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fjamigoгæ (СÓÐÃûÆø)
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̼Æ×£º 21.9, 30.9, 39.5, 39.7, 39.8, 40.6, 41.3, 46.1, 49.1, 50.9, 57.4, 60.4, 79.7, 101.5, 108.3, 110.6, 115, 127.5, 128.1, 130.0, 132.9, 136.0, 145.7, 146.2, 147.6, 149.0, 172.6, |
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²éѯ½á¹û£º¹²²éµ½30¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (1S)-1-[3,4-Dimethoxy-2-(S)-p-tolylsulfinyl]benzyl-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline C26H27NO5S ÏàËÆ¶È:59.2% Tetrahedron 2012 68 1266-1271 Asymmetric synthesis of (S)-(− -tetrahydropalmatine and (S)-(− -canadine via a sulfinyl-directed Pictet¨CSpengler cyclizationVirginia M. Mastranzo, Jos¨¦ Luis Olivares Romero, Francisco Yuste, Benjam¨ªn Ortiz, Rub¨¦n S¨¢nchez-Obreg¨®n, Jos¨¦ L. Garc¨ªa Ruano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 4'-O-demethyl-4¦Â-N-[(5-FU-N1-)-propyl L-phenylalanyl]-4-desoxy-podophyllotoxin C37H36FN3O11 ÏàËÆ¶È:56.2% Bioorganic & Medicinal Chemistry 2009 17 3111-3117 Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents Shi-Wu Chen, Rong Xiang, Jian Liu, Xuan Tian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . bargustanine C29H34N2O7 ÏàËÆ¶È:55.1% Chemistry of Natural Compounds 1996 32 216-334 ALKALOIDS. PLANTS, STRUCTURE, PROPERTIES R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 4'-O-demethyl-4¦Â-N-[(5-FU-N1-)-propyl L-valinyl]-4-desoxy-podophyllotoxin C33H36FN3O11 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2009 17 3111-3117 Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents Shi-Wu Chen, Rong Xiang, Jian Liu, Xuan Tian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 5e C36H31NO8 ÏàËÆ¶È:53.3% Journal of Natural Products 2012 75 1578-1583 Cytotoxic Lignans from Fruits of Cleistanthus indochinensis: Synthesis of Cleistantoxin Derivatives Van Trinh Thi Thanh, Van Cuong Pham, Huong Doan Thi Mai, Marc Litaudon, Françoise Gu¨¦ritte, Pascal Retailleau, Van Hung Nguyen, and Van Minh Chau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . noscomin ÏàËÆ¶È:51.8% Journal of Natural Products 1999 62 502-503 A Novel Extracellular Diterpenoid with Antibacterial Activity from the Cyanobacterium Nostoc commune Birgit Jaki, Jimmy Orjala, and Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . endiandric acid L C26H30O4 ÏàËÆ¶È:51.8% Journal of Natural Products 2011 74 1875-1880 Anti-inflammatory Endiandric Acid Analogues from the Roots of Beilschmiedia tsangii Yun-Ting Huang, Hsun-Shuo Chang, Guei-Jane Wang, Ming-Jen Cheng, O Chu-Huang Chen, Yi-Jen Yang, and Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . endiandramide B C26H33NO3 ÏàËÆ¶È:51.8% Journal of Natural Products 2011 74 1875-1880 Anti-inflammatory Endiandric Acid Analogues from the Roots of Beilschmiedia tsangii Yun-Ting Huang, Hsun-Shuo Chang, Guei-Jane Wang, Ming-Jen Cheng, O Chu-Huang Chen, Yi-Jen Yang, and Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (2S,3S) N-{1-[N-(tertButoxycarbonyl)-(S)-phenylalanyl]-3-ethoxycarbonyl aziridine-2-yl]carbonyl}-(S)-leucyl-(S)-proline C31H44N4O9 ÏàËÆ¶È:51.8% Bioorganic & Medicinal Chemistry 2000 8 1281-1291 aziridinyl peptides as inhibitors of cysteine proteases: Effect of a free carboxylic acid function on inhibition T. Schirmeister, M. Peric Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . N-(4-amino-2,6-diisopropylphenyl)-N'-{[1-[3-(3-hydroxypropoxy)pyridin-2-yl]-4-(3-methoxyphenyl)piperidin-4-yl]methyl}urea dihydrochloride C34H47N5O4 ÏàËÆ¶È:51.8% Bioorganic & Medicinal Chemistry 2009 17 4636-4646 Synthesis and structure¨Cactivity relationships of N-(4-amino-2,6-diisopropylphenyl)-N¡¯-(1,4-diarylpiperidine-4-yl)methylureas as anti-hyperlipidemic agents Shigehiro Asano, Hitoshi Ban, Koichi Kino, Katsuhisa Ioriya, Masami Muraoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . ethyl 1'-(2H-1,3-benzodioxol-5-ylmethyl)-1-benzyl-2,5'-dioxo-1,2-dihydrospiro[indole-3,3'-pyrrolidine]-2'-carboxylate C29H26N2O6 ÏàËÆ¶È:51.8% European Journal of Organic Chemistry 2011 5303-5310 Diastereoselective Access to Tri- and Pentacyclic Spiro--lactam-oxindole Cores through a Tandem Aza-Michael Initiated Ring Closure Sequence Iyad Allous, S¨¦bastien Comesse, Morgane Sanselme and Adam Daïch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 1'-(2H-1,3-benzodioxol-5-ylmethyl)-1-benzyl-2,5'-dioxo-1,2-dihydrospiro[indole-3,3'-pyrrolidine]-2'-carboxylic acid ÏàËÆ¶È:51.8% European Journal of Organic Chemistry 2011 5303-5310 Diastereoselective Access to Tri- and Pentacyclic Spiro--lactam-oxindole Cores through a Tandem Aza-Michael Initiated Ring Closure Sequence Iyad Allous, S¨¦bastien Comesse, Morgane Sanselme and Adam Daïch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 16 C28H29NO7 ÏàËÆ¶È:51.8% Journal of the American Chemical Society 2006 128 10370-10371 Strain-Release Rearrangement of N-Vinyl-2-Arylaziridines. Total Synthesis of the Anti-Leukemia Alkaloid (− -DeoxyharringtonineJoseph D. Eckelbarger, Jeremy T. Wilmot, and David Y. Gin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . compound 3a C32H42N2O10S ÏàËÆ¶È:51.8% Bioorganic & Medicinal Chemistry 2012 20 6285-6295 Synthesis and biological evaluation of a series of podophyllotoxins derivatives as a class of potent antitubulin agents Yingqian Liu, Dongfeng Wei, Yonglong Zhao, Weidong Cheng, Yan Lu, Yaqiong Ma, Xin Li, Chao Han, Yanxia Wei, Huiming Cao, Chunyan Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . bargustanine ÏàËÆ¶È:51.7% Chemistry of Natural Compounds 1993 29 35-38 Berberis ALKALOIDS.XV. STRUCTURE OF BARGUSTANINE A. Karimov, M. M. Yusupov,and R. Shakirov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 14a ÏàËÆ¶È:51.7% Helvetica Chimica Acta 1980 63 1335-1346 Synth¨¨se partielle et propri¨¦t¨¦s oncostatiques des pseudo-tubulosines, analogues de l'¨¦m¨¦tine et de la tubulosine Elisabeth Seguin, Michel Koch, Evelyne Chenu, Marcel Hayat Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 2-trifluoroacetyl-1-(2-bromo-4,5-methylenedioxybenzyl)-7-benzyloxy-5,6-dimethoxy-1,2,3,4-tetrahydroisoquinoline C28H25BrF3NO6 ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 2009 57 368-376 First Total Syntheses of (¡À)-Isopiline, (¡À)-Preocoteine, (¡À)-Oureguattidine and (¡À)-3-Methoxynordomesticine and the Biological Activities of (¡À)-3-Methoxynordomesticine Surachai Nimgirawath, Phansuang Udomputtimekakul, Thongchai Taechowisan, Asawin Wanbanjob and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 8h ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 2009 57 368-376 First Total Syntheses of (¡À)-Isopiline, (¡À)-Preocoteine, (¡À)-Oureguattidine and (¡À)-3-Methoxynordomesticine and the Biological Activities of (¡À)-3-Methoxynordomesticine Surachai Nimgirawath, Phansuang Udomputtimekakul, Thongchai Taechowisan, Asawin Wanbanjob and Yuemao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (Z)-(1R*,5S*)-1,2,3,4,5,6-Hexahydro-7-hydroxy-2-[3,4-dimethoxy-3-methyl-2-[(4-methylphenyl)sulfoxyphenyl]methylene]-9,10-dimethoxy-8-methyl-4-oxo-1,5-imino-3-benzazocine C31H34N2O9S ÏàËÆ¶È:51.7% Tetrahedron 2012 68 4166-4181 Chemistry of renieramycins. Part 12: An improved total synthesis of (¡À)-renieramycin G Original Research Article Masashi Yokoya, Kimiko Shinada-Fujino, Saiko Yoshida, Masahiro Mimura, Hiroki Takada, Naoki Saito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 4'-O-demethyl-4¦Â-N-[(5-FU-N1-)-propyl L-threonyl]-4-desoxy-podophyllotoxin C32H34FN3O12 ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 2009 17 3111-3117 Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents Shi-Wu Chen, Rong Xiang, Jian Liu, Xuan Tian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound XIX ÏàËÆ¶È:51.7% Russian Journal of Organic Chemistry 2005 41 1132-1144 Thebaine Adducts with Maleimides. Synthesis and Transformations E.E. Shults, M.M. Shakirov, G.A. Tolstikov, V.N. Kalinin and G. Schmidhammer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 4'-O-demethyl-4¦Â-N-[(5-FU-N1-)-propyl L-leucyl]-4-desoxy-podophyllotoxin C34H38FN3O11 ÏàËÆ¶È:51.6% Bioorganic & Medicinal Chemistry 2009 17 3111-3117 Synthesis and biological evaluation of novel conjugates of podophyllotoxin and 5-FU as antineoplastic agents Shi-Wu Chen, Rong Xiang, Jian Liu, Xuan Tian Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . cephaeline ÏàËÆ¶È:50% Phytochemistry 1999 52 1169-1176 Ipecac alkaloids from Cephaelis acuminata Atsuko Itoh, Yuki Ikuta, Yoshikazu Baba, Takao Tanahashi, Naotaka Nagakura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . tubulosine C29H37N3O3 ÏàËÆ¶È:50% Journal of Natural Products 1990 Vol 53 1009 Tubulosine: An Antitumor Constituent of Pogonopus speciosus W.-W. Ma, J. E. Anderson, A. T. McKenzie, S. R. Byrn, J. L. McLaughlin, M. S. Hudson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . sculponeatin O C28H40O4 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2009 57 525-527 New Terpenoids from Isodon sculponeata Fei Wang, Xiang-Mei Li and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 8,9-Dimethoxy-3-(7-methyl-2-(4-methylphenyl)-2H-pyrazolo[3,4-d]pyridazin-4-yl)-1-(4-methylphenyl)-1,5,6,10btetrahydro[1,2,4]triazolo[3,4-a]isoquinoline C32H31N7O2 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2011 66 299-310 Synthesis, Reactions and Antibacterial Activity of 3-Acetyl[1,2,4]triazolo[3,4-a]isoquinoline Derivatives using Chitosan as Heterogeneous Catalyst under Microwave Irradiation H. M. Hassaneen, H. M. E. Hassaneen, Y. S. Mohammed, R. M. Pagni Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . (1R*,2S*,5S*)-1,2,3,4,5,6-Hexahydro-7-hydroxy-2-[3,4-dimethoxy-3-methyl-2-[(4-methylphenyl)sulfoxy]-phenyl]methyl]-9,10-dimethoxy-8,11-dimethyl-4-oxo-1,5-imino-3-benzazocine C32H38N2O9S ÏàËÆ¶È:50% Tetrahedron 2012 68 4166-4181 Chemistry of renieramycins. Part 12: An improved total synthesis of (¡À)-renieramycin G Original Research Article Masashi Yokoya, Kimiko Shinada-Fujino, Saiko Yoshida, Masahiro Mimura, Hiroki Takada, Naoki Saito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 3-N-methyl-N-[4-(11¦Â,17¦Â)-17-hydroxy-3-oxo-17¦Á-(1-propynyl)estra-4,9-dien-11-yl]-phenylaminopropionic acid C31H37NO4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 1891-1898 Synthesis, in vitro progesterone receptors affinity of gadolinium containing mifepristone conjugates and estimation of binding sites in human breast cancer cells Pijus Saha, Claudia Hödl, Wolfgang S.L. Strauss, Rudolf Steiner, Walter Goessler, Olaf Kunert, Alexander Leitner, Ernst Haslinger, H. Wolfgang Schramm Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . 4'-O-demethyl-4¦Â-[4''-(4''-fluorobenzoyl)anilino]-4-desoxypodophyllotoxin C34H28FNO8 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 8493-8500 Synthesis of 4¦Â-N-polyaromatic substituted podophyllotoxins: DNA topoisomerase inhibition, anticancer and apoptosis-inducing activities Ahmed Kamal, B. Ashwini Kumar, Paidakula Suresh, Satyam Kumar Agrawal, Gousia Chashoo, Shashank K. Singh, A.K. Saxena Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . secoaconitine C32H43NO9 ÏàËÆ¶È:50% Phytochemistry Letters 2011 4 166-169 Three new C19-diterpenoid alkaloids from Aconitum pendulum Yu-Jie Wang, Jing Zhang, Chen-Juan Zeng, Zhe Yao, Yi Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |

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