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13C NMR (101 MHz, CDCl3) ¦Ä 199.79, 164.68, 156.32, 135.14, 134.24, 132.67, 124.59, 123.09, 77.16, 55.83, 44.46, 44.14, 43.01, 39.43, 36.91, 35.72, 34.26, 33.23, 27.86, 25.51, 21.36, 20.13, 19.80, 19.12, 17.78, 16.79. лл |
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yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
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hycome: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллŶ 2015-03-31 09:56:33
hycome: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ллŶ 2015-03-31 09:56:33
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1 . ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:96.1% Journal of Natural Products 1998 61 1421-1422 Steroidal Constituents of Ganoderma applanatum and Ganoderma neo-japonicum Kim-Hong Gan, Shieh-Hsieh Kuo, and Chun-Nan Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . ergosta-4,6,8(14),22E-tetraen-3-one ÏàËÆ¶È:96.1% China Journal of Chinese Materia Medica 2009 34 2197-2199 Chemical constituents from fruits of Ailanthus altissima ZHAO Chunchao, SHAO Jianhua, LIXian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Ergosta-4,6,8(14),22-tetraene-3-one ÏàËÆ¶È:96.1% Archives of Pharmacal Research 2002 25 851-855 Cytotoxic ergosterols from paecilomyces sp. J300 Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . ergota-4,6,8(14),22E-tetraene-3-one ÏàËÆ¶È:96.1% Chinese Pharmaceutical Journal 2013 48 1343-1346 Chemical Constituents in the Petroleum Ether Extract of the Whole Herb of Flickingeria fimbriata WANG Jing, FEI Jiao-dong, DING Gang, LI Rong-tao, YU Chang-yuan*, ZOU Zhong-mei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ergosta-4,6,8(14),22-tetraen-3-one C28H40O ÏàËÆ¶È:92.5% Chinese Journal of New Drugs 2013 22 2168-2173 Isolation and identification of endophytic fungus LM033 obtained from Moringaoleifera Lam. and biological activity of the metabolites CAI Qing-xiu, ZHAO Jin-hao, WANG Jia-ying, WANG Li-wei, ZHANG Chu-long Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ergosta-4,6,8(14),22-tetraen-3-one C28H40O ÏàËÆ¶È:89.2% Chemical & Pharmaceutical Bulletin 2004 52(8) 1005-1008 Six Immunosuppressive Features from an Ascomycete, Zopfiella longicaudata, Found in a Screening Study Monitored by Immunomodulatory Activity Haruhiro FUJIMOTO,Etsuko NAKAMURA, Emi OKUYAMA, and Masami ISHIBASHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (22E,24R)-Ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:89.2% Steroids 2001 66 771-775 A novel sterol from Chinese truffles Tuber indicum Gao Jinming, Hu Lin, Liu Jikai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ergosta-4,6,8(14),22-tetraen-3-one C28H40O ÏàËÆ¶È:89.2% Natural Product Research 2008 22 901-906 Ergosta-4,6,8(14),22-tetraen-3-one from Vietnamese Xylaria sp. possessing inhibitory activity of nitric oxide production Dang Ngoc Quang; Dang Dinh Bach Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2015-03-30 19:25:59
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
2Â¥2015-03-30 16:47:43
hycome
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- ³æºÅ: 50805
- ×¢²á: 2004-07-14
- רҵ: ÉúÎﻯ¹¤ÓëʳƷ»¯¹¤

3Â¥2015-03-30 17:15:45














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