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ÈܼÁ£ºë®´úßÁठ13C NMR (151 MHz, Pyr) ¦Ä 140.70, 121.70, 102.36, 78.39, 78.26, 77.90, 75.12, 71.49, 62.62, 56.61, 56.03, 50.13, 45.83, 42.26, 39.73, 39.12, 37.26, 36.71, 36.17, 33.99, 31.95, 31.84, 30.04, 29.25, 28.32, 26.18, 24.29, 23.18, 21.06, 19.75, 19.20, 18.99, 18.79, 11.94, 11.75. |
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ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
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2Â¥2013-06-26 17:11:00
Óð»¯ÐÂÉú
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- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 149.1
- Ìû×Ó: 57
- ÔÚÏß: 37.1Сʱ
- ³æºÅ: 1058826
- ×¢²á: 2010-07-16
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
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²»ºÃÒâ˼£¬Ö±½ÓÔÚmestrenovaÖÐÉú³ÉµÄ£¬»¹²»ÖªµÀÔõô¸ÄÅÅÁÐ˳Ðò£¬ÒÔΪû¹ØÏµ¾ÍÖ±½Ó·¢ÁË£¬ºÙºÙ ²ÑÀ¢¡¡ 11.75, 11.94,18.79, 18.99, 19.20, 19.75, 21.06, 23.18, 24.29, 26.18, 28.32, 29.25, 30.04, 31.84, 31.95, 33.99, 36.17, 36.71, 37.26, 39.12, 39.73, 42.26, 45.83, 50.13, 56.03, 56.61, 62.62, 71.49, 75.12, 77.90, 78.26, 78.39, 102.36, 121.70, 140.70. |
3Â¥2013-06-26 17:24:53
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
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ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
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Óð»¯ÐÂÉú: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-26 20:57:46
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°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½5770¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-Sitosterol ¦Â-D-glucopyranoside C35H60O6 ÏàËÆ¶È:100% Chemistry of Natural Compounds 2007 43 358-359 TRITERPENE GLYCOSIDES FROM Astragalus AND THEIR GENINS.LXXV. STEROLS AND TRITERPENOIDS FROM Astragalus orbiculatus I. M. Isaev, R. P. Mamedova, M. A. Agzamova, and M. I. Isaev Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-Sitosterol Glucoside ÏàËÆ¶È:100% Chemistry of Natural Compounds 1991 27 603-606 TRITERPENE GLYCOSIDES OF Hedera taurica VII. STRUCTURES OF TAUEOSIDES A AND D FROM THE LEAVES OF CRIMEAN IVY V. I. Grishkovets, N. V. Tolkacheva, A. S. Shashkov,and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . daucosterol ÏàËÆ¶È:100% Acta Botanica Sinica 1999 41 107-110 Chemical constituents of the Anemone tomentosa Root Wang Jun-Ru, Peng Shu-Lin, Wang Ming-Kui, Feng Jun-Tao, Ding Li-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . daucosterol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2005 30 1340-1342 Studies on chemical constituents from flowers of Apocynum venetum CHEN Long, DU Lijun, DING Yi, XISNG Dongming , WANG Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ºúÂܲ·ÜÕ ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2005 30 153-154 ²ØÒ©¶ÌËëÍöú²Ý»¯Ñ§³É·ÖÑо¿ ÑîÔÆÉÑ, ºÎ Àó, Ñ÷, Ê·¸ß·å, ³Èó»ª Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . daucosterol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2004 29 741-758 Studies on chemical constituents in root of Paeonia sinjiangensis SONG Zhaohui, WANG Baode, BA Hang, TONG Xiaotian, ZHU Dayuan, JIANG Fuxiang Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2001 26 43-47 Studies on Chemical Constituents from Buddleja lindleyana Fert LU Jianghai, ZHAO Yuying, QIAO Liang, FANG Yiou, HUANG Qinan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . daucosterol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 2001 26 45-46 Chemical Constituents of Gymnotheca involucrata Pei YANG Weili, TIAN Jun, DING Lisheng Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 1996 21 104-105 Chemical Constituents of Coleus carnosifolius Dunn. Mu Qing, Li Chaoming and Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . daucosterol C35H60O6 ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 1992 17 36-38 Studies on the Chemical Constituents of Actinidia arguta(Sieb.et Zuce.)Planch.ex Miquel Shi Yue and Wang Huili, Ma Bingru Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . daucosterol ÏàËÆ¶È:100% China Journal of Chinese Materia Medica 1992 17 737-739 Studies on the Chemical Constituents of Drynotria propinqua(Wall)J.Sm Liu Songqiang and Xiao Zhuoyin Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ¦Â-sitosterol-3-O-glucoside ÏàËÆ¶È:100% Natural Product Sciences 1998 4 263-267 Constituents from Syzygium aromaticum Merr. et Perry Son, Kun-Ho; Kwon, Soon-Youl; Kim, Hyun-Pyo; Chang, Hyeun-Wook; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ¦Â-sitosterol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:100% Natural Product Sciences 2000 6 135-138 Antioxidative Constituents from the Seeds of Cuscuta chinensis Kwon, Yong-Soo; Chang, Bok-Sim; Kim, Chang-Min Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Daucosterol ÏàËÆ¶È:100% Natural Product Sciences 2007 13 332-336 Norsesquiterpene and Steroid Constituents of Humulus japonicus Yu, Byung-Chul; Yang, Min-Cheol; Lee, Kyu-Ha; Kim, Ki-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-O-¦Â-Glucosylsitosterol ÏàËÆ¶È:100% Phytochemistry 1994 36 221-223 Furocoumarins from the rhizomes of Dorstenia brasiliensis Ricardo M. Kuster, Robson R. Bernardo, Antonio J.R. Da Silva, Jos¨¦ P. Parente, Walter B. Mors Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-06-26 18:16:33













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