±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 271  |  »Ø¸´: 1

sunshine_»¶

ľ³æ (ÖøÃûдÊÖ)

[ÇóÖú] ΢Æ×ÇóÖú

ÈܼÁ£ºßÁà¤
̼Æ×Êý¾Ý£º16.45,16.72,17.45,21.18,23.86,26.78,27.03,28.35,30.63,30.98,32.43,34.43,35.24,35.55,37.01,37.14,40.29,40.41,40.69,41.25,56.43,62.46,62.85,64.03,70.32,71.74,72.77,74.54,75.22,75.38,75.51,76.90,78.45,78.61,81.24,103.91,105.14,110.63
·Ç³£¸Ðл£¡
»Ø¸´´ËÂ¥
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
sunshine_»¶: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-09-28 21:30:37
²éѯ½á¹û£º¹²²éµ½4019¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)  
--------------------------------------------------------------------------------



1 .     Timosaponin BII-a
C39H66O14     ÏàËÆ¶È:97.4%
Journal of Asian Natural products Research          2010          12          955-961
Hydrolysis of timosaponin BII by the crude enzyme from Aspergillus niger AS 3.0739
Wen-Bin Zhou; Bing Feng; Hong-Zhi Huang; Ping Liu; He-Shui Yu; Yang Zhao; Yu-Juan Qin; Li-Ping Kang; Bai-Ping Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


2 .     prototokoronin
     ÏàËÆ¶È:84.2%
Phytochemistry          1983          22          203-206
Protoyonogenin and protoneoyonogenin from the aerial parts and tissue cultures of Dioscorea tokoro
Astsuko Uomori, Shujiro Seo, Kazuo Tori, Yutaka Tomita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


3 .     prototokoronin
     ÏàËÆ¶È:84.2%
Journal of the Chemical Society, Perkin Transactions 1          1984                   869-874
Biosynthesis of (25S)- and (25R)-furostanol glycosides from [1,2-13C2] acetate in Dioscorea tokoro tissue cultures
Shujiro Seo, Atsuko Uomori, Yohko Yoshimura and Kazuo Tori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


4 .     (25S)-26-O-¦Â-D-glucopyranosyl-furost-1¦Â,3¦Â,22¦Á,26-tetraol3-O-¦Â-D-glucoside
C39H66O15     ÏàËÆ¶È:82.0%
Magnetic Resonance in Chemistry          2009          47          87-91
Structural elucidation of four new furostanol saponins from Tupistra chinensis by 1D and 2D NMR spectroscopy (pages 87¨C91)
Kun Zou, Jun-zhi Wang, Zhi-yong Guo, Ming Du, Jun Wu, Yuan Zhou, Fei-jun Dan and Chuang Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


5 .     (25R)-26-O-¦Â-D-glucopyranosyl-furost-1¦Â,3¦Â,22¦Á,26-tetraol3-O-¦Â-D-glucoside
C39H66O15     ÏàËÆ¶È:82.0%
Magnetic Resonance in Chemistry          2009          47          87-91
Structural elucidation of four new furostanol saponins from Tupistra chinensis by 1D and 2D NMR spectroscopy (pages 87¨C91)
Kun Zou, Jun-zhi Wang, Zhi-yong Guo, Ming Du, Jun Wu, Yuan Zhou, Fei-jun Dan and Chuang Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


6 .     aspafilioside A
C38H62O12     ÏàËÆ¶È:81.5%
Acta Pharmaceutica Sinica          1990          Vol 25          509-514
STEROIDAL SAPONINS FROM ASPARAGUS FILICINUS
Y Ding and CR Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


7 .     (25R)-5¦Â-spirost-3¦Â‑ol 3-O-¦Â‑D-xylopyranosyl-(1¡ú6)-¦Â‑D-glucopyranoside
C38H62O12     ÏàËÆ¶È:81.5%
Planta Medica          2012          78          276¨C285
Spirostanol Saponins Derivated from the Seeds of Trigonella foenum-graecum by ¦Â-Glucosidase Hydrolysis and Their Inhibitory Effects on Rat Platelet Aggregation
Xu Pang, Yue Cong, He-Shui Yu, Li-Ping Kang, Bing Feng, Bing-Xing Han, Yang Zhao, Cheng-Qi Xiong,Da-Wei Tan,Wei Song, Bin Liu, Yu-Wen Cong, Bai-Ping Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


8 .     (25R)-5¦Â-spirostan-3¦Â-yl O-¦Â-D-glucopyranosyl-(1¡ú3)-¦Â-D-galactopyranoside
C39H64O13     ÏàËÆ¶È:79.4%
Journal of Natural Products          2009          72          1399-1404
Steroidal Glycosides from Agave utahensis and Their Cytotoxic Activity
Akihito Yokosuka,Maki Jitsuno,Satoru Yui, Masatoshi Yamazaki, and Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


9 .     timosaponin A-III
     ÏàËÆ¶È:79.4%
Chemical & Pharmaceutical Bulletin          1994          42          2342-2345
New Steroidal Saponins from the Rhizomes of Anemarrhena asphodeloides BUNGE (Liliaceae)
Setsuo SAITO,Satoshi NAGASE and Koki ICHINOSE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


10 .     compound 6
     ÏàËÆ¶È:79.4%
Chinese Chemical Letters          1993          4          141-144
STUDIES ON TWO NEW FUROSTANOL GLYCOSIDES FROM ALLIUM MACROSTEMON BUNGE
JUN PENG PENG,XUAN WANG AND XIN SHENG YAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


11 .     compound 2
     ÏàËÆ¶È:79.4%
Acta Pharmaceutica Sinica          2003          Vol 38          433-437
Study on the active spirostanol saponins of Gualou xiebai baijiutang
HE Xiang-jiu; WANG Nai-li; QIU Feng; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


12 .     Ys-II
     ÏàËÆ¶È:79.4%
Phytochemistry          1989          28          1215-1217
The steroidal glycosides from the caudex of Yucca gloriosa
Kimiko Nakano,Tokushi Yamasaki,Yukiko Imamura,K¨­tar¨­ Murakami,Yoshihisa Takaishi,Toshiaki Tomimatsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


13 .     Filiasparoside F
C43H70O17     ÏàËÆ¶È:79.0%
Steroids          2010          75          734-739
Steroidal saponins and ecdysterone from Asparagus filicinus and their cytotoxic activities
Jia-Jun Wu, Ka-Wing Cheng, Xiao-Feng Zuo, Ming-Fu Wang, Ping Li, Lu-Yong Zhang, Hao Wang, Wen-Cai Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


14 .     protoyonogenin
     ÏàËÆ¶È:78.9%
Phytochemistry          1983          22          203-206
Protoyonogenin and protoneoyonogenin from the aerial parts and tissue cultures of Dioscorea tokoro
Astsuko Uomori, Shujiro Seo, Kazuo Tori, Yutaka Tomita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


15 .     Timosaponin BII-b
C33H56O9     ÏàËÆ¶È:78.9%
Journal of Asian Natural products Research          2010          12          955-961
Hydrolysis of timosaponin BII by the crude enzyme from Aspergillus niger AS 3.0739
Wen-Bin Zhou; Bing Feng; Hong-Zhi Huang; Ping Liu; He-Shui Yu; Yang Zhao; Yu-Juan Qin; Li-Ping Kang; Bai-Ping Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


16 .     aspafilioside A
     ÏàËÆ¶È:78.9%
Chinese Traditional and Herbal Drugs          2012          43          1716-1720
Steroids from tubers of Asparagus filicinus
TAO Hua-ming; WANG Li-shu; ZHAO Da-qing; ZHU Quan-hong; YIN Yong-guan; LIU Yong-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


17 .     Timosaponin AIII
     ÏàËÆ¶È:78.9%
Natural Product Research and Development          2012          24          1497-1501
Steroidal Saponins from Anemarrhena asphodeloides Bge.
ZHU Fu-tao; HUANG Xue-feng; KONG Ling-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


18 .     (25R)-5¦Â-spirostan-3¦Â-yl O-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-galactopyranoside
C39H64O13     ÏàËÆ¶È:76.9%
Journal of Natural Products          2009          72          1399-1404
Steroidal Glycosides from Agave utahensis and Their Cytotoxic Activity
Akihito Yokosuka,Maki Jitsuno,Satoru Yui, Masatoshi Yamazaki, and Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


19 .     (25R)-5¦Â-spirostan-3¦Â-ol 3-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glu-copyranoside
C39H64O13     ÏàËÆ¶È:76.9%
Planta Medica          2006          72          667-670
Bioactive Steroidal Saponins from Smilax medica
Sautour, M.; Miyamoto, T.; Lacaille-Dubois, M.-A.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


20 .     anemarrhenasaponin I
C39H66O14     ÏàËÆ¶È:76.9%
Chemical & Pharmaceutical Bulletin          1994          42          2342-2345
New Steroidal Saponins from the Rhizomes of Anemarrhena asphodeloides BUNGE (Liliaceae)
Setsuo SAITO,Satoshi NAGASE and Koki ICHINOSE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


21 .     smilageninoside
     ÏàËÆ¶È:76.9%
Chinese Chemical Letters          2007          18          171-174
Two new saponins from Anemarrhena asphodeloides Bge
Ying Peng, Yu Jing Zhang , Zhi Qiang Ma, Wei San Pan, Yu Qing Sun,Shao Jiang Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


22 .     smilagenin 3-O-[¦Â-D-glucopyranosyl(1¡ú2)]-¦Â-D-mannopyranoside
     ÏàËÆ¶È:76.9%
Acta Pharmaceutica Sinica          1991          26          619-621
NOVEL TRITERPENOIDS FROM CYNANCHUM HANCOCKIANUM
HX Lou; X Li and TR Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


23 .     compound II
C39H64O14     ÏàËÆ¶È:76.9%
Acta Pharmaceutica Sinica          1992          27          26-32
STUDIES ON THE ACTIVE CONSTITUENTES OF ANEMARRHENA ASPHODELOIDES BUNGE
JX Dong; GY Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------


24 .     compound 6
     ÏàËÆ¶È:76.9%
Acta Pharmaceutica Sinica          1993          28          526-531
STUDIES ON TWO NEW FUROSTANOL GLYCOSIDES FROM ALLIUM MACROSTEMON BUNGE
JP Peng; X Wang and XS Yao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-28 21:17:50
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ sunshine_»¶ µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á +15 ÐܶþÏëÉϰ¶ 2026-04-04 16/800 2026-04-07 13:54 by oooqiao
[¿¼ÑÐ] ÉúÎïѧ363µ÷¼ÁÇóÖú +5 fanzhang6666 2026-04-06 6/300 2026-04-07 11:13 by ºÃÔËÀ´2024
[˶²©¼ÒÔ°] 0856²ÄÁÏ»¯¹¤Çóµ÷¼Á£¬Ò»Ö¾Ô¸211£¬³õÊԳɼ¨349 +4 ½­»´±±Ô 2026-04-05 4/200 2026-04-06 22:44 by chenzhimin
[¿¼ÑÐ] Ò»Ö¾Ô¸°²»Õij211 0703»¯Ñ§×Ü·Ö339Çóµ÷¼Á +7 Íí·ç²»Íí 2026-04-04 7/350 2026-04-06 14:06 by houyaoxu
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á +5 asdasdassda 2026-04-05 5/250 2026-04-06 09:32 by dongzh2009
[¿¼ÑÐ] 372·Ö£¬²ÄÁÏÓ뻯¹¤£¬Ò»Ö¾Ô¸ºþÄÏ´óѧ£¬Çóµ÷¼Á +3 À¶¼ãƬ 2026-04-01 3/150 2026-04-06 09:04 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 285Çóµ÷¼Á +4 ¶ñ·¨´ó¶þµÄÆøÎ¶ß 2026-04-05 5/250 2026-04-05 20:32 by 286640313
[¿¼ÑÐ] ²ÄÁÏÇóµ÷¼Á +10 ÄØÄØÄÝÄÝ 2026-04-01 10/500 2026-04-04 23:12 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 277Çóµ÷¼Á +4 12A3 2026-04-02 5/250 2026-04-04 20:28 by À¶ÔÆË¼Óê
[¿¼ÑÐ] ²ÄÁÏרҵ383Çóµ÷¼Á +8 ¹ùÑôÑôÑô³É 2026-04-03 8/400 2026-04-04 10:29 by Rednal.
[¿¼ÑÐ] 294Çóµ÷¼Á +6 Grey_Ey 2026-04-03 6/300 2026-04-03 20:46 by ÐÀϲ777
[¿¼ÑÐ] 366Çóµ÷¼Á +7 sbdnd 2026-04-03 7/350 2026-04-03 12:40 by cymywx
[¿¼ÑÐ] 303Çóµ÷¼Á +3 һɫÇåÓð 2026-04-02 4/200 2026-04-03 10:22 by À¶ÔÆË¼Óê
[¿¼ÑÐ] Ò»Ö¾Ô¸ÉÂÎ÷ʦ·¶´óѧÉúÎïѧ317·Ö +5 1563ÈÕ¡£ 2026-04-02 5/250 2026-04-03 06:58 by ilovexiaobin
[¿¼ÑÐ] 08¿ªÍ·¿´¹ýÀ´£¡£¡£¡ +4 wwwwffffff 2026-03-31 6/300 2026-04-02 11:42 by ¾ùÖµ»Ø¹é
[¿¼ÑÐ] 324Çóµ÷¼Á +5 ÏëÉÏѧÇóµ÷ 2026-04-01 6/300 2026-04-02 10:16 by sanrepian
[¿¼ÑÐ] 0710ÉúÎïѧÇóµ÷¼Á +9 manman511 2026-04-01 9/450 2026-04-02 10:00 by zxl830724
[¿¼ÑÐ] 266Çóµ÷¼Á +4 ѧԱ97LZgn 2026-04-02 4/200 2026-04-02 09:52 by yulian1987
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +11 Ò»ÑùYWY 2026-03-31 11/550 2026-04-01 11:35 by wangjy2002
[¿¼ÑÐ] Ò»Ö¾Ô¸ ÄϾ©º½¿Õº½Ìì´óѧ £¬080500²ÄÁÏ¿ÆÑ§Ó빤³Ìѧ˶ +10 @taotao 2026-03-31 11/550 2026-04-01 09:43 by xiayizhi
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û