| ²é¿´: 454 | »Ø¸´: 2 | |||
zyh256389½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú A ÒÑÓÐ2È˲ÎÓë
|
| 21.0,56.0,56.1,94.8,95.3,106.9,108.0,109.9,121.0,133.3,137.3,162.4,164.0,165.6,182.5,186.3 |
» ²ÂÄãϲ»¶
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211µç×ÓÐÅÏ¢347Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
±¾¿ÆÎ÷¹¤´ó 0856 324Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
µ÷¼Á
ÒѾÓÐ8È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´

Ô¹¬ÕÛ¹ð
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 335 (´óѧÉú)
- ½ð±Ò: 3183.7
- ºì»¨: 3
- Ìû×Ó: 360
- ÔÚÏß: 57.9Сʱ
- ³æºÅ: 3524428
- ×¢²á: 2014-11-07
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zyh256389(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10, ok 2015-04-22 16:18:12
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zyh256389(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+10, ok 2015-04-22 16:18:12
|
²éѯ½á¹û£º¹²²éµ½379¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ascomycone A C16H14O6 ÏàËÆ¶È:100% Journal of Natural Products 2008 71(11) 1973-1976 Ascomycones A#C, Heptaketide Metabolites from an Unidentified Ascomycete Till Opatz, Heinz Kolshorn, Eckhard Thines, and Heidrun Anke Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ascomycone B C15H12O6 ÏàËÆ¶È:81.2% Journal of Natural Products 2008 71(11) 1973-1976 Ascomycones A#C, Heptaketide Metabolites from an Unidentified Ascomycete Till Opatz, Heinz Kolshorn, Eckhard Thines, and Heidrun Anke Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1,3-Dihydroxy-6-methoxy-2-methyl-9,10-anthraquinone C16H12O5 ÏàËÆ¶È:68.7% Journal of Asian Natural Products Research 2011 13 1023-1029 Anthraquinones from the roots of Knoxia valerianoides Feng Zhao, Su-Juan Wang*, Sheng Lin, Cheng-Gen Zhu, Shao-Peng Yuan, Xiao-Yu Ding, Zheng-Gang Yue, Yang Yu, Bo Liu, Xiu-Li Wu, Qi Hou and Jian-Gong Shi* Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 1a C16H12O5 ÏàËÆ¶È:68.7% Indian Journal of Chemistry Section B 2000 39B 796-798 A new anthraquinone glycoside from the roots of Plumbago zeylanica Aditi Gupta, I R Siddiqui, J Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . physcion ÏàËÆ¶È:68.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 127-131 Studies on Chemical Constituents of Glycosides from Syringa pubenscens LIU Pu, YANG You-liang, DENG Rui-xue, ZHAO Tian-zeng, YIN Wei-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-hydroxy-3,6,7-trimethoxy-8-methylanthraquinone C18H16O6 ÏàËÆ¶È:66.6% Asian Journal of Chemistry 2011 23 609-613 Phytochemical Studies on the Toxic Compounds of Gladiolus segetum D. ABDESSEMED, *, N. ALLOUI and A. DIBI Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Emodin ÏàËÆ¶È:62.5% Molecules 2003 8 614-621 Constituents from Moghat, the Roots of Glossostemon bruguieri (Desf.) Meselhy R. Meselhy Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,7,-dimethoxy-4'-methyl-flavone C18H16O4 ÏàËÆ¶È:62.5% Indian Journal of Chemistry Section B 2006 45B 1478-1486 Cytotoxic and antimicrobial activities of some synthetic flavones Mostahar,Sohel; Alam,Sayed; Islam,Azizul Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . questin ÏàËÆ¶È:62.5% Journal of Shenyang Pharmaceutical University 2009 26 536-538 Chemical cnstituents of Caulis Polygoni Multiflori (the stem of Polygonum multif lorum Thunb.) LIANG Yan, TIAN Wei-xi, MA Xiao-feng Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . physcion ÏàËÆ¶È:62.5% Journal of China Pharmaceutical University 2003 34 216-219 Steroids and Anthraquinones from Astragalus hoantchy ZHAO Ming; DUAN Jin-Ao; HUANG Wen-Zhe; ZHOU Rong-Han; CHE Chun-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . physcion ÏàËÆ¶È:62.5% Natural Product Research and Development 2001 13(6) 16-18 STUDIES ON THE CHEMICAL CONSTITUENTS OF HYPOESTES TRIFLORA JIANG Bei; ZHAO Qin-shi; LIN Zhong-wen; LU Yang; ZHENG Qi-tai; SUN Han-dong Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-O-methylemodin ÏàËÆ¶È:62.5% Chemistry and Industry of Forest Products 2009 29 100-102 Study on Anthraquinone Constituents in the Seed of Cassia tora L. JIA Zhen-bao, CHEN Wen-wei, JIANG Jia-xin, DING Xiao-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ´ó»ÆËؼ×ÃÑ ÏàËÆ¶È:62.5% Chinese Tladitional Patent Medicine 2011 33 514-516 Ò¹½»ÌÙ¸ÄÉÆË¯Ãß»îÐԳɷÖÑо¿ ¼³¹ãÈ«, Ñî¾ê, ÑîСÉú Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . physcion ÏàËÆ¶È:62.5% Chinese Tladitional Patent Medicine 2012 34 892-895 Chemical constituents of the ethyl acetate extract from Rumex hastatus D.Don ZHANG Lan-sheng, CHENG Yong-xian, LIU Guang-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (-)-1-epi-ventiloquinone L C16H16O5 ÏàËÆ¶È:62.5% Organic & Biomolecular Chemistry 2012 10 4462-4466 Stereoselective synthesis of (− -1-epi-ventiloquinone L and (+)-ventiloquinone L, the monomeric unit of cardinalin 3Rodney A. Fernandes, Arun B. Ingle and Vijay P. Chavan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . physcion-8-O-¦Â-D-glucopyranoside C22H22O10 ÏàËÆ¶È:62.5% Journal of Chinese Medicinal Materials 2011 34 893-895 Study on the Chemical Constituents of Rumex patientia LIU Jing, XIA Zhong-ting, ZHOU Gui-rong, ZHANG Lan-lan, KONG Ling-yi Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1,3-dihydroxy-2-hydroxymethyl-6-methoxy-9,10-anthraquinone ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2011 36 2980-2986 Anthraquinones from the Roots of Knoxia valerianoides ZHAO, Feng, WANG, Sujuan, WU, Xiuli, YU, Yang, YUE, Zhenggang, LIU, Bo, LIN, Sheng, Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . physcion ÏàËÆ¶È:62.5% Journal of Chinese Medicinal Materials 2013 36 752-755 Chemical Constituents from Flowers of Gardenia jasminoides SONG Jia-ling, YANG Yong-jian, QI Huan-yang, LI Qiang Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-18 21:35:29
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½379¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ascomycone A C16H14O6 ÏàËÆ¶È:100% Journal of Natural Products 2008 71(11) 1973-1976 Ascomycones A#C, Heptaketide Metabolites from an Unidentified Ascomycete Till Opatz, Heinz Kolshorn, Eckhard Thines, and Heidrun Anke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ascomycone B C15H12O6 ÏàËÆ¶È:81.2% Journal of Natural Products 2008 71(11) 1973-1976 Ascomycones A#C, Heptaketide Metabolites from an Unidentified Ascomycete Till Opatz, Heinz Kolshorn, Eckhard Thines, and Heidrun Anke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1,3-Dihydroxy-6-methoxy-2-methyl-9,10-anthraquinone C16H12O5 ÏàËÆ¶È:68.7% Journal of Asian Natural Products Research 2011 13 1023-1029 Anthraquinones from the roots of Knoxia valerianoides Feng Zhao, Su-Juan Wang*, Sheng Lin, Cheng-Gen Zhu, Shao-Peng Yuan, Xiao-Yu Ding, Zheng-Gang Yue, Yang Yu, Bo Liu, Xiu-Li Wu, Qi Hou and Jian-Gong Shi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 1a C16H12O5 ÏàËÆ¶È:68.7% Indian Journal of Chemistry Section B 2000 39B 796-798 A new anthraquinone glycoside from the roots of Plumbago zeylanica Aditi Gupta, I R Siddiqui, J Singh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . physcion ÏàËÆ¶È:68.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 127-131 Studies on Chemical Constituents of Glycosides from Syringa pubenscens LIU Pu, YANG You-liang, DENG Rui-xue, ZHAO Tian-zeng, YIN Wei-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-hydroxy-3,6,7-trimethoxy-8-methylanthraquinone C18H16O6 ÏàËÆ¶È:66.6% Asian Journal of Chemistry 2011 23 609-613 Phytochemical Studies on the Toxic Compounds of Gladiolus segetum D. ABDESSEMED, *, N. ALLOUI and A. DIBI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Emodin ÏàËÆ¶È:62.5% Molecules 2003 8 614-621 Constituents from Moghat, the Roots of Glossostemon bruguieri (Desf.) Meselhy R. Meselhy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5,7,-dimethoxy-4'-methyl-flavone C18H16O4 ÏàËÆ¶È:62.5% Indian Journal of Chemistry Section B 2006 45B 1478-1486 Cytotoxic and antimicrobial activities of some synthetic flavones Mostahar,Sohel; Alam,Sayed; Islam,Azizul Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . questin ÏàËÆ¶È:62.5% Journal of Shenyang Pharmaceutical University 2009 26 536-538 Chemical cnstituents of Caulis Polygoni Multiflori (the stem of Polygonum multif lorum Thunb.) LIANG Yan, TIAN Wei-xi, MA Xiao-feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . physcion ÏàËÆ¶È:62.5% Journal of China Pharmaceutical University 2003 34 216-219 Steroids and Anthraquinones from Astragalus hoantchy ZHAO Ming; DUAN Jin-Ao; HUANG Wen-Zhe; ZHOU Rong-Han; CHE Chun-Tao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . physcion ÏàËÆ¶È:62.5% Natural Product Research and Development 2001 13(6) 16-18 STUDIES ON THE CHEMICAL CONSTITUENTS OF HYPOESTES TRIFLORA JIANG Bei; ZHAO Qin-shi; LIN Zhong-wen; LU Yang; ZHENG Qi-tai; SUN Han-dong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-O-methylemodin ÏàËÆ¶È:62.5% Chemistry and Industry of Forest Products 2009 29 100-102 Study on Anthraquinone Constituents in the Seed of Cassia tora L. JIA Zhen-bao, CHEN Wen-wei, JIANG Jia-xin, DING Xiao-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . ´ó»ÆËؼ×ÃÑ ÏàËÆ¶È:62.5% Chinese Tladitional Patent Medicine 2011 33 514-516 Ò¹½»ÌÙ¸ÄÉÆË¯Ãß»îÐԳɷÖÑо¿ ¼³¹ãÈ«, Ñî¾ê, ÑîСÉú Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . physcion ÏàËÆ¶È:62.5% Chinese Tladitional Patent Medicine 2012 34 892-895 Chemical constituents of the ethyl acetate extract from Rumex hastatus D.Don ZHANG Lan-sheng, CHENG Yong-xian, LIU Guang-ming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . (-)-1-epi-ventiloquinone L C16H16O5 ÏàËÆ¶È:62.5% Organic & Biomolecular Chemistry 2012 10 4462-4466 Stereoselective synthesis of (− -1-epi-ventiloquinone L and (+)-ventiloquinone L, the monomeric unit of cardinalin 3Rodney A. Fernandes, Arun B. Ingle and Vijay P. Chavan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . physcion-8-O-¦Â-D-glucopyranoside C22H22O10 ÏàËÆ¶È:62.5% Journal of Chinese Medicinal Materials 2011 34 893-895 Study on the Chemical Constituents of Rumex patientia LIU Jing, XIA Zhong-ting, ZHOU Gui-rong, ZHANG Lan-lan, KONG Ling-yi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1,3-dihydroxy-2-hydroxymethyl-6-methoxy-9,10-anthraquinone ÏàËÆ¶È:62.5% China Journal of Chinese Materia Medica 2011 36 2980-2986 Anthraquinones from the Roots of Knoxia valerianoides ZHAO, Feng, WANG, Sujuan, WU, Xiuli, YU, Yang, YUE, Zhenggang, LIU, Bo, LIN, Sheng, Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . physcion ÏàËÆ¶È:62.5% Journal of Chinese Medicinal Materials 2013 36 752-755 Chemical Constituents from Flowers of Gardenia jasminoides SONG Jia-ling, YANG Yong-jian, QI Huan-yang, LI Qiang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . physcion ÏàËÆ¶È:62.5% Journal of Chinese Medicinal Materials 2013 36 57-60 Chemical Constituents from Aerial Part of Rumex patientia ZENG Yong, LUO Jian-jun, LI Chong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-03-18 21:36:12













»Ø¸´´ËÂ¥
-1-epi-ventiloquinone L and (+)-ventiloquinone L, the monomeric unit of cardinalin 3