Znn3bq.jpeg
±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 191  |  »Ø¸´: 2

linkus1988

ľ³æ (ÕýʽдÊÖ)

[ÇóÖú] ÇóÖú΢Æ×Êý¾Ý

ÈܼÁ£º¼×´¼
ÏàËÆ¶È>=50%
̼Æ×Êý¾Ý£º
55.3,55.5,55.5,56.4,56.7,62.5,71.3,72.7,74.9,77.8,78.2,87.0,87.1,87.5,102.8,110.9,111.6,116.1,117.9,119.8,120.0,133.7,137.4,147.3,147.4,149.1,150.9
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lhwppkk

½ð³æ (ÕýʽдÊÖ)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
linkus1988: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¶àл 2013-09-16 16:30:03
²éѯ½á¹û£º¹²²éµ½363¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     4, 4'-dimethoxy-3'-hydroxy-7, 9'¡Ã7', 9-diepoxylignan-3-O-¦Â-D-glucopyranoside
C26H32O11     ÏàËÆ¶È:92.5%
Acta Botanica Yunnanica          2003          25(6)          711-715
A New Lignan Glycoside from Curculigo capitulata
LI Ning,TAN Ning-Hua,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     pinoresinol-4-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:92.5%
Chinese Traditional and Herbal Drugs          2008          39          654-656
Chemical constituents of Selaginella sinensis
FENG Wei-sheng; CHEN Hui; ZHENG Xiao-ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (+)-pinoresinol-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:92.5%
Chinese Traditional and Herbal Drugs          2008          39          343-346
ÏãÁÛëާÖÐÄ¾Ö¬ËØÀ࿹Ñõ»¯»îÐԳɷֵÄÑо¿
ÕÅÑåÁú;ÔøÎ°Ãñ;Íõ»ÛÈÙ;ÖìÀö;ÐìºéÁÁ;¿ïº£Ñ§
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     Pinoresinol-4-O-glucoside
    ÏàËÆ¶È:92.5%
Archives of Pharmacal Research          2005          28          39-43
Antitumor and antiinflammatory constituents from celtis sinensis
Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (+)-pinoresinol-4'-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:92.5%
Acta Pharmaceutica Sinica          2013          48          521-525
Chemical constituents from Pachysandra terminalis
XIAO Hui-jun, LI Chen-yang, TANG Sheng-an, QIN Nan, DUAN Hong-quan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (-)-pinoresinol 4-O-¦Â-D-glucopyranosid
    ÏàËÆ¶È:92.5%
Journal of Tropical and Subtropical Botany          2012          20          206-208
Five Glycosides from the Seeds of Litchi chinensis
XU Xin-ya, XIE Hai-hui, WEI Xiao-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (+)-Pinoresinol-O-¦Â-D-glucopyranoside
C26H32O11     ÏàËÆ¶È:88.8%
Acta Botanica Yunnanica          2006          28(4)          429-432
Non2alkaloid Constituents of Buxus sinica (Buxaceae)
LIN Yun-Liang, QIU Ming-Hua, LI Zhong-Rong,ZHOU Lin,LIU Jian-Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (+)-pinoresinol O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.8%
Phytochemistry          2009          70          1277-1285
Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside,macarangiosides E, and F isolated from the leaves of Macaranga tanarius
Katsuyoshi Matsunami, Hideaki Otsuka, Kazunari Kondo, Takakazu Shinzato, Masatoshi Kawahata, Kentaro Yamaguchi, Yoshio Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (-)-pinoresinol 4-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:88.8%
China Journal of Chinese Materia Medica          2006          31          133-135
Chemical constituents from root of Lasianthus acuminatissimus I
LI Bin, ZHANG Dongming, LUO Yongming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Pinoresinol-4-O-¦Â-D-glucopyranoside
C26H32O11     ÏàËÆ¶È:88.8%
Natural Product Research and Development          2012          24          298-302
Vasorelaxant Effect on Isolated Rabbit Aortic Rings and Chemical Constituents of n-Butanol Fraction from Leaves of Magnolia officinalis Rehd et Wils.
YANG Zhu-ya; WEI Ying-fang; ZHOU Zhi-hong; LONG Fei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (-)-Pinoresinol 4-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:85.1%
Phytochemistry          1994          35          479-483
Lignans and a stilbene from Festuca argentina
Adriana C. Casabuono, Alicia B. Pomillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     4,4'-dimethoxy-3'-hydroxy-7,9',7',9-diepoxyligan-3-O-¦Â-D-glucopyranoside
    ÏàËÆ¶È:85.1%
Natural Product Research and Development          2010          22          731-735
Studies on the Chemical Constituents of Euphorbia helioscopia
HE Jiang-bo;LIU Guang-ming; CHENG Yong-xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (+)-pinoresinol 4-O-glucoside
    ÏàËÆ¶È:85.1%
Natural Medicines          1995          49          475-477
Studies on the Constituents of Chinese Medicine "Luobumaye" : On Phenolic Compounds of Poacynum hendersonii Leaves
LEI ZHEN-HUAN,YAHARA SHOJI, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ËÉÖ¬ËØ-4-O-¦Â-D-ÆÏÌÑÌÇÜÕ
    ÏàËÆ¶È:85.1%
Journal of Chinese Medicinal Materials          2007          30          792-794
Non-saponins from Solanum nigrum L.
WANG Li-ye, WANG Nai-li, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3'-demethyl-phillyrin
C26H32O11     ÏàËÆ¶È:81.4%
Natural Product Research and Development          2008          20          278-279
Chemical constituents from Tinospora sinensis
REN Yan-li;TANG Qian-rui; ZHANG Zhen; CHEN Li; HE Hong-ping; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ËÉÓÍ´¼-4-O-¦Â-D-ÇÛ²ËÌÇ»ù-(1¡ú2)-¦Â-D-ßÁà«ÆÏÌÑÌÇß°
    ÏàËÆ¶È:78.5%
Journal of Tropical and Subtropical Botany          2005          13          171-174
°åÀ¶¸ùÖÐß°Àà³É·ÖµÄÑо¿
κ»¶»¶, ÎâÆ¼, κТÒå, ¼ªÌïÑÅÖ®, лº£»Ô
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     pinoresinol 4-O-¦Á-L-rhamnopyranosyl (1¡ú 2)-¦Â-D-gluco-pyranoside
C32H42O15     ÏàËÆ¶È:78.1%
Journal of Natural Medicines          2009          63          100-101
Lignan and flavonoid glycosides from Urtica laetevirens Maxim.
Yuan Zhou, Wei Wang, Ling Tang, Xing-guo Yan and Li-ying Shi, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     lanicepside B
    ÏàËÆ¶È:77.7%
Helvetica Chimica Acta          2007          Vol. 90          951
Two New Lignan Glycosides from Saussurea laniceps
Zhi-Wang Zhou, Sheng Yin, Xiao-NingWang, Cheng-Qi Fan, Hui Li, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (+)-isoeucommin A
    ÏàËÆ¶È:77.7%
Natural Product Communications          2011          6          1901-1904
Two New Phenolic Glycosides from Viburnum plicatum var. plicatum f. plicatum
Saki Katagiri, Yoshiki Watanabe, Yasunori Yaoita, Masao Kikuchi and Koichi Machida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (+)-epipinoresinolmethyl ether-¦Â-D-glucoside
C21H24O6     ÏàËÆ¶È:77.7%
Pharmaceutical Biology          2002          40          96-102
The First Report on the Occurrence of Furofuranoid Lignan Glucosides in Acanthaceae
El-Domiaty M.M., El-Shafae A.M., Abdel-Aal M.M., Abou-Hashem M.M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (-)-(7R,7'R,8S,8'R)-4,4'-Dihydroxy-3,3'-dimethoxy-7,7'-epoxylignan-4-O-¦Â-D-glucopyranoside
C26H34O10     ÏàËÆ¶È:77.7%
Journal of Asian Natural Products Research          2013          15          482-491
Glycosides from the bark of Machilus robusta
Peng-Bin Bu, Yan-Ru Li, Ming Jiang, Fang Wang, Xiao-Liang Wang, Sheng Lin, Cheng-Gen Zhu & Jian-Gong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (-)-(7R,7'R,8S,8'R)-4,4'-Dihydroxy-3,3'-dimethoxy-7,7'-epoxylignan-4'-O-¦Â-D-glucopyranoside
C26H34O10     ÏàËÆ¶È:77.7%
Journal of Asian Natural Products Research          2013          15          482-491
Glycosides from the bark of Machilus robusta
Peng-Bin Bu, Yan-Ru Li, Ming Jiang, Fang Wang, Xiao-Liang Wang, Sheng Lin, Cheng-Gen Zhu & Jian-Gong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     (+)-Pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside
C33H36O15     ÏàËÆ¶È:74.1%
Phytochemistry          2009          70          1277-1285
Absolute configuration of (+)-pinoresinol 4-O-[6''-O-galloyl]-¦Â-D-glucopyranoside,macarangiosides E, and F isolated from the leaves of Macaranga tanarius
Katsuyoshi Matsunami, Hideaki Otsuka, Kazunari Kondo, Takakazu Shinzato, Masatoshi Kawahata, Kentaro Yamaguchi, Yoshio Takeda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     neoarctin A
C26H34O12     ÏàËÆ¶È:74.0%
Journal of Asian Natural Products Research          2007          9          541-544
A new lignan from the seeds of Arctium lappa
MIN YONG, GU KUN and MIN-HUA QIU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     7R,7' R,8S,8'S-( +)-neo-olivil 4-O-¦Â-D-Glucopyranoside
C26H34O12N     ÏàËÆ¶È:74.0%
Chemical & Pharmaceutical Bulletin          2005          53          48-51
Studies on the Constituents of Swertia japonica MAKINO II. On the Structures of New Glycosides
Masafumi Kikuchi and Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     erythro-1-(4-O-¦Â-glucopyranosyl-3-methoxyphenyl)-2-{2-methoxyl-4-[1-(E)-propene-3-ol]-phenoxyl}-propane-1,3-diol
C27H34O13     ÏàËÆ¶È:74.0%
Turkish Journal of Chemistry          2005          29          71-81
Secondary Metabolites of Phlomis viscosa and Their Biological Activities
İHSAN ÇALIŞ, HASAN KIRMIZIBEKMEZ, JOHN A. BEUTLER, ALİ ARSLAN DÖNMEZ, FUNDA NURAY YALÇIN, EKREM KILIÇ, MERAL ÖZALP, PETER R¨¹EDI, DENİZ TAŞDEMİR
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Hyuganoside IIIa
C26H34O12     ÏàËÆ¶È:74.0%
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   Ì¼Æ×Ä£Äâͼ
28 .     Hyuganoside IIIb
C26H34O12     ÏàËÆ¶È:74.0%
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   Ì¼Æ×Ä£Äâͼ
29 .     Pinoresinol-4-O-rutinoside
    ÏàËÆ¶È:71.8%
Archives of Pharmacal Research          2005          28          39-43
Antitumor and antiinflammatory constituents from celtis sinensis
Dae Keun Kim, Jong Pil Lim, Jin Wook Kim, Hee Wook Park and Jae Soon Eun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     lanicepside A
C26H34O12     ÏàËÆ¶È:70.3%
Helvetica Chimica Acta          2007          Vol. 90          951
Two New Lignan Glycosides from Saussurea laniceps
Zhi-Wang Zhou, Sheng Yin, Xiao-NingWang, Cheng-Qi Fan, Hui Li, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-16 16:26:30
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

linkus1988

ľ³æ (ÕýʽдÊÖ)

3Â¥2013-09-16 16:29:03
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ linkus1988 µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á +4 Áõīī 2026-04-05 4/200 2026-04-08 06:22 by lijunpoly
[¿¼ÑÐ] 0703»¯Ñ§µ÷¼Á 348·Ö +10 °¦ÎÒ³¬ÕæÃ»ÕÐÁË 2026-04-06 10/500 2026-04-08 00:45 by JourneyLucky
[¿¼ÑÐ] Çóµ÷¼Á +11 wwwwabcde 2026-04-07 11/550 2026-04-07 23:16 by JourneyLucky
[¿¼ÑÐ] 22408 һ־Ը˫һÁ÷È˹¤ÖÇÄÜ300·Ö ËÄÁù¼¶£¬Êý¾Ý·ÖÎö¹ú½± +4 zzfeng123 2026-04-06 6/300 2026-04-07 21:02 by zzfeng123
[¿¼ÑÐ] 085602µ÷¼Á ³õÊÔ×Ü·Ö335 +10 19123253302 2026-04-05 10/500 2026-04-07 15:23 by СÇÇͬѧya
[¿¼ÑÐ] 328Çóµ÷¼Á +4 ghhh88888 2026-04-06 5/250 2026-04-07 14:45 by ghhh88888
[ÂÛÎÄͶ¸å] Decision: Revise for Editor»¹»áËÍÉóÂð 100+3 CccccccccFD 2026-04-04 5/250 2026-04-07 10:58 by ±±¾©À³ÒðÈóÉ«
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +10 Ò»ÑùYWY 2026-04-06 10/500 2026-04-06 21:05 by lbsjt
[¿¼ÑÐ] 287Çóµ÷¼Á +3 ͨÐÅѧ˶081000 2026-04-03 4/200 2026-04-06 21:03 by going home
[¿¼ÑÐ] Ò»Ö¾Ô¸¹ú¿Æ´óÐŹ¤Ëù,Ó¢¶þÊý¶þ408×Ü·Ö293·ÖÇóµ÷¼Á +3 ilcyuan 2026-04-02 4/200 2026-04-06 16:35 by likeihood
[¿¼ÑÐ] 285Çóµ÷¼Á +8 AZMK 2026-04-04 11/550 2026-04-06 13:56 by BruceLiu320
[¿¼ÑÐ] ¹¤¿Æ370Çóµ÷¼Á +3 äçÐļ弦µ° 2026-04-05 3/150 2026-04-06 10:55 by ÕâÊÇÒ»¸öÎÞÁĵÄê
[¿¼ÑÐ] ²ÄÁÏÓ뻯¹¤371Çóµ÷¼Á +14 ÅãÁÕ¿´º£ 2026-04-04 15/750 2026-04-06 06:59 by houyaoxu
[¿¼ÑÐ] 262Çóµ÷¼Á +7 ÌìϵÚÒ»ÎÄ 2026-04-04 8/400 2026-04-05 21:31 by ¼¤Á÷Ó¶É
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +12 Ò»ÑùYWY 2026-04-02 13/650 2026-04-04 20:49 by À¶ÔÆË¼Óê
[¿¼ÑÐ] µ÷¼Á0855-288 +5 xÐܶþa 2026-04-03 5/250 2026-04-04 00:19 by Öí»á·É
[¿¼ÑÐ] Ò»Ö¾Ô¸Äϲý´óѧ324Çóµ÷¼Á +13 hanamiko 2026-04-01 13/650 2026-04-03 18:30 by lsÁõ˧
[¿¼ÑÐ] 071000ÉúÎïѧµ÷¼Á +8 ÖªÕÑÂû 2026-04-02 8/400 2026-04-03 10:36 by macy2011
[¿¼ÑÐ] Ò»Ö¾Ô¸±±¾©¿Æ¼¼´óѧ085601²ÄÁϹ¤³ÌÓ¢Ò»Êý¶þ³õÊÔ×Ü·Ö335Çóµ÷¼Á +8 Ë«ÂíβƦÀϰå2 2026-04-02 9/450 2026-04-02 14:45 by 5896
[¿¼ÑÐ] 283Çóµ÷¼Á +3 jiouuu 2026-04-02 4/200 2026-04-02 14:08 by ßÕßÕßÕßÉßÉßÉ
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û