±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 1050  |  »Ø¸´: 11
¡¾Óн±½»Á÷¡¿»ý¼«»Ø¸´±¾Ìû×Ó£¬²ÎÓë½»Á÷£¬¾ÍÓлú»á·ÖµÃ×÷Õß liufang0378 µÄ 90 ¸ö½ð±Ò £¬»ØÌû¾ÍÁ¢¼´»ñµÃ 1 ¸ö½ð±Ò£¬Ã¿ÈËÓÐ 1 ´Î»ú»á
µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû

liufang0378

½ð³æ (СÓÐÃûÆø)


[½»Á÷] ΢Æ×ÇóÖú

p01
115.53,130.95,161.98,199.29
p02
64.32,70.11,71.76
p03
20.95,61.01,64.00,67.27,69.69,71.25,71.93,72.02,76.05,77.60,83.10,103.07,106.00,116.42,121.93,129.13,129.13,144.21,151.00,152.68,161.83,164.55,170.80,182.86
p04
20.90,58.25,60.99,63.92,67.39,69.68,71.29,71.89,71.97,76.01,77.53,82.66, 99.79,100.38,102.74,103.82,106.00,112.54,113.66,119.40,123.54,127.98,144.37,147.23,151.14,151.78,152.67,164.41,170.76,182.83
p05
35.63,42.27,56.03,56.23,58.63,66.35,70.74,73.89,76.88,93.38,98.29,102.24,111.62,112.21,121.81,123.96,141.57,148.95,153.70,165.96
p06
35.64,42.27,58.57,58.86,61.88,66.36,70.73,73.89,76.88,77.93,80.63,93.39,98.32,102.14,129.33,129.83,134.14,141.64,166.20
¹²6¸ö»¯ºÏÎdmsoÈÜ´òÆ×£¬Ð»Ð»
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ÇÀ½ð±ÒÀ²£¡»ØÌû¾Í¿ÉÒԵõ½:

²é¿´È«²¿É¢½ðÌù

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

asdjnjkk

гæ (³õÈëÎÄ̳)


P01:
1 .     p-hydroxy benzaldehyde
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2014          39          4811-4815
Chemical constituents from traditional Chinese medicine Siegesbeckia pubescens
WANG Rui£¬SHI Yan-ping£¬WANG Qing-zhong£¬CAO Hui
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report    Ïà¹ØÑ§ÊõÑо¿
2 .     4,4'-dihydroxy-Z-stilbene
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2013          44          2493-2497
Chemical constituents of Swertia macrosperma
ZHAO Sheng-kui, PU Jie, CHEN Yong-dui, LI Shang-xiu, ZHU Yong-xian, LI Gan-peng*
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
3 .     4-bromophenol
C6H5BrO     ÏàËÆ¶È:75%
South African Journal of Botany          2017          112          527-532
Isolation and characterization of 2-hydroxy-3-[4-hydroxyphenyl]-2-propenoic acid and 4-bromophenol from anti-diabetic extract of the root bark of Uvaria afzelii
M.D. Ayoola, J.O. Balogun, F.G. Famuyiwa, S.O. Yeboah, S.O. Famuyiwa
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
4 .     pyrocatechol
    ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2018          49          3226-3231
Chemical constituents from twig and leaves of Taxus media
LI Zhen-lin, LV Xu-hui, WANG Xin-jie, ZHOU Xiao-ju, LI Jie, QIAN Shi-hui
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   


P02:
1 .     D-galacitol
    ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2006          31          1078-1080
Chemical constituents from branch of Broussonetia papyrifera
CHAO Jianfei, YIN Zhiqi, YE Wencai, ZHAO Shou xun
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report    Ïà¹ØÑ§ÊõÑо¿
2 .     D-mannitol
    ÏàËÆ¶È:100%
China Journal of Chinese Materia Medica          2004          29          52-54
Studies on the chemical constituents of Bombyx batryticatus
YIN Zhiqi, YE Wencai, ZHAO Shou xun
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
3 .     D-mannitol
    ÏàËÆ¶È:100%
Acta Pharmaceutica Sinica          2005          Vol 40          533-535
A new flavonoid glycoside from the roots and stems of Sphaerophysa salsula
HOU Bai-ling; LI Zhan-lin; LI Xian
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
4 .     mannitol
    ÏàËÆ¶È:100%
Acta Pharmaceutica Sinica          2000          Vol 35          587-591
CHEMICAL STUDIES ON THE CONSTITUENTS OF PLAGIOCHASM INTERMEDIUM L.
WANG Feng-qiang; LOU Hong-xiang
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
5 .     ¸Ê¶´¼(mannitol)
    ÏàËÆ¶È:100%
Chinese Traditional and Herbal Drugs          2011          42(5)          856-858
Chemical constituents in Guizhi Fuling Capsula (I)
WANG Zhen-zhong, LI Cheng,LI Jia-chun,XIAO Wei
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report

©ÁËÁ©
8Â¥2021-05-14 13:22:53
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
²é¿´È«²¿ 12 ¸ö»Ø´ð

asdjnjkk

гæ (³õÈëÎÄ̳)


¡ï
liufang0378(½ð±Ò+1): лл²ÎÓë
P03:
1 .     isoscutellarein 7-O-(6'''-Oacetyl)-¦Â-allopyranosyl(1'''¡ú2'')-¦Â-glucopyranoside
    ÏàËÆ¶È:82.7%
Phytochemistry          2003          64          1295-1301
Acylated flavone glycosides from Veronica
Dirk C. Albach, Ren¨¦e J. Grayer, Søren Rosendal Jensen, Fevzi Özgö kce,Nigel C. Veitch
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
2 .     isoscutellarein 7-O-[6''-acetylallopyranosyl(1¡ú2)glucopyranoside]
    ÏàËÆ¶È:82.7%
Phytochemistry          1991          30          1169-1173
Flavonoid constituents of Stachys aegyptiaca
M.A. El-Ansari, M.F. Abdalla, N.A.M. Saleh, D. Barron, J.L. Le Qu¨¦r¨¦
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
3 .     isosutellarein 7-O-[6'''-O-acetyl-¦Â-D-allopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:82.7%
Phytochemistry          1987          26          1185-1187
Acetylated allose-containing flavonoid glucosides from Stachys anisochila
Andreas Lenherr,Tom J. Mabry
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
4 .     isoscutellarein7-O-(2''-O-6'''-O-acetyl-¦Â-D-allopyranosyl-¦Â-D-glucopyranoside
    ÏàËÆ¶È:82.7%
Phytochemistry          1984          23          2343-2345
Three flavonoid glycosides containing acetylated allose from stachys recta
Andreas Lenherr, Mohammed F. Lahloub, Otto Sticher
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
5 .     isoscutellarein 7-O-(6'''-O-acetyl)-¦Â-D-allopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:82.7%
Natural Product Sciences          2018          24          259-265
Isolation of Flavonoid Glycosides with Cholinesterase Inhibition Activity and Quantification from Stachys japonica
Agung Nugroho, Jae Sue Choi, Su Hui Seong, Byong-Min Song, Kyoung-Sik Park, and Hee-Juhn Park
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report    Ïà¹ØÑ§ÊõÑо¿


P04£º
1 .     3'-hydroxy-4'-O-methylisoscutellarein 7-O-[6'''-O-acetyl-¦Â-D-allopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside
    ÏàËÆ¶È:96.6%
Phytochemistry          1987          26          1185-1187
Acetylated allose-containing flavonoid glucosides from Stachys anisochila
Andreas Lenherr,Tom J. Mabry
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
2 .     3-hydroxy-4'-O-methylisoscutellarein 7-O-(2''-O-6'''-O-acetyl-¦Â-D-allopyranosyl-¦Â-D-glucopyranoside)
    ÏàËÆ¶È:96.6%
Phytochemistry          1984          23          2343-2345
Three flavonoid glycosides containing acetylated allose from stachys recta
Andreas Lenherr, Mohammed F. Lahloub, Otto Sticher
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
3 .     3-hydroxy-4'-O-methylisoscutel-larein 7-O-[6'''-O-acetyl-¦Â-D-allopyranosyl-(1¡ú2)-6''-O-acetyl-¦Â-D-glucopyransoide
    ÏàËÆ¶È:84.3%
Phytochemistry          1987          26          1185-1187
Acetylated allose-containing flavonoid glucosides from Stachys anisochila
Andreas Lenherr,Tom J. Mabry
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
4 .     isoscutellarein 4'-methyl ether 7-O-(6'''-O-acetyl)-ballopyranosyl(1'''¡ú2'')-¦Â-glucopyranoside
    ÏàËÆ¶È:83.3%
Phytochemistry          2003          64          1295-1301
Acylated flavone glycosides from Veronica
Dirk C. Albach, Ren¨¦e J. Grayer, Søren Rosendal Jensen, Fevzi Özgö kce,Nigel C. Veitch
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
5 .     4'-O-methylisoscutellarem7-O-(2''-O-6'''-O-acetyl-¦Â-D-allo-pyranosyl-¦Â-D-glucopyranoside
    ÏàËÆ¶È:83.3%
Phytochemistry          1984          23          2343-2345
Three flavonoid glycosides containing acetylated allose from stachys recta
Andreas Lenherr, Mohammed F. Lahloub, Otto Sticher
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
6 .     4'-O-methylhypolaetin-7-O-[6'''-O-acetyl-¦Â-D-allopyranosyl-(1¡ú2)]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:83.3%
Turkish Journal of Chemistry          2013          37          464 - 472
Flavonoid constituents of Sideritis caesarea
BELKIS HALFON, ECE ÇİFTÇİ, G¨¹LAÇTI TOPÇU
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
7 .     isoscutellarein 4'-methyl ether 7-O-¦Â-(6"'-O-acetyl-2"-allosyl)gluco-slde
C30H34O17     ÏàËÆ¶È:83.3%
Yakugaku Zasshi          1985          105          955-959
On the Glycosidic Constituents of Stachys sieboldi MIQ. and Their Effects on Hyarulonidase Activity
YOSHIO TAKEDA, TETSURO FUJITA, TOSHIO SATOH, HISAO KAKEGAWA
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
8 .     hypolaetin 7-O-[6'''-O-acetyl-¦Â-D-allopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:80%
Phytochemistry          1987          26          1185-1187
Acetylated allose-containing flavonoid glucosides from Stachys anisochila
Andreas Lenherr,Tom J. Mabry
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   

P05£º
1 .     6-O-veratroylcatalposide
    ÏàËÆ¶È:83.3%
Acta Botanica Boreali-Occidentalia Sinica          2003          23          633-636
Chemical constituents of Veronica ciliate, as a psychrophyte from Northwest China
GAO Kun, LI Xu qin, LIU An, JIA Zhong -jian
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
2 .     Eremoside B
C25H33O13     ÏàËÆ¶È:72%
Helvetica Chimica Acta          2012          95          586-593
Eremosides A-C,New Iridoid Glucosides from Eremostachys loasifolia
Bakhat Ali,Rashad Mehmood,Uzma Rasheed Mughal,Abdul Malik,Muhammad Safder,Riaz Hussain,Muhammad Imran,and Rasool Bakhsh Tareen
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
3 .     Pakiside B
C25H32O13     ÏàËÆ¶È:72%
Helvetica Chimica Acta          2010          93          2245-2250
New Glycosidic Constituents of Abutilon pakistanicum
Bakhat Ali, Itrat Fatima, Abdul Malik and Zaheer Ahmed
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   


P06£º
1 .     veronicoside
    ÏàËÆ¶È:86.3%
Archives of Pharmacal Research          2009          32          207-213
Antioxidative iridoid glycosides and phenolic compounds from Veronica peregrina
Jong Hwan Kwak, Hyun Jung Kim, Kwang Ho Lee, Se Chan Kang and Ok Pyo Zee
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report    Ïà¹ØÑ§ÊõÑо¿
2 .     veronicoside
    ÏàËÆ¶È:86.3%
Chemistry Central Journal          2016          10          1−8
Bioactivity-guided isolation of antioxidant and anti-hepatocarcinoma constituents from Veronica ciliata
Li Yin, Qiuxia Lu, Shancai Tan, Lisheng Ding, Yiran Guo, Fang Chen, and Lin Tang
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report    Ïà¹ØÑ§ÊõÑо¿
3 .     veronicoside
C22H26O11     ÏàËÆ¶È:81.8%
Chemistry of Natural Compounds          1995          31          632-633
Iridoids from Catalpa bignonioides
M. S. Maksudov, R. U. Umarov, Z. Saatov
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
4 .     5''-methoxy-ampicoside
C24H30O14     ÏàËÆ¶È:76.1%
Natural Product Research          2017          31          181−189
Iridoid glycosides from Callicarpa nudiflora Hook
Shi-Xiu Feng, Bo Yi, Min Zhang, Jing Xu, Hai Lin & Wen-Tong Xu
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report    Ïà¹ØÑ§ÊõÑо¿
5 .     6-O-(pcoumaroyl)-catalpol
    ÏàËÆ¶È:72.7%
Planta Medica          1982          46          42-44
Isolation of 6-O-(p-Coumaroyl)-Catalpol from Tabebuia rosea
C. M. Compadre, J. F. Jauregui, P. Joseph Nathan and A. G. Enriquez
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report   
6 .     catalposide
    ÏàËÆ¶È:72.7%
Acta Botanica Boreali-Occidentalia Sinica          2003          23          633-636
Chemical constituents of Veronica ciliate, as a psychrophyte from Northwest China
GAO Kun, LI Xu qin, LIU An, JIA Zhong -jian
Structure      13C NMR    ÆÚ¿¯µØÖ·     Data Report
7Â¥2021-05-14 13:19:41
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

20092290

ľ³æ (Ö°Òµ×÷¼Ò)


¡ï
liufang0378(½ð±Ò+1): лл²ÎÓë
л¯ºÏÎïÀ÷º¦ÁË

·¢×ÔСľ³æAndroid¿Í»§¶Ë
12Â¥2021-06-28 19:08:53
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
¼òµ¥»Ø¸´
huading5Â¥
2021-05-14 06:37   »Ø¸´  
liufang0378(½ð±Ò+1): лл²ÎÓë
·¢×ÔСľ³æAndroid¿Í»§¶Ë
bjdxyxy11Â¥
2021-05-20 11:26   »Ø¸´  
liufang0378(½ð±Ò+1): лл²ÎÓë
¡£ ·¢×ÔСľ³æAndroid¿Í»§¶Ë
Ìáʾ: Èç¹ûÄúÔÚ30·ÖÖÓÄڻظ´¹ýÆäËûÉ¢½ðÌù£¬Ôò¿ÉÄÜÎÞ·¨ÁìÈ¡´ËÌù½ð±Ò
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Çó»¯Ñ§µ÷¼Á +11 wulanna 2026-03-28 11/550 2026-03-30 10:59 by ̽123
[¿¼ÑÐ] 300Çóµ÷¼Á£¬²ÄÁÏ¿ÆÑ§Ó¢Ò»Êý¶þ +15 leaflight 2026-03-24 15/750 2026-03-30 10:54 by 1172367218
[¿¼ÑÐ] 0856Çóµ÷¼Á +8 —öèñ 2026-03-28 8/400 2026-03-30 10:00 by wzy-lxz
[¿¼ÑÐ] Ò»Ö¾Ô¸211£¬335·Ö£¬0856£¬Çóµ÷¼ÁԺУºÍµ¼Ê¦ +7 Çã____Ïô 2026-03-27 8/400 2026-03-30 09:37 by longlotian
[¿¼ÑÐ] »¯Ñ§0703 µ÷¼Á 306·Ö Ò»Ö¾Ô¸211 +7 26ÒªÉϰ¶ 2026-03-28 7/350 2026-03-29 20:04 by Î޼ʵIJÝÔ­
[¿¼ÑÐ] 299Çóµ÷¼Á +10 15188958825 2026-03-25 10/500 2026-03-29 17:51 by ÍõÁÁ_´óÁ¬Ò½¿Æ´ó
[¿¼ÑÐ] Ò»Ö¾Ô¸Ö£ÖÝ´óѧ£¬080500ѧ˶£¬×Ü·Ö317·ÖÇóµ÷¼Á +8 ¾Ù¸öÀõ×Óoi 2026-03-24 9/450 2026-03-29 13:08 by peike
[¿¼ÑÐ] 305Çóµ÷¼Á +8 RuiFairyrui 2026-03-28 8/400 2026-03-29 08:22 by fmesaito
[¿¼ÑÐ] 292Çóµ÷¼Á +14 ¶ì¶ì¶ì¶î¶î¶î¶î¶ 2026-03-25 15/750 2026-03-28 08:45 by WYUMater
[¿¼ÑÐ] 265Çóµ÷¼Á11408 +3 ÁõС¹lu 2026-03-27 3/150 2026-03-27 20:53 by nihaoar
[¿¼ÑÐ] Ò»Ö¾Ô¸211ԺУ 344·Ö ¶«±±Å©Òµ´óѧÉúÎïѧѧ˶£¬Çóµ÷¼Á +5 ؼ·çѩҹ¹éÈËØ¼ 2026-03-26 8/400 2026-03-27 19:22 by ؼ·çѩҹ¹éÈËØ¼
[¿¼ÑÐ] 315µ÷¼Á +4 0860Çóµ÷¼Á 2026-03-26 5/250 2026-03-27 11:23 by wangjy2002
[¿¼ÑÐ] Çóµ÷¼Á323²ÄÁÏÓ뻯¹¤ +7 1124361 2026-03-24 7/350 2026-03-27 10:22 by wangjy2002
[¿¼ÑÐ] 336²ÄÁÏÇóµ÷¼Á +7 ³ÂäÞÓ¨ 2026-03-26 9/450 2026-03-27 00:20 by wxiongid
[¿¼ÑÐ] Çóµ÷¼Á Ò»Ö¾Ô¸ ±¾¿Æ ±±¿Æ´ó »¯Ñ§ 343 +6 13831862839 2026-03-24 7/350 2026-03-26 22:57 by ²»³Ôô~µÄ؈
[¿¼ÑÐ] 321Çóµ÷¼Á +6 wasdssaa 2026-03-26 6/300 2026-03-26 20:57 by sanrepian
[¿¼ÑÐ] 0703»¯Ñ§Çóµ÷¼Á +3 µ¤ÇàÄÌ¸Ç 2026-03-26 5/250 2026-03-26 20:11 by macy2011
[¿¼ÑÐ] ²ÄÁÏÓ뻯¹¤304ÇóBÇøµ÷¼Á +3 Çñgl 2026-03-25 3/150 2026-03-25 19:03 by Ainin_
[¿¼ÑÐ] 0854AI CV·½ÏòÕÐÊÕµ÷¼Á +4 ÕÂСÓã567 2026-03-23 4/200 2026-03-25 17:04 by CoderLoser
[¿¼ÑÐ] 284Çóµ÷¼Á +3 yanzhixue111 2026-03-23 6/300 2026-03-23 22:58 by pswait
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û