| ²é¿´: 268 | »Ø¸´: 1 | ||
µØ¹ÏµØ¹Ï½ð³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| DMSO-d6£ºC18: 30.67,31.07,31.15,32.95,33.03,33.69,35.70,36.03,37.41,37.94,44.06,46.81,53.63,54.47,54.84,54.85,55.00,61.12,69.10,70.12,73.44,73.74,73.85,76.81,76.83,78.94,102.91,102.96,109.59,111.83,212.71 |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-21 16:19:40
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
µØ¹ÏµØ¹Ï: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-21 16:19:40
|
1 . Agavoside A ÏàËÆ¶È:63.6% Journal of Asian Natural Products Research 2003 5 95-103 THREE NEW HECOGENIN GLYCOSIDES FROM FERMENTED LEAVES OF AGAVE AMERICANA JIAN-MING JIN, XI-KUI LIU and CHONG-REN YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . longipenane 26-O-¦Â-D-glucopyranoside C33H54O10 ÏàËÆ¶È:60.6% Bioorganic & Medicinal Chemistry Letters 2013 23 1771-1775 Steroidal constituents from the leaves of Hosta longipes and their inhibitory effects on nitric oxide production Chung Sub Kim, Sun Yeou Kim, Eunjung Moon, Mi Kyeong Lee, Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 26-O-¦Â-D-glucopyranoside-3¦Â,26-dihydroxy-(25R)-5¦Á-furostan-20(22)-en-6-one C33H52O9 ÏàËÆ¶È:60.6% Molecules 2014 19 20975-20987 Four New Furostanol Saponins from the Rhizomes and Roots of Smilax scobinicaulis and Their Cytotoxicity Jing Xu, Shixiu Feng, Qi Wang, Yingli Cao, Miao Sun and Cunli Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (25R)-3¦Â,6¦Á-dihydroxy-5¦Á-spirostan-12-one C27H42O5 ÏàËÆ¶È:58.0% Planta Medica 2000 66 393-396 A New Steroidal Saponin from the Leaves of Agave americana Akihito Yokosuka,Yoshihiro Mimaki,Minpei Kuroda,Yutaka Sashida Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 4b ÏàËÆ¶È:58.0% Chemical & Pharmaceutical Bulletin 1995 43 1190-1196 Steroidal Saponins from the Underground Parts of Hosta longipes and Their Inhibitory Activity on Tumor Promoter-Induced Phospholipid Metabolism Yoshihiro MIMAKI,Toshihiro KANMOTO,Minpei KURODA,Yutaka SASHIDA,Atsuko NISHINO,Yoshiko SATOMI and Hoyoku NISHINO Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5¦Á(25R)-spirostan-2¦Á,3¦Â-diol 12-one(manogenin) C27H42O5 ÏàËÆ¶È:58.0% Phytochemistry 1991 30 633-636 12-Keto steroidal glycosides from the caudex of Yucca gloriosa Kimiko Nakano, Yukari Midzuta, Yumiko Hara, Ktar Murakami, Yoshihisa Takaishi, Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Manogenin ÏàËÆ¶È:58.0% Phytochemical Analysis 1994 5 24-26 Isolation and quantitation of manogenin and kammogenin from callus cultures of Agave amaniensis Gunawan Indrayanto, Herra Studiawan and Noor Cholies Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (22R,25S)-22-Hydroxy-12-oxo-5a-furostane-3b,26-diyl diacetate C31H48O7 ÏàËÆ¶È:58.0% Steroids 2012 77 59-66 Rapid conversion of spirostans into furostan skeletons at room temperature Omar Viñas-Bravo, Roxana Martinez-Pascual, Jos¨¦ Luis Vega-Baez, V¨ªctor G¨®mez-Calvario, Jes¨²s Sandoval-Ram¨ªrez, Sara Montiel-Smith, Socorro Meza-Reyes, Alejandra L¨®pez-De Rosas, M¨®nica Mart¨ªnez-Montiel, Mayra Reyes, Jos¨¦ A. Ruiz Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 26-O-¦Â-D-glucopyranoside-3¦Â,26-dihydroxy-(25R)-5¦Á-furostan-22-methoxyl-6-one C34H56O10 ÏàËÆ¶È:55.8% Molecules 2014 19 20975-20987 Four New Furostanol Saponins from the Rhizomes and Roots of Smilax scobinicaulis and Their Cytotoxicity Jing Xu, Shixiu Feng, Qi Wang, Yingli Cao, Miao Sun and Cunli Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-28 10:12:36














»Ø¸´´ËÂ¥