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²éѯ½á¹û£º¹²²éµ½1493¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (+)-norboldine acetate ÏàËÆ¶È:70% Natural Product Communications 2009 4 43-46 Alkaloids from Lindera aggregata Li-She Gan, Wei Yao, Jian-Xia Mo and Chang-Xin Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 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Nichols and Stephanie Kidd, Marcel Hadorn and Franz Baumberger Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . cycloolivil ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 2009 34 1225-1227 Lignans from stems of Sambucus williamsii OUY ANG Fu, LIU Yuan, XI AO Huihui, YU Haiyang, WANG Naili, YAO Xinsheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . norboldine ÏàËÆ¶È:65% Phytochemistry 1993 32 897-903 Unusual methyl transfer in the biosynthesis of aporphine and protoberberine alkaloids Bernd Schneider, Meinhart H. Zenk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (Z)-3'-Amino-5,6,7,4'-tetramethoxy-aurone C19H19NO6 ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2012 20 1231-1239 Influence of the skeleton on the cytotoxicity of flavonoids Guy Lewin,Genevi¨¨ve Aubert,Sylviane Thoret,Joëlle Dubois,Thierry Cresteil Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . norboldine ÏàËÆ¶È:65% Phytochemistry 1989 28 1083-1086 (S)-norcoclaurine is the central intermediate in benzylisoquinoline alkaloid biosynthesis Richard Stadler,Toni M. Kutchan,Meinhart H. Zenk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . coryternatines B C20H21NO6 ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry Letters 2010 20 4487-4490 Benzylisoquinoline alkaloids from the tubers of Corydalis ternata and their cytotoxicity Ki Hyun Kim, Il Kyun Lee, Cheng Jie Piao, Sang Un Choi, Jei Hyun Lee, Yeong Shik Kim, Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 8-O-4-Dehydrodiferulic Acid C20H18O8 ÏàËÆ¶È:65% Chemistry of Natural Compounds 2010 46 499-501 Triterpene saponins and other constituents from Fatsia japonica Hak-Ju Lee, Hyun-Jung Lee, Kyoungtae Lee, Ha-Young Kang and Dongho Lee, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . ((8R,8'S)-7-(4-hydroxy-3-methoxyphenyl)-8'-methylbutan-8-yl)-3'-methoxybenzene-4',5'-diol C19H24O5 ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry Letters 2011 21 6884-6887 Inhibitory effect on NO production of phenolic compounds from Myristica fragrans To Dao Cuong, Tran Manh Hung, MinKyun Na, Do Thi Ha, Jin Cheol Kim, Dongho Lee, SungWoo Ryoo, Jeong Hyung Lee, Jae Sue Choi, Byung Sun Min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . laurolitsine C18H19NO4 ÏàËÆ¶È:65% Journal of the Chinese Chemical Society 1992 39 189-194 Isoquinoline Alkaloids from Neolitsea Konishii Àîˮʢ(Shoei-Sheng Lee);—îÐн¡(Hsih-Chin Yang) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . stepholidine C19H21NO4 ÏàËÆ¶È:65% Journal of Pharmacy and Pharmacology 2006 58 695-700 Acetylcholinesterase inhibitors from Stephania venosa tuber Kornkanok Ingkaninan, Preeda Phengpa, Supreeya Yuenyongsawad and Nantaka Khorana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 6-amino-11-(3,4,5-trimethoxyphenyl)-11,12-dihydropyrido[3,4-c][1,9]phenanthroline C24H22N4O3 ÏàËÆ¶È:65% Tetrahedron 2012 68 9105-9112 Synthesis and physicochemical characterization of novel 6-aminopyrido[3,4-c][1,9]phenanthrolines as aza-analogs of benzo[c]phenanthridines Christopher Meier, Joscha Kotthaus, Lars Stenzel, Ulrich Girreser, Dieter Heber, Bernd Clement Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (-)-stepholidine ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2013 21 856-868 Asymmetric total synthesis and identification of tetrahydroprotoberberine derivatives as new antipsychotic agents possessing a dopamine D1, D2 and serotonin 5-HT1A multi-action profile Haifeng Sun, Liyuan Zhu, Huicui Yang, Wangke Qian, Lin Guo, Shengbin Zhou, Bo Gao, Zeng Li, Yu Zhou, Hualiang Jiang, Kaixian Chen, Xuechu Zhen, Hong Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (+)-cycloolivil ÏàËÆ¶È:65% Chinese Chemical Letters 2011 22 85-87 A new aryltetrahydronaphthalene lignan from Epimedium brevicornum Hai Zhou Li, Guo Jun Luo, Hong Mei Li, Xiao Lei Li, Rong Tao Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 3-ôÇ»ù-4-¼×Ñõ»ù±½¼×Ëá ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 2012 37 2092-2099 Non-anthraquinones constituents from the roots of Knoxia valerianoides ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 2-demethylcolchifoline C21H23NO7 ÏàËÆ¶È:61.9% Acta Botanica Yunnanica 1999 21(3) 364-368 Alkaloids from the Flowers of Colchicum autumnale HE Hong-Ping,LIU Fu-Chu, HU Lin,ZHU Hong-You Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 4-(5-phenyl-1,3,4-oxadiazol-2-yl-thio)-3-methoxybenzene-1,2-diol ÏàËÆ¶È:61.9% Journal of Heterocyclic Chemistry 2009 46 443-446 A facile electrochemical method for the synthesis of 5-phenyl-1,3,4-oxadiazol-2-ylthio-benzene-1,2-diol derivatives Ali Reza Fakhari,Saied Saeed Hosseiny Davarani,Hamid Ahmar,Kobra Hasheminasab and Hamid Reza Khavasi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . Threo-1-(4-hydroxy-3-methoxyphenyl)-1-methoxy-2-{4-[1-formyl-(E)-vinyl]-2-methoxyphenoxy}-3-propanol C21H24O7 ÏàËÆ¶È:61.9% Journal of Asian Natural products Research 2010 12 874-878 Two new 8-O-4¡ä-type lignans from the stem of Schima superba and their cell growth inhibitory activities against human cancer cell lines Wen Xu; Hui Wang; Guang-Xiong Zhou; Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . balanophonin E C21H24O7 ÏàËÆ¶È:61.9% Molecules 2013 18 10397-10403 Three New Phenolics and Other Constituents from the Seeds of Lithocarpus pachylepis Yong Xie, Guoxu Ma, Hua Wei, Jingquan Yuan, Haifeng Wu, Xiaolei Zhou, Junshan Yang and Xudong Xu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . litseglutine B C20H23NO4 ÏàËÆ¶È:60% Helvetica Chimica Acta 2005 Vol. 88 2523 Two New Aporphine Alkaloids from Litsea glutinosa Jing-Hua Yang, Liang Li, Yun-Song Wang, Jing-Feng Zhao, Hong-Bin Zhang, and Shi-De Luo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 8'-epi-cleomiscosin A C20H18O8 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2004 52(12) 1458-1461 Tyrosinase Inhibitors from Rhododendron collettianum and Their Structure¨CActivity Relationship (SAR) Studies Viqar Uddin AHMAD,Farman ULLAH, Javid HUSSAIN, Umar FAROOQ, Muhammad ZUBAIR,Mahmud Tareq Hassan KHAN, and Muhammad Iqbal CHOUDHARY Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . Compound 2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2001 49(7) 930-931 A Novel Quinoline Alkaloid Possessing a 7-Benzyl Group from the Centipede, Scolopendra subspinipes Naoki NODA,Yuji YASHIKI,Takafumi NAKATANI,Kazumoto MIYAHARA,and Xiao-Ming DU Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . laetanine ÏàËÆ¶È:60% Planta Medica 1998 64 58-62 Alkaloids of Hernandia voyronhi: Chloroquine-Potentiating Activity and Structure Elucidation of Herveline D P. Rasoanaivo, S. Ratsimamanga-Urverg, H. Rafatro, D. Ramanitrahasimbola, G. Palazzino, C. Galeffi and M. Nicoletti Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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