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13C NMR (101 MHz, DMSO) ¦Ä 213.11 (s), 173.28 (s), 163.81 (s), 152.07 (s), 143.79 (s), 141.03 (s), 123.91 (s), 119.15 (s), 109.32 (s), 89.55 (s), 70.96 (s), 51.10 (s), 44.56 (s), 41.03 (s), 39.32 (s), 35.95 (s), 32.85 (s), 29.50 (s), 23.56 (s), 21.47 (s).
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djcs0411

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ÒýÓûØÌû:
2Â¥: Originally posted by lifeliuyan at 2014-11-14 13:10:45
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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3Â¥2014-11-14 13:30:37
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lifeliuyan

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È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
2Â¥2014-11-14 13:10:45
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djcs0411

½ð³æ (СÓÐÃûÆø)

ÒýÓûØÌû:
2Â¥: Originally posted by lifeliuyan at 2014-11-14 13:10:45
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺
È磺21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

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21.47,23.56,29.50,32.85,35.95,39.32,41.03,44.56,51.10,70.96,  89.55,109.32,119.15,123.91,141.03,143.79,152.07,163.81,173.28,
213.11

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4Â¥2014-11-14 13:56:15
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

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²éѯ½á¹û£º¹²²éµ½106¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     isojateorin
    ÏàËÆ¶È:60%
Planta Medica          1987          53          271-273
Isolation and 13C-NMR Studies on Three New Furanoditerpenyl Glucosides from Jateorrhiza columba
Hideji Itokawa, Kenji Mizuno, Yoshitatsu Ichihara, and Koichi Takey
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     seco-chiliolidic acid
    ÏàËÆ¶È:60%
Phytochemistry          2010          71          1395-1399
Cytotoxic terpenoids from Nardophyllum bryoides
Marianela S¨¢nchez, Marcia Mazzuca, Mar¨ªa Jos¨¦ Veloso, Luc¨ªa R. Fern¨¢ndez, Gast¨®n Siless, Lydia Puricelli, Jorge A. Palermo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     isojateorin
    ÏàËÆ¶È:60%
European Journal of Organic Chemistry          1987          1987          193-197
Studies on the Constituents of Jateorhiza palmata Miers (Colombo Root), II. Separation and Structure of Six New Furanoid Diterpene Glucosides: Palmatoside B, C, D, E, F, and G
Michiko Yonemitsu, Naomichi Fukuda, Takeatsu Kimura and Tetsuya Komori
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     compound 3
    ÏàËÆ¶È:57.1%
Phytochemistry          2010          71          1395-1399
Cytotoxic terpenoids from Nardophyllum bryoides
Marianela S¨¢nchez, Marcia Mazzuca, Mar¨ªa Jos¨¦ Veloso, Luc¨ªa R. Fern¨¢ndez, Gast¨®n Siless, Lydia Puricelli, Jorge A. Palermo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     fibrauretin A
C20H22O8     ÏàËÆ¶È:55%
Journal of Natural Products          2007          70          1930-1933
Cytochrome P3A4 Inhibitors and Other Constituents of Fibraurea tinctoria
Chung-Ren Su,Yune-Fang Ueng, Nguyen Xuan Dung, M. Vijaya Bhaskar Reddy,and Tian-Shung Wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     polystachyne D
C20H22O5     ÏàËÆ¶È:55%
Phytochemistry          2000          53          103-109
Polystachynes A-E,five cis-neo-clerodane diterpenoids from Salvia polystachya
Emma Maldonado, Alfredo Ortega
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Cardiophyllidin
C20H20O6     ÏàËÆ¶È:55%
Tetrahedron Letters          1988          29          363-366
Cardiophyllidin, a seco-ent-neoclerodane diterpenoid from Salvia cardiophylla
A.G. Gonz¨¢lez, J.R. Herrera, J.G. Luis, A.G. Ravelo, M.L. Rodriguez, E. Ferro
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     1,10¦Â-dihydroxy-4¦ÁH-1,10-secoeudesma-5(6),11(13)-dien-12,8¦Â-olide
C15H22O4     ÏàËÆ¶È:55%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     19-hydroxy-seco-chiliolide acid methyl ester
C21H28O6     ÏàËÆ¶È:55%
Tetrahedron          1986          42          1305-1313
New diterpenes from chiliotrichium rosmarinifolium and nardophyllum lanatum
J. Jakupovic, S. Banerjee, F. Bohlmann, R.M. King, H. Robinson
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (-)-4-[(4aS,8aS)-2,5,5,8a-tetramethyl-4a,5,6,7,8,8a-hexahydro-1-naphthalenyl]-2-methyl-2-butanol
C19H32O     ÏàËÆ¶È:55%
Tetrahedron          2002          58          5275-5285
The synthesis of Ambra oxide related compounds starting from (+)-larixol. Part 3
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     compound 4
C20H30N3O10P     ÏàËÆ¶È:55%
The Journal of Antibiotics          2007          60          752-756
Isolation of 8'-Phosphate Ester Derivatives of Amicoumacins: Structure-activity Relationship of Hydroxy Amino Acid Moiety FREE
Makoto Hashimoto, Takaaki Taguchi, Satoshi Nishida, Kouji Ueno, Kaio Koizumi, Masaki Aburada and Koji Ichinose
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     amicoumacin A
C20H29N3O7     ÏàËÆ¶È:55%
Agricultural and Biological Chemistry          1982          46          2659-2665
Chemical Structures of Amicoumacins Produced by Bacillus pumilus
Jiro ITOH, Shoji OMOTO, Nobusuke NISHIZAWA, Yoshio KODAMA, Shigeharu INOUYE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     N-pentanoyl-1-(aminomethyl)-4-methyl-1,2,3,4-tetrahydrocyclopentindole
C18H24N2O     ÏàËÆ¶È:55%
Journal of Medicinal Chemistry          1998          41          451-467
Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles
David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     4,4'-((5-(decahydroquinoline-1-carbonyl)-1,3-phenylene)bis(oxy))dibenzimidamide
    ÏàËÆ¶È:55%
Bioorganic & Medicinal Chemistry          2014          22          3187-3203
Structure-guided discovery of 1,3,5 tri-substituted benzenes as potent and selective matriptase inhibitors exhibiting in vivo antitumor efficacy
Rajeev Goswami, Subhendu Mukherjee, Chakshusmathi Ghadiyaram, Gerd Wohlfahrt, Ramesh K. Sistla, Jwala Nagaraj, Leena K. Satyam, Krishnaprasad Subbarao, Rajendra K. Palakurthy, Sreevalsam Gopinath, Narasimha R. Krishnamurthy, Tarja Ikonen, Anu Moilanen, Ho
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     isojateorin
C20H22O7     ÏàËÆ¶È:55%
European Journal of Organic Chemistry          1986          1986          1327-1333
Studies on the Constituents of Jateorhiza palmata Miers (Colombo root), I Separation and Structure of a New Furanoid Diterpene Glucoside (Palmatoside A)
Michiko Yonemitsu, Naomichi Fukuda, Takeatsu Kimura and Tetsuya Komori
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     O-acetyltalpinine
C22H26N2O3     ÏàËÆ¶È:54.5%
Journal of Natural Products          2014          77          2068-2080
Oxidized Derivatives of Macroline, Sarpagine, and Pleiocarpamine Alkaloids from Alstonia angustifolia
Shin-Jowl Tan, Jun-Lee Lim, Yun-Yee Low, Kae-Shin Sim, Siew-Huah Lim, and Toh-Seok Kam
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     compound 4
C23H34O5     ÏàËÆ¶È:54.1%
Journal of Natural Products          2007          70          1551-1557
Induction of Apoptosis by Diterpenes from the Soft Coral Xenia elongata
Eric H. Andrianasolo,Liti Haramaty, Kurt Degenhardt, Robin Mathew,Eileen White,Richard Lutz,and Paul Falkowski
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     borapetol B diacetate
    ÏàËÆ¶È:54.1%
Chemical & Pharmaceutical Bulletin          1986          34          2868-2872
Studies on the Constituents of the Stems of Tinospora tuberculata BEUMEE, III. : New Diterpenoids, Borapetoside B and Borapetol B
NAOMICHI FUKUDA,MICHIKO YONEMITSU and TAKEATSU KIMURA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     (13R)-13-hydroxy-1(10),14-ent-halimadien-18-oic Acid Methyl Ester
    ÏàËÆ¶È:52.3%
Journal of Natural Products          2002          65          11-15
Isolation and Absolute Configuration of ent-Halimane Diterpenoids from Hymenaea courbaril from the Suriname Rain Forest1
Maged Abdel-Kader,John M. Berger,Carla Slebodnick,Jeannine Hoch,Stan Malone, Jan H. Wisse,Marga C. M. Werkhoven, Steven Mamber,O and David G. I. Kingston
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     tinophyllol
    ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          1985          33          479-487
Indonesian Medicinal Plants. I. New Furanoditerpenes from Arcangelisia flava MERR. (1)
TOSHINOBU KUNII,KENGO KAGEI,YOSHIYUKI KAWAKAMI,YASUSHI NAGAI,YUKUO NEZU and TADASHI SATO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     methyl 13R-hydroxy-1(10),14-ent-halimadien-18-oate
    ÏàËÆ¶È:52.3%
Phytochemistry          1994          37          1359-1361
Minor diterpenoids from Halimium viscosum
Julio G. Urones, Isidro S. Marcos, Pilar Basabe, Maria Jose Sexmero, Herminio Carrillo, Maria Jose Melchor
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5Â¥2014-11-14 16:40:11
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