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²éѯ½á¹û£º¹²²éµ½812¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . teucrolivin H ÏàËÆ¶È:63.6% Chemical & Pharmaceutical Bulletin 2004 52(12) 1497-1500 Neoclerodanes from Teucrium orientale Maurizio BRUNO,Sergio ROSSELLI, Antonella MAGGIO,Franco PIOZZI,Leonardo SCAGLIONI,Nelly A. ARNOLD,and Monique S. J. SIMMONDS Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . alstophyllal C22H26N2O3 ÏàËÆ¶È:63.6% Journal of Natural Products 2004 67 547-552 New Indole Alkaloids from Alstonia macrophylla Toh-Seok Kam, and Yeun-Mun Choo Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 5,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-3-(3-methylbut-2-en-1-yl)-6-(3-methylbutanoyl)-4H-chro-men-4-one C26H26O7 ÏàËÆ¶È:60% Tetrahedron 2013 69 5850-5858 Total syntheses of norartocarpin and artocarpin Wen-Jing Zhang, Jing-Fang Wu, Peng-Fei Zhou, Yang Wang, Ai-Jun Hou Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Verruculogen C27H33N3O7 ÏàËÆ¶È:59.2% Chemistry of Natural Compounds 2004 40 615-617 FUMITREMORGINS FROM THE MARINE ISOLATE OF THE FUNGUS Aspergillus fumigatus Sh. Sh. Afiyatullov, A. I. Kalinovskii, M. V. Pivkin,P. S. Dmitrenok, and T. A. Kuznetsova Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . spiranthol-B C21H24O3 ÏàËÆ¶È:59.0% Chemical & Pharmaceutical Bulletin 1989 37 3195-3199 Studies on the Constituents of Orchidaceous Plants. VIII. : Constituents of Spiranthes sinensis (PERS.) AMES var. amoena (M. BIEBERSON) HARA. (1). Isolation and Structure Elucidation of Spiranthol-A, Spiranthol-B, and Spirasineol-A, New Isopentenyldihydro Yasuhiro TEZUKA,Midori UEDA and Tohru KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . dimethyl 8a-acetyl-3,4,5,6,7,8,8a,9-octahydro-9-methylene- 2H-fluorene-2,2-dicarboxylate C20H24O5 ÏàËÆ¶È:59.0% Helvetica Chimica Acta 2009 92 1729-1740 Palladium-Catalyzed Cascade Oligocyclizations Involving Competing Elementary Steps Such as Thermal [1,5]-Acyl Shifts Wajdi M. Tokan, Stefan Schweizer, Claudia Thies, Frank. E. Meyer, Philip J. Parsons, Armin de Meijere Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Irciformonin K C22H30O5 ÏàËÆ¶È:59.0% Helvetica Chimica Acta 2009 92 2101-2110 Irciformonins E - K, C22-Trinorsesterterpenoids from the Sponge Ircinia formosana Ya-Ching Shen, Pei-Show Shih, Yun-Sheng Lin, Yu-Chi Lin, Yao-Haur Kuo, Yuh-Chi Kuo, Ashraf Taha Khalil Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . alstonerinal C21H24N2O2 ÏàËÆ¶È:59.0% Phytochemistry 1999 51 839-844 Alkaloids from the stem-bark of Alstonia macrophylla Toh-Seok Kam, Ing-Ho Iek, Yeun-Mun Choo Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 12R,13S-Dihydroxyfumitremorgin C ÏàËÆ¶È:59.0% Natural Product Sciences 2007 13 251-254 12,13-Dihydroxyfumitremorgin C, Fumitremorgin C, and Brevianamide F, Antibacterial Diketopiperazine Alkaloids from the Marine-Derived Fungus Pseudallescheria sp. Zhang, Dahai; Noviendri, Dedi; Nursid, Muhammad; Yang, Xiu-Dong; Son, Byeng-Wha Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 6c ÏàËÆ¶È:59.0% Phytochemistry 1993 32 433-438 Stilbenes and other constituents of Knema austrosiamensis Maria Jos¨¦ T. G. Gonzal¨¦z, Madalena M. M. Pinto, Anake Kijjoa, Choojit Anantachoke, Werner Herz Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . dihydroxy-fumitremorgin C C22H25N3O5 ÏàËÆ¶È:59.0% 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 12 . trans-1-acetoxy-2-bromo-1,2-dihydroisoacronycine C22H22NO5Br ÏàËÆ¶È:59.0% Heterocycles 2002 57 341-351 Synthesis and Cytotoxic Activity of Isoacronycine and Its Derivatives Prokopios Magiatis, Sofia Mitaku,* Alain Pierr¨¦, and Ghanem Atassi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ethyl 5-(6-methoxy-7-(3-(4-methylpiperidin-1-yl)propoxy)-quinazolin-4-ylamino)benzo thiophene-2-carboxylate ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2010 18 3812-3822 Design and synthesis of novel Gefitinib analogues with improved anti-tumor activity Xiaoqing Wu, Mingdong Li, Yang Qu, Wenhua Tang, Youguang Zheng, Jiqin Lian, Min Ji, Liang Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 8,8-dimethyldihydroberberine C22H23NO4 ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2010 18 5915-5924 8, 8-Dimethyldihydroberberine with improved bioavailability and oral efficacy on obese and diabetic mouse models Zhe Cheng, An-Feng Chen, Fang Wu, Li Sheng, Han-Kun Zhang, Min Gu, Yuan-Yuan Li, Li-Na Zhang, Li-Hong Hu, Jing-Ya Li, Jia Li Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . macrogentine C21H26N2O3 ÏàËÆ¶È:59.0% Tetrahedron 2000 56 6143-6150 Novel Macroline Oxindoles from a Malayan Alstonia Toh-Seok Kam, Yeun-Mun Choo Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 14 C42H63O12P ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2009 17 1325-1338 Synthesis and biological evaluation of extraordinarily potent C-10 carba artemisinin dimers against P. falciparum malaria parasites and HL-60 cancer cells James Chadwick, Amy E. Mercer, B. Kevin Park, Richard Cosstick, Paul M. O¡¯Neill Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . tryprostation A C22H27N3O3 ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2008 16 4626-4651 Synthesis and structure¨Cactivity relationship studies on tryprostatin A, an inhibitor of breast cancer resistance protein Hiteshkumar D. Jain, Chunchun Zhang, Shuo Zhou, Hao Zhou, Jun Ma, Xiaoxiang Liu, Xuebin Liao, Amy M. Deveau, Christine M. Dieckhaus, Michael A. Johnson, Kirsten S. Smith, Timothy L. Macdonald, Hideaki Kakeya, Hiroyuki Osada, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . oxindole-bridged[2.2.3]bicycle C21H23NO4 ÏàËÆ¶È:59.0% Tetrahedron 2013 69 5588-5603 Studies toward welwitindolinones: formal syntheses of N-methylwelwitindolinone C isothiocyanate and related natural products Tsung-hao Fu, William T. McElroy, Mariam Shamszad, Richard W. Heidebrecht Jr., Brian Gulledge, Stephen F. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Cochliomycin A C22H28O7 ÏàËÆ¶È:59.0% Journal of Natural Products 2011 74 629-633 Potent Antifouling Resorcylic Acid Lactones from the Gorgonian-Derived Fungus Cochliobolus lunatus Chang-Lun Shao, Hui-Xian Wu, Chang-Yun Wang, Qing-Ai Liu, Ying Xu, Mei-Yan Wei, Pei-Yuan Qian, Yu-Cheng Gu, Cai-Juan Zheng, Zhi-Gang She, and Yong-Cheng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . N-Methylwelwitindolimne B isothiocymete C21H23ClN2O2S ÏàËÆ¶È:59.0% Journal of the American Chemical Society 1994 116 9935-9942 Welwitindolinones, Unusual Alkaloids from the Blue-Green Algae Hapalosiphon welwitschii and Westiella intricata. Relationship to Fischerindoles and Hapalinodoles Klemens Stratmann, Richard E. Moore, Rosanne Bonjouklian, Jack B. Deeter, Gregory M. L. Patterson, Stacey Shaffer, Charles D. Smith, Tim A. Smitka Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Methyl-2-(9-demethoxyberberine bromide-9-yl)hydroxyacetate C22H20NO6 ÏàËÆ¶È:59.0% Chemistry of Natural Compounds 2013 48 1047-1053 Synthesis of berberine bromide analogs containing tertiary amides of acetic acid in the 9-O-position I. V. Nechepurenko, N. I. Komarova, V. G. Vasil¡¯ev Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . compound anti-3f C27H32N2O7 ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2012 2359-2366 Diastereoselective Synthesis of ¦Â-Lactam¨COxindole Hybrids Through a Three-Component Reaction of Azetidine-2,3-diones, -Diazo-oxindoles, and Alcohols Catalyzed by [Rh2(OAc)4] Benito Alcaide, Pedro Almendros, Cristina Aragoncillo, Ricardo Callejo, M. Pilar Ruiz and M. Rosario Torres Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . cycloaltilisin C26H26O7 ÏàËÆ¶È:57.6% Journal of Natural Products 1993 Vol 56 1594-1597 Three New Prenylflavones from Artocarpus altilis Chien-Chih Chen, Yu-Lin Huang, Jun-Chih Ou, Chwan-Fwu Lin, Tzu-Ming Pan Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (2R)-(1,2:5,6-di-O-isopropylidene-¦Á-D-glucofuranos-3-O-yl) 2-isoproprenyl-5,9-dimethyldeca-4,8-dienoate C27H42O7 ÏàËÆ¶È:57.6% Tetrahedron 2000 56 9647-9653 Structure and Synthesis of Anhydrobisfarnesol from Euphorbia lateriflora and Asymmetric Synthesis of (R)-Sesquilavandulol Sophie Faure, Joseph D. Connolly, Christopher O. Fakunle, Olivier Piva Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . compound 3 C24H31NO9 ÏàËÆ¶È:56.5% Canadian Journal of Chemistry 2008 86 138-141 Synthesis of isoxazole conjugates of sugars via 1,3-dipolar cycloaddition Vipraja V. Vaidya, Karuna S. Wankhede, Manikrao M. Salunkhe, and Girish K. Trivedi Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 11-methoxy-O-acetylisoretuline ÏàËÆ¶È:56.5% Phytochemistry 1990 29 686-687 Alkaloids from seeds of Strychnos variabilis and S. longicaudata Philippe Thepenier,Marie-Jose Jacquier,Georges Massiot,Louisette Le Men-Olivier,Clement Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . methyl 12R-acetoxy-lambertianate ÏàËÆ¶È:56.5% Phytochemistry 1985 24 2041-2046 Diterpenes from the seed of Sciadopitys verticillata Shinichi Hasegawa, Yoshiyuki Hirose Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound anti-3b ÏàËÆ¶È:56.5% European Journal of Organic Chemistry 2012 2359-2366 Diastereoselective Synthesis of ¦Â-Lactam¨COxindole Hybrids Through a Three-Component Reaction of Azetidine-2,3-diones, -Diazo-oxindoles, and Alcohols Catalyzed by [Rh2(OAc)4] Benito Alcaide, Pedro Almendros, Cristina Aragoncillo, Ricardo Callejo, M. Pilar Ruiz and M. Rosario Torres Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound anti-3c C25H28N2O6 ÏàËÆ¶È:56.5% European Journal of Organic Chemistry 2012 2359-2366 Diastereoselective Synthesis of ¦Â-Lactam¨COxindole Hybrids Through a Three-Component Reaction of Azetidine-2,3-diones, -Diazo-oxindoles, and Alcohols Catalyzed by [Rh2(OAc)4] Benito Alcaide, Pedro Almendros, Cristina Aragoncillo, Ricardo Callejo, M. Pilar Ruiz and M. Rosario Torres Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . macrocarpine C C23H30N2O3 ÏàËÆ¶È:56.5% Tetrahedron 2004 60 3957-3966 Unusual spirocyclic macroline alkaloids, nitrogenous derivatives, and a cytotoxic bisindole from Alstonia Toh-Seok Kam, Yeun-Mun Choo, Kanki Komiyama Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . compound 5 C23H26O6 ÏàËÆ¶È:56.5% Journal of Natural Products 2012 75 1299-1304 Busseihydroquinones A¨CD from the Roots of Pentas bussei Milkyas Endale, Annabel Ekberg, Hoseah M. Akala, John Patrick Alao, Per Sunnerhagen, Abiy Yenesew, and M¨¢t¨¦ Erd¨¦lyi Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 17-hydroxypseudolaric acid B C23H28O9 ÏàËÆ¶È:56.5% Chinese Traditional and Herbal Drugs 2012 43 220-222 Antifungal constituents of Pseudolaricis Cortex XU Yun-hui; ZHANG Shuai; ZHANG Nian; KONG De-yun; HUA Mo-li Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . methylpseud olarate A2 C23H30O7 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2003 11 4577-4584 Antifungal diterpenoids of Pseudolarix kaempferi, and their structure¨Cactivity relationship study Sheng-Ping Yang, Lei Dong, Ying Wang, Yan Wu, Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . gallomyrtucommulone D C27H36O13 ÏàËÆ¶È:56% Journal of Natural Products 2006 69(2) 251-254 Antibacterial Galloylated Alkylphloroglucinol Glucosides from Myrtle (Myrtus communis) Giovanni Appendino, Lucia Maxia, Piergiorgio Bettoni, Monica Locatelli, Carola Valdivia, Mauro Ballero, Michael Stavri, Simon Gibbons, and Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 4e C26H30F2N6O9P ÏàËÆ¶È:56% Canadian Journal of Chemistry 2010 88 35-41 Synthesis and electrochemical behavior of triazole-containing nicotinamide adenine dinucleotide analogs Wujun Liu, Shuhua Hou, and Zongbao Kent Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . exiguamine A C25H25N5O6 ÏàËÆ¶È:56% Journal of the American Chemical Society 2006 128 16046-16047 Exiguamine A, an Indoleamine-2,3-dioxygenase (IDO) Inhibitor Isolated from the Marine Sponge Neopetrosia exigua Harry C. Brastianos, Eduardo Vottero, Brian O. Patrick, Rob Van Soest, Teatulohi Matainaho, A. Grant Mauk, and Raymond J. Andersen Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . methyl 4-cyano-3,4,4a,5,6,7-hexahydro-5'-methyl-2',2''-dioxodispiro[3'H-indole-3',2-pyrrolizine-3,3''[3''H]-indoline]-4-carboxylate C25H22N4O4 ÏàËÆ¶È:56% Tetrahedron 2013 69 2062-2069 Synthesis and stereochemical investigation of highly functionalized novel dispirobisoxindole derivatives via [3+2] cycloaddition reaction in ionic liquid Anshu Dandia, Anuj K. Jain, Ashok K. Laxkar, Dharmendra S. Bhati Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 1'-cyclohexyl-7',7'-dimethyl-2,5'-dioxo-1',5',6',7',8',9'-hexahydrospiro[indoline-3,4'-pyrrolo[2,3-b]quinoline]-3'-carbonitrile C27H28N4O2 ÏàËÆ¶È:56% Tetrahedron 2013 69 5955-5967 Novel and efficient synthesis of 4,7-dihydro-1H-pyrrolo[2,3-b]pyridine derivatives via one-pot, three-component approach from N-substituted 5-amino-3-cyanopyrroles, various carbonyl and active methylene compounds Marcelo Vilches-Herrera, Anke Spannenberg, Peter Langer, Viktor O. Iaroshenko Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . verruculogen ÏàËÆ¶È:55.5% Natural Product Research and Development 2013 25 64-67 Studies on Secondary Metabolites Produced by Endophytic Aspergillus fumigatus from Trifolium repens YANG Yong-xun, DONG Xiao-ping, YAN Yong-ming, TAO Ming, LUO Qian Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . NA-209A C27H33N3O7 ÏàËÆ¶È:55.5% Chinese Journal of Antibiotics 2000 25 257-271 ΢ÉúÎïÀ´Ô´µÄµ¨¹Ì´¼õ£»ù×ªÒÆÃ¸ÒÖÖÆ¼ÁÑо¿¢ò. NA-209A, B µÄÀí»¯ÌØÕ÷ºÍ½á¹¹¼ø±ð ÌÆÓÂ, Ñî´ó¾ü, Ò¦Ìì¾ô Structure 13C NMR ̼Æ×Ä£Äâͼ |
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