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C:21.0,21.6,22.1,22.6,25.0,26.2,26.6,28.2,28.6,32.6,32.9,33.8,34.1,34.6,37.9,38.2,41.8,47.3,50.6,75.3,108.5,108.6,110.1,172.2,173.8,173.8,192.3,192.5
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yangyinhe

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

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Ö¾´º(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+5 2015-05-19 09:55:37
1 .     Dysoxyhainic acid I
C30H50O3     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          2011          21          125-129
Ring ¦Á-seco triterpenoids with antibacterial activity from Dysoxylum hainanense
Xiu-Feng He, Xiao-Ning Wang, Sheng Yin, Lei Dong, Jian-Min Yue
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     macrocarpal-am-1
    ÏàËÆ¶È:64.2%
Bioscience, Biotechnology, and Biochemistry          1995          59          2330-2332
New Macrocarpal-am-1 from Eucalyptus amplifolia
Inder Singh Pal, Hideo Etoh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     baurenyl acetate
C32H49O2     ÏàËÆ¶È:63.3%
Phytochemistry          1994          37          1729-1735
Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     3¦Á,12¦Á,16¦Â-Trihydroxy-5¦Â-cholan-24-oic acid
C24H40O5     ÏàËÆ¶È:60.7%
Steroids          2010          75          506-512
Synthesis, aggregation behavior and cholesterol solubilization studies of 16-epi-pythocholic acid (3¦Á,12¦Á,16¦Â-trihydroxy-5¦Â-cholan-24-oic acid)
Nonappa, Uday Maitra
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     matlystatin A
C27H47O8N5S     ÏàËÆ¶È:60.7%
The Journal of Antibiotics          1994          47          1473-1480
MATLYSTATINS, NEW INHIBITORS OF TYPE IV COLLAGENASES FROM Actinomadura atramentaria III. STRUCTURE ELUCIDATION OF MATLYSTATINS A TO F
HIDEYUKI HARUYAMA, YOSHIKO OHKUMA, HIDEMI NAGAKI, TAKESHI OGITA, KAZUHIKO TAMAKI, TAKESHI KINOSHITA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     compound 2b
    ÏàËÆ¶È:60.7%
The Journal of Antibiotics          1994          47          1473-1480
MATLYSTATINS, NEW INHIBITORS OF TYPE IV COLLAGENASES FROM Actinomadura atramentaria III. STRUCTURE ELUCIDATION OF MATLYSTATINS A TO F
HIDEYUKI HARUYAMA, YOSHIKO OHKUMA, HIDEMI NAGAKI, TAKESHI OGITA, KAZUHIKO TAMAKI, TAKESHI KINOSHITA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     N-acetyl 15-acetoxy-1,20-cyclo-16,17-didehydro-4-methylatidane
C24H33NO3     ÏàËÆ¶È:60.7%
Canadian Journal of Chemistry          1992          70          1397-1405
Formation, reactions, and NMR spectra of 1,20-cycloatidanes
Oliver E. Edwards, Dusan Dvornik, Ralph J. Kolt, Barbara A. Blackwell
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     24-epi-makisterone A
C28H46O7     ÏàËÆ¶È:60.7%
Steroids          2013          78          1098-1102
Ecdysteroids from the flowers of Aerva javanica
Muhammad Saleem, Sara Musaddiq, Naheed Riaz, Momina Zubair, Muhammad Ashraf, Rumana Nasar, Abdul Jabbar
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     12¦Â-hydroxy-cholaniic acid methyl ester
    ÏàËÆ¶È:60.7%
Organic Magnetic Resonance          1983          21          305-309
Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers
Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     eucalmaidial B
C28H38O7     ÏàËÆ¶È:60.7%
RSC Advances          2014          4          21373-21378
Eucalmaidials A and B, phloroglucinol-coupled sesquiterpenoids from the juvenile leaves of Eucalyptus maideni
Li-Wen Tian, Min Xu, Xing-Cong Li, Chong-Ren Yang, Hua-Jie Zhu and Ying-Jun Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     24-Methylene-26-acetoxycycloartan-3-one
    ÏàËÆ¶È:60.6%
Phytochemistry          1996          42          795-798
A cycloartane triterpenoid and ¦Ø-phenyl alkanoic and alkenoic acids from Trichilia claussenii
Mônica T. Pupo, Paulo C. Vieira, João B. Fernandes, M. F¨¢tima das G. F. da Silva
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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12 .     21,24(¦ÁS)-dihydroxycycloart-25-en-3-one
C30H46O2     ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          636-642
Phytochemical Investigation of Aglaia rubiginosa
S. Weber, J. Puripattanavong, V. Brecht, and A. W. Frahm
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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13 .     cashmirol A
C31H50O2     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2009          6          1471-1476
Cashmirols A and B, New Lipoxygenase Inhibiting Triterpenes from Sorbus cashmiriana
Mehdi Hassan Kazmi, Ejaz Ahmed, Saira Hameed, Abdul Malik, Itrat Fatima, and Muhammad Ashraf
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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14 .     20(S),24(R)-epoxy-3¦Á,17¦Á,25-trihydroxydammarane
C30H52O4     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1996          44          1748-1753
Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-01-09 18:50:31
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