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²éѯ½á¹û£º¹²²éµ½3964¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . garcidepsidone C C28H34O8 ÏàËÆ¶È:67.7% Journal of Natural Products 2000 63 1361-1363 Cytotoxic Prenylated Depsidones from Garcinia parvifolia Yuan-Jian Xu,Pui-Yii Chiang, Yee-Hing Lai, J. J. Vittal, Xiao-Hua Wu, B. K. H. Tan,Z. Imiyabir, and Swee-Hock Goh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 17-(N,N-(1-methoxycarbonyl-butan-1,4-diyl)-carboxamido-androst-4,16-diene-3-one C26H35O4N ÏàËÆ¶È:64.7% Steroids 2011 76 280-290 Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation P¨¦ter ¨¢cs, Attila Tak¨¢cs, Merc¨¦desz Kiss, No¨¦mi P¨¢link¨¢s, S¨¢ndor Mah¨®, L¨¢szl¨® Koll¨¢r Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (¡À)-(8¦Â,9¦Â,14¦Á)-N-Methoxycarbonyl-3,11-diaza-17¦Á-vinylgona-1,3,5(10)-trien-13¦Á-o C19H24N2O3 ÏàËÆ¶È:64.5% Steroids 2012 77 157-167 Synthesis and characterization of (¡À)-13-hydroxy-3,11-diaza steroids Malika Ibrahim-Ouali, Eug¨¦nie Romero Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Longipedlactone F C30H38O6 ÏàËÆ¶È:64.5% Tetrahedron 2006 62 6073-6081 Longipedlactones A¨CI, nine novel triterpene dilactones possessing a unique skeleton from Kadsura longipedunculata Jian-Xin Pu, Rong-Tao Li, Wei-Lie Xiao, Ning-Bo Gong, Sheng-Xiong Huang, Yang Lu, Qi-Tai Zheng, Li-Guang Lou, Han-Dong Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . methyl isomariesiate C C31H44O4 ÏàËÆ¶È:64.5% Tetrahedron 1987 43 1775-1784 Further new rearranged lanostanoids from the seeds of Abies mariesii and A. firma Shinichi Hasegawa, Tadayoshi Miura, Nobutada Kaneko, Yoshiyuki Hirose, Yoichi Iitaka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl (1S,4aR,5S,8aS)-5-{2-(2-[N-benzyl-N-(2-methylprop-2-enoyl)aminomethyl]furan-3-yl)-ethyl}-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate {methyl 16-[N-benzyl-N-(2-methylprop-2-enoyl)aminomethyl]-15,16-epoxy-labda-8(17),13(16),14-trien C33H43NO4 ÏàËÆ¶È:64.5% Russian Journal of Organic Chemistry 2008 44 516-523 Synthetic transformations of higher terpenoids: XVII. Intramolecular cyclization of N -furfuryl amides of the labdane series Yu. V. Kharitonov, E. E. Shul¡¯ts, M. M. Shakirov and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 22E,24R-3-acetylstigmasta-5,22-diene-7,11-dione C31H46O3 ÏàËÆ¶È:64.5% Zeitschrift f¨¹r Naturforschung B 2013 68 924-930 Steroids and Ceramide from the Stem Bark of Odyendyea gabonensis Emmanuel Ngeufa Happi, Simone V¨¦ronique Fannang, Marie Fomani, Suzye Mireille Moladje Donkwe, Nkoungou Yomzak Carine Nicaise, Jean Duplex Wansi, and Norbert Sewald Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 27bb C33H38N2O8 ÏàËÆ¶È:64.5% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . amotsangin D C32H40O10 ÏàËÆ¶È:62.5% Journal of Natural Products 2008 71(1) 93-97 Limonoids and Sesquiterpenoids from Amoora tsangii Hua-Dong Chen, Sheng-Ping Yang, Shang-Gao Liao, Bo Zhang, Yan Wu, and Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . methyl ester of globostellatic acid E C35H52O7 ÏàËÆ¶È:62.5% Journal of Natural Products 2000 63 943-946 New Isomalabaricane Derivatives from a New Species of Jaspis Sponge Collected at the Vanuatu Islands Angela Zampella,Maria Valeria D¡¯Auria, C¨¦cile Debitus, and Jean-Louis Menou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . dimethyl abiesonate C32H46O5 ÏàËÆ¶È:62.5% Chemistry of Natural Compounds 1986 22 548-552 TRITERPENOIDS FROM Abies SPECIES. I. ABIESONIC ACID - A TRITERPENOID WITH A NEW CARBON SKELETON FROM THE OLEORESIN OF Abies sibirica V. A. Raldugin, Yu. V. Gatilov,I. Yu. Bagryanskaya, and N. I. Yaroshenko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-cyano-3-[(3'¦Â,17'¦Â)-3'-(acetyloxy)androst-5'-en-17'-yl]-5-(4''-furyl)-(2E,4E)-penta-2,4-dienoicacidamide C31H38N2O4 ÏàËÆ¶È:62.5% Steroids 2013 78 1134-1140 Stereoselective synthesis of novel antiproliferative steroidal (E, E) dienamides through a cascade aldol/cyclization process Bin Yu, Xiao-Nan Sun, Xiao-Jing Shi, Ping-Ping Qi, Yuan Fang, En Zhang, De-Quan Yu, Hong-Min Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 15-veratroyl-17-acetyl-19-oxodictizine C32H41NO3 ÏàËÆ¶È:61.2% Phytochemistry 2005 66 837-846 Norditerpene and diterpene alkaloids from Aconitum variegatum Jes¨²s G. D¨ªaz, Juan Garc¨ªa Ruiza, Werner Herz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . xyloccensin Z2 C31H40O12 ÏàËÆ¶È:61.2% Journal of Natural Products 2006 69 1083-1085 Polyhydroxylated Phragmalins from the Fruit of a Chinese Mangrove, Xylocarpus granatum Yuan Zhou, Fan Cheng, Jun Wu, and Kun Zou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . N6,O',O',O',O'-pentaacetyl-14,15-dihydrohiselosamide C31H39N3O13 ÏàËÆ¶È:61.2% Journal of Natural Products 2002 65 649-655 Investigation of Pictet-Spengler Type Reactions of Secologanin with Histamine and Its Benzyl Derivative Gyula Beke, L¨¢szl¨® F. Szab¨®, and Benjamin Pod¨¢nyi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 11¦Â-hydroxyhomodeoxyharringtonine C29H39NO9 ÏàËÆ¶È:61.2% Journal of Natural Products 1996 59 1192-1195 New Oxygenated Cephalotaxus Alkaloids from Cephalotaxus harringtonia var. drupacea Ichiro Takano, Ichiro Yasuda, and Motohiro Nishijima, Yukio Hitotsuyanagi, Koichi Takeya, and Hideji Itokawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . iyengadione C29H44O2 ÏàËÆ¶È:61.2% Natural Product Research 2002 16 407-413 Steroid and Antibacterial Steroidal Glycosides from Marine Green Alga Codium Iyengarii Borgesen Muhammad Shaiq Ali; Muhammad Saleem; Raghav Yamdagni; Muhammad Ashfaq Ali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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