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19.32,21.91,28.83,29.21,30.00,31.85,32.32,32.65,33.23,34.03,35.51,35.62,37.46,37.81,40.42,40.50,40.63,44.33,45.04,45.74,46.45,46.55,46.73,48.28,59.66,64.32,66.45,67.82,70.90,70.99,73.00,81.41,92.97,121.20,128.41,145.78,151.59,172.84
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1 .     wattoside B
C34H57O12     ÏàËÆ¶È:57.8%
Acta Botanica Yunnanica          2001          23(3)          373-380
New Steroidal Glycosides from Tupistra wattii
YANG Fan, SHEN Ping,WANG Yi-Fei,ZHANG Ren-Yan, YANG Chong-Ren
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-amyrin-3-palmitate
C46H80O2     ÏàËÆ¶È:57.8%
Chinese Journal of Natural Medicines          2007          5          259-262
Non-alkaline Constituents From the Leaf of Alstonia scholaris
DU Guo-Shun; CAI Xiang-Hai; SHANG Jian-Hua; LUO Xiao-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Olean-12-en-3¦Â,16¦Â-diol-3-O-palmitate
    ÏàËÆ¶È:57.8%
Pharmazie          2006          61          70-73
Triterpenoids from Pyrethrum tatsienense
Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     N'-[N-(2¦Á,3¦Â-dihydroxy-12-oleanen-28-oyl)-L-alanyl]-glycine
C35H56N2O6     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2009          17          1139-1145
Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides
Andres Parra, Francisco Rivas, Pilar E. Lopez, Andres Garcia-Granados, Antonio Martinez, Fernando Albericio, Nieves Marquez, Eduardo Muñoz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     caulophyllogenin-3-O-¦Á-L-arabinopyranoside
C35H56O9     ÏàËÆ¶È:57.8%
Journal of Anhui Agricultural Sciences          2012          40          745-747
Study on the Chemical Constitutes of C. robustum root
MA Yang-min et al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     pukeensine
C44H64N2O3     ÏàËÆ¶È:57.5%
Acta Pharmaceutica Sinica          1992          27          394-396
A NEW SKELETON BISDITERPENOID ALKALOID FROM ACONITUM PUKEENSE
LS Ding; FE Wu; YZ Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     3-O-¦Â-D-galactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl quillaic acid
    ÏàËÆ¶È:57.1%
Phytochemistry          1995          40          509-514
Acylated triterpene saponins from Silene jenisseensis
Marie-Aleth Lacaille-Dubois, Bernard Hanquet, Zhen-Hua Cui, Zhi-Cen Lou, Hildebert Wagner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Lilioglycoside C
C39H60O13     ÏàËÆ¶È:56.4%
Chemistry of Natural Compounds          1997          33          658-662
sTRuCTURES OF SOME LILIOGLYCOSIDES FROM THE BULBS OF Lilium regale
P. K. Kintya, A. S. Gur'eva, N. E. Mashchenko,and A. S. Shashkov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     N-[3-(6-aminohexyl)aminocarbonyl]propyl-2-cyano-3,12-dioxooleana-1,9(11)-dien-28-amide trifluoroacetate
C41H62N4O4     ÏàËÆ¶È:56.4%
Journal of Medicinal Chemistry          2004          47          4923-4932
Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets
Tadashi Honda, Tomasz Janosik, Yukiko Honda, Jie Han, Karen T. Liby, Charlotte R. Williams, Robin D. Couch, Amy C. Anderson, Michael B. Sporn, and Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N''-[N'-[N-(2¦Á,3¦Â-dihydroxy-12-oleanen-28-oyl)-6-aminohexanoyl]-L-alanyl]-glycine
C41H67N3O7     ÏàËÆ¶È:56.0%
Bioorganic & Medicinal Chemistry          2009          17          1139-1145
Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides
Andres Parra, Francisco Rivas, Pilar E. Lopez, Andres Garcia-Granados, Antonio Martinez, Fernando Albericio, Nieves Marquez, Eduardo Muñoz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2¦Á,3¦Â,21¦Â-trihydroxyolean-12-en-28-oic acid 28-O-¦Â-D-glucopyranoside
C36H58O10     ÏàËÆ¶È:55.2%
Planta Medica          2009          75          522-527
Antimicrobial Pentacyclic Triterpenoids from Terminalia superba
Turibio Kuiate Tabopda, Joseph Ngoupayo, Sheraz A. Khan Tanoli, Anne-Claire Mitaine-Offer,Bonaventure Tchaleu Ngadjui, Muhammad Shaiq Ali, Bang Luu, Marie-Aleth Lacaille-Dubois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     brevicuspisaponin 2
C35H56O10     ÏàËÆ¶È:55.2%
Phytochemistry          2000          53          901-904
Triterpenoid glycosides and a triterpene from Ilex brevicuspis
Alexandre T. Cardoso Taketa, Tatjana Schmittmann-Schlager, Dominique Guillaum, Grace Gosmann, Eloir Paulo Schenkel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (22S,25R)-Furost-5-ene-3¦Â,22,26-triol 22-O-(¦Á-D-glucopyranoside)
C33H54O9     ÏàËÆ¶È:55.2%
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
14 .     (22R,25R)-Furost-5-ene-3¦Â,22,26-triol 22-O-(¦Á-D-glucopyranoside)
C33H54O9     ÏàËÆ¶È:55.2%
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
15 .     olean-12-en-3¦Â,15¦Á-yl diacetate
    ÏàËÆ¶È:55.2%
Phytochemistry          1988          27          3653-3657
Alkaloids from Alstonia macrophylla
Atta-ur-rahman,Gulzar Ahmed,M.Iqbal Choudhary,Habib-ur-rehman,K.T. De Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     23-hydroxyimberbic acid-23-O-¦Á-L-4-acetyl-rhamnopyranoside
    ÏàËÆ¶È:55.2%
Chinese Traditional and Herbal Drugs          2008          39          512-514
é­Ðη糵×ÓÒ¶ÖÐÝÆÀ໯ºÏÎïµÄÑо¿
ÎâÏþÅô;³Â¹âÓ¢;½¯²ÅÎä;Öì¹úÔª;·½ºêÑ«
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ÉßÝÔËØ A
    ÏàËÆ¶È:55.2%
Chinese Traditional and Herbal Drugs          2005          36          830-831
˼éÉßÝԵĻ¯Ñ§³É·ÖÑо¿(¢ñ)
´÷ÖÒ,Íõ¸ÖÁ¦,Íõ·å,ÂíË«³É,ÁÖÈð³¬
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Pinnatoxin B
    ÏàËÆ¶È:55.2%
Tetrahedron Letters          2001          42          3491-3494
Pinnatoxins B and C, the most toxic components in the pinnatoxin series from the Okinawan bivalve Pinna muricata
Noboru Takada, Naoyoshi Umemura, Kiyotake Suenaga, Tong Chou, Akito Nagatsu, Takeharu Haino, Kaoru Yamada, Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Pinnatoxin C
    ÏàËÆ¶È:55.2%
Tetrahedron Letters          2001          42          3491-3494
Pinnatoxins B and C, the most toxic components in the pinnatoxin series from the Okinawan bivalve Pinna muricata
Noboru Takada, Naoyoshi Umemura, Kiyotake Suenaga, Tong Chou, Akito Nagatsu, Takeharu Haino, Kaoru Yamada, Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ¦Â-amyrin 3-palmitate
C46H50O2     ÏàËÆ¶È:55.2%
Natural Product Research and Development          1998          10(3)          20-23
TWO NEW TRITERPENE ESTER FROM PRATIA BEGONIFOLIA
Liu Xikui; Chiu Minghua; Li Zhongrong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     22-methoxy-5¦Â-furostane-1¦Â,3¦Â,4¦Â,5¦Â,26-pentaol 26-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:55.2%
Natural Product Research and Development          1995          7(1)          19-23
STEROIDAL GLYCOSTDES FROM ASPIDISTRA SICHUANENSTS K. Y. LANG ET Z. Y. ZHU
Chen Mengjing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     4''-O-[3-(1,2,3,4-tetrahydro-3-quinolinyl)propanoyl]-8a-aza-8a-homoerythromycin A
C49H81N3O14     ÏàËÆ¶È:55.2%
The Journal of Antibiotics          2009          62          133-144
Synthesis and biological properties of 4"-O-acyl derivatives of 8a-Aza-8a-homoerythromycin
Vlado Stimac, Sulejman Alihodzic, Gorjana Lazarevski, Stjepan Mutak, Zorica Marusic Istuk, Andrea Fajdetic, Ivana Palej, Hana Cipcic Paljetak, Jasna Padovan, Branka Tavcar and Vesna Erakovic Haber
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     (4R,4¦ÁR,4¦ÂR,6¦ÁR,7R,8R,10¦ÁR,10¦ÂR,12¦ÁR)-hexadecahydro-¦Á8,¦Á8,3,3,7,10¦Á,10¦Â-heptamethyl-13-oxo-7-{2-oxo-2-[(2-phenylethyl)amino]ethyl}-1H-4,12¦Á-(epoxymethano)chrysene-8-acetic acid
C38H55NO5     ÏàËÆ¶È:55.2%
Helvetica Chimica Acta          2013          96          1757-1781
Synthesis of Nitrogen-Containing Derivatives of (18,19¦Â)-19-Hydroxy-2,3-secooleanane-2,3,28-trioic Acid 28,19-Lactone
Andrey V. Shernyukov, Ilya Ya. Mainagashev, Dina V. Korchagina, Alexander M. Genaev, Nina I. Komarova, Nariman F. Salakhutdinov and Genrikh A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (4'R,4''R,2'''S,¦ÁR)-1-[2'-Oxo-4'-pentyl-N(5')-methyl-1',5'-diazocan-N(1')-yl]-4-{2''-oxo-4''-[2'''-(benzyloxy)heptyl]-N(5'')-(¦Á-methylbenzyl)-1'',5''-diazocan-N(1')-yl}butane
C44H70N4O3     ÏàËÆ¶È:55.2%
The Journal of Organic Chemistry          2012          77          9724-9737
Absolute Configuration Assignment by Asymmetric Syntheses of the Homalium Alkaloids (−-(R,R,R)-Hoprominol and (−-(4¡äS,4¡åR,2‴R)-Hopromalinol
Stephen G. Davies, James A. Lee, Paul M. Roberts, Jeffrey P. Stonehouse, and James E. Thomson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 10c
C38H64O7     ÏàËÆ¶È:55.2%
Steroids          2013          78          651-661
Synthesis of various secosteroidal macrocycles by ring-closing metathesis
Malika Ibrahim-Ouali, Eug¨¦nie Romero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     3¦Â-Acetoxy-28-oxo-28-[3-acetyl-(3-aminopropyl)-amino]lup-20(29)-ene
C37H60N2O2     ÏàËÆ¶È:55.2%
Russian Journal of Bioorganic Chemistry          2013          39          329-337
Synthesis of aminopropylamino derivatives of betulinic and oleanolic acids
G. V. Giniyatullina, O. B. Kazakova, N. I. Medvedeva, I. V. Sorokina, N. A. Zhukova, T. G. Tolstikova, G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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