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yjl2007

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yjl2007: ½ð±Ò+10 2012-06-12 16:15:04
1 .     1-O-acetyl-4R,6S-britannilactone
C17H24O5     ÏàËÆ¶È:100%
Natural Product Sciences          2003          9          28-30
X-Ray Crystallography of New Sesquiterpene Lactone isolated from Inula britannica var.chinensis
Han, Ah-Reum; Mar, Woong-Chon; Seo, Eun-Kyoung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     1-O-Acetyl-4R,6S-britannilactone
C17H15O5     ÏàËÆ¶È:100%
Archives of Pharmacal Research          2004          27          83-85
The inhibitory principle of lipopolysaccharide-induced nitric oxide production from inula britannica var. chinensis
Kang-Hoon Je, Ah-Reum Han, Hyun-Tai Lee, Woongchon Mar and Eun-Kyoung Seo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     1-acetoxy-6¦Á-hydroxyeriolanolide
C17H24O5     ÏàËÆ¶È:94.1%
Phytochemistry          1993          34          1647-1649
Secoeudesmanolides from Inula japonica
F. Jeske, S. Huneck, J. Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1,6-O,O-diacetylbritannilactone
C17H22O4     ÏàËÆ¶È:78.9%
Phytochemistry          1993          34          249-252
Sesquiterpene lactones from Inula britannica
Zhou Bing-Nan, Bai Nai-Sheng, Lin Long-Ze, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     6¦Á-acetoxy-1-hydroxy-4¦ÁH-1,10-secoeudesma-5(10),11(13)-dien-12,8¦Â-olide
C17H24O5     ÏàËÆ¶È:64.7%
Tetrahedron          2010          66          9379-9388
New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages
Jiang-Jiang Qin, Hui-Zi Jin, Jia-Xian Zhu, Jian-Jun Fu, Qi Zeng, Xiang-Rong Cheng, Yan Zhu, Lei Shan, Shou-De Zhang, Yue-Xing Pan, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Cespihypotin Y
C20H26O4     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2010          93          281-289
Verticillane-Type Diterpenoids and an Eudesmanolide-Type Sesquiterpene from the Formosan Soft Coral Cespitularia hypotentaculata
Yu-Chi Lin, Mohamed H. Abd El-Razek and Ya-Ching Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     eupatorone
C16H20O4     ÏàËÆ¶È:58.8%
Helvetica Chimica Acta          2006          Vol. 89          3104
Cadinene Derivatives from Eupatorium adenophorum
Ming-Zhong Wang, Yan-Yan Zhang , Shun-Lin Li, Xiang-Hai Cai, and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     2-deoxo-2-(acetyloxy)- 9-oxoageraphorone
C17H26O3     ÏàËÆ¶È:58.8%
Helvetica Chimica Acta          2006          Vol. 89          3104
Cadinene Derivatives from Eupatorium adenophorum
Ming-Zhong Wang, Yan-Yan Zhang , Shun-Lin Li, Xiang-Hai Cai, and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     tiomanene
C17H25BrO     ÏàËÆ¶È:58.8%
Phytochemistry          2008          69          2490-2494
Antibacterial activity of halogenated sesquiterpenes from Malaysian Laurencia spp.
Charles Santhanaraju Vairappan, Minoru Suzuki,Takahiro Ishii, Tatsufumi Okino,Tsuyoshi Abe,Michio Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (S)-5-Cyclohexyl-3-isopropyl-1H-benzo[e][1,4]diazepin-2(3H)-one
C18H24N2O     ÏàËÆ¶È:58.8%
Bioorganic & Medicinal Chemistry          2011          19          1802-1815
Synthesis and biological evaluation of 1,4-benzodiazepin-2-ones with antitrypanosomal activity
John Spencer, Rajendra P. Rathnam, Alan L. Harvey, Carol J. Clements, Rachel L. Clark,Michael P. Barrett, Pui Ee Wong, Louise Male, Simon J. Coles, Simon P. Mackay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (1R,2R,3R,6R,7S)-1-acetoxy-2,3-dihydroxy-2,3-dihydrobisabolene
C17H30O4     ÏàËÆ¶È:58.8%
Natural Product Communications          2011          Vol. 6, No. 9          1225-1228
A New Bisabolene from Stevia tomentosa
Alejandro Valdez-Calder¨®n, J. Mart¨ªn Torres-Valencia, J. Jes¨²s Manr¨ªquez-Torres, Ren¨¦ Vel¨¢zquez-Jim¨¦nez, Mario A. G¨®mez-Hurtado, Luisa U. Rom¨¢n-Mar¨ªn, Juan D. Hern¨¢ndez-Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     2¦Á-acetoxy-7¦Á-hydroxysphaerantholide
C15H18O3     ÏàËÆ¶È:58.8%
Phytochemistry          1990          29          1213-1217
Carvotacetone derivatives and eudesman-12,6¦Â-olides from Sphaeranthus species
J. Jakupovic,M. Grenz,F. Bohlmann,G.M. Mungai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (6S,7¦Á,8S)-8,15-diacetoxy-14-hydroxymelampa-1(10),4,11(13)-trien-12,6-olide
C19H24O7     ÏàËÆ¶È:57.8%
Journal of Natural Products          2000          63          305-307
Preparation, Stereochemistry, and Cytotoxic Activity of the Melampolides from Mikania minima
Alejandro F. Barrero,J. Enrique Oltra, Ignacio Rodr¨ªguez-Garc¨ªa,Armando Barrag¨¢n, and M¨ªriam Âlvarez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 6
    ÏàËÆ¶È:57.8%
Tetrahedron Letters          2003          44          2641-2643
A synthetic approach to bicyclo[6.2.1]undecane ring systems
Mauricio Gomes Constantino, Kleber Thiago de Oliveira, Adilson Beatriz, Gil Valdo Jos¨¦ da Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (Z)-3,8-Diacetoxy-1,9,14-pentadecatriene-4,6-diyne
C19H22O4     ÏàËÆ¶È:57.8%
Heterocycles          2011          83          1067-1076
New Antibacterial Polyacetylenes from Sunflower (Helianthus annuus L.) Seedlings
Fumie Seshimoto, Si Won Hong, Haruyuki Nakajyo, and Hideyuki Shigemori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     triacetate derivative of Pestalotioprolide A
    ÏàËÆ¶È:55%
Phytochemistry Letters          2012          5          13-17
¦Á-Pyrone and seiricuprolide derivatives from the mangrove-derived fungi Pestalotiopsis spp. PSU-MA92 and PSU-MA119
Vatcharin Rukachaisirikul,Aekkachai Rodglin,Souwalak Phongpaichit,Jirayu Buatong,Jariya Sakayaroj
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     Diacetyl crucigasterin D
C20H35NO3     ÏàËÆ¶È:55%
Tetrahedron          2010          66          7533-7538
Crucigasterins A¨CE, antimicrobial amino alcohols from the Mediterranean colonial ascidian Pseudodistoma crucigaster
M. Letizia Ciavatta, Emiliano Manzo, Genoveffa Nuzzo, Guido Villani, Mario Varcamonti, Margherita Gavagnin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (1R*,3S*,4R*,6S*)-4-(hydroxy)-9-(acetoxy)-1-[(2Z)-2-methyl-but-2-enoyloxy]-bisabol-10(11)-ene or (1R*,2S*,4R*,6S*)-4-(hydroxy)-2-[3-(acetoxy)-1,5-dimethylhex-4-enyl]-5-methyl-cyclohexyl-(2Z)-2-methyl but-2-enoate
C22H36O5     ÏàËÆ¶È:54.5%
Planta Medica          2004          70          978-985
New Constituents of Leontopodium alpinum and their in vitro Leukotriene Biosynthesis Inhibitory Activity
Stefan Schwaiger£¬Michael Adams£¬Christoph Seger£¬Ernst P. Ellmerer£¬Rudolf Bauer£¬Hermann Stuppner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 20c
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2010          18          3656-3667
Hybrids of sugars and aromatics: A Pd-catalyzed modular approach to chromans and isochromans
Markus Leibeling, Dennis C. Koester, Martin Pawliczek, Daniel Kratzert, Birger Dittrich, Daniel B. Werz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (1R,2E,4R,5R,7E,10S,11S,12R)-5-acetoxy-10,18-dihydroxy-2,7-dolabelladiene
C22H36O4     ÏàËÆ¶È:54.5%
Tetrahedron          1997          53          8675-8688
New diterpenoids from the alga Dictyota dichotoma
Rosario Dur¨¢n, Eva Zub¨ªa, Mar¨ªa J. Ortega, Javier Salv¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     compound 2
C22H24O7     ÏàËÆ¶È:54.5%
Phytochemistry          2011          72          265-275
Phytotoxic clerodane diterpenes from Salvia miniata Fernald (Lamiaceae)
Angela Bisio, Gianluca Damonte, Daniele Fraternale, Emanuela Giacomelli, Annalisa Salis, Giovanni Romussi, Sergio Cafaggi, Donata Ricci, Nunziatina De Tommasi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     3¦Â-acetoxy,5¦Á,11,12,13-tetrahydroxyeudesm-4(15)-ene
C17H28O6     ÏàËÆ¶È:52.9%
Phytochemistry          2002          59          851-856
Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea
Ahmed A. Ahmed, Ahmed A. Mahmoud, Eptehal T. Ali, Olga Tzakou,Maria Couladis, Tom J. Mabry, Tam¨¢s G¨¢tid, G¨¢bor T¨®th
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     (1R*,6R*,7S*,10S*)-10-isothiocyanatocadin-4-ene
C16H25NS     ÏàËÆ¶È:52.9%
Journal of Natural Products          2004          67          833-837
Terpene Isocyanides, Isocyanates, and Isothiocyanates from the Okinawan Marine Sponge Stylissa sp.
Hidemichi Mitome, Nao Shirato, Hiroaki Miyaoka, Yasuji Yamada, and Rob W. M. van Soest
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     (1S*,2S*,5S*,6S*,7R*,8S*)-13-isothiocyanatocubebane
C16H25NS     ÏàËÆ¶È:52.9%
Journal of Natural Products          2004          67          833-837
Terpene Isocyanides, Isocyanates, and Isothiocyanates from the Okinawan Marine Sponge Stylissa sp.
Hidemichi Mitome, Nao Shirato, Hiroaki Miyaoka, Yasuji Yamada, and Rob W. M. van Soest
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     semiplenamide E
C24H45NO3     ÏàËÆ¶È:52.9%
Journal of Natural Products          2003          66          1364-1368
Semiplenamides A-G, Fatty Acid Amides from a Papua New Guinea Collection of the Marine Cyanobacterium Lyngbya semiplena
Bingnan Han,Kerry L. McPhail,Alessia Ligresti, Vincenzo Di Marzo, and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     macrophyllic acid e
C15H22O3     ÏàËÆ¶È:52.9%
Journal of Natural Products          2001          64          466-471
Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla
Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     (3e)-6-acetoxy-3,11-dimethyl-7-methylidendodeca-1,3,10-triene
C17H26O2     ÏàËÆ¶È:52.9%
Journal of Natural Products          2001          64          401-405
New Acyclic Sesquiterpenes and Norsesquiterpenes from the Caribbean Gorgonian Plexaurella grisea
Ana Rueda, Eva Zub¨ªa, Mar¨ªa J. Ortega, and Javier Salv¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     3-acetoxy-E-¦Ã-bisabolene
C17H26O2     ÏàËÆ¶È:52.9%
Journal of Natural Products          1997          60          967-970
Laurencia rigida: Chemical Investigations of Its Antifouling Dichloromethane Extract
Gabriele M. König and Anthony D. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     9-Oxo-4(5)¦Á-epoxy-6,7¦Á(H)-eudesm-12,6-olide
C15H18O4     ÏàËÆ¶È:52.9%
Chemistry of Natural Compounds          2009          45          503-506
EPOXIDATION OF SESQUITERPENE LACTONES TOURNEFORIN AND LUDARTIN
R. I. Dzhalmakhanbetova, M. A. Rodichev Yu. V. Gatilov, M. M. Shakirov, G. A. Atazhanova,and S. M. Adekenov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     7,10-diisopropyl-4R,13R-dimethyl-1-oxa-8,9-diaza-7,9-cyclopentadecadien-2-one
    ÏàËÆ¶È:52.9%
Chemistry of Natural Compounds          2009          45          470-473
SYNTHESIS FROM L-MENTHOL OF OPTICALLY ACTIVEMACROLIDES WITH N-CONTAINING(AZINE OR HYDRAZIDE) GROUPS
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva,R. R. Muslukhov, E. M. Vyrypaev, E. G. Galkin,and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-06-12 15:18:56
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