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×ÏÒÂÇáÆï: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-09 21:09:54
1 .     (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-7-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-13-oxo-1H-4,12¦Á-(epoxymethano)chrysene-8-acetic acid
C35H56O6N2     ÏàËÆ¶È:72.9%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (4R,4¦ÁR,4¦ÂR,6¦ÁR,7R,8R,10¦ÁR,10¦ÂR,12¦ÁR)-7-[2-(4-ethylpiperazin-1-yl)-2-oxoethyl]hexadecahydro-¦Á8,¦Á8,3,3,7,10¦Á,10¦Â-heptamethyl-13-oxo-1H-4,12¦Á-(epoxymethano)chrysene-8-acetic acid
C36H58N2O5     ÏàËÆ¶È:72.9%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3¦Â-Acetoxy-28-oxo-28-[3-acetyl-(3-aminopropyl)-amino]lup-20(29)-ene
C37H60N2O2     ÏàËÆ¶È:72.9%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     spirasine V/VI
    ÏàËÆ¶È:71.0%
Journal of Integrative Plant Biology          2005          47          120-123
Two New Diterpenoid from Spiraea japonica L.F. var. fortunei (Planchon)Rehd
Li-Ming FAN, Hong-Ping HE, Yue-Mao SHENand Xiao-Jiang HAO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     3-O-[¦Á-D-mannopyranosyl-(1¡ú2)-¦Á-D-mannopyranosyl]oleanolic acid
C42H68O13     ÏàËÆ¶È:70.7%
Bioorganic & Medicinal Chemistry          2009          17          5207-5218
Mannosylated saponins based on oleanolic and glycyrrhizic acids. Towards synthetic colloidal antigen delivery systems
Alison M. Daines, Ben W. Greatrex, Colin M. Hayman, Sarah M. Hook, Warren T. McBurney, Thomas Rades, Phillip M. Rendle, Ian M. Sims
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (3¦Â,22E)-stigmasta-5,22-dien-3-yl 4-(piperazin-1-yl)-4-oxobutanoate
C37H60N2O3     ÏàËÆ¶È:70.7%
Steroids          2012          77          1212-1218
Polyamine conjugates of stigmasterol
Norbert Vida, Hana Svobodov¨¢, Lucie R¨¢rov¨¢, Pavel Drašar, David Šaman, Josef Cvačka, Zden¨§k Wimmer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     compound 6
C51H66O5     ÏàËÆ¶È:70.2%
Bioorganic & Medicinal Chemistry Letters          2011          21          338-341
Efficient synthesis and biological evaluation of epiceanothic acid and related compounds
Pu Zhang, Li Xu, Keduo Qian, Jun Liu, Luyong Zhang, Kuo-Hsiung Lee , Hongbin Sun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3-O-(3',3'-dimethylsuccinyl)betulin
C36H58O5     ÏàËÆ¶È:70.2%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     plagiospirolide B
C15H20O2     ÏàËÆ¶È:70.2%
Tetrahedron          1989          45          5003-5014
Novel C - 35 terpenoids from the Panamanian liverwort plagiochila moritziana
J. Spörle, H. Becker, M.P. Gupta, M. Veith, V. Huch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (4R,4¦ÁR,4¦ÂR,6¦ÁR,7R,8R,10¦ÁR,10¦ÂR,12¦ÁR)-hexadecahydro-7-{2-{[(4-methoxyphenyl)methyl]ami-no}-2-oxoethyl}-¦Á8,¦Á8,3,3,7,10¦Á,10¦Â-heptamethyl-13-oxo-1H-4,12¦Á-(epoxymethano)chrysene-8-acetic acid
    ÏàËÆ¶È:70.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     (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:70.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     (4R,4¦ÁR,4¦ÂR,6¦ÁR,7R,8R,10¦ÁR,10¦ÂR,12¦ÁR)-8-{1,1-dimethyl-2-oxo-2-[(2-phenylethyl)amino]ethyl}-hexadecahydro-3,3,7,10¦Á,10¦Â-pentamethyl-13-oxo-1H-4,12¦Á-(epoxymethano)chrysene-7-acetic acid
C38H55NO5     ÏàËÆ¶È:70.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     (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-(tricyclo[3.3.1.1(3,7)]dec-1-ylamino)ethyl]-1H-4,12¦Á-(epoxymethano)chrysene-8-acetic acid
    ÏàËÆ¶È:70.2%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     Methyl 3-oxo-3'S-(chloromethyl)-4'R-(nitromethyl)spiro[2(1')R-cyclopentane]-dihydrobetulonate
C37H58ClNO5     ÏàËÆ¶È:70.2%
Tetrahedron Letters          2012          53          217-221
The first synthesis of spirocyclopentyl derivatives of lupane triterpenoids by radical nitrocyclization of C-2-diallyl substituted betulonates
Anna Yu. Spivak, Elvira R. Shakurova, Darya A. Nedopekina, Sergey L. Khursan, Michail Yu. Ovchinnikov, Leonard M. Khalilov, Victor N. Odinokov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     Methyl (3¦Â)-3-[(L)-lysyloxy]-11-oxoolean-12-en-30-oate
C37H60N2O5     ÏàËÆ¶È:70.2%
Zeitschrift f¨¹r Naturforschung B          2012          67          731-746
Synthesis and Cytotoxic Activity of Methyl Glycyrrhetinate Esterified with Amino Acids
Ren¨¦ Csuk, Stefan Schwarz, Bianka Siewert, Ralph Kluge, and Dieter Ströhl
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     3-O-(3',3'-dimethylglutaryl)-28-O-tritylbetulin
C56H74O5     ÏàËÆ¶È:69.0%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     28-[1-(¦Â-D-Mannopyranosyl)-1H-1,2,3-triazol-4-yl]-lup-20(29)-en-3,28-dione
C38H57N3O7     ÏàËÆ¶È:68.4%
Archiv der Pharmazie          2011          1          37-49
Synthesis, Encapsulation and Antitumor Activity of New Betulin Derivatives
Ren¨¦ Csuk, Alexander Barthel, Ronny Sczepek, Bianka Siewert, and Stefan Schwarz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3-O-acetylbetulinic acid Chorohexyl ester
    ÏàËÆ¶È:68.4%
Archiv der Pharmazie          2010          343          449-457
Synthesis and Anticancer Activity of Novel Betulinic acid and Betulin Derivatives
Harish Kommera, Goran N. Kaluđerović, Jutta Kalbitz and Reinhard Paschke
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     10¦Á-hydroxy-9¦Á-methyl-15-oxo-20-nor-kauran-19-oic acid methyl ester-16¦Á-yl-14'¦Á,16'¦Á,17'-trihydroxy-15'-oxo-ent-kaur-11'-en-19'-oate
C41H58O10     ÏàËÆ¶È:68.2%
Planta Medica          2004          70          540-550
Structure of Kaurane-Type Diterpenes from Parinari sprucei and their Potential Anticancer Activity
Alessandra Braca,Annahil Armenise, Ivano Morelli,Jeannette Mendez,Qiuwen Mi,Hee-Byung Chai,Steven M. Swanson ,A. Douglas Kinghorn,Nunziatina De Tommasi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     3-O-(3',3'-dimethylsuccinyl)-28-O-tritylbetulin
C55H72O5     ÏàËÆ¶È:68.2%
Bioorganic & Medicinal Chemistry          2010          18          6451-6469
Conjugates of betulin derivatives with AZT as potent anti-HIV agents
Juan Xiong, Yoshiki Kashiwada, Chin-Ho Chen, Keduo Qian, Susan L. Morris-Natschke, Kuo-Hsiung Lee, Yoshihisa Takaishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-03-09 16:00:49
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