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13C NMR (75 MHz, MeOD) ¦Ä    14.49, 17.63,18.50,20.26, 21.49,22.61,23.57,  24.45, 24.65,28.96, 29.47, 31.75, 32.17,32.87,35.15, 37.33, 38.73,39.22,42.22, 51.32, 51.78,  66.65, 68.42, 68.70, 71.10, 84.89, 85.24, 85.41,105.35, 122.14,  127.36,  129.00,  129.82, 131.10,132.31, 133.59, 167.63,  206.45
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1 .     ecdysterone 22,25-Di-O-benzoate
    ÏàËÆ¶È:63.1%
Chemistry of Natural Compounds          1990          26          301-303
PHYTOECDYSTEROIDS OF PLANTS OF THE GENUS Silene.XVII. ECDYSTERONE 22,25-DI-O-BENZOATE FROM Silene scabrifolia
A. Saatov, N. D. Abdullaev,M. B. Gorovits, and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Momordicoside V
C36H58O8     ÏàËÆ¶È:63.1%
Magnetic Resonance in Chemistry          2010          48          392-396
Cucurbitane-type triterpene glycosides from the fruits of Momordica charantia (pages 392¨C396)
Nguyen Xuan Nhiem, Phan Van Kiem, Chau Van Minh, Ninh Khac Ban, Nguyen Xuan Cuong, Le Minh Ha, Bui Huu Tai, Tran Hong Quang, Nguyen Huu Tung and Young Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 7
    ÏàËÆ¶È:63.1%
Tetrahedron Letters          2003          44          6673-6677
Degradation of triterpenic compounds from olive-pressing residues. Synthesis of trans-decalin type chiral synthons
Andr¨¦s Garcı́a-Granados, Pilar E L¨®pez, Enrique Melguizo, Andr¨¦s Parra, Yolanda Sime¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 8
C37H56O3     ÏàËÆ¶È:60.5%
Journal of Natural Products          2007          70          147-153
Chemical Transformation and Biological Activities of Ambrein, a Major Product of Ambergris from Physeter macrocephalus (Sperm Whale)
Ya-Ching Shen,Shi-Yie Cheng,Yao-Haur Kuo,Tsong-Long Hwang,Michael Y. Chiang,and Ashraf Taha Khalil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3'-O-benzoyl-13do decanoylingenol
    ÏàËÆ¶È:60.5%
Chinese Traditional and Herbal Drugs          2010          41          877-881
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Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 5
C42H65BO7Si     ÏàËÆ¶È:60.5%
Journal of Asian Natural Products Research          2011          13          297-303
Synthesis of a novel phosphate analog of 20-hydroxylecdysone with potent hypoglycemic activity
Dan Zhang; Min Zhang; Bao Ding; Xiao-Lin Wang; Zong-Yin Qiu; Yong Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3¦Â-(E)-cinnamoyleuphorbol
    ÏàËÆ¶È:60.5%
Journal of the Brazilian Chemical Society          2011          22          1880-1887
Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br.
Rosalina C. S. Mata, Dina I. M. D. de Mendonça, Liliana Vieira, Aldenir F. dos Santos, Luciana A. da Silva, Jorge F. Gaspar, C¨¦lia Martins, Jos¨¦ Rueff and Antônio E. G. Sant¡¯Ana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     5,15-bis(4-dioxylborylphenyl)porphyrin with 20-hydroxyecdysone
C86H104B2N4O14     ÏàËÆ¶È:60.5%
Steroids          2012          77          1169-1175
Design and studies of novel polyoxysterol-based porphyrin conjugates
Halina A. Zhylitskaya, Vladimir N. Zhabinskii, Raisa P. Litvinovskaya, Raffaella Lettieri, Donato Monti, Mariano Venanzi, Vladimir A. Khripach, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     21-cis,cis,cis-9,12,15-Octadecatrienoyloxy-11¦Â,17¦Á-dihydroxypregn-4-en-3,20-dione
C39H58O6     ÏàËÆ¶È:58.9%
Steroids          2009          74          1007-1014
Lipase-catalyzed regioselective preparation of fatty acid esters of hydrocortisone
Paula G. Quintana, Alicia Baldessari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     28-(2'-Methyl-1H-imidazol-1-yl)-3,28-dioxours-12-en-2-(2'-methyl-1H-imidazol-1-yl)-methylene
C39H54N4O2     ÏàËÆ¶È:58.9%
Bioorganic & Medicinal Chemistry          2012          20          5774-5786
Synthesis of novel ursolic acid heterocyclic derivatives with improved abilities of antiproliferation and induction of p53, p21waf1 and NOXA in pancreatic cancer cells
Ana S. Leal, Rui Wang, Jorge A.R. Salvador, Yongkui Jing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Garcimultiflorone C
C38H52O7     ÏàËÆ¶È:57.8%
Journal of Natural Products          2009          72          253-258
Benzophenone Derivatives from the Fruits of Garcinia multiflora and Their Anti-inflammatory Activity
Jih-Jung Chen, Chia-Wei Ting, Tsong-Long Hwang, and Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     carteriosulfonic acid B
C38H69NO12S     ÏàËÆ¶È:57.8%
Journal of Natural Products          2009          72          1651-1656
Carteriosulfonic Acids A-C, GSK-3¦ÂInhibitors from a Carteriospongia sp.
Malcolm W. B. McCulloch, Tim S. Bugni, Gisela P. Concepcion, Gary S. Coombs, Mary Kay Harper, Simran Kaur,Gina C. Mangalindan, Misha M. Mutizwa, Charles A. Veltri, David M. Virshup, and Chris M. Ireland
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-O-benzoyl-13-octanoyloxyingenol
C35H46O8     ÏàËÆ¶È:57.8%
Phytochemistry          2008          69          812-819
Ingenane diterpenoids from Euphorbia esula
Zhi-Qiang Lu, Min Yang, Jin-Qiang Zhang, Guang-Tong Chen, Hui-Lian Huang,Shu-Hong Guan, Chao Ma, Xuan Liu, De-An Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3,20-O-diacetylingenol 5-O-(2' E,4' Z)-tetradecadienoate
C38H54O8     ÏàËÆ¶È:57.8%
Planta Medica          1996          62          260-262
Ingenane Diterpenes from Euphorbia petiolata
Yan-Ping Shi, Zhong-Jian Jia, Bin Ma, Sadiq Saleh, and Jamil Lahham
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     makisterone C
C35H56O7     ÏàËÆ¶È:57.8%
Helvetica Chimica Acta          2009          92          753-761
Ecdysteroids from Silene viridiflora
Andr¨¢s Simon, No¨¦mi T¨®th, G¨¢bor T¨®th, Zolt¨¢n Kele, Judit Groska, M¨¢ria B¨¢thori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     15-Hydroxyponasterone A
C27H44O7     ÏàËÆ¶È:57.8%
Steroids          2008          73          502-514
Additional minor ecdysteroid components of Leuzea carthamoides
Miloš Bud¨§š¨ªnsky, Karel Vok¨¢č, Juraj Harmatha, Josef Cvačka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     roylenine
C37H58O12     ÏàËÆ¶È:57.8%
Journal of Asian Natural Products Research          2008          10          1023-1028
A new pregnane glycoside from Marsdenia roylei as potential antioxidant and antidyslipidemic agents
Arun Seth, Sudha Paswan, Sanjay Srivastav, Naveen Kumar Khare, Akriti Bhatia,Alok Kumar, Geetik Bhatia, Mohamm Mubin Khan, Ashok Kumar Khann and Jitendr Kumar Saxen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 1a
    ÏàËÆ¶È:57.8%
Journal of Natural Products          1995          Vol 58          1570-1574
Triterpenoids from the Aerial Parts of Lantana camara
Sabira Begum, Syed Mohammad Raza, Bina Shaheen Siddiqui, Salimuzzaman Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     camarilic acid
C36H54O6     ÏàËÆ¶È:57.8%
Journal of Natural Products          1995          Vol 58          1570-1574
Triterpenoids from the Aerial Parts of Lantana camara
Sabira Begum, Syed Mohammad Raza, Bina Shaheen Siddiqui, Salimuzzaman Siddiqui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (25R)-26-acetyloxy-3¦Â-benzoyloxycholest-5-ene-16,22-dione
C36H48O6     ÏàËÆ¶È:57.8%
Steroids          2011          76          18-27
The synthesis of cholestane and furostan saponin analogues and the determination of sapogenin¡¯s absolute configuration at C-22
Haixing Wang, Yanshen Guo, Yuyao Guan, Liang Zhou, Pingsheng Lei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Citrinadin A
C35H52O6N4     ÏàËÆ¶È:57.8%
Organic Letters          2004          Vol. 6, No. 18          3087-3089
Citrinadin A, a Novel Pentacyclic Alkaloid from Marine-Derived Fungus Penicillium citrinum
Masashi Tsuda, Yuu Kasai, Kazusei Komatsu, Teruo Sone, Michiko Tanaka,Yuzuru Mikami, and Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     niuxixinsterone A
C34H50O9     ÏàËÆ¶È:57.8%
Molecules          2011          16          5989-5997
Three New Phytoecdysteroids Containing a Furan Ring from the Roots of Achyranthes bidentata Bl.
Qiu-Hong Wang, Liu Yang, Hai Jiang, Zhi-Bin Wang, Bing-You Yang and Hai-Xue Kuang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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