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1 . 1-O-acetyl-4R,6S-britannilactone C17H24O5 ÏàËÆ¶È:100% Natural Product Sciences 2003 9 28-30 X-Ray Crystallography of New Sesquiterpene Lactone isolated from Inula britannica var.chinensis Han, Ah-Reum; Mar, Woong-Chon; Seo, Eun-Kyoung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 1-O-Acetyl-4R,6S-britannilactone C17H15O5 ÏàËÆ¶È:100% Archives of Pharmacal Research 2004 27 83-85 The inhibitory principle of lipopolysaccharide-induced nitric oxide production from inula britannica var. chinensis Kang-Hoon Je, Ah-Reum Han, Hyun-Tai Lee, Woongchon Mar and Eun-Kyoung Seo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 1-acetoxy-6¦Á-hydroxyeriolanolide C17H24O5 ÏàËÆ¶È:94.1% Phytochemistry 1993 34 1647-1649 Secoeudesmanolides from Inula japonica F. Jeske, S. Huneck, J. Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 1,6-O,O-diacetylbritannilactone C17H22O4 ÏàËÆ¶È:78.9% Phytochemistry 1993 34 249-252 Sesquiterpene lactones from Inula britannica Zhou Bing-Nan, Bai Nai-Sheng, Lin Long-Ze, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 6¦Á-acetoxy-1-hydroxy-4¦ÁH-1,10-secoeudesma-5(10),11(13)-dien-12,8¦Â-olide C17H24O5 ÏàËÆ¶È:64.7% Tetrahedron 2010 66 9379-9388 New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages Jiang-Jiang Qin, Hui-Zi Jin, Jia-Xian Zhu, Jian-Jun Fu, Qi Zeng, Xiang-Rong Cheng, Yan Zhu, Lei Shan, Shou-De Zhang, Yue-Xing Pan, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Cespihypotin Y C20H26O4 ÏàËÆ¶È:60% Helvetica Chimica Acta 2010 93 281-289 Verticillane-Type Diterpenoids and an Eudesmanolide-Type Sesquiterpene from the Formosan Soft Coral Cespitularia hypotentaculata Yu-Chi Lin, Mohamed H. Abd El-Razek and Ya-Ching Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . eupatorone C16H20O4 ÏàËÆ¶È:58.8% Helvetica Chimica Acta 2006 Vol. 89 3104 Cadinene Derivatives from Eupatorium adenophorum Ming-Zhong Wang, Yan-Yan Zhang , Shun-Lin Li, Xiang-Hai Cai, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 2-deoxo-2-(acetyloxy)- 9-oxoageraphorone C17H26O3 ÏàËÆ¶È:58.8% Helvetica Chimica Acta 2006 Vol. 89 3104 Cadinene Derivatives from Eupatorium adenophorum Ming-Zhong Wang, Yan-Yan Zhang , Shun-Lin Li, Xiang-Hai Cai, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . tiomanene C17H25BrO ÏàËÆ¶È:58.8% Phytochemistry 2008 69 2490-2494 Antibacterial activity of halogenated sesquiterpenes from Malaysian Laurencia spp. Charles Santhanaraju Vairappan, Minoru Suzuki,Takahiro Ishii, Tatsufumi Okino,Tsuyoshi Abe,Michio Masuda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (S)-5-Cyclohexyl-3-isopropyl-1H-benzo[e][1,4]diazepin-2(3H)-one C18H24N2O ÏàËÆ¶È:58.8% Bioorganic & Medicinal Chemistry 2011 19 1802-1815 Synthesis and biological evaluation of 1,4-benzodiazepin-2-ones with antitrypanosomal activity John Spencer, Rajendra P. Rathnam, Alan L. Harvey, Carol J. Clements, Rachel L. Clark,Michael P. Barrett, Pui Ee Wong, Louise Male, Simon J. Coles, Simon P. Mackay Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (1R,2R,3R,6R,7S)-1-acetoxy-2,3-dihydroxy-2,3-dihydrobisabolene C17H30O4 ÏàËÆ¶È:58.8% Natural Product Communications 2011 Vol. 6, No. 9 1225-1228 A New Bisabolene from Stevia tomentosa Alejandro Valdez-Calder¨®n, J. Mart¨ªn Torres-Valencia, J. Jes¨²s Manr¨ªquez-Torres, Ren¨¦ Vel¨¢zquez-Jim¨¦nez, Mario A. G¨®mez-Hurtado, Luisa U. Rom¨¢n-Mar¨ªn, Juan D. Hern¨¢ndez-Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2¦Á-acetoxy-7¦Á-hydroxysphaerantholide C15H18O3 ÏàËÆ¶È:58.8% Phytochemistry 1990 29 1213-1217 Carvotacetone derivatives and eudesman-12,6¦Â-olides from Sphaeranthus species J. Jakupovic,M. Grenz,F. Bohlmann,G.M. Mungai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . (6S,7¦Á,8S)-8,15-diacetoxy-14-hydroxymelampa-1(10),4,11(13)-trien-12,6-olide C19H24O7 ÏàËÆ¶È:57.8% Journal of Natural Products 2000 63 305-307 Preparation, Stereochemistry, and Cytotoxic Activity of the Melampolides from Mikania minima Alejandro F. Barrero,J. Enrique Oltra, Ignacio Rodr¨ªguez-Garc¨ªa,Armando Barrag¨¢n, and M¨ªriam Âlvarez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . compound 6 ÏàËÆ¶È:57.8% Tetrahedron Letters 2003 44 2641-2643 A synthetic approach to bicyclo[6.2.1]undecane ring systems Mauricio Gomes Constantino, Kleber Thiago de Oliveira, Adilson Beatriz, Gil Valdo Jos¨¦ da Silva Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (Z)-3,8-Diacetoxy-1,9,14-pentadecatriene-4,6-diyne C19H22O4 ÏàËÆ¶È:57.8% Heterocycles 2011 83 1067-1076 New Antibacterial Polyacetylenes from Sunflower (Helianthus annuus L.) Seedlings Fumie Seshimoto, Si Won Hong, Haruyuki Nakajyo, and Hideyuki Shigemori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . triacetate derivative of Pestalotioprolide A ÏàËÆ¶È:55% Phytochemistry Letters 2012 5 13-17 ¦Á-Pyrone and seiricuprolide derivatives from the mangrove-derived fungi Pestalotiopsis spp. PSU-MA92 and PSU-MA119 Vatcharin Rukachaisirikul,Aekkachai Rodglin,Souwalak Phongpaichit,Jirayu Buatong,Jariya Sakayaroj Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Diacetyl crucigasterin D C20H35NO3 ÏàËÆ¶È:55% Tetrahedron 2010 66 7533-7538 Crucigasterins A¨CE, antimicrobial amino alcohols from the Mediterranean colonial ascidian Pseudodistoma crucigaster M. Letizia Ciavatta, Emiliano Manzo, Genoveffa Nuzzo, Guido Villani, Mario Varcamonti, Margherita Gavagnin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (1R*,3S*,4R*,6S*)-4-(hydroxy)-9-(acetoxy)-1-[(2Z)-2-methyl-but-2-enoyloxy]-bisabol-10(11)-ene or (1R*,2S*,4R*,6S*)-4-(hydroxy)-2-[3-(acetoxy)-1,5-dimethylhex-4-enyl]-5-methyl-cyclohexyl-(2Z)-2-methyl but-2-enoate C22H36O5 ÏàËÆ¶È:54.5% Planta Medica 2004 70 978-985 New Constituents of Leontopodium alpinum and their in vitro Leukotriene Biosynthesis Inhibitory Activity Stefan Schwaiger£¬Michael Adams£¬Christoph Seger£¬Ernst P. Ellmerer£¬Rudolf Bauer£¬Hermann Stuppner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 20c ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2010 18 3656-3667 Hybrids of sugars and aromatics: A Pd-catalyzed modular approach to chromans and isochromans Markus Leibeling, Dennis C. Koester, Martin Pawliczek, Daniel Kratzert, Birger Dittrich, Daniel B. Werz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (1R,2E,4R,5R,7E,10S,11S,12R)-5-acetoxy-10,18-dihydroxy-2,7-dolabelladiene C22H36O4 ÏàËÆ¶È:54.5% Tetrahedron 1997 53 8675-8688 New diterpenoids from the alga Dictyota dichotoma Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 2 C22H24O7 ÏàËÆ¶È:54.5% Phytochemistry 2011 72 265-275 Phytotoxic clerodane diterpenes from Salvia miniata Fernald (Lamiaceae) Angela Bisio, Gianluca Damonte, Daniele Fraternale, Emanuela Giacomelli, Annalisa Salis, Giovanni Romussi, Sergio Cafaggi, Donata Ricci, Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 3¦Â-acetoxy,5¦Á,11,12,13-tetrahydroxyeudesm-4(15)-ene C17H28O6 ÏàËÆ¶È:52.9% Phytochemistry 2002 59 851-856 Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea Ahmed A. Ahmed, Ahmed A. Mahmoud, Eptehal T. Ali, Olga Tzakou,Maria Couladis, Tom J. Mabry, Tam¨¢s G¨¢tid, G¨¢bor T¨®th Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . (1R*,6R*,7S*,10S*)-10-isothiocyanatocadin-4-ene C16H25NS ÏàËÆ¶È:52.9% Journal of Natural Products 2004 67 833-837 Terpene Isocyanides, Isocyanates, and Isothiocyanates from the Okinawan Marine Sponge Stylissa sp. Hidemichi Mitome, Nao Shirato, Hiroaki Miyaoka, Yasuji Yamada, and Rob W. M. van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . (1S*,2S*,5S*,6S*,7R*,8S*)-13-isothiocyanatocubebane C16H25NS ÏàËÆ¶È:52.9% Journal of Natural Products 2004 67 833-837 Terpene Isocyanides, Isocyanates, and Isothiocyanates from the Okinawan Marine Sponge Stylissa sp. Hidemichi Mitome, Nao Shirato, Hiroaki Miyaoka, Yasuji Yamada, and Rob W. M. van Soest Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . semiplenamide E C24H45NO3 ÏàËÆ¶È:52.9% Journal of Natural Products 2003 66 1364-1368 Semiplenamides A-G, Fatty Acid Amides from a Papua New Guinea Collection of the Marine Cyanobacterium Lyngbya semiplena Bingnan Han,Kerry L. McPhail,Alessia Ligresti, Vincenzo Di Marzo, and William H. Gerwick Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . macrophyllic acid e C15H22O3 ÏàËÆ¶È:52.9% Journal of Natural Products 2001 64 466-471 Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . (3e)-6-acetoxy-3,11-dimethyl-7-methylidendodeca-1,3,10-triene C17H26O2 ÏàËÆ¶È:52.9% Journal of Natural Products 2001 64 401-405 New Acyclic Sesquiterpenes and Norsesquiterpenes from the Caribbean Gorgonian Plexaurella grisea Ana Rueda, Eva Zub¨ªa, Mar¨ªa J. Ortega, and Javier Salv¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 3-acetoxy-E-¦Ã-bisabolene C17H26O2 ÏàËÆ¶È:52.9% Journal of Natural Products 1997 60 967-970 Laurencia rigida: Chemical Investigations of Its Antifouling Dichloromethane Extract Gabriele M. König and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 9-Oxo-4(5)¦Á-epoxy-6,7¦Á(H)-eudesm-12,6-olide C15H18O4 ÏàËÆ¶È:52.9% Chemistry of Natural Compounds 2009 45 503-506 EPOXIDATION OF SESQUITERPENE LACTONES TOURNEFORIN AND LUDARTIN R. I. Dzhalmakhanbetova, M. A. Rodichev Yu. V. Gatilov, M. M. Shakirov, G. A. Atazhanova,and S. M. Adekenov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 7,10-diisopropyl-4R,13R-dimethyl-1-oxa-8,9-diaza-7,9-cyclopentadecadien-2-one ÏàËÆ¶È:52.9% Chemistry of Natural Compounds 2009 45 470-473 SYNTHESIS FROM L-MENTHOL OF OPTICALLY ACTIVEMACROLIDES WITH N-CONTAINING(AZINE OR HYDRAZIDE) GROUPS G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva,R. R. Muslukhov, E. M. Vyrypaev, E. G. Galkin,and A. G. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ |
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