| ²é¿´: 380 | »Ø¸´: 2 | |||
maheffÌú³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ2È˲ÎÓë
|
|
56.00,61.8,69.31,70.59,73.98,77.24,77.37,102.49,110.23,115.89,120.22,123.42,128.50,132.36,147.00,148.18 ÈܼÁ d-DMSO |
» ²ÂÄãϲ»¶
071000ÉúÎïѧµ÷¼ÁÇóÖú
ÒѾÓÐ12È˻ظ´
¿¼ÑжþÂÖµ÷¼Á
ÒѾÓÐ7È˻ظ´
µ÷¼Á
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ9È˻ظ´
0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£
ÒѾÓÐ14È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ23È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ41È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ21È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ28È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
maheff: ½ð±Ò+5, ¡ïÓаïÖú 2015-05-15 08:41:27
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
maheff: ½ð±Ò+5, ¡ïÓаïÖú 2015-05-15 08:41:27
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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%) ̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½1183¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ÒÒ»ùËɰØÜÕ ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . coniferine C16H22O8 ÏàËÆ¶È:81.2% Turkish Journal of Chemistry 2009 33 667-675 Secondary metabolites from Nepeta heliotropifolia Z¨¹HAL G¨¹VENALP, HİLAL ÖZBEK, AYŞE KURU¨¹Z¨¹M-UZ, CAVİT KAZAZ, L. ÖM¨¹R DEMİREZER Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Coniferin C16H22O8 ÏàËÆ¶È:75% Acta Botanica Yunnanica 2000 22(2) 214-218 The Chemical Constituents from Toricellia angulata WU Shao-Hua,MA Yun-Bao,LUO Xiao-Dong,WU Da-Gang,LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-methoxy-4-(3'-hydroxy-propenyl)-phenol-1-O-¦Â-D-glucopyranoside ÏàËÆ¶È:75% Journal of Asian Natural Products Research 2002 4 43-46 PHENOLIC GLUCOSIDES FROM OXYTROPIS MYRIOPHYLLA JIANG-HAI LU, YI LIU, GUANG-ZHONG TU and YU-YING ZHAO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . trans-isoconiferin ÏàËÆ¶È:75% Heterocycles 2004 63 2573-2580 New Neolignan and Phenylpropanoid Glycosides in Juniperus communis var. Depressa Tsutomu Nakanishi, Naoki Iida, Yuka Inatomi, Hiroko Murata, Akira Inada, Jin Murata, Frank A. Lang, Munekazu Iinuma, Toshiyuki Tanaka* Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . coniferin C16H22O8 ÏàËÆ¶È:75% Chinese Journal of Pharmaceuticals 2007 38 221-226 Two New Compounds from Picrorhiza scrophulariiflora XIE Zhi-yong, HU Hong-xia, KONG De-yun, YANG Pei-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ·´Ê½ÒìËɰØÜÕ C16H22O8 ÏàËÆ¶È:75% Natural Product Research and Development 2012 24 1007-1013 Chemical Constituents from the Stems of Dipteronia dyeriana Henry GUO Rong; WANG Yue-hu; SHI Ya-na; LI Xing-yu; LI Wen-chang; LONG Chun-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-(4-hydroxy-3-methoxyphenyl)-1-glucosyl-2-propene ÏàËÆ¶È:75% Nippon N¨geikagaku Kaishi 1988 62 1067-1071 The Structure and Physiological Activity of Phenyl Propanoid Glycosides in the Lemon (Citrus limon Burum f.), Unshiu (Citrus unshiu) and Kinkan (Fortunella japonica) Peelings Akiyoshi SAWABE, Yoshiharu MATSUBARA, Yoshitomi IIZUKA, Kozo OKAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . coniferin ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2013 38 3520-3524 Non-alkaloid components from Sophora flavescens ZHANG Chi, MA Yue, GAO Hui-min, LIU Xiao-qian, CHEN Liang-mian, ZHANG Qi-wei, WANG Zhi-min, LI An-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . junipediol A-8-O-¦Â-D-glucoside ÏàËÆ¶È:75% Food Chemistry 2014 165 92-97 Identification of a new angiotensin-converting enzyme (ACE) inhibitor from Thai edible plants Arunee Simaratanamongkol, Kaoru Umehara , Hiroshi Noguchi, Pharkphoom Panichayupakaranant Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-05-15 07:59:35
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
¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
maheff: ½ð±Ò+3 2015-05-15 08:41:36
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
maheff: ½ð±Ò+3 2015-05-15 08:41:36
|
²éѯ½á¹û£º¹²²éµ½125¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ÒÒ»ùËɰØÜÕ ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . coniferine C16H22O8 ÏàËÆ¶È:81.2% Turkish Journal of Chemistry 2009 33 667-675 Secondary metabolites from Nepeta heliotropifolia Z¨¹HAL G¨¹VENALP, HİLAL ÖZBEK, AYŞE KURU¨¹Z¨¹M-UZ, CAVİT KAZAZ, L. ÖM¨¹R DEMİREZER Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Coniferin C16H22O8 ÏàËÆ¶È:75% Acta Botanica Yunnanica 2000 22(2) 214-218 The Chemical Constituents from Toricellia angulata WU Shao-Hua,MA Yun-Bao,LUO Xiao-Dong,WU Da-Gang,LIU Ji-Kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-methoxy-4-(3'-hydroxy-propenyl)-phenol-1-O-¦Â-D-glucopyranoside ÏàËÆ¶È:75% Journal of Asian Natural Products Research 2002 4 43-46 PHENOLIC GLUCOSIDES FROM OXYTROPIS MYRIOPHYLLA JIANG-HAI LU, YI LIU, GUANG-ZHONG TU and YU-YING ZHAO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . trans-isoconiferin ÏàËÆ¶È:75% Heterocycles 2004 63 2573-2580 New Neolignan and Phenylpropanoid Glycosides in Juniperus communis var. Depressa Tsutomu Nakanishi, Naoki Iida, Yuka Inatomi, Hiroko Murata, Akira Inada, Jin Murata, Frank A. Lang, Munekazu Iinuma, Toshiyuki Tanaka* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . coniferin C16H22O8 ÏàËÆ¶È:75% Chinese Journal of Pharmaceuticals 2007 38 221-226 Two New Compounds from Picrorhiza scrophulariiflora XIE Zhi-yong, HU Hong-xia, KONG De-yun, YANG Pei-ming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ·´Ê½ÒìËɰØÜÕ C16H22O8 ÏàËÆ¶È:75% Natural Product Research and Development 2012 24 1007-1013 Chemical Constituents from the Stems of Dipteronia dyeriana Henry GUO Rong; WANG Yue-hu; SHI Ya-na; LI Xing-yu; LI Wen-chang; LONG Chun-lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-(4-hydroxy-3-methoxyphenyl)-1-glucosyl-2-propene ÏàËÆ¶È:75% Nippon N¨geikagaku Kaishi 1988 62 1067-1071 The Structure and Physiological Activity of Phenyl Propanoid Glycosides in the Lemon (Citrus limon Burum f.), Unshiu (Citrus unshiu) and Kinkan (Fortunella japonica) Peelings Akiyoshi SAWABE, Yoshiharu MATSUBARA, Yoshitomi IIZUKA, Kozo OKAMOTO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . coniferin ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2013 38 3520-3524 Non-alkaloid components from Sophora flavescens ZHANG Chi, MA Yue, GAO Hui-min, LIU Xiao-qian, CHEN Liang-mian, ZHANG Qi-wei, WANG Zhi-min, LI An-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . junipediol A-8-O-¦Â-D-glucoside ÏàËÆ¶È:75% Food Chemistry 2014 165 92-97 Identification of a new angiotensin-converting enzyme (ACE) inhibitor from Thai edible plants Arunee Simaratanamongkol, Kaoru Umehara , Hiroshi Noguchi, Pharkphoom Panichayupakaranant Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . oniferyl alcohol 9-O-¦Â-D-glucopyranoside C16H22O8 ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2014 45 1367-1372 Chemical constituents from roots of Sambucus williamsii (I) YANG Bing-you, SONG Dan-dan, HAN Hua, YANG Liu, LIU Yan, WANG Qiu-hong, KUANG Hai-xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . coniferin ÏàËÆ¶È:68.7% Acta Botanica Yunnanica 2000 22(3) 343-350 Chemical Constituents of Crude Green Tea ,the Material of Pu - er Tea in Yunnan ZHOU Zhi-Hong,YANG Chong-Ren Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 2-(3-hydroxy-4-methoxyphenyl)ethyl 1-O-¦Â-D-glucopyranoside C15H22O8 ÏàËÆ¶È:68.7% Chemical & Pharmaceutical Bulletin 1991 39 1047-1050 Studies on the Nepalese Crude Drugs. XII. On the Phenolic Compounds from the Root of Scutellaria prostrata JACQ. ex BENTH. Yuichi KIKUCHI,Yukinori MIYAICHI,Yumi YAMAGUCHI,Haruhisa KIZU and Tsuyoshi TOMIMORI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . coniferin C16H22O8 ÏàËÆ¶È:68.7% Chemical & Pharmaceutical Bulletin 1991 39 865-870 Studies on the Constituents of the Bark of Kalopanax pictus NAKAI Kazuko SANO,Shuichi SANADA,Yoshiteru IDA and Junzo SHOJI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-(3-Hydroxy-4-methoxyphenyl)ethyl-1-O-¦Â-D-glucopyranoside C15H22O8 ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 2-(3-Hydroxy-4-methoxyphenyl)ethyl-1-O-¦Â-D-glucopyranoside C15H22O8 ÏàËÆ¶È:68.7% Chemistry of Natural Compounds 2002 38 473-519 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS.DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 3a ÏàËÆ¶È:68.7% Acta Botanica Sinica 2001 43 193-197 Three New Phenolic Glycosides from the Fertile Sprouts of Equisetu Marvense CHANG Jun, XUAN Li-Jiang, XU Ya-Ming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . coniferin ÏàËÆ¶È:68.7% Phytochemistry 1993 33 1215-1219 Lignan and phenylpropanoid glycosides from Osmanthus asiaticus Masataka Sugiyama, Eiko Nagayama, Masao Kikuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-05-15 07:59:55













»Ø¸´´ËÂ¥
5