Znn3bq.jpeg
²é¿´: 370  |  »Ø¸´: 1

ÑöÁ«

½ð³æ (СÓÐÃûÆø)

[ÇóÖú] ΢Æ×ÇóÖú£¬Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë

13C NMR (101 MHz, DMSO) ¦Ä48.59,54.74,55.57,55.63,63.36,100.86,109.06,110.77,113.28,114.13,114.38,139.52,152.23,154.16,158.64,160.13
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

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

׿Խ_ÏÈ·æ

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

ºýÍ¿³æ

ÓÅÐã°æÖ÷

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ÑöÁ«: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú, лл 2015-04-13 19:22:06
²éѯ½á¹û£º¹²²éµ½188¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     herpetolide A
C16H14O6     ÏàËÆ¶È:87.5%
Chemical & Pharmaceutical Bulletin          2008          56(2)          192-193
Two New Coumarins from Herpetospermum caudigerum
Mei ZHANG,Yun DENG, Hong-Bin ZHANG, Xiao-Lin SU, Hu-Lan CHEN, Tian YU, and Ping GUO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     herpetolide A
    ÏàËÆ¶È:87.5%
Journal of Chinese Medicinal Materials          2012          35          1080-1082
Study on the Chemical Constituents of Herpetospermum caudigerum
XU Bing, YANG Pan-pan, WANG Pei-long, LING Hu-lang, CHEN Min
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     3,3',4'-tri-O-methylellagic acid
    ÏàËÆ¶È:70.5%
Natural Product Research          2001          15          35-42
Vanillic Acid 4-O-¦Â-D-(6'-O-Galloyl) Glucopyranoside and Other Constituents from the Bark of Terminalia macroptera Guill. Et Perr
J¨¹rgen Conrad; Bernhard Vogler; Iris Klaiber; Sabine Reeb; Jan-Hinrich Guse; Gudrun Roos; Wolfgang Kraus
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     3,3',4'-trimethoxyellagic acid
C19H21NO4     ÏàËÆ¶È:70.5%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 8          1019-1023
Study on chem ical constituents from ethyl acetate extract ofMyricaria bracteata
ZHANG Ying, YUAN Yi, CUI Baosong, LI Shuai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     Dimethyl Ether
    ÏàËÆ¶È:70.5%
Journal of the Chemical Society, Perkin Transactions 1          1984                   2919-2925
The biosynthesis of rubrofusarin, a polyketide naphthopyrone from Fusarium culmorum: 13C n.m.r. assignments and incorporation of 13C- and 2H-labelled acetates
Finian J. Leeper and James Staunton
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     3,3',4'-trimethyl ellagic acid
    ÏàËÆ¶È:70.5%
Natural Product Research and Development          2009          21          73-75
Studies on the Chemical Constituents of Polygonum runcinatum Buch.-Ham.var.sinense Hemsl.
WANG Li-ning;XU Bi-xue; CAO Pei-xue; LIANG Guang-yi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     3,3',4'-O-trimethylellagicacid
    ÏàËÆ¶È:70.5%
Journal of Integrative Plant Biology          2005          47          251-256
Two New Triterpenoids from the Roots of Sanguisorba officinalis L.
Fan ZHANG, Tie-Jun FU, Shu-Lin PENG, Zhong-Rong LIU and Li-Sheng DING*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3,4,3'-trimethoxy ellagic acid
    ÏàËÆ¶È:70.5%
Zeitschrift f¨¹r Naturforschung C          2007          62          196-200
Bioactive Phenolic Compounds from Aerial Parts of Plinia glomerata
C. Serafin, V. Nart, A. Malheiros, M. M. d. Souza, L. Fischer, G. D. Monache, F. D. Monache, and V. C. Filho
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     3,3',4-tri-O-methylellagic acid
C17H12O8     ÏàËÆ¶È:70.5%
Journal of Chinese Medicinal Materials          2014          37          1801-1803
Chemical Constituents from Canarium pimela Fruits
LV Zhen-cheng,YIN Yan,LIN Li-jing,PENG Yong-hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     herpetolide B
C16H12O6     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2008          56(2)          192-193
Two New Coumarins from Herpetospermum caudigerum
Mei ZHANG,Yun DENG, Hong-Bin ZHANG, Xiao-Lin SU, Hu-Lan CHEN, Tian YU, and Ping GUO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     xanthoxyletin
    ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          1990          38          1230-1232
New Binary Coumarins from Citues Plants
Chihiro ITO,Miyuki MATSUOKA,Takahiro OKA,Motoharu JU-ICHI,Masatake NIWA,Mitsuo OMURA and Hiroshi FURUKAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     isopimpinellin
C15H14O4     ÏàËÆ¶È:68.7%
China Journal of Chinese Materia Medica          2003          28          344-346
Studies on the Coumarins in the Root of Zanthoxylum dimorphophyllum
TAO ZhaoYang, CHEN WanSHeng, ZHANG Wei Dong, SUN Lian Na, ZHENG Shui Qing, YOU Liang, QIAO ChuanZhuo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     7-{2-[4-(4-Chlorophenyl)piperazin-1-yl]ethoxy}-4-methyl-2H-chromen-2-one
    ÏàËÆ¶È:68.7%
Chemistry & Biodiversity          2011          Vol.8          1052-1064
Rational Design, Synthesis, Biological Evaluation, Homology and Docking Studies of Coumarin Derivatives as ¦Á1-Adrenoceptor Antagonists
Xiang Zhou, Ya-Dong Chen, Tao Wang, Xiao-Bing Wang, and Ling-Yi Kong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     N,N'-diethyl-N,N'-di-(7-methoxy-4-coumarinmethyl)-2-butene-1,4-diamine
C30H34N2O6     ÏàËÆ¶È:68.7%
Heterocycles          2005          65          2937-2947
A Convenient Procedure for the Synthesis of Substituted 4-Methylaminocoumarins
Khadeejh H. A. Al-Zghoul, Kifah S. M. Salih, Mikdad T. Ayoub,* and Mohammad S. Mubarak*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     Xanthoxyletin
    ÏàËÆ¶È:68.7%
Journal of Natural Medicines          2009          63          21-27
Inhibitory effect of oxycoumarins isolated from the Thai medicinal plant Clausena guillauminii on the inflammation mediators, iNOS, TNF-¦Á, and COX-2 expression in mouse macrophage RAW 264.7
Tomonori Nakamura, Naoko Kodama, Yu Arai, Takuya Kumamoto and Yoshihiro Higuchi, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     3,3',4'-Èý¼×Ñõ»ù÷·»¨Ëá
    ÏàËÆ¶È:68.7%
Chinese Traditional and Herbal Drugs          2007          38          348-350
Æ¿»¨Ä¾»¯Ñ§³É·ÖµÄÑо¿
ÌÕÊïºì;Å˽£Óî;ÆáÊ绪;ÀîÇìÐÀ;ÕÅ‚Æ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     6-chloro-4-(p-methoxyphenyl)-7-methoxy-2(1H)-quinolinone
C17H14ClNO3     ÏàËÆ¶È:68.7%
Heterocycles          2012          85          1933-1940
Synthesis and Evaluation of 4-Aryl-2(1H)-quinolinones as Potent Amyloid ¦Â Fibrillogenesis Inhibitors
Yoko Shimokawa, Masamichi Nakakoshi, Setsu Saito, Hideharu Suzuki, Yuusaku Yokoyama, Akihito Ishigami, Hideo Nishioka, and Masayoshi Tsubuki*
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     gnetucleistol E
C16H16O4     ÏàËÆ¶È:68.7%
Acta Chimica Sinica          2003          61          1331-1334
Stilbenes from Gnetum cleistostachyum
YAO, Chun-Suo LIN, Mao LIU, Xin WANG, Ying-Hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     N-methoxy-1-(4'-methoxyphenyl)-3-(2'',5''-dimethoxyphenyl)-1H-pyrazole-4-carboxamide
C20H21N3O5     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2010          18          4338-4350
Novel pyrazole derivatives: Synthesis and evaluation of anti-angiogenic activity
Michael S. Christodoulou, Sandra Liekens, Konstantinos M. Kasiotis, Serkos A. Haroutounian
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     7-{2-[4-(3-Methoxyphenyl)piperazin-1-yl]ethoxy}-4-methyl-2H-chromen-2-one
    ÏàËÆ¶È:65%
Chemistry & Biodiversity          2011          Vol.8          1052-1064
Rational Design, Synthesis, Biological Evaluation, Homology and Docking Studies of Coumarin Derivatives as ¦Á1-Adrenoceptor Antagonists
Xiang Zhou, Ya-Dong Chen, Tao Wang, Xiao-Bing Wang, and Ling-Yi Kong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     Compound 8
C22H25N3O3     ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry Letters          2003          13          175-178
New arylpiperazine derivatives with high affinity for ¦Á1A, D2 and 5-HT2A receptors
J. C. Gonz¨¢lez-G¨®mez, L. Santana, E. Uriarte, J. Brea, M. Villaz¨®n, M. I. Loza, M. De Luca, M. E. Rivas, G. Y. Montenegro, J. A. Fontenla
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     N-(3,9,10-trimethoxy-7-oxo-6,7-dihydro-5H-dibenzo[a,c][7]cyclohepten-5-yl)-2,2,2-trifluoroacetamide
C20H18F3NO5     ÏàËÆ¶È:65%
Bioorganic & Medicinal Chemistry          2012          20          2614-2623
Synthesis of novel 7-oxo and 7-hydroxy trifluoroallocolchicinoids with cytotoxic effect
Elizabeth Chosson, Francesca Santoro, Christophe Rochais, Jana Sopkova-de Oliveira Santos, R¨¦mi Legay, Sylviane Thoret, Thierry Cresteil, Maria Stefania Sinicropi, Thierry Besson, Patrick Dallemagne
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     Compound 7b
C20H10FN3O4     ÏàËÆ¶È:65%
Indian Journal of Chemistry Section B          2014          53          1442-1447
Novel and thermally stable ionic liquid (TBA acetate) for domino reaction: Synthesis of spirooxindoles via new mechanistic way
Riyaz, Sd; Indrasena, A; Naidu, A; Dubey, P K
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     7,2',5'-trimethoxyflavone
C18H16O5     ÏàËÆ¶È:64.7%
Chemical & Pharmaceutical Bulletin          2003          51(12)          1374-1376
Flavonoids from Andrographis viscosula
Yerra Koteswara RAO,Amooru Gangaiah DAMU,Alahari Janardhan RAO,Shanmuganathan VENKATESAN, Ping-Chung KUO,Chunduri Venkata RAO,and Tian-Shung WU
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     3,3',4'-Tri-O-methylellagic acid
    ÏàËÆ¶È:64.7%
Chemistry of Natural Compounds          2007          43          125-127
ELLAGIC ACID DERIVATIVES FROM THE STEM BARK OF Dipentodon sinicus
Guan Ye, Hua Peng, Mingsong Fan,and Cheng-Gang Huang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
26 .     3,3',4'-tri-O-methylellagic acid
    ÏàËÆ¶È:64.7%
China Journal of Chinese Materia Medica          2009          34          414-418
Chemical constituents in roots of Osbeckia opipara
WANG Hongsheng, WANG Yuehu, SHI Yana, LI Xingyu, LONG Chunlin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
27 .     3,3',4-tri-O-methylellagic acid
    ÏàËÆ¶È:64.7%
China Journal of Chinese Materia Medica          2008          33          158-160
Studies on chemical constituents of fruits of Bridelia tomentosa
DENG Anjun, QIN Hailin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
×·Çó׿Խ£¬¸ÒΪÏÈ·æ
2Â¥2015-04-12 22:15:27
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ ÑöÁ« µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] ũѧ0904 312Çóµ÷¼Á +3 Say Never 2026-04-10 3/150 2026-04-10 23:24 by babysonlkd
[¿¼ÑÐ] 314Çóµ÷¼Á +18 xhhdjdjsjks 2026-04-09 19/950 2026-04-10 18:53 by HPUCZ
[¿¼ÑÐ] 336²ÄÁÏÓ뻯¹¤085600Çóµ÷¼Á +21 Ë®ÐǼÇinfp 2026-04-05 24/1200 2026-04-10 15:28 by luoyongfeng
[¿¼ÑÐ] Çóµ÷¼Á +9 ôæôæÒ»ÊéÉú 2026-04-09 9/450 2026-04-10 11:43 by wp06
[¿¼ÑÐ] Çóµ÷¼Á +11 ôæôæÒ»ÊéÉú 2026-04-09 13/650 2026-04-10 10:27 by liuhuiying09
[¿¼ÑÐ] µ÷¼Á +19 ²»·ê´º 2026-04-05 20/1000 2026-04-10 10:15 by may_ÐÂÓî
[¿¼ÑÐ] 292Çóµ÷¼Á +9 ЦЦԬ 2026-04-09 9/450 2026-04-10 10:05 by LHGeng
[¿¼ÑÐ] Ò»Ö¾Ô¸Öпƴó070300»¯Ñ§£¬314·ÖÇóµ÷¼Á +12 wakeluofu 2026-04-09 12/600 2026-04-10 09:57 by liuhuiying09
[¿¼ÑÐ] 293Çóµ÷¼Á +5 ÓÂÔ¶¿â°®314 2026-04-08 5/250 2026-04-10 08:46 by vgtyfty
[¿¼ÑÐ] 305Çóµ÷¼Á +4 77Qi 2026-04-07 4/200 2026-04-09 17:27 by wp06
[¿¼ÑÐ] 280Çóµ÷¼Á +7 wzzzÍõ 2026-04-09 7/350 2026-04-09 15:32 by ÊÍ·ÅÌìÐÔ
[¿¼ÑÐ] 283µç×ÓÐÅÏ¢Çóµ÷¼Á +4 ÈýʯWL 2026-04-08 4/200 2026-04-09 10:21 by wp06
[¿¼ÑÐ] Çóµ÷¼Á +13 Æâluck 2026-04-07 13/650 2026-04-08 22:46 by Öí»á·É
[¿¼ÑÐ] »¯Ñ§308·ÖÇóµ÷¼Á +21 ÄãºÃÃ÷ÌìÄãºÃ 2026-04-07 23/1150 2026-04-08 22:32 by ¿­¿­Òª±ä˧
[¿¼ÑÐ] 298Çóµ÷¼Á +4 ²ÐºÉÐÂÁø 2026-04-07 4/200 2026-04-07 23:02 by lbsjt
[¿¼ÑÐ] ²ÄÁϵ÷¼Á +17 СÁõͬѧ߹߹ 2026-04-06 18/900 2026-04-07 11:41 by Ê«Óë×ÔÓÉ
[¿¼ÑÐ] 302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601 +12 zyxÉϰ¶£¡ 2026-04-04 12/600 2026-04-07 02:09 by BruceLiu320
[¿¼ÑÐ] 327Çóµ÷¼Á +4 ʰ¹âÈÎȾ 2026-04-05 4/200 2026-04-05 20:16 by ÄϺ½~ÍòÀÏʦ
[¿¼ÑÐ] 22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ +3 hannnnnnn 2026-04-04 3/150 2026-04-04 14:35 by ÍÁľ˶ʿÕÐÉú
[¿¼ÑÐ] Çóµ÷¼Á +3 ũҵ¹¤³ÌÓëÐÅÏ¢¼ 2026-04-04 3/150 2026-04-04 12:19 by Éá¶øºóµÃ
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û