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1 .     buxaminol B
C27H46N2O     ÏàËÆ¶È:65.3%
Journal of Natural Products          1986          Vol 49          106
Alkaloids from the Leaves of Buxus papilosa
Atta-ur-Rahman, M. Iqbal Choudhary, Irshad Ali, Habib-ur-Rehman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2S-hydroxyisobromosphaerol
C20H32Br2O2     ÏàËÆ¶È:62.5%
Journal of Natural Products          2008          71(8)          1386-1392
Brominated Diterpenes with Antibacterial Activity from the Red Alga Sphaerococcus coronopifolius
Vangelis Smyrniotopoulos, Constantinos Vagias, M.Mukhlesur Rahman, Simon Gibbons, and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     kahukuene B
C20H32OBr2     ÏàËÆ¶È:62.5%
Journal of Natural Products          1993          Vol 56          76
Kahukuenes, New Diterpenoids from the Marine Alga Laurencia majuscula
Mary Roger Brennan, In Kyu Kim, Karen L. Erickson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     grayanoside D
    ÏàËÆ¶È:62.5%
Phytochemistry          1980          19          2159-2162
Grayanoside D, A diterpene glucoside from Leucothoe Grayana
Jinsaku Sakakibara, Naohiro Shirai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-oxo-6¦Â-hydroxyolean-18-en-28-oic acid methyl ester
C31H48O4     ÏàËÆ¶È:62.0%
Phytochemistry          1983          22          1828-1830
3-oxo-6¦Â-hydroxyolean-18-en-28-oic acid from orthopterygium huancuy
Antonio G. Gonz¨¢lez, Jos¨¦ Amaro, Braulio M. Fraga, Javier G. Luis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Buxaminol A
    ÏàËÆ¶È:61.5%
Journal of Natural Products          2010          73          1858-1862
Triterpenoidal Alkaloids from Buxus natalensis and Their Acetylcholinesterase Inhibitory Activity
Wadim L. Matochko, Abin James, Cheuk W. Lam, Daniel J. Kozera, Athar Ata, and Robert M. Gengan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     stigmast-5-en-3-ol
C29H50O     ÏàËÆ¶È:60.7%
Journal of Medicinal Plants Research          2012          6          3923-3930
Isolation and identification of phytochemical constituents from Scrophularia takesimensis
Hye Min Kim, Mi-Jeong Ahn and Sanghyun Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3',4',5',5,7-pentamethoxy-4-acetyldelphinidin-3-O-¦Á-L-rhamnoside
C28H36O13     ÏàËÆ¶È:60.7%
Asian Journal of Chemistry          2008          20          6027-6032
Isolation and Antimicrobial Studies of the Compounds Isolated from the Stem Bark of Ficus hispida Linn.
BIMOLA D. ASEM and WARJEET S. LAITONJAM
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (+)-muqubilone B diol
C25H46O6     ÏàËÆ¶È:60%
Journal of Natural Products          2009          72          218-222
The Marine Sponge Diacarnus bismarckensis as a Source of Peroxiterpene Inhibitors of Trypanosoma brucei, the Causative Agent of Sleeping Sickness
Brent K. Rubio, Karen Tenney, Kean-Hooi Ang, Maha Abdulla, Michelle Arkin, James H. McKerrow, and Phillip Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     cladosporide A
C25H40O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2000          48(10)          1422-1426
A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated form Cladosporium sp.
Tomoo HOSOE,Hideaki OKADA,Takeshi ITABASHI,Koohei NOZAWA,Kaoru OKADA,Galba Maria de CAMPOS TAKAKI,Kazutaka FUKUSHIMA,Makoto MIYAJI and Ken-ichi KAWAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     cladosporide A
C25H40O3     ÏàËÆ¶È:60%
The Journal of Antibiotics          2001          54          747-750
New Pentanorlanostane Derivatives, Cladosporide B-D, as Characteristic Antifungal Agents Against Aspergillus fumigatus, Isolated from Cladosporium sp.
TOMOO HOSOE,SHIGERU OKAMOTO,KOOHEI NOZAWA,KEN-ICHI KAWAI,KAORU OKADA,GALBA MARIA DE CAMPOS TAKAKI,KAZUTAKA FUKUSHIMA and MAKOTO MIYAJI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ophiobora-3(20),7,18-triene
    ÏàËÆ¶È:60%
Organic Letters          2013          15          594-597
Identification of Ophiobolin F Synthase by a Genome Mining Approach: A Sesterterpene Synthase from Aspergillus clavatus
Ryota Chiba, Atsushi Minami, Katsuya Gomi, and Hideaki Oikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     cycloart-24-en-3¦Â,26-diol
    ÏàËÆ¶È:59.2%
Chinese Journal of Natural Medicines          2012          10          36-39
Chemical constituents of Allophylus longipes
Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (22E)-2¦Â,3¦Â-dihydroxy-5¦Á-stigmast-22-en-6-one
C29H48O3     ÏàËÆ¶È:58.6%
Steroids          1994          59          463-467
Synthesis of new brassinosteroids with potential activity as antiecdysteroids
Carme Brosa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     phlomistetraol B
    ÏàËÆ¶È:58.6%
China Journal of Chinese Materia Medica          2012          37          2088-2091
A new C-28 nortriterpenoid from fruits of Leonurus japonicus
ZHENG Yuqing; YAN He; HAN Jing; TAN Ninghua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     secolincomolide B Keto form
C23H40O5     ÏàËÆ¶È:58.3%
Planta Medica          2002          68          142-145
Cytotoxic Butanolides and Secobutanolides from the Stem Wood of Formosan Lindera communis
Ian-Lih Tsai,Chao-Hui Hung ,Chang-Yih Duh,Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     20,22-isovaleriate-5¦Â-cholest-7-ene-2¦Â,3¦Â,14¦Á,20R,22R,25-hexahydroxy-6-one
C32H5207     ÏàËÆ¶È:58.3%
Chemistry of Natural Compounds          2001          37          262-265
ECDYSTEROIDS FROM Silene claviformis
Z. Sadikov,1 Z. Sa atov, M. G arcia,J.-P. Girault, and R. Lafont
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     14¦Á-hydroxycortisol
C21H32O5     ÏàËÆ¶È:58.3%
Natural Product Research          1996          9          1-5
Fungal Metabolism of Cortisol. Major Formation of a 5¦Â-Dihydro-Derivative by Curvularia Lunata
Bertrand Leblond; Robert Azerad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2013-10-15 22:52:03
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