methylpyrrolidine-2-carboxamido)-4-methyl pentanoate C39H60N6O9 ÏàËÆ¶È:54.2% Tetrahedron 2012 68 1918-1925 Rhodium-catalyzed reductive cyclization of 1,6-enynes and stereoselective synthesis of the putative structure of lucentamycin A and its stereoisomers Young Jin Ham, Hana Yu, Nam Doo Kim, Jung-Mi Hah, Khalid B. Selim, Hwan Geun Choi, Taebo Sim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Diaporthalasin C32H39NO3 ÏàËÆ¶È:52.9% Phytochemistry Letters 2014 10 5-9 An antibacterial cytochalasin derivative from the marine-derived fungus Diaporthaceae sp. PSU-SP2/4 Nanthaphong Khamthong, Vatcharin Rukachaisirikul, Souwalak Phongpaichit, Sita Preedanon, Jariya Sakayaroj Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-Hydroxy-1,3,5(10)-estratrien-17¦Â-O,17¦Á-(3' (R/S)-allylbutanolactone C25H32O3 ÏàËÆ¶È:52.6% Steroids 2004 69 325-342 Inhibition of type 2 17¦Â-hydroxysteroid dehydrogenase by estradiol derivatives bearing a lactone on the D-ring: structure¨Cactivity relationships Patrick Bydal, Serge Auger, Donald Poirier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-D-glucoside of ¦Á-spinasterol ÏàËÆ¶È:51.4% Acta Pharmaceutica Sinica 2005 Vol 40 994-996 Isolation and structure identification of the chemical constituents from Gypsophila oldhamiana SUN Jing-yong ZHONG Ying ZUO Chun-xu YIN Jun-ting WANG Bin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . benzyl 2¦Â,3¦Á-Dihydroxyurs-12-en-28-oate C37H54O4 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(11) 1877-1880 Practical Synthesis of Bredemolic Acid, a Natural Inhibitor of Glycogen Phosphorylase Keguang Cheng, Pu Zhang, Jun Liu, Juan Xie, and Hongbin Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . gilvsin B C31H50O4 ÏàËÆ¶È:50% Phytochemistry 2009 70 558-563 Lanostane-triterpenoids from the fungus Phellinus gilvus Hui-Kang Liu, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . gilvsin D C30H48O3 ÏàËÆ¶È:50% Phytochemistry 2009 70 558-563 Lanostane-triterpenoids from the fungus Phellinus gilvus Hui-Kang Liu, Tung-Hu Tsai, Tun-Tschu Chang, Cheng-Jen Chou, Lie-Chwen Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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