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totti8963½ð³æ (³õÈëÎÄ̳)
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΢Æ×ÇóÖú
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| 13C NMR 27.68,49.01,57.05,57.13,62.24,69.24,115.08,118.00,118.29,119.24,126.84,132.01,135.96,136.98,137.15,138.07,150.69,150.97,158.03,158.24. |
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- Ó¦Öú: 105 (¸ßÖÐÉú)
- ½ð±Ò: 2190.7
- É¢½ð: 1870
- ºì»¨: 15
- Ìû×Ó: 538
- ÔÚÏß: 120.8Сʱ
- ³æºÅ: 1337209
- ×¢²á: 2011-07-04
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ

2Â¥2012-07-07 21:04:41
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½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 105 (¸ßÖÐÉú)
- ½ð±Ò: 2190.7
- É¢½ð: 1870
- ºì»¨: 15
- Ìû×Ó: 538
- ÔÚÏß: 120.8Сʱ
- ³æºÅ: 1337209
- ×¢²á: 2011-07-04
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
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totti8963: ½ð±Ò+1, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-07-09 20:21:25
totti8963: ½ð±Ò+1, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-07-09 20:21:25
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1 . taspine C20H19NO6 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1991 39 1041-1042 A Cytotoxic Substance from Sangre de Grado Hideji ITOKAWA,Yoshitatsu ICHIHARA,Miwako MOCHIZUKI,Tamami ENOMORI,Hiroshi MORITA,Osamu SHIROTA,Mutsumi INAMATSU and Koichi TAKEYA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ÒùÑòÞ½¼îA C20H20O6N ÏàËÆ¶È:55% Chemical Journal of Chinese Universities 2003 24 2215-2217 Isolation and Structure Identif ication of the Novel Alkaloid Constituent from Ep imed ium Koreanum Naki LIU Chun-Ming, LIU Zhi-Qiang, DOU Jian-Peng, LI Li, LIU Shu-Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 2-Amino-50 -bromo-20 ,5,10-trioxo-5,10-dihydrospiro[benzo[g] chromene-4,30 -indoline]-3-carbonitrile C21H10BrN3O4 ÏàËÆ¶È:55% Journal of Heterocyclic Chemistry 2009 46 1266-1270 An efficient,three-component synthesis of spiro[benzo[g]chromene-4,3'-indoline]-3-carbonitrile and spiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile derivatives Ramin Ghahremanzadeh,Tayebeh Amanpour and Ayoob Bazgir Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5,6-Dimethoxy-1-(3,4-dimethoxybenzyl)isoquinoline hydrochloride ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 1996 4 781-791 Coralyne and related compounds as mammalian topoisomerase I and topoisomerase II poisons Darshan Makhey, Barbara Gatto, Chiang Yu, Angela Liu, Leroy F. Liu, Edmond J. LaVoie Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (Z)-3-[3-Ethoxy-1-(3,4,5-trimethoxyphenyl)prop-1-en-1-yl]-4-(methoxymethoxy)benzonitrile C23H27NO6 ÏàËÆ¶È:55% European Journal of Organic Chemistry 2012 1603-1615 A One-Pot Three-Step Synthesis of Z-Trisubstituted Olefins from Arylalkynes and Their Cyclization into 4-Aryl-2H-chromenes Evelia Rasolofonjatovo, Bret Tr¨¦guier, Olivier Provot, Abdallah Hamze, Jean-Daniel Brion and Mouad Alami Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-methyl-3-[(thiomorpholin-4-yl)-methyl]-5-[2-(methoxy)phenyl]-1-[4-(?uoro)phenyl]-1H-pyrrole C23H24FNOS ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2010 18 8076-8084 Identification of a novel pyrrole derivative endowed with antimycobacterial activity and protection index comparable to that of the current antitubercular drugs streptomycin and rifampin Mariangela Biava, Giulio Cesare Porretta, Giovanna Poce, Claudio Battilocchio, Salvatore Alfonso, Alessandro De Logu, Nadia Serra, Fabrizio Manetti, Maurizio Botta Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-methyl-3-[(thiomorpholin-4-yl)-methyl]-5-[4-(?uoro)phenyl]-1-[2-(methoxy)phenyl]-1H-pyrrole C23H24FNOS ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2010 18 8076-8084 Identification of a novel pyrrole derivative endowed with antimycobacterial activity and protection index comparable to that of the current antitubercular drugs streptomycin and rifampin Mariangela Biava, Giulio Cesare Porretta, Giovanna Poce, Claudio Battilocchio, Salvatore Alfonso, Alessandro De Logu, Nadia Serra, Fabrizio Manetti, Maurizio Botta Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . tert-Butyl 3-[2-(3-Methyl-1,2-5,6-tetrahydropyridin-1-yl)ethyl]indole-1-carboxylate C21H28N2O2 ÏàËÆ¶È:55% European Journal of Organic Chemistry 2012 1147-1157 Synthesis of the Indolic Pentacyclic Core of Manadomanzamine A Following Biogenetically Based Strategies Lok-Hang Yan, Philippe Nuhant, Isabelle Sinigaglia, Yann Fromentin, Christian Marazano, Bernard Delpech and Erwan Poupon Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . lissoclibadin 6 C24H34N2O4S3 ÏàËÆ¶È:54.5% Journal of Natural Products 2007 70 439-442 Lissoclibadins 4-7, Polysulfur Aromatic Alkaloids from the Indonesian Ascidian Lissoclinum cf. badium Takahiro Nakazawa,Jingzhon Xu,Teruaki Nishikawa,Taiko Oda, Ayako Fujita, Kazuyo Ukai,Remy E. P. Mangindaan, Henki Rotinsulu,Hisayoshi Kobayashi, and Michio Namikoshi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-[1-(3-Dimethylaminopropyl)-1H-indol-3-yl]-3-(4-phenylpyrimidin-2-yl)urea C24H26N6O ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 2742-2750 The synthesis and evaluation of indolylureas as PKC¦Á inhibitors Jane F. Djung, Richard. J. Mears, Christian A. G. N. Montalbetti, Thomas S. Coulter,Adam Golebiowski, Andrew N. Carr, Oliver Barker, Kenneth D. Greis, Songtao Zhou,Elizabeth Dolan, Gregory F. Davis Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-Amino-50 -bromo-10 -methyl-20 ,5,10-trioxo-5,10-dihydrospiro [benzo[g]chromene-4,30 -indoline]-3-carbonitrile C22H12BrN3O4 ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2009 46 1266-1270 An efficient,three-component synthesis of spiro[benzo[g]chromene-4,3'-indoline]-3-carbonitrile and spiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile derivatives Ramin Ghahremanzadeh,Tayebeh Amanpour and Ayoob Bazgir Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Lavendustin A C21H19NO6 ÏàËÆ¶È:52.3% Journal of Natural Products 1989 Vol 52 1252 Isolation of a Novel Tyrosine Kinase Inhibitor, Lavendustin A, from Streptomyces griseolavendus Toshihiko Onoda, Hironobu Iinuma, Yumi Sasaki, Masa Hamada, Kunio Isshiki, Hiroshi Naganawa, Tomio Takeuchi, Kuniaki Tatsuta, Kazuo Umezawa Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5'-O-demethylhamatine C24H27NO4 ÏàËÆ¶È:50% Phytochemistry 2008 69 1065-1075 Six naphthylisoquinoline alkaloids and a related benzopyranone from a Congolese Ancistrocladus species related to Ancistrocladus congolensis Gerhard Bringmann, Joanna Spuziak, Johan H. Faber, Tanja Gulder, Inga Kajahn,Michael Dreyer, G¨¹nther Heubl, Reto Brun, Virima Mudogo Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 5,6,2',3',6'-pentamethoxyflavone ÏàËÆ¶È:50% Phytochemistry 2005 66 649-652 A furanocoumarin and polymethoxylated flavonoids from the Yucatec Mayan plant Casimiroa tetrameria Bilkis Heneka, Horst Rimpler, Anita Ankli, Otto Sticher, Simon Gibbons,Michael Heinrich Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . narcotohline ÏàËÆ¶È:50% Planta Medica 1993 59 477-478 5' -O-Demethylnarcotine:A New Alkaloid from Papa ver somniferum J¨¢nos R¨¦pdsi , S¨¢ndor Hosztafi, and Zolt¨¢n Szab¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . isoimerubrine ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1993 41 1418-1422 Structures and Solid State Tautomeric Forms of Two Novel Antileukemic Tropoloisoquinoline Alkaloids, Pareirubrines A and B, from Cissampelos pareira Hiroshi MORITA,Kouji MATSUMOTO,Koichi TAKEYA,Hideji ITOKAWA and Yoichi IITAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . columbamine ÏàËÆ¶È:50% Biochemical Systematics and Ecology 1991 19 433-437 Constituants chimiques de trois especes de Burasaia (Menispermacees) endemiques de Madagascar Ph. Rasoanaivo, S. Ratsimamanga-Urverg, A. Rakoto-Ratsimamanga, A. Raharisololalao Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-hydroxy-2,9,11-trimethoxy-5,6-dihydro isoquino[3,2-a]isoquinolinylium C20H20NO4 ÏàËÆ¶È:50% Natural Product Research 2009 23 1134-1143 Constituents of Tinospora sinensis and their antileishmanial activity against Leishmania donovani Rakesh Maurya; Prasoon Gupta; Kailash Chand; Manmeet Kumar; Preety Dixit; Nasib Singh; Anuradha Dube Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . jatrorrhizine ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2009 34 1097-1100 A new flavonoid glucoside from Huanglian jiedutang decoction MA Zhaotang, YANG Xiuwei, ZHONG Guoyue Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 2 ÏàËÆ¶È:50% Phytochemistry 1998 49 2137-2139 Glochidioboside, a glucoside of (7S,8R)-dihydrodehydrodiconiferyl alcohol from leaves of glochidion obovatum Yoshio Taked¦Á, Chieko Mim¦Á, Toshiya Masud¦Á, Eiji Hirat¦Á, Anki Takushi, Hideaki Otsuka Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2',4',5'-trimethoxy-2",2"-dimethylpyrano[5",6": 6,7]isoflavone C23H22O6 ÏàËÆ¶È:50% Phytochemistry 1998 48 557-579 Flavones and isoflavones from Millettia ichthyochtona Christine Kamperdick, Nguyen Minh Phuong, Tran Van Sung, G¨¹nter Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3',4-O-dimethylcedrusin C21H26O6 ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 884 Modified Taxols, 8. Deacylation and Reacylation of Baccatin III Gamini Samaranayake, Kurt A. Neidigh, David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . taspine ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 884 Modified Taxols, 8. Deacylation and Reacylation of Baccatin III Gamini Samaranayake, Kurt A. Neidigh, David G. I. Kingston Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 1-(tert-Butoxycarbonyl)-6-(4-cyanophenyl)-2-(5-cyanopyridin-2-yl)-1H-indole C26H20N4O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2156-2167 Exploration of larger central ring linkers in furamidine analogues:Synthesis and evaluation of their DNA binding, antiparasitic and fluorescence properties Abdelbasset A. Farahat, Ekaterina Paliakov, Arvind Kumar, Alaa-Eldin M. Barghash ,Fatma E. Goda ,Hassan M. Eisa,Tanja Wenzler , Reto Brun , Yang Liu ,W. David Wilson , David W. Boykin Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 1-(tert-Butoxycarbonyl)-6-(4-cyanophenyl)-2-(6-cyanopyridin-3-yl)-1H-indole C26H20N4O2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2156-2167 Exploration of larger central ring linkers in furamidine analogues:Synthesis and evaluation of their DNA binding, antiparasitic and fluorescence properties Abdelbasset A. Farahat, Ekaterina Paliakov, Arvind Kumar, Alaa-Eldin M. Barghash ,Fatma E. Goda ,Hassan M. Eisa,Tanja Wenzler , Reto Brun , Yang Liu ,W. David Wilson , David W. Boykin Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2012-07-07 21:08:30













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