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13C NMR (126 MHz, dmso) ¦Ä 10.70,18.52,29.91,30.13,36.60,43.18,43.95,49.04,56.08,69.72,70.74, 80.32,106.43,111.71,126.31, 128.73,128.92,131.74,132.12,132.94,133.79,137.62,139.66,143.82,157.68,167.87,
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wangcong123: ½ð±Ò+10, ¡ïÓаïÖú 2015-05-11 21:28:13
1 .     trienomycinol
    ÏàËÆ¶È:65.3%
The Journal of Antibiotics          1988          41          1223-1230
STRUCTURE-ACTIVITY RELATIONSHIP OF A NOVEL ANTITUMOR ANSAMYCIN ANTIBIOTIC TRIENOMYCIN A AND RELATED COMPOUNDS
SHINJI FUNAYAMA, YUMI ANRAKU, AKIRA MITA, Zm-Bo YANG, KIYOSHI SHIBATA, KANKI KOMIYAMA, IWAO UMEZAWA, SATOSHI OMURA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     4-hydroxy-4-{9-hydroxy-9-[2-(1-hydroxy-6-methyl-octa-2,4-dienylidene)-3,6-dioxo-cyclohexylidene]-nona-1,3,5,7-tetraenyl}-6-oxa-bicyclo[3.1.0]hex-2-ene-2-carboxylic acid
C30H32O8     ÏàËÆ¶È:65.3%
Microbiological Research          2013          168          223-230
Taxonomy and chemical characterization of new antibiotics produced by Saccharothrix SA198 isolated from a Saharan soil
D. Boubetra, N. Sabaou, A. Zitouni, C. Bijani, A. Lebrihi, F. Mathieu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     17¦Â-estradiol-3-benzyl ether 17-tosylate
C32H36O4S     ÏàËÆ¶È:59.2%
Steroids          2011          76          1141-1148
Synthesis of novel steroidal 17 -triazolyl derivatives via Cu(I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro
Éva Frank∗, Judit Moln¨¢r, Istv¨¢n Zupk¨®, Zal¨¢n K¨¢d¨¢r, J¨¢nos Wölfling
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     compound 2b
C26H40O3     ÏàËÆ¶È:57.6%
Journal of Medicinal Chemistry          1995          38          4529-4537
1.alpha.,25-Dihydroxyvitamin D3 Analogs Featuring Aromatic and Heteroaromatic Rings: Design, Synthesis, and Preliminary Biological Testing
Gary H. Posner, Zhengong Li, M. Christina White, Victoria Vinader, Kazuhiro Takeuchi, Sandra E. Guggino, Patrick Dolan, Thomas W. Kensler
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     17-(1-p-chlorophenyl-5-pyrazolyl)androsta-5,16-dien-3¦Â-ol
C28H33ClN2O     ÏàËÆ¶È:57.6%
Steroids          2012          77          1152-1159
Novel series of 17¦Â-pyrazolylandrosta-5,16-diene derivatives and their inhibitory effect on 17¦Á-hydroxylase/C17,20-lyase
Zolt¨¢n Iv¨¢nyi, Nikoletta Szab¨®, J¨¢nos Wölfling, Mih¨¢ly Sz¨¦csi, J¨¢nos Julesz, Gyula Schneider
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     reblastatin
C28H42N2O8     ÏàËÆ¶È:55.5%
The Journal of Antibiotics          2000          53          657-663
Discovery of Novel Ansamycins Possessing Potent Inhibitory Activity in a Cell-based Oncostatin M Signalling Assay
PAUL STEAD,SHAZIA LATIF,ANDREW P. BLACKABY,PHILIP J. SIDEBOTTOM,ANGELA DEAKIN,NICHOLAS L. TAYLOR,PAUL LIFE,JOHN SPAULL,FIONA BURRELL,ROSIE JONES,JANE LEWIS,IAN DAVIDSON and THOMAS MANDER
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     biselyngbyolide A
C27H42O5     ÏàËÆ¶È:55.5%
Chemistry Letters          2012          41          165-167
Biselyngbyolide A, a Novel Cytotoxic Macrolide from the Marine Cyanobacterium Lyngbya sp.
Maho Morita, Osamu Ohno, and Kiyotake Suenaga
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     17-O-demethyllebstatin
    ÏàËÆ¶È:55.5%
China Journal of Chinese Materia Medica          2011          36          1763-1768
Isolation and structural elucidation of secondary metabolites from marine Streptomyces sp. SCSIO 1934
NIU, Siwen, LI, Sumei, TIAN, Xinpeng, HU, Tao, JU, Jianhua, YNAG, Xiaohong, ZHANG, Si, ZHANG, Changsheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     biselyngbyolide B
C27H40O4     ÏàËÆ¶È:55.5%
Chemistry Letters          2014          43          287-289
Biselyngbyolide B, a Novel ER Stress-inducer Isolated from the Marine Cyanobacterium Lyngbya sp.
Osamu Ohno, Ayane Watanabe, Maho Morita, and Kiyotake Suenaga*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     3-Methoxy-2'-oxo-2'-phenoxy-3'-propyl[1',3',2' ]oxazaphosphorino[5',6'-e:16¦Â,17¦Â]estra-1,3,5(10)-triene 24a
    ÏàËÆ¶È:55.1%
Steroids          2007          72          446-458
New steroid-fused P-heterocycles: Part II. Synthesis and conformational study of oxazaphosphorino[16,17-e]estrone derivatives
Éva Frank, Brigitta Kazi, Zolt¨¢n Mucsi, Krisztina Lud¨¢nyi, György Keglevich
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-05-11 21:10:33
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