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»¯ºÏÎï1 ²éѯ½á¹û£º¹²²éµ½204¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . angeloyl gomisin H ÏàËÆ¶È:89.2% Natural Product Sciences 2006 12 134-137 Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (R-biar)-12-angeloyloxy-6,7,8,9-tetrahydro-1,2,3,13,14-pentamethoxy-7,8-dimethyl-7-dibenzo[a,c]cyclooctenol C28H36O8 ÏàËÆ¶È:88.8% Journal of Asian Natural Products Research 2012 14 159-164 Two new lignans from Celastrus flagellaris Rupr. Xue-Mei Zhao, Fu-Jiang Guo, Yi-Ming Li & Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Neglschisandrin C C32H36O8 ÏàËÆ¶È:76.6% Molecules 2008 13 1148-1155 Neglschisandrins C-D: Two New Dibenzocyclooctadiene Lignans from Schisandra neglecta Min Chen, Zhihua Liao, Xiumei Xu, Yan Wen, Min Sun, Haoxiang Zhang and Wenhui Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (R-biar)-12-benzoyloxy-6,7,8,9-tetrahydro-1,2,3,13,14-pentamethoxy-7,8-dimethyl-7-dibenzo[a,c]cyclooctenol C30H34O8 ÏàËÆ¶È:75.8% Journal of Asian Natural Products Research 2012 14 159-164 Two new lignans from Celastrus flagellaris Rupr. Xue-Mei Zhao, Fu-Jiang Guo, Yi-Ming Li & Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . gomisin T C23H30O7 ÏàËÆ¶È:73.0% Chemical & Pharmaceutical Bulletin 1988 36 3811-3815 Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . schisandrin C24H32O7 ÏàËÆ¶È:73.0% Natural Product Sciences 2005 11 248-252 Dibenzocyclooctene lignan compounds isolated from the fruits of Schisandra chinensis Baill Piao, LongZhu; Lee, Yu-Joung; PhamPhu, ThanhTruc; Shin, Jae-Kyoon Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . schizandrin ÏàËÆ¶È:73.0% Natural Product Sciences 2006 12 134-137 Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . gomisin T ÏàËÆ¶È:73.0% Tetrahedron Letters 2005 46 8467-8470 Regio- and stereoselective 12-O-demethylation of schizandrin into gomisin T, an important intermediate to gomisin A, by Mortierella sp. (TM-I1104) Hirotoshi Kanatani, Susumu Terabayashi, Shuichi Takeda, Wei Li, Kazuo Koike, Tamotsu Nikaido Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gomisin H ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1980 28 2414-2421 The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 12 ÏàËÆ¶È:69.2% Journal of Asian Natural products Research 2010 12 549-556 Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . methyl schisantherin F ÏàËÆ¶È:67.8% Journal of Natural Products 2009 72 1133-1141 Lignans with Anti-HIV Activity from Schisandra propinqua var. sinensis Xiao-Nian Li, Jian-Xin Pu, Xue Du, Liu-Meng Yang, Hui-Mei An, Chun Lei, Fei He, Xiao Luo, Yong-Tang Zheng,Yang Lu, Wei-Lie Xiao, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . met A-I C22H26O7 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1988 36 2061-2069 Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix. YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 5a C24H28O8 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1988 36 2061-2069 Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix. YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . schizandrin C24H32O7 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1988 36 3811-3815 Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 14 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1988 36 3811-3815 Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . schizandrin ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1978 26 3257-3260 The Constituents of Schizandra chinensis BAILL. The Structures of Two New Lignans, Gomisin N and Tigloylgomisin P YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,ITIRO YOSIOKA and HIROSHI KOBAYASHI Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . schizandrin ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1980 28 2414-2421 The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . gomisin A C23H28O7 ÏàËÆ¶È:65.3% Natural Product Sciences 2005 11 248-252 Dibenzocyclooctene lignan compounds isolated from the fruits of Schisandra chinensis Baill Piao, LongZhu; Lee, Yu-Joung; PhamPhu, ThanhTruc; Shin, Jae-Kyoon Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . gomisin A ÏàËÆ¶È:65.3% Natural Product Sciences 2006 12 134-137 Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . schizandrin ÏàËÆ¶È:65.3% Phytochemistry 1988 27 569-573 A lignan from Schizandra chinensis Yukinobu Ikeya,Heihachiro Taguchi,Hiroshi Mitsuhashi,Shigefumi Takeda,Yoshio Kase,Masaki Aburada Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . schizandrin ÏàËÆ¶È:65.3% Korean Journal of Pharmacognosy 2011 42 233-239 Quantitative Determination of Lignans from Schizandra chinensis by HPLC Koo, Dong-Chil; Suh, Won-Se; Baek, So-Yoon; Shim, Sang-Hee Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (+)-14-tigloylgomisin K3 C28H36O7 ÏàËÆ¶È:64.2% Helvetica Chimica Acta 2008 Vol. 91 1053 Four New Dibenzocyclooctadiene Lignans from Schisandra rubriflora Hong-Mei Li, Yong-Ming Luo, Jian-Xin Pu, Xiao-Nian Li, Chun Lei, Rui-Rui Wang, Yong-Tang Zheng, Han-Dong Sun and Rong-Tao Li Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Neglschisandrin D C30H34O7 ÏàËÆ¶È:64.2% Molecules 2008 13 1148-1155 Neglschisandrins C-D: Two New Dibenzocyclooctadiene Lignans from Schisandra neglecta Min Chen, Zhihua Liao, Xiumei Xu, Yan Wen, Min Sun, Haoxiang Zhang and Wenhui Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 20 C28H38O8 ÏàËÆ¶È:64.2% Journal of Asian Natural products Research 2010 12 549-556 Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . tiegusanin C C30H34O8 ÏàËÆ¶È:63.3% Journal of Natural Products 2009 72 1133-1141 Lignans with Anti-HIV Activity from Schisandra propinqua var. sinensis Xiao-Nian Li, Jian-Xin Pu, Xue Du, Liu-Meng Yang, Hui-Mei An, Chun Lei, Fei He, Xiao Luo, Yong-Tang Zheng,Yang Lu, Wei-Lie Xiao, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 15 C27H36O8 ÏàËÆ¶È:62.9% Journal of Asian Natural products Research 2010 12 549-556 Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . Kadsufolin A C29H38O8 ÏàËÆ¶È:62.0% Helvetica Chimica Acta 2011 94 519-527 Kadsufolins A ¨C D and Related Cytotoxic Lignans from Kadsura oblongifolia Zehao Huang, Yan Lu, Yinan Liu, Kenneth F. Bastow, Kuohsiung Lee and Daofeng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . pyramidatin C ÏàËÆ¶È:61.5% Phytochemistry 2000 55 653-661 Dibenzocyclooctadiene-type lignans from Magnolia pyramidata Qi Song, Frank R. Fronczek, Nikolaus H. Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . gomisin A ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 1990 38 136-141 Studies on the Metabolism of Gomisin A (TJN-101). II. : Structure Determination of Biliary and Urinary Metabolites in Rat Yukinobu IKEYA,Hiroshi MITSUHASHI,Hiromi SASAKI,Yutaka MATSUZAKI,Tamae MATSUZAKI and Eikichi HOSOYA Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . gomisin A ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 1988 36 2061-2069 Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix. YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . met B C22H28O7 ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 1988 36 2061-2069 Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix. YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . gomisin A ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 1980 28 2414-2421 The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (-)-gomisin K1 acetate ÏàËÆ¶È:61.5% Chemical & Pharmaceutical Bulletin 1980 28 2414-2421 The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . isoschizandrin C24H32O7 ÏàËÆ¶È:61.5% Phytochemistry 1988 27 569-573 A lignan from Schizandra chinensis Yukinobu Ikeya,Heihachiro Taguchi,Hiroshi Mitsuhashi,Shigefumi Takeda,Yoshio Kase,Masaki Aburada Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (Sa)-3',4,4',5,5'-pentamethoxy-3-hydroxypyramidatin C23H28O7 ÏàËÆ¶È:61.5% Phytochemistry 2010 71 1787-1795 Dibenzocyclooctadiene lignans from Magnolia and Talauma (Magnoliaceae): Their absolute configuration ascertained by circular dichroism and X-ray crystallography and re-evaluation of previously published pyramidatin structures Wolfgang Sch¨¹hly, Barbara Gröblacher, Judith Neyer, Walter M.F. Fabian, Frank R. Fronczek, Olaf Kunert Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 6 ÏàËÆ¶È:61.5% Journal of Asian Natural products Research 2010 12 549-556 Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . compound 10 ÏàËÆ¶È:61.5% Journal of Asian Natural products Research 2010 12 549-556 Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . gomisin A ÏàËÆ¶È:61.5% Chinese Traditional and Herbal Drugs 2009 40 1707-1710 Îåζ×ÓÌÙ¾¥»¯Ñ§³É·ÖµÄÑо¿ Ê·ÁÕ;ºÎÏþϼ;ÅËÓ¢;º«Áè;ÍõÖ¾³É;ÕÔÓàÇì Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . compound II ÏàËÆ¶È:61.5% Archives of Pharmacal Research 1990 13 278-281 Lingans from Korean red ginseng Bong Hee Huh, Ihn Ran Lee and Byung Hoon Han Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . Kadsufolin B C26H34O8 ÏàËÆ¶È:61.5% Helvetica Chimica Acta 2011 94 519-527 Kadsufolins A ¨C D and Related Cytotoxic Lignans from Kadsura oblongifolia Zehao Huang, Yan Lu, Yinan Liu, Kenneth F. Bastow, Kuohsiung Lee and Daofeng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . gomisin A ÏàËÆ¶È:61.5% Journal of Chinese Medicinal Materials 2009 32 1054-1056 Study on the Chemical Constituents of the Fruit Handles from Schizandra chinensis SHI Lin, HE Xiao-xia, PAN Ying, HAN Ling, YANG Xiao-ou, ZHAO Yu-qing Structure 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï2 ²éѯ½á¹û£º¹²²éµ½61¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . gliotoxin C13H14N2O4S2 ÏàËÆ¶È:92.3% Chinese Pharmaceutical Journal 2011 46 569-575 Antitumor Metabolites from Fungus Aspergillus sydowi D2-6 REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . gliotoxin ÏàËÆ¶È:92.3% Marine Drugs 2014 12 69-87 Gliotoxin Isolated from Marine Fungus Aspergillus sp. Induces Apoptosis of Human Cervical Cancer and Chondrosarcoma Cells Van-Tinh Nguyen, Jung Suck Lee, Zhong-Ji Qian, Yong-Xin Li, Kil-Nam Kim, Soo-Jin Heo, You-Jin Jeon, Won Sun Park, Il-Whan Choi, Jae-Young Je and Won-Kyo Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . gliotoxin C13H14N2O4S2 ÏàËÆ¶È:84.6% Journal of Natural Products 1990 Vol 53 717 Gliotoxin: Uncommon 1H Couplings and Revised 1H- and 13C-nmr Assignments Mourad Kaouadji, Regine Steiman, Françoise Seigle-Murandi, Serge Krivobok, Lucile Sage Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . trans-4-propenylphenol (anol) glucoside ÏàËÆ¶È:58.3% Phytochemistry 2006 67 1029-1033 Clerodanes and other constituents of Cleidion spiciflorum Waree Naengchomnong, Paulo M. Pinho, Anake Kijjoa, Pichan Sawangwong,Maria Jos¨¦ Gonzalez, Artur M.S. Silva, Graham Eaton, Werner Herz Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . tert-butyl [3-(ethoxycarbonyl)phenyl]carbamate C10H11NO4 ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2010 3704-3710 Amination of Aryl Iodides Using a Fluorous-Tagged Ammonia Equivalent Simon Dalsgaard Nielsen, Garrick Smith, Mikael Begtrup and Jesper Langgaard Kristensen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . A26771A C14H16N2O3S2 ÏàËÆ¶È:58.3% Marine Drugs 2012 10 2912-2935 Isolation, Structure Elucidation and Total Synthesis of Lajollamide A from the Marine Fungus Asteromyces cruciatus Tobias A. M. Gulder, Hanna Hong, Jhonny Correa, Ekaterina Egereva, Jutta Wiese, Johannes F. Imhoff and Harald Gross Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . p-bromobenzoate of menisdaurilide C15H11O4Br ÏàËÆ¶È:53.8% Phytochemistry 1993 33 389-392 Butenolides from Sinomenium acutum Hideaki Otsuka, Aiko Ito, Naomi Fujioka, Ken' Ichiro Kawamata, Ryoji Kasai, Kazuo Yamasaki, Tomohiro Satoh Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 11 C21H18F3O9S ÏàËÆ¶È:53.8% Tetrahedron Letters 2001 42 1321-1324 1,6-Anhydro-¦Â-l-hexopyranoses as valuable building blocks toward the synthesis of l-gulosamine and l-altrose derivatives Shang-Cheng Hung, Cheng-Chung Wang, Shu-Wen Chang, Chien-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 19 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 1996 4 1949-1961 Macromolecular recognition: Effect of multivalency in the inhibition of binding of yeast mannan to concanavalin A and pea lectins by mannosylated dendrimers Daniel Pag¨¦, Diana Zanini, Ren¨¦ Roy Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1D-1,4,5-Tri-O-benzoyl-2,3,6-trideoxy-myo-inositol ÏàËÆ¶È:53.8% Journal of the American Chemical Society 1993 115 4429-4434 Synthesis of 1D-3-deoxy-, 1D-2,3-dideoxy-, and 1D-2,3,6-trideoxy-myo-inositol 1,4,5-trisphosphate from quebrachitol, their binding affinities, and calcium release activity A. P. Kozikowski, V. I. Ognyanov, A. H. Fauq, S. R. Nahorski, R. A. Wilcox Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . bisdethiobis(methylthio)gliotoxin C15H20N2O4S2 ÏàËÆ¶È:53.3% Chinese Journal of Marine Drugs 2008 27(4) 14-20 Bioactive alkaloids from sponge-derived actinomyces sh6004 FU Hai-chao, ZHAO Wen-ying, ZHONG Hui-min, HONG Kui, GU Qian-qun, ZHU Wei-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2,2-dimethyl-6-vinylchromene ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2001 49(9) 1207-1209 Isolation and Structures of Two New Compounds from the Essential Oil of Brazilian Propolis Toshihide KUSUMOTO,Tomofumi MIYAMOTO,Ryuichi HIGUCHI,Shima DOI,Hiroyuki SUGIMOTO,and Hideo YAMADA Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 7-benzoyloxy-6-oxo-2,4Z-heptadiene-1,4-olide C14H10O5 ÏàËÆ¶È:50% Phytochemistry 2001 58 1311-1315 Oxidized heptenes from flowers of Melodorum fruticosum Chaiyo Chaichantipyuth, Supachai Tiyaworanan, Somchai Mekaroonreung, Nattaya Ngamrojnavanich, Sophon Roengsumran, Songchan Puthong,Amorn Petsom, Tsutomu Ishikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl 4-(1,1-dimethyl-2-propynyloxy)benzoate ÏàËÆ¶È:50% Journal of Natural Products 2003 66 169-176 Synthesis and Structure−Phytotoxicity Relationships of Acetylenic Phenols and Chromene Metabolites,and Their Analogues, from the Grapevine Pathogen Eutypa lata Leverett R. Smith, Noreen Mahoney, and Russell J. Molyneux Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-phenylaminobenzoate C15H15NO2 ÏàËÆ¶È:50% Molecules 2005 10 226-237 A Survey on the Reactivity of Phenyliodonium Ylide of 2-Hydroxy-1, 4-Naphthoquinone with Amino Compounds Konstantina Spagou, Elizabeth Malamidou-Xenikaki and Spyros Spyroudis Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-(Oxiranecarbonyl-amino)-benzoic acid tert-butyl ester C14H17NO4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 145-155 Investigation of ¦Á-phenylnorstatine and ¦Á-benzylnorstatine as transition state isostere motifs in the search for new BACE-1 inhibitors Fredrik Wångsell, Patrik Nordeman, Jonas Sävmarker, Rikard Emanuelsson, Katarina Jansson,Jimmy Lindberg, Åsa Rosenquist, Bertil Samuelsson, Mats Larhed Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (2S,3R,4E)-2-N-(2'-hydroxytetracosanoyl) octadecasphinga-4-ene ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2003 58b 1128-1132 A New Tetranortriterpenoid from Dysoxylum lenticellatum Shu-Hua Qi, Da-Gang Wu, Si Zhang, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 5 ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 8311-8315 The cooperative effect of electrostatic and hydrophobic forces in the complexation of cationic molecules by a water-soluble resorcin[4]arene derivative Seong Jin Park, Jong-In Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . methyl (Z)-5-(2-fluoro-5-nitrophenyl)-2-pentenoate C12H12FNO4 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2010 47 1176-1182 Ester- and ketone-substituted (¡À)-1-alkyl-6-nitro-1,2,3,4-tetrahydroquinolines by a tandem SNAr-Michael reaction Richard A. Bunce and Eric J. Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 11 C20H21NO2 ÏàËÆ¶È:50% Heterocycles 2005 65 2871-2884 Stereoselective Functionalization of Alkenyl-¦Â-lactams Luigino Troisi,* Emanuela Pindinelli, Luisella De Vitis, Catia Granito, and Ludovico Ronzini Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (E)-4-(2-Ethoxycarbonylvinyl)benzoic acid ethyl ester C14H16O4 ÏàËÆ¶È:50% Molecules 2010 15 315-330 Palladium(II)/Cationic 2,2¡¯-Bipyridyl System as a Highly Efficient and Reusable Catalyst for the Mizoroki-Heck Reaction in Water Shao-Hsien Huang, Jun-Rong Chen and Fu-Yu Tsai Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (2S,5S,6R)-6-(1,3-dioxoisoindolin-2-yl)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid C16H14N2O5S ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2007 45 819-829 Comparison of various density functional methods for distinguishing stereoisomers based on computed 1H or 13C NMR chemical shifts using diastereomeric penam ¦Â-lactams as a test set (pages 819¨C829) Keith W. Wiitala, Christopher J. Cramer and Thomas R. Hoye Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . deoxyradicinol ÏàËÆ¶È:50% Phytochemistry 1985 24 729-731 Phytotoxins from Alternaria helianthi: radicinin, and the structures of deoxyradicinol and radianthin Beni Tal, David J. Robeson, Basil A. Burke, Arne J. Aasen Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (2S,3R,4E)-2-N-(2'-hydroxy-tetracosanoyl)octadecasphinga-4-ene ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2008 39 1606-1609 Chemical constituents of Amtipathes dichotoma SU Guo-chen; ZHANG Si; QI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound ent-7 C14H14NO4 ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 1209-1212 Synthesis of (2R,4R)- and (2S,4S)-4-hydroxypipecolic acid derivatives and (2S,4S)-(− -SS20846AMark Sabat, Carl R Johnson Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . N,N',N''-tris(4-ethoxycarbonylphenyl)-1,3,5-benzenetricarboxamide C36H33N3O9 ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 4717-4720 A new prearranged tripodant ligand N,N',N¡å-trimethyl-N,N',N¡å-tris(3-pyridyl)-1,3,5-benzene tricarboxamide is easily obtained via the N-methyl amide effect Mikkel Jørgensen, Frederik C Krebs Structure 13C NMR ̼Æ×Ä£Äâͼ |

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