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9.4,10.2,18.5,19.4,25.6,33.1,35.2,36.1,37.5,39.8,42.1,42.9,48.5,54.8,56.3,56.6,57.5,59.2,83.5,88.9,117.6,121.1,122.5,128.6,133.6,138.3,139.3,143.4,153.5,159.1,196.6,202.4
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jiangchunyong: ½ð±Ò+2, лл 2012-09-14 15:17:54
1 .     6'-Chloro-(24R)-24-ethyl-cholest[3,4-b]pyridin-5,22-diene
C32H46NCl     ÏàËÆ¶È:53.1%
Steroids          2008          73          1137-1142
Convenient preparation of A-ring fused pyridines from steroidal enamides
Madan G. Barthakur, Moyurima Borthakur, Romesh C. Boruah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     amaranzole B
C37H48N2O15S3     ÏàËÆ¶È:51.4%
The Journal of Organic Chemistry          2010          75          2453-2460
Amaranzoles B−F, Imidazole-2-carboxy Steroids from the Marine Sponge Phorbas amaranthus. C24-N-and C24-O-Analogues from a Divergent Oxidative Biosynthesis
Brandon I. Morinaka, Joseph R. Pawlik and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     norselic acid A
C29H40O4     ÏàËÆ¶È:50%
Journal of Natural Products          2009          72          1842-1846
Norselic Acids A-E, Highly Oxidized Anti-infective Steroids that Deter Mesograzer Predation, from the Antarctic Sponge Crella sp.
Wai S. Ma,Tina Mutka,Brian Vesley, Margaret O. Amsler, James B. McClintock, Charles D. Amsler, Jason A. Perman,Maya P. Singh, William M. Maiese, Michael J. Zaworotko, Dennis E. Kyle, and Bill J. Baker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     plakinamine F
C31H48N2O     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          1474-1476
New Steroidal Alkaloids from an Undescribed Sponge of the Genus Corticium
Hyi-Seung Lee,Youngwan Seo,Jung-Rae Rho, Jongheon Shin,and Valerie J. Paul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     schleicheol 1
C30H52O2     ÏàËÆ¶È:50%
Journal of Natural Products          2000          63          72-78
Isolation and Structures of Schleicherastatins 1-7 and Schleicheols 1 and 2 from the Teak Forest Medicinal Tree Schleichera oleosa1
George R. Pettit,Atsushi Numata, Gordon M. Cragg, Delbert L. Herald, Tamie Takada,Chika Iwamoto,Roland Riesen, Jean M. Schmidt, Dennis L. Doubek, and Animesh Goswami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     acoseptine
C32H44N2O7     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1999          35          91-93
STRUCTURE OF ACOSEPTINE m A REPRESENTATIVE OF A NEW TYPE OF NORDITERPENOID ALKALOIDS
S. K. Usmanova, L A. Bessonova,N. D. Abduilaev, and M. G. Levkovich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     1' ,4' ,16,17-Tetrahydro-3¦Â-hydroxy-6 '-methoxy-4' -methyl-(16¦Â,17¦Á)-androsta-5,16-dieno[17,16-b]quinoline
C28H39NO2     ÏàËÆ¶È:50%
Steroids          2004          69          301-312
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions
Ang¨¦la Magyar, J¨¢nos Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     1' ,4' ,16,17-Tetrahydro-3¦Â-hydroxy-6 '-methoxy-4 '-methyl-(16¦Á,17¦Á)-androsta-5,16-dieno[17,16-b]quinoline
C28H39NO2     ÏàËÆ¶È:50%
Steroids          2004          69          301-312
Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions
Ang¨¦la Magyar, J¨¢nos Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, P¨¦ter Forg¨®, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     17¦Â-[3-(N-4-Methoxyphenyl)tetrahydrooxazin-2-on-6-yl]androst-5-en-3¦Â-ol
C30H41O4N     ÏàËÆ¶È:50%
Steroids          2004          69          451-460
Neighboring group participation: Part 15. Stereoselective synthesis of some steroidal tetrahydrooxazin-2-ones, as novel presumed inhibitors of human 5¦Á-reductase
J¨¢nos Wölfling, L¨¢szl¨® Hackler, Erzs¨¦bet Merny¨¢k, Gyula Schneider, Istv¨¢n T¨®th, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, P¨¢l Soh¨¢r, Antal Cs¨¢mpai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     2'-Phenyl-(24R)-24-ethyl-cholest[3,2-d]pyrimidin-4,22-diene
C37H50N2     ÏàËÆ¶È:50%
Steroids          2009          74          730-734
A facile three-component solid phase synthesis of steroidal A-ring fused pyrimidines under microwave irradiation
Madan G. Barthakur, Shyamalee Gogoi, Mandakini Dutta, Romesh C. Boruah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     ¦Á-spinasterol
    ÏàËÆ¶È:50%
Natural Product Research          2001          15          339-344
A New Oleanane Triterpenoid from Gordonia ceylanica
H. M. T. B. Herath; P. S. Athukoralage; Joanne F. Jamie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     29-nor-3¦Â-methoxyserrat-14-en-21-one
    ÏàËÆ¶È:50%
Phytochemistry          1995          38          1467-1471
21¦Á-hydroxy-3¦Â-methoxyserrat-14-en-30-al and other triterpenoids from the cuticle of Picea jezoensis
Reiko Tanaka, Harumi Senba, Toshie Minematsu, Osamu Muraoka, Shunyo Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     N-{4-[(6-methoxyquinolin-8-yl)amino]pentyl}-N2-({4-[(6-methoxyquinolin-8-yl)amino]pentyl}carbamoyl)-N5-{N-[(2,2,5,7,8-pentamethyl-3,4-dihydro-2H-chromen-6-yl)sulfonyl]carbamimidoyl}-L-ornithinamide
C51H70N10O7S     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          197-210
Synthesis, antiprotozoal, antimicrobial, b-hematin inhibition, cytotoxicity and methemoglobin (MetHb) formation activities of bis(8-aminoquinolines)
Kirandeep Kaur, Meenakshi Jain, Shabana I. Khan, Melissa R. Jacob, Babu L. Tekwani, Savita Singh,Prati Pal Singh, Rahul Jain
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     compond 6b
C31H50O     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2006          54          1473-1477
C-24 Stereochemistry of Marine Sterols: (22E)-24-(Isopropenyl)-22-dehydrocholesterol and 24-Isopropenylcholesterol
Shizue Echigo, Noriyuki Hara, Gladys Jeanette Carderon, Carmenza Duque and Yoshinori Fujimoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     Ethyl ent-16¦Â-Hydroxy-15a-[(nicotinoyloxy)methyl]beyeran-19-oate
C29H41NO5     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2010          93          2052-2069
Stereoselective Synthesis, Characterization, and Antibacterial Activities of Novel Isosteviol Derivatives with D-Ring Modification
Ya Wu, Cong-Jun Liu, Xu Liu, Gui-Fu Dai, Jin-Yu Du and Jing-Chao Tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     Ethyl ent-16¦Â-Hydroxy-15¦Á-{[(4-toluenesulfonyl)oxy]methyl}beyeran-19-oate
C30H44O6S     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2010          93          2052-2069
Stereoselective Synthesis, Characterization, and Antibacterial Activities of Novel Isosteviol Derivatives with D-Ring Modification
Ya Wu, Cong-Jun Liu, Xu Liu, Gui-Fu Dai, Jin-Yu Du and Jing-Chao Tao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     gagamine
    ÏàËÆ¶È:50%
Chinese Journal of Medicinal Chemistry          2009          19          140-143
C-21 steroidal glycosides from Cynanchum wallichiiW ight
CHEN Gang, LI Zhi-feng, ZHANG Qi-hu, Pei Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     16 ¦Á-Fluorine-scutione
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1996          4          815-820
Scutione, a new bioactive norquinonemethide triterpene from Maytenus scutioides (Celastraceae)
Antonio G. Gonz¨¢lez, Nelson L. Alvarenga, Angel G. Ravelo, Isabel L. Bazzocchi, Esteban A. Ferro, Angel G. Navarro, Laila M. Moujir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     Phyllofolactone D
C27H42O3     ÏàËÆ¶È:50%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1998          37(3)          81-84
The Secondary Metabolites of Marine Sponge Phallospongia foliascens
Wan Yiqian Li Qing Zeng Longmei Su Jingyu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     Phyllofolactone E
C27H42O3     ÏàËÆ¶È:50%
Acta Scientiarum Naturalium Universitatis Sunyatseni          1998          37(3)          81-84
The Secondary Metabolites of Marine Sponge Phallospongia foliascens
Wan Yiqian Li Qing Zeng Longmei Su Jingyu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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