| ²é¿´: 334 | »Ø¸´: 1 | |||
huadong1227ľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
LY-21-1 ΢Æ×Êý¾ÝÇóÖúÒÑÓÐ1È˲ÎÓë
|
|
MEODÈÜ£¬13C-NMRÈçÏ£º 16.26,18.00,18.13,18.71,19.89,21.97,27.27,30.90,31.69, 32.79,33.42,36.15,38.24,38.64,39.69,47.46,52.32,58.00, 62.07,69.24,69.94,70.60,72.30,72.53,72.57,73.07,73.10, 74.00,74.09,76.84,78.13,79.43,79.64,81.00,100.64,102.51, 102.78,103.34,22.60,125.74,142.46,156.53,199.55 |
» ²ÂÄãϲ»¶
Ö°³ÆÆÀÉóû¹ý£¬Çó°²Î¿
ÒѾÓÐ21È˻ظ´
À¬»øÆÆ¶þ±¾Ö°³ÆÆÀÉó±ê×¼
ÒѾÓÐ15È˻ظ´
Ͷ¸åElsevierµÄNeoplasiaÔÓÖ¾£¬µ½×îºóÑ¡publishing optionsÊ±Ò³Ãæ¿Õ°×£¬²»ÄÜÍê³ÉͶ¸å
ÒѾÓÐ20È˻ظ´
ESTͶ¸å״̬ÎÊÌâ
ÒѾÓÐ7È˻ظ´
±ÏÒµºóµ±¸¨µ¼Ô±ÁË£¬ÌìÌì¸÷ÖÖѧÉú³¬·³
ÒѾÓÐ4È˻ظ´
ƸU VÈÈÈÛ½ºÑо¿ÈËÔ±
ÒѾÓÐ10È˻ظ´
ÇóÖúÎÄÏ×
ÒѾÓÐ3È˻ظ´
Ͷ¸å·µÐÞºóÊÕµ½ÕâÑùµÄ»Ø¸´£¬»¹ÓÐÏ£ÍûÂð
ÒѾÓÐ8È˻ظ´
ÈýÎÞ²úÆ·»¹Óлú»áÂð
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÁ½¸ö΢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»df12
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý YC-8
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú´óÉñ΢Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
zzb7855
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 235 (´óѧÉú)
- ½ð±Ò: 4054.1
- É¢½ð: 5
- ºì»¨: 4
- Ìû×Ó: 720
- ÔÚÏß: 150.1Сʱ
- ³æºÅ: 225506
- ×¢²á: 2006-03-23
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
huadong1227: ½ð±Ò+5, ¡ïÓаïÖú 2014-11-10 15:33:58
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
huadong1227: ½ð±Ò+5, ¡ïÓаïÖú 2014-11-10 15:33:58
|
²éѯ½á¹û£º¹²²éµ½1610¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . pregna-5,16-diene-3b-ol-20-one 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Á-L-rhamnopyranosyl-(1¡ú4)]-¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside C45H70O19 ÏàËÆ¶È:91.1% Magnetic Resonance in Chemistry 2012 50 813-817 Steroidal saponins and pregnane glycosides from Smilax microphylla Tao Lin, Hui-Lian Huang, Rong-Hua Liu, Ji-Cheng Shu, Gang Ren, Feng Shao and Li-sha Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . hypoglaucin H ÏàËÆ¶È:86.0% China Journal of Chinese Materia Medica 2014 39 2034-2038 Chemical constituents from Solanum rostratum HAO Li-juan, WANG Shan, ZHU Jing-jing, WANG Zhi-min, WEI Shou-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (3¦Â-dihydroxy pregn-5,16-dien-20-one 3-O-¦Â-chacotrioside ÏàËÆ¶È:83.7% Phytochemistry 1999 50 481-484 Steroidal saponins from Asparagus dumosus Viqar Uddin Ahmad, Syed Muhammad Khaliq-uz-Zaman, Simin Shameel, Shaista Perveen, Zulfiqar Ali Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-O-¦Â-D-glucopyranosyl-22-O-methyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Î,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú6'')-O-¦Â-D-galactopyranoside ÏàËÆ¶È:82.6% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-O-[bis-¦Á-L-rhamnopyranosyl-(1¡ú4 and 1¡ú2)¦Â-D-glucopyranosyl]-(25R)-furosta-5,2O-dien-3¦Â,26-diol ÏàËÆ¶È:82.2% Planta Medica 1988 54 344-346 Oligofurostanosides from Asparagus cochinchinensis Zhou Zhong Liang, Rita Aquino, Francesco De Simone, Antonio Dini, Oreste Schettino, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1-O-¦Â-D-glucopyranosyl-(25R)-fur-ost-5(6)-en-1¦Â,3¦Â,22¦Â,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú6'')-O-¦Â-D-galactopyranoside ÏàËÆ¶È:82.2% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . solamargine C45H73NO15 ÏàËÆ¶È:81.8% Bioorganic & Medicinal Chemistry Letters 2011 21 2930-2933 Total synthesis of solamargine Guohua Wei, Jing Wang, Yuguo Du Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (25R)-26-O-¦Â-D-glucopyranosyl-22¦Á-methoxy-furost-5-ene-1¦Â,3¦Â,26-triol 1-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-6-O-acetyl¦Â-D-glucopyranoside and ÏàËÆ¶È:80.4% Phytochemistry 2011 72 651-661 Steroidal glycosides from Ruscus ponticus Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-solamarine ÏàËÆ¶È:80% Phytochemistry 2002 59 79-84 Bioactive steroidal alkaloid glycosides from Solanum aculeastrum Alphonse W. Wanyonyi, Sumesh C. Chhabra, Gerald Mkoji, Udo Eilert,Wilson M. Njue Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . solamargine ÏàËÆ¶È:80% Phytochemistry 2002 59 79-84 Bioactive steroidal alkaloid glycosides from Solanum aculeastrum Alphonse W. Wanyonyi, Sumesh C. Chhabra, Gerald Mkoji, Udo Eilert,Wilson M. Njue Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . dioscin ÏàËÆ¶È:80% Natural Product Research 2003 17 287-292 A New Steroidal Saponin from Dioscorea Zingiberensis Wright Wenji Sun; Guangzhong Tu; Yongmin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . dioscin ÏàËÆ¶È:80% Natural Product Research 2003 17 287-292 A New Steroidal Saponin from Dioscorea Zingiberensis Wright Wenji Sun; Guangzhong Tu; Yongmin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . tribol ÏàËÆ¶È:80% Fitoterapia 2004 75 117-122 Anovel furostanol saponin from Tribulus terrestris of Bulgarian origin J. Conrad , D. Dinchev , I. Klaiber , S. Mika , I. Kostova,W. Kraus Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . dioscoreanoside C C45H72O19 ÏàËÆ¶È:80% Phytochemistry 2013 95 341-350 Steroidal saponins from the flowers of Dioscorea bulbifera var. sativa L¨¦on Azefack Tapondjou, Kristina Jenett-Siems, Stefan Böttger, Matthias F. Melzig Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . dioscoreanoside E C45H72O19 ÏàËÆ¶È:80% Phytochemistry 2013 95 341-350 Steroidal saponins from the flowers of Dioscorea bulbifera var. sativa L¨¦on Azefack Tapondjou, Kristina Jenett-Siems, Stefan Böttger, Matthias F. Melzig Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1-O-¦Â-D-glucopyranosyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Á,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú2'')-O-¦Á-L-arabinopyranoside ÏàËÆ¶È:79.5% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-O-¦Â-D-glucopyranosyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Â,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú2'')-O-¦Á-L-arabinopyranoside ÏàËÆ¶È:79.5% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (25R)-26-O-¦Â-D-glucopyranosyl-furost-5-ene-3¦Â,22¦Á,26-triol 3-O-[¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside] ÏàËÆ¶È:79.5% Phytochemistry 2011 72 651-661 Steroidal glycosides from Ruscus ponticus Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ÊíÝ÷ÔíÜÕ ÏàËÆ¶È:79.0% Chinese Traditional and Herbal Drugs 2001 32 18,38 ÊÖÕÆ²ÎµÄ»¯Ñ§³É·ÖÑо¿ Àî˧,Íõ¶°,¿ïº£Ñ§,¸ÔÌï¼ÎÈÊ,°Âɽ?Ø Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1-O-[¦Á-L-rhamnopyranosyl-(1)-6-O-acetyl-¦Â-D-galactopyranosyl]-1¦Â,3¦Â,22¦Î-26-tetrahydroxyfurost-5(6)-ene-26-O-¦Â-D-glucopyranoside ÏàËÆ¶È:78.7% Chemistry of Natural Compounds 2009 45 756-758 Analysis and isolation of saponins from Limoniastrum feei by LC-UV N. Belboukhari, A. Cheriti Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . (25R,26R)-3¦Â,17¦Á-dihydroxy-26-methoxyspirostan-5-ene-3¦Â-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside C47H76O18 ÏàËÆ¶È:78.2% Chinese Traditional and Herbal Drugs 2011 42 21-24 Steroidal saponins and phenylic constituents from Lilium lancifolium and their anti-oxidant activities ZHOU Zhong-liu, SHI Ren-bing, LIU Bin, ZOU Jie-ming, YIN Wen-qing, XIA Jing-min Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (23S,25R)-23-hydroxyspirost-5-en-3¦Â-yl O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[¦Â-D-glucopyranosyl-(1¡ú6)]-¦Â-D-glucopyranoside C45H72O18 ÏàËÆ¶È:77.7% Phytochemistry 1999 51 567-573 Steroidal saponins from the bulbs of Lilium candidum Yoshihiro Mimaki, Tadaaki Satou, Minpei Kuroda, Yutaka Sashida, Yoshio Hatakeyama Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . asparasaponin II ÏàËÆ¶È:77.7% Chinese Traditional and Herbal Drugs 1999 30(12) 888-890 Studies on the Chemical Constituents of Commmon Asparagus Bark (Asparagus officinalis) Sun Jianhua; Zuo Chunxu; Yang Shangjun Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . compound 5 C45H72O ÏàËÆ¶È:77.7% Zeitschrift f¨¹r Naturforschung C 2002 57 33-38 Two New Sulfated Furostanol Saponins from Tribulus terrestris I. Kostova, D. Dinchev, G. Hopp Rentsch, V. Dimitrov, and A. Ivanova Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 1-O-¦Â-D-glucopyranosyl-22-O-methyl-(25R)-furost-5(6)-en-1¦Â,3¦Â,22¦Î,26-tetraol-26-O-¦Á-L-rhamnopyranosyl-(1'''¡ú2'')-O-¦Á-L-arabinopyranoside ÏàËÆ¶È:77.7% Food Chemistry 2005 93 205-214 Furostanol saponins in Allium caepa L. Var. tropeana seeds Irene Dini, Gian Carlo Tenore, Elena Trimarco, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . hauptsaponine S2 ÏàËÆ¶È:77.7% Pharmazie 1987 42 143-143 Steroidsaponine aus Dioscorea hispida L. Ng. X. Cuong, D. Zeigan, Gabriele Voigt, und K. Hiller Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ascalonicoside A1 C45H74O19 ÏàËÆ¶È:77.7% Journal of Agricultural and Food Chemistry 2002 50 5686-5690 Chemical Composition of Shallot (Allium ascalonicum Hort.) Ernesto Fattorusso, Maria Iorizzi, Virginia Lanzotti, and Orazio Taglialatela-Scafati Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . ascalonicoside A2 C45H74O19 ÏàËÆ¶È:77.7% Journal of Agricultural and Food Chemistry 2002 50 5686-5690 Chemical Composition of Shallot (Allium ascalonicum Hort.) Ernesto Fattorusso, Maria Iorizzi, Virginia Lanzotti, and Orazio Taglialatela-Scafati Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (3¦Â,5¦Á,6¦Â)-5,6-dihydroxysolanidan-3-yl 6-deoxy-¦Á-l-mannopyranosyl-(1¡ú2)-[6-deoxy-¦Á-l-mannopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside C45H75NO16 ÏàËÆ¶È:77.7% Helvetica Chimica Acta 2013 96 931-940 Five New Steroidal Alkaloid Glycosides from Solanum tuberosum Zhi-Qiang Zhang, Jian-Guang Luo, Jun-Song Wang and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . dioscin ÏàËÆ¶È:77.7% China Journal of Chinese Materia Medica 2014 39 2034-2038 Chemical constituents from Solanum rostratum HAO Li-juan, WANG Shan, ZHU Jing-jing, WANG Zhi-min, WEI Shou-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (23S,25R)-spirost-5-en-3,23-diol 3-O-¦Á-L-rhamnopyranosyl-(1¡ú2)-O-[¦Á-L-rhamnopyranosyl-(1¡ú4)]-¦Â-D-glucopyranoside C45H72O17 ÏàËÆ¶È:77.7% Records of Natural Products 2015 9 94-104 Chemical Constituents from Solanum glabratum Dunal var. sepicula Essam Abdel-Sattar, Mohamed A Farag and Engy A Mahrous Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (6S,13S)-13-O[¦Á-L-rhamnopyranosyl-(1¡ú4)-¦Â-D-fucopyranosyl]-6-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Á-L-rhamnopyranosyl]cleroda-3,14-diene-6,13-diol ÏàËÆ¶È:77.2% Phytochemistry 1997 46 839-844 Biologically active clerodane-type diterpene glycosides from the root-stalks of Dicranopteris pedata Tadashi Aoki, Tadashi Ohro, Yoshikazu Hiraga, Takayuki Suga, Mihoko Uno, Shinji Ohta Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . Solamargine C45H73NO15 ÏàËÆ¶È:77.2% Fitoterapia 2010 81 767-771 Evaluation of the biological activity of the molluscicidal fraction of Solanum sisymbriifolium against non target organisms Jean-Jacques M. Bagalwa, Laurence Voutquenne-Nazabadioko, Charlotte Sayagh, Augustin S. Bashwira Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ¦Â-solamarine C45H73NO15 ÏàËÆ¶È:77.2% Fitoterapia 2010 81 767-771 Evaluation of the biological activity of the molluscicidal fraction of Solanum sisymbriifolium against non target organisms Jean-Jacques M. Bagalwa, Laurence Voutquenne-Nazabadioko, Charlotte Sayagh, Augustin S. Bashwira Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (25S)-26-O-¦Â-D-glucopyranoyl-20(22)-en-furost-1¦Â,3¦Â,5¦Â,26-tetraol-1-O-¦Â-D-arabinopyranoside-3-O-¦Á-L-rhamnopyranoside C44H72O19 ÏàËÆ¶È:77.2% Natural Product Research 2013 27 85-92 Three new steroidal glycosides from roots of Reineckia carnea Qian Wang, Qune Hou, Zhiyong Guo, Kun Zou, Yanhong Xue, Nianyu Huang, Fan Cheng & Yuan Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 26-O-¦Â-D-glucopyranosyl-furost¦Á-5,25(27)-diene-3¦Â,22¦Á,26-triol 3-O-[¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside] ÏàËÆ¶È:77.2% Phytochemistry 2011 72 651-661 Steroidal glycosides from Ruscus ponticus Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . (25R)-26-O-¦Â-D-glucopyranosyl-furost¦Á-5,20(22)-diene-3¦Â,26-diol 3-O-[¦Á-L-arabinopyranosyl-(1¡ú4)-O-¦Â-D-glucopyranoside] ÏàËÆ¶È:77.2% Phytochemistry 2011 72 651-661 Steroidal glycosides from Ruscus ponticus Assunta Napolitano, Tamar Muzashvili, Angela Perrone, Cosimo Pizza, Ether Kemertelidze, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . Ceposide A C44H72O18 ÏàËÆ¶È:77.2% Phytochemistry 2012 74 133-139 Antifungal saponins from bulbs of white onion, Allium cepa L. Virginia Lanzotti, Adriana Romano, Stefania Lanzuise, Giuliano Bonanomi, Felice Scala Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . digitoxigenin 3-O-[O-¦Â-D-glucopyranosyl-(1¡ú6)-O-¦Â-D-glucopyranosyl-(1¡ú4)-2-O-acetyl-¦Â-D-digitalopyranoside] C44H69O19 ÏàËÆ¶È:77.2% Phytochemistry 2013 88 105-111 Cardenolide glycosides from root of Streptocaulon juventas Rui Xue, Na Han, Chun Ye, Hai-bo Wang, Jun Yin Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 3-O-[¦Á-L-rhamnopyranosyl-(1¡ú2)-¦Â-Dgalactopyranosyl-(1¡ú2)-¦Â-D-glucuronopyranosyl]-3¦Â,16¦Â,22¦Á-trihydroxy-olean-12-ene C48H78O18 ÏàËÆ¶È:77.0% Journal of Natural Products 2007 70 979-983 Oleanane Saponins from Stylosanthes erecta Marinella De Leo,Rokia Sanogo, Nunziatina De Tommasi, and Alessandra Braca Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . incanumine C49H79NO19 ÏàËÆ¶È:77.0% Journal of Natural Products 1990 Vol 53 513 The Cytotoxic Principles of Solanum incanum Chun-Nan Lin, Chai-Ming Lu, Ming-Kung Cheng, Kim-Hong Gan, Shen-Jeu Won Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . ent-14-labden-8¦Â-ol 13¦Á-O-[¦Â-D-quinovopyranosyl-(1¡ú2)-3'-O-acetyl-¦Á-L-rhamnopyranosyl]-19-O-¦Á-L-rhamnopyranoside C40H68O16 ÏàËÆ¶È:76.7% Journal of Natural Products 2007 70 1837-1845 Diterpenoid Glycosides from the Bitter Fern Gleichenia quadripartita Cecilia Socolsky,Yoshinori Asakawa,and Alicia Bard¨®n Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . macrophyllosaponin C C42H72O14 ÏàËÆ¶È:76.7% Journal of Natural Products 1996 59 1019-1023 Four Novel Cycloartane Glycosides from Astragalus oleifolius I¨²hsan Çalış, Murat Zor, İclal Saracoğlu, Aşkın Işımer, and Heinz R¨¹egger Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 26-O-¦Â-D-glucopyranosyl-22-O-methylfurosta-5,25(27)-diene-1¦Â,3¦Â,22¦Î,26-tetrol 1-O-{O-¦Á-L-rhamnopyranosyl-(1¡ú2)-3-O-acetyl-4-O-sulfo-¦Á-L-arabinipyranoside} ÏàËÆ¶È:76.5% Chemical & Pharmaceutical Bulletin 1998 46 298-303 New Steroidal Constituents of the Underground Parts of Ruscus aculeatus and Their Cytostatic Activity on HL-60 Cells Yoshihiro MIMAKI,Minpei KURODA,Aiko KAMEYAMA,Akihito YOKOSUKA and Yutaka SASHIDA Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . Acankoreoside J C47H73O20 ÏàËÆ¶È:76.5% Planta Medica 2010 76 189-194 Lupane-Type Triterpene Glycosides from the Leaves of Acanthopanax koreanum and Their In Vitro Cytotoxicity Nhiem, Nguyen Xuan; Kiem, Phan Van; Minh, Chau Van; Ha, Do Thi; Tai, Buu Huu; Yen, Pham Hai; Tung, Nguyen Huu; Hyun, Jae-Hee; Kang, Hee-Kyoung; Kim, Young Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . Acanthifolioside G C47H80O17 ÏàËÆ¶È:76.5% Journal of Natural Products 2012 75 2094-2100 Isolation of Steroidal Glycosides from the Caribbean Sponge Pandaros acanthifolium Fabrice Berru¨¦, Malcolm W. B. McCulloch, Patricia Boland, Saskia Hart, Mary Kay Harper, James Johnston, and Russell Kerr Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . compound 19 C46H76O22 ÏàËÆ¶È:76.0% Tetrahedron 2002 58 5837-5848 New pregnane glycosides from Caralluma negevensis Alessandra Braca, Ammar Bader, Ivano Morelli, Roberto Scarpato, Gino Turchi, Cosimo Pizza, Nunziatina De Tommasi Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 26-O-¦Â-D-glucopyranosyl-furost-3¦Â,26-diol-22-methoxy-3-O-¦Á-L-rhamnopyranosy(1¡ú4)-O-¦Â-D-glucopyranoside C46H78O18 ÏàËÆ¶È:76.0% Academic Journal of Second Military Medical University 2007 28 1241-1244 Studies on chemical constituents of Asparagus cochinchinensis SHEN Yang, CHEN Hai-sheng, WANG Qiong Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . solamargine ÏàËÆ¶È:75.5% Planta Medica 1993 59 483-484 Solamargine: The Main Glycoalkaloid from the Fruits of Solanum paludosum Mich¨¨le Valverde, CatherineLavaud, Joel Boustie,Houriya El Badaoui, BrunoMuguet, and Max Henr Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 3-O-[¦Á-L- rhamnopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl]-26-O-(¦Â-D-glucopyranosyl)-(25R)-furosta-5,20-dien-3¦Â,26-diol ÏàËÆ¶È:75.5% Planta Medica 1988 54 344-346 Oligofurostanosides from Asparagus cochinchinensis Zhou Zhong Liang, Rita Aquino, Francesco De Simone, Antonio Dini, Oreste Schettino, and Cosimo Pizza Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-11-10 14:54:03













»Ø¸´´ËÂ¥