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2Â¥: Originally posted by jasminelw at 2013-07-30 19:32:22
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1 .     teucrolivin H
    ÏàËÆ¶È:63.6%
Chemical & Pharmaceutical Bulletin          2004          52(12)          1497-1500
Neoclerodanes from  ...

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-07-30 19:32:22
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