| ²é¿´: 310 | »Ø¸´: 1 | ||
ÏÄéªéª4940гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÐÂÊÖ½âÆ×ÇóÖú£¬¶àл£¡£¡ ÒÑÓÐ1È˲ÎÓë
|
|
̼Æ×£º36.56,37.92,73.58,84.77,112.62,114.62,114.81,114.85,115.62,116.12,117.46,120.34,121.53,122.56,128.03,128.35,133.23,143.47,143.60,143.78,144.70,145.03,145.05,146.86,167.00,,172.59 ÈܼÁ£ºë®´ú¼×´¼ |
» ²ÂÄãϲ»¶
085602µ÷¼Á ³õÊÔ×Ü·Ö335
ÒѾÓÐ7È˻ظ´
»¯Ñ§357·Ö£¬¿¼Ñе÷¼Á
ÒѾÓÐ7È˻ظ´
278Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
085400µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ6È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
26¿¼Ñе÷¼Á0710 0860
ÒѾÓÐ13È˻ظ´
296²ÄÁÏר˶Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
½âÆ×ÐÂÊÖ£¬¶àлÀ²
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¨307-75a£©
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
Çó½âÆ×¸ßÊÖ¿´¿´Õâ¸ö¼òµ¥½á¹¹ÊÇ·ñÕýÈ·
ÒѾÓÐ4È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ5È˻ظ´
Çó½âºË´ÅÇâÆ×£¡£¡£¡¶àл¶àл£¡£¡
ÒѾÓÐ19È˻ظ´
NMR½âÆ×ÇóÖú£¡¼±£¡
ÒѾÓÐ12È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú£ººË´Å¹²ÕñÁׯ׽âÎöµÄÊé»òÕß×ÊÁÏ£¡
ÒѾÓÐ7È˻ظ´
ÇëºË´Å¸ßÊÖ°ïæ¿´¸öÎïÖʵÄÇâÆ×
ÒѾÓÐ26È˻ظ´
ÇóÖúESR¸ßÊÖ½âÆ×
ÒѾÓÐ14È˻ظ´
²âÁËһδ֪ÎïµÄºË´ÅͼÆ×Çë°ïæ·ÖÎöÒ»ÏÂͼ°É£¬ÈçÐèÒª½øÐÐÆäËû²âÊÔ£¬Çë¸æÖª£¬¶àлÀ²¡£
ÒѾÓÐ18È˻ظ´
ºË´Å/ÖÊÆ×½âÆ×¸ßÊÖ°ïæ¿´¿´Õâ¸ö»¯ºÏÎï½á¹¹Ôõô½âÎö
ÒѾÓÐ12È˻ظ´
Çó½âÆ×£¬ÓÐÖÊÆ×¡¢ÇâÆ×¡¢Ì¼Æ×£¬¶àл£¡
ÒѾÓÐ14È˻ظ´
°ïæ·ÖÎöϺ˴ÅHÆ×
ÒѾÓÐ16È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÆ×CÆ×ºÍHÆ×
ÒѾÓÐ22È˻ظ´
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 ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÏÄéªéª4940: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2014-09-13 10:09:41
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÏÄéªéª4940: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2014-09-13 10:09:41
|
²éѯ½á¹û£º¹²²éµ½292¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 1 C26H22O11 ÏàËÆ¶È:76.9% Fitoterapia 2011 82 260-266 Isolation and identification of degradation products of salvianolic acid A by NMR and LC-MS Jinzhong Xu, Shanshan Zeng, Xueying Chen, Haibin Qu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 2 ÏàËÆ¶È:76.9% Fitoterapia 2011 82 260-266 Isolation and identification of degradation products of salvianolic acid A by NMR and LC-MS Jinzhong Xu, Shanshan Zeng, Xueying Chen, Haibin Qu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (R)-norsalvianolic acid L C26H22O10 ÏàËÆ¶È:73.0% Molecules 2014 19 1786-1794 A Pair of New Antioxidant Phenolic Acid Stereoisomers Isolated from Danshen Injection (Lyophilized Powder) Jing Liu, Jianfeng Zhao, Zhong Dai, Ruichao Lin, Gangli Wang and Shuangcheng Ma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (S)-norsalvianolic acid L C26H22O10 ÏàËÆ¶È:73.0% Molecules 2014 19 1786-1794 A Pair of New Antioxidant Phenolic Acid Stereoisomers Isolated from Danshen Injection (Lyophilized Powder) Jing Liu, Jianfeng Zhao, Zhong Dai, Ruichao Lin, Gangli Wang and Shuangcheng Ma Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . schizotenuin C1 C27H20O12 ÏàËÆ¶È:70.3% Natural Medicines 1996 50 204-211 The 3¦Á-Hydroxysteroid Dehydrogenase Inhibitory Active Flabonoids and Phenylpropanoids from Schizonepeta Spikes MATSUTA MUNETO,KANITA RIE,SAITO YUJI,YAMASHITA AKIRA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . salvianolic acid A ÏàËÆ¶È:69.2% Chinese Traditional and Herbal Drugs 2010 41 1060-1065 Chemical components of active fractions from Qili Qiangxin Capsula LIU Yi-xun; YU He-shui; KANG Li-ping; ZOU Peng; JIA Ji-ming; WANG Hong-tao ZHENG Ya-jie; TIAN Shu-yan; WU Yi-ling; MA Bai-ping Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5,6-dihydroxy-3-(3,4-dihydroxyphenyl)-1-methyl-2-benzopyran-4-carboxylic acid 4-[1-carboxy-2-(3,4-dihydroxyphenyl)] ethyl ester ÏàËÆ¶È:69.2% Fitoterapia 2012 83 1196-1204 Chemical conversions of salvianolic acid B by decoction in aqueous solution Hyoung Jae Lee, Jeong-Yong Cho, Jae-Hak Moon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . salvianolic acid C ÏàËÆ¶È:69.2% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 90-94 Studies on Chemical Constituents of Mianyi Composite Decoction ( ¢ò ) XU Nan, CAO Yue, ZHOU Ling, XIE Xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl lithospermate ÏàËÆ¶È:67.8% Chinese Journal of Natural Medicines 2007 5 27-30 Water-Soluble Constituents of Clerodendranthus spicatus WANG Min; LIANG Jing-Yu; CHEN Xue-Ying Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . yunnaneic acid E C27H24O14 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1997 45 1596-1600 Four New Caffeic Acid Metabolites, Yunnaneic Acids E-H, from Salvia yunnanensis Takashi TANAKA,Akiko NISHIMURA,Isao KOUNO,Gen-ichiro NONAKA and Chong-Ren YANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . salvianolic acid K C27H24O13 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1998 46 107-112 Constituents of Roots of Salvia deserta SCHANG. (Xinjiang-Danshen) Yasuhiro TEZUKA,Rena KASIMU,Jian Xin LI,Purusotam BASNET,Ken TANAKA,Tsuneo NAMBA and Shigetoshi KADOTA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Clinopodic acid N C27H22O12 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2012 60 499-507 Caffeic Acid Oligomers with Hyaluronidase Inhibitory Activity from Clinopodium gracile Hiroaki Aoshima,Toshio Miyase,and Tsutomu Warashina Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 7'R,7''S,8''S-Salvianolic acid P C27H22O12 ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2010 58 6064-6068 Depsides and Other Polar Constituents from Origanum dictamnus L. and Their in Vitro Antimicrobial Activity in Clinical Strains Aliki Chatzopoulou, Anastasia Karioti, Chrysoula Gousiadou, Vanesa Lax Vivancos, Panagiotis Kyriazopoulos, Stamatina Golegou and Helen Skaltsa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . schizotenuin F C28H24O12 ÏàËÆ¶È:66.6% Natural Medicines 1996 50 204-211 The 3¦Á-Hydroxysteroid Dehydrogenase Inhibitory Active Flabonoids and Phenylpropanoids from Schizonepeta Spikes MATSUTA MUNETO,KANITA RIE,SAITO YUJI,YAMASHITA AKIRA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . cissalvianolic acid J C27H22O12 ÏàËÆ¶È:66.6% Journal of Food Science 2010 75 359-362 Polyphenolic Acids from Mint (the Aerial of Mentha haplocalyx Briq.) with DPPH Radical Scavenging Activity G.-M. SHE, C. XU, B. LIU, AND R.-B. SHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . lithospermic acid ÏàËÆ¶È:66.6% Chinese Archives of Traditional Chinese Medicine 2013 31 1240-1242 Study of Chemical Components from Qili Qiangxin Capsule (I) QIAO Li, WANG Zongquan, MENG Zuohuan, JIANG Xingang, JIA Jiming, SONG Jian Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . salvianolic acid K C27H22O13 ÏàËÆ¶È:66.6% Journal of Xinjiang Medical University 2002 25 233-234 Research on the water-soluble component of the roots of Salvia deserta Schang Rena, Halmurat, DU Nian-Sheng, et al Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . salvianolic acid K ÏàËÆ¶È:66.6% Journal of Xinjiang Medical University 2003 26 583-585 Studies on the chemical constituents of the flowers of salvia deserta schang WANG Xin-ling, Rena, Zaoranmu, et al Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . eritrichin C26H21O10 ÏàËÆ¶È:65.3% Planta Medica 2005 71 446-451 Caffeic Acid Metabolites from Eritrichium sericeum Cell Cultures Fedoreyev, Sergey A.; Veselova, Marina V.; Krivoschekova, Olga E.; Mischenko, Natalia P.; Denisenko, Vladimir A.; Dmitrenok, Pavel S.; Glazunov, Valery P.; Bulgakov, Victor P.; Tchernoded, Galina K.; Zhuravlev, Yury N. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . isolithospermic acid C27H22O12 ÏàËÆ¶È:65.3% Natural Product Communications 2012 7 885-888 Biotransformation of Salvianolic acid B by Fusarium oxysporum f. sp. Cucumerinum and Its Two Degradation Routes Shidong Kan, Huimin Lin, Ji¡¯an Li, Lei Shao and Daijie Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-09-12 21:29:38














»Ø¸´´ËÂ¥
10