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1 .     sendanin
C32H40O12     ÏàËÆ¶È:67.7%
Tetrahedron letters          1976          17          2877-2880
Sendanin, a new limonoid from melia azedarach linn. var. japonica makino
Masamitsu Ochi, Hiyoshizo Kotsuki, Ken Hirotsu, Takashi Tokoroyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     sendanin
    ÏàËÆ¶È:67.7%
Heterocycles          1985          23          2321-2325
Azadirachtanin, a New Limonoid from the Leaves of Azadirachta indicca
Gurudas Podder and Shashi B. Mohato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     9-deoxo-9a-aza-9a-ethyl-9a-homoerythromycin A
C39H74O12N2     ÏàËÆ¶È:67.6%
The Journal of Antibiotics          1988          41          1029-1047
SYNTHESIS, IN VITRO AND IN VIVO ACTIVITY OF NOVEL 9-DEOXO-9a-AZA-9a-HOMOERYTHROMYCIN A DERIVATIVES; A NEW CLASS OF MACROLIDE ANTIBIOTICS, THE AZALIDES
G. MICHAEL BRIGHT, ARTHUR A. NAGEL, JON BORDNER, KISHOR A. DESAI, JOSEPH N. DIBRINO, JOLANTA NOWAKOWSKA, LAWRENCE VINCENT, RICHARD M. WATROUS, FRANK C. SCIAVOLINO, ARTHUR R. ENGLISH, JAMES A. RETSEMA, MARGARET R. ANDERSON, LORI A. BRENNAN, ROBERTA J. BORO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Azedarachin A
C33H44O11     ÏàËÆ¶È:66.6%
Phytochemistry          1996          41          117-120
Limonoid antifeedants from Melia toosendan
Jian-Bo Zhou, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     azedarachin A
C33H44O11     ÏàËÆ¶È:66.6%
Bulletin of the Chemical Society of Japan          1994          67          2468-2472
The Structures of Azedarachins, Limonoid Antifeedants from Chinese Melia azedarach Linn
Ruo Chun Huang, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     azedarachin A
    ÏàËÆ¶È:66.6%
Heterocycles          1999          50          595-609
Limonoids from Melia toosendan (Meliaceae) and Their Antifeedant Activity
Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     16¦Á-acetoxycalactin
C31H42O11     ÏàËÆ¶È:64.5%
Phytochemistry          1994          37          801-806
Cardenolide glycosides from Asclepias fruticosa
Tsutomu Warashina, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Trichilin L
C33H44O11     ÏàËÆ¶È:63.6%
Phytochemistry          1996          41          117-120
Limonoid antifeedants from Melia toosendan
Jian-Bo Zhou, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     trichilin L
    ÏàËÆ¶È:63.6%
Heterocycles          1999          50          595-609
Limonoids from Melia toosendan (Meliaceae) and Their Antifeedant Activity
Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (22S,23S)-3¦Â ,5,22,23-Tetrahydroxy-5 ¦Á-stigmastan-6-one
C29H50O5     ÏàËÆ¶È:63.3%
Steroids          2004          69          713-720
In vitro and in vivo antiherpetic activity of three new synthetic brassinosteroid analogues
Flavia M. Michelini, Javier A. Ram¨ªrez, Alejandro Berra, Lydia R. Galagovsky, Laura E. Alch¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 341
    ÏàËÆ¶È:63.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     17¦Â-hydroxyafroside
C29H42O10     ÏàËÆ¶È:63.3%
Phytochemistry          1994          37          217-226
Steroidal glycosides and cardenolide glycosides from Asclepias fruticosa
Tsutomu Warashina, Tadataka Noro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 1b
    ÏàËÆ¶È:63.3%
Australian Journal of Chemistry          1987          40          1713-1721
A 13C N.M.R. Study of Some Oxygenated Hopane Triterpenes
AL Wilkins, KJ Ronaldson, PM Jager and PW Bird
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     sendanlin
    ÏàËÆ¶È:62.5%
Bulletin of the Chemical Society of Japan          1994          67          2468-2472
The Structures of Azedarachins, Limonoid Antifeedants from Chinese Melia azedarach Linn
Ruo Chun Huang, Hiroaki Okamura, Tetsuo Iwagawa, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 9
C34H54O11     ÏàËÆ¶È:61.7%
Journal of Natural Products          1994          Vol 57          348
Insect Inhibitory Steroidal Saccharide Esters from Physalis peruviana
Carl A. Elliger, William F. Haddon, Leslie Harden, Anthony C. Waiss Jr., Rosalind Y. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     6'-hydroxy-16¦Á-acetoxycalactin
C31H42O12     ÏàËÆ¶È:61.2%
Journal of Natural Products          2009          72          1087-1091
Cardenolides from Pergularia tomentosa Display Cytotoxic Activity Resulting from Their Potent Inhibition of Na+/K+-ATPase
Sonia Piacente, Milena Masullo, Nancy De Neve, Janique Dewelle,Arafa Hamed, Robert Kiss, and Tatjana Mijatovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (-)-ent-12¦Â-hydroxykaur-16-en-19-oic acid, 19-O-¦Â-D-xylopyranosyl-(1¡ú6)-O-¦Â-D-glucopyranoside
C31H48O12     ÏàËÆ¶È:61.2%
Journal of Asian Natural Products Research          2008          10          77-683
Terpenoids from the tuber of Cremastra appendiculata
Shuai Li, Zhen Xue, Su-Juan Wang, Yong-Chun Yang and Jian-Gong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ¦Â-D-glucopyranosyl-15¦Á-(3-hydroxy-3-methylbutanoyloxy)-ent-16-kauren-19-oate
C31H48O10     ÏàËÆ¶È:61.2%
Phytochemistry Letters          2013          6          425-428
Two new ent-kaurene diterpene glucosides from the roots of Mikania micrantha
Qiaolin Xu, Haihui Xie, Huilin Xiao, Lidong Lin, Xiaoyi Wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     12-Deacetyltrichilin I
    ÏàËÆ¶È:60.6%
Bioorganic & Medicinal Chemistry          1996          4          1355-1359
Cytotoxic trichilin-type limonoids from Melia azedarach
Koichi Takeya, Zhi-Sheng Qiao, Chieko Hirobe, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     4,28-dihydroxy-3,4-secolup-20(29)-en-3-oic acid
C30H50O4     ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          278-282
Microbial Transformations of Two Lupane-Type Triterpenes and Anti-Tumor-Promoting Effects of the Transformation Products
Toshihiro Akihisa,Yoshio Takamine, Kazuo Yoshizumi, Harukuni Tokuda, Yumiko Kimura,Motohiko Ukiya, Toro Nakahara,Toshihiro Yokochi,Eiichiro Ichiishi, and Hoyoku Nishino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     18-¦Â-D-3',6'-diacetoxyglucopyrano-syl-ent-kaur-16-ene
C30H44O9     ÏàËÆ¶È:60%
Planta Medica          2007          73          84-90
Antibacterial Diterpenoids from Sagittaria pygmaea
Xue-Ting Liu1,Yao Shi,Biao Yu,Ian D. Williams,Herman H.-Y. Sung Qiong Zhang,Jing-Yu Liang,Nancy Y. Ip,Zhi-Da Min
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     3¦Â-O-(¦Â-D-diginosyl)-14,15¦Á-dihydroxy-5¦Á-card-20(22)-enolide
C30H46O8     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2009          6          431-435
Nematicidal Cardenolides from Nerium indicum Mill.
Xing-BiaoWang, Guo-Hong Li, Li-Jun Zheng, Kai-Yan Ji, Hua L , Fang-Fang Liu, Li-Zhi Dang, Ming-He Mo, and Ke-Qin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     ajugamarin D1
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1989          37          354-357
Neo-clerodane Diterpenes from Ajuga nipponensis
Hiroko SHIMOMURA,Yutaka SASHIDA and Kazunori OGAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (22S,23S)-3¦Â -Bromo-5,22,23-trihydroxy-5¦Á-stigmastan-6-one
C29H49BrO4     ÏàËÆ¶È:60%
Steroids          2004          69          713-720
In vitro and in vivo antiherpetic activity of three new synthetic brassinosteroid analogues
Flavia M. Michelini, Javier A. Ram¨ªrez, Alejandro Berra, Lydia R. Galagovsky, Laura E. Alch¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (22S,23S)-2¦Á-fluoro-3¦Â,22,23-trihydroxy-5¦Á-stigmastan-6-one
C29H49FO4     ÏàËÆ¶È:60%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     (20S)-5-Ergostene-3¦Â,7¦Á,16¦Â,20-tetrol
C28H48O4Na     ÏàËÆ¶È:60%
Steroids          2009          74          761-765
Steroids from the leaves of Chinese Melia azedarach and their cytotoxic effects on human cancer cell lines
Shi-Biao Wu, Yan-Ping Ji, Jing-Jing Zhu, Yun Zhao, Gang Xia, Ying-He Hu, Jin-Feng Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     16¦Â,22-diacetoxy-12¦Â-hydroxy-24-methylscalaran-25,24-olide
C30H46O7     ÏàËÆ¶È:60%
Journal of Natural Products          1991          Vol 54          364
Metabolites of Porifera, Part III. New 24-Methylscalaranes from Phyllospongia dendyi of the Indian Ocean
Ch. Bheemasankara Rao, Raju S. H. S. N. Kalidindi, G. Trimurtulu, D. Venkata Rao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     16,22-diacetylhomoscalaralactone IIB
C30H46O7     ÏàËÆ¶È:60%
Journal of Natural Products          1992          Vol 55          859
Homoscalarane Sesterterpenes from Lendenfeldia frondosa
K. A. Alvi, Phillip Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     Scandenogenin D
C30H46O7     ÏàËÆ¶È:60%
Phytochemistry          1996          41          1169-1174
Cucurbitane glycosides from Hemsleya panacis-scandens rhizomes
Hideo Kubo, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Rui-Lin Nie, Osamu Tanaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     16¦Â-hydroxy-17-acetoxy-(-)-kauran-19-oic acid-¦Â-D-glucopyranosyl ester
C28H44O10     ÏàËÆ¶È:60%
Phytochemistry          1993          33          1181-1183
Kaurane diterpenoids from Aster ageratoides
Cheng Dong-Liang, Cao Xiao-Ping, Wei Han-Xun, He Lan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     affinoside R
C30H40O10     ÏàËÆ¶È:60%
Phytochemistry          1992          31          3547-3551
Reinvestigation of cardenolide glycosides from seeds of Anodendron affine
Rikako Hanada, Fumiko Abe, Y¨±jir¨­ M¨­ri, Tatsuo Yamauchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     affinoside T
C29H38O10     ÏàËÆ¶È:60%
Phytochemistry          1992          31          3547-3551
Reinvestigation of cardenolide glycosides from seeds of Anodendron affine
Rikako Hanada, Fumiko Abe, Y¨±jir¨­ M¨­ri, Tatsuo Yamauchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     anemonolide(²ÝÓñ÷ÄÚõ¥)
C30H48O5     ÏàËÆ¶È:60%
Chemical Journal of Chinese Universities          2001          22          1338-1341
The Chemical Constituents from Anemone Rivularis
LIAO Xun, LIBo-Gang, WANG Ming-Kui, DING Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     (12S,2'S)-12,19-diacetoxy-18-chloro-4¦Á,6¦Á,-dihydroxy-1¦Â-(2-methylbutanoyloxy)-neo-clerod-13-en-15,16-olide
C29H43ClO10     ÏàËÆ¶È:60%
Fitoterapia          2011          82          1123-1127
neo-Clerodane diterpenes from Ajuga ciliata Bunge and their neuroprotective activities
Ping Guo, Yushan Li, Jing Xu, Yuanqiang Guo, Da-Qing Jin, Jie Gao, Wenbin Hou, Tiejun Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     Meliarachin B
C30H36O11     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2011          Vol. 94          1515-1526
Meliarachins A¨CK: Eleven Limonoids from the Twigs and Leaves of Melia azedarach
Zu-Shang Su, Sheng-Ping Yang, Sheng Zhang, Lei Dong, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     3¦Â-Acetoxy-5-hydroxy-5¦Á-cholestan-6-one
    ÏàËÆ¶È:60%
Steroids          2012          77          461-466
Synthesis and plant growth promoting activity of polyhydroxylated ketones bearing the 5a-hydroxy-6-oxo moiety and cholestane side chain
Anielka Rosado-Ab¨®n, Guadalupe de Dios-Bravo ,Rogelio Rodr¨ªguez-Sotres ,Mart¨ªn A. Iglesias-Arteaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     ¦Á-onocerin
    ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2010          41          1960-1963
Éì½î²ÝµÄ»¯Ñ§³É·ÖÑо¿
ëø´ä´ä;ºÎÓÀÖ¾;·ë½ðÀÚ;°ÍÏþÓê;Àî¶«Ó°
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Hirsutosterol E
C30H50O5     ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2011          9          3272-3278
Hirsutosterols A¨CG, polyoxygenated steroids from a Formosan soft coral Cladiella hirsuta
Bo-Wei Chen, Shu-Ming Chang, Chiung-Yao Huang, Jui-Hsin Su, Zhi-Hong Wen, Yang-Chang Wu and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     Hirsutosterol G
C29H46O5     ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2011          9          3272-3278
Hirsutosterols A¨CG, polyoxygenated steroids from a Formosan soft coral Cladiella hirsuta
Bo-Wei Chen, Shu-Ming Chang, Chiung-Yao Huang, Jui-Hsin Su, Zhi-Hong Wen, Yang-Chang Wu and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     Eremophiloside C
C40H68O14     ÏàËÆ¶È:60%
Tetrahedron          2008          64          5061-5071
Unusual cycloartane glycosides from Astragalus eremophilus
Angela Perrone, Milena Masullo, Carla Bassarello, Elena Bloise, Arafa Hamed, Patrizia Nigro, Cosimo Pizza, Sonia Piacente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     epi-reevesioside F
C30H46O8     ÏàËÆ¶È:60%
Phytochemistry          2013          87          86-95
Cytotoxic cardenolide glycosides from the root of Reevesia formosana
Hsun-Shuo Chang, Michael Y. Chiang, Hsing-Yu Hsu, Cheng-Wei Yang, Chu-Hung Lin, Shiow-Ju Lee, Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     sendanin
    ÏàËÆ¶È:59.3%
Chemical & Pharmaceutical Bulletin          1995          43          1171-1175
Cytotoxic Limonoids and Tetranortriterpenoids from Melia azedarach
Hideji ITOKAWA,Zhi-Sheng QIAO,Chieko HIROBE and Koichi TAKEYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     Chisiamol F
C32H54O7     ÏàËÆ¶È:59.3%
Chinese Journal of Chemistry          2009          27          1805-1810
Chisiamols A¨CF, Triterpenoids from Chisocheton siamensis
Bojun Xie, Shengping Yang, Chen Zhang and Jianmin Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     (9R)-9-deoxo-9-(N,N-dimethylamino)-12,21-epoxy-erythromycin B
C39H72N2O12     ÏàËÆ¶È:59.3%
Journal of Medicinal Chemistry          1991          34          3390-3395
Synthesis and antibacterial activities of C-21 functionalized derivatives of (9R)-9-amino-9-deoxoerythromycins A and B
Paul A. Lartey, Shari L. DeNinno, Ramin Faghih, Dwight J. Hardy, Jacob J. Clement, Jacob J. Plattner, Richard L. Stephens
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     azedarachin B
    ÏàËÆ¶È:59.3%
Heterocycles          1999          50          595-609
Limonoids from Melia toosendan (Meliaceae) and Their Antifeedant Activity
Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     azedarachin B
C32H42O11     ÏàËÆ¶È:59.3%
Heterocycles          1997          45          1781-1786
Antifeeding Limonoids from Melia toosendan
Jian-Bo Zhou, Yuji Minami, Fumio Yagi, Kenjiro Tadera, and Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     hippuristerol F
C31H52O6     ÏàËÆ¶È:58.0%
Journal of Natural Products          2005          68          1366-1370
Steroids from the Gorgonian Isis hippuris
Chih-Hua Chao, Long-Fei Huang, Shwu-Li Wu, Jui-Hsin Su, Ho-Cheng Huang, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     trichilin C
C35H46O13     ÏàËÆ¶È:58.0%
Journal of Natural Products          1998          61          179-184
Limonoids Showing Selective Toxicity to DNA Repair-Deficient Yeast and Other Constituents of Trichilia emetica
A. A. Leslie Gunatilaka, Vanderlan da S. Bolzani, Ermias Dagne, Glenn A. Hofmann, Randall K. Johnson, Francis L. McCabe, Michael R. Mattern, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     compound 5
    ÏàËÆ¶È:58.0%
Chemistry of Natural Compounds          2001          37          343-346
13C NMR SPECTRA OF 5- AND 7-BROMO-6-KETOSTEROIDS AND RELATED COMPOUNDS
N. V. Kovganko, S. N. Sokolov, and V. L. Survilo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     2¦Á,5¦Á,10¦Â-triacetoxy-14¦Â-(2-hydroxyl-3-methyl-butyryl)oxytaxa-4(20),11-diene
C31H46O9     ÏàËÆ¶È:58.0%
Journal of Asian Natural Products Research          2009          11          490-497
Four new minor taxanes from cell cultures of Taxus chinensis
Dan Xiea, Hong-Ting Jiaab, Yi Zhanga, Jian-Hua Zoua, Da-Li Yina, Xiao-Guang Chena,Yu-Ning Yanb and Jun-Gui Daia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     monoglycoside 19-acetylfrugoside
    ÏàËÆ¶È:58.0%
Phytochemistry          1996          42          523-529
Re-investigation of the cardenolide glycosides from Gomphocarpus sinaicus
Nahla S. Abdel-Azim, Faiza M. Hammouda, Dieter Hunkler, Horst Rimpler
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     ajugamacrin B
C31H44O11     ÏàËÆ¶È:58.0%
Phytochemistry          1993          33          887-889
Two neo-clerodane diterpenoids from Ajuga macrosperma
Xiaoyu Shen, Akira Isogai, Kazuo Furihata, Handong Sun, Akinori Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     ajugamacrin B
    ÏàËÆ¶È:58.0%
Phytochemistry          1993          34          1091-1094
Neo-clerodane diterpenoids from ajuga macrosperma and ajuga pantantha
Shien Xiaoyu, Akira Isogai, Kazuo Furihata, Sun Handong, Akinori Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     3-Decladinosyl-9-deoxo-9-dihydro-9a-(N'-benzylthiocarbamoyl)-6-O-methyl-9a-aza-9a-homoerythromycin A
C38H66N3O9S     ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          2011          19          556-566
Novel 9a,11-bridged azalides: One-pot synthesis of N'-substituted 2-imino-1,3-oxazolidines condensed to an azalide aglycone
Zorica Marušić Ištuk, Ana Čikoš, Dubravka Gembarovski, Gorjana Lazarevski, Ivica Ðilović,Dubravka MatkovićČalogović, Goran Kragol
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     ajugaciliatin B
C31H45ClO11     ÏàËÆ¶È:58.0%
Journal of Natural Products          2011          84          1575-1583
Bioactive neo-Clerodane Diterpenoids from the Whole Plants of Ajuga ciliata Bunge
Ping Guo,Yushan Li, Jing Xu, Cuizhou Liu,Yonggang Ma, and Yuanqiang Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     ajugaciliatin D
C31H45ClO11     ÏàËÆ¶È:58.0%
Journal of Natural Products          2011          84          1575-1583
Bioactive neo-Clerodane Diterpenoids from the Whole Plants of Ajuga ciliata Bunge
Ping Guo,Yushan Li, Jing Xu, Cuizhou Liu,Yonggang Ma, and Yuanqiang Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     Ajugamacrin B
    ÏàËÆ¶È:58.0%
Phytochemical Analysis          2002          13          372-380
NMR shift data of neo-clerodane diterpenes from the genus Ajuga
Josep Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     2¦Á,5¦Á,10¦Â-triacetoxy-14¦Â-(2'-methyl)butyryloxy-4(20),11-taxadiene
    ÏàËÆ¶È:58.0%
Journal of Shenyang Pharmaceutical University          2009          26          956-961
Isolation and identification of the taxoids from a callus culture of Taxus cuspidata
BAI Jiao, SUN Dong-xue, LI Zhan-lin, SAKA I Jun-ich i, ANDO M asa-yo shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     sinenxane C
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