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14.19,15.30,15.88,29.90,34.26,40.66,41.95,56.03,56.05,60.62,60.78,60.96,71.98,110.09,112.75,122.87,127.63,133.09,133.86,137.32,139.67,140.32,142.26,151.69,151.80,152.56

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27.54,36.57,60.42,69.75,73.11,75.65,120.17,123.38,129.80,130.79,165.14,166.06
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1 .     angeloyl gomisin H
    ÏàËÆ¶È:89.2%
Natural Product Sciences          2006          12          134-137
Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis
An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (R-biar)-12-angeloyloxy-6,7,8,9-tetrahydro-1,2,3,13,14-pentamethoxy-7,8-dimethyl-7-dibenzo[a,c]cyclooctenol
C28H36O8     ÏàËÆ¶È:88.8%
Journal of Asian Natural Products Research          2012          14          159-164
Two new lignans from Celastrus flagellaris Rupr.
Xue-Mei Zhao, Fu-Jiang Guo, Yi-Ming Li & Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     Neglschisandrin C
C32H36O8     ÏàËÆ¶È:76.6%
Molecules          2008          13          1148-1155
Neglschisandrins C-D: Two New Dibenzocyclooctadiene Lignans from Schisandra neglecta
Min Chen, Zhihua Liao, Xiumei Xu, Yan Wen, Min Sun, Haoxiang Zhang and Wenhui Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (R-biar)-12-benzoyloxy-6,7,8,9-tetrahydro-1,2,3,13,14-pentamethoxy-7,8-dimethyl-7-dibenzo[a,c]cyclooctenol
C30H34O8     ÏàËÆ¶È:75.8%
Journal of Asian Natural Products Research          2012          14          159-164
Two new lignans from Celastrus flagellaris Rupr.
Xue-Mei Zhao, Fu-Jiang Guo, Yi-Ming Li & Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     gomisin T
C23H30O7     ÏàËÆ¶È:73.0%
Chemical & Pharmaceutical Bulletin          1988          36          3811-3815
Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II
FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     schisandrin
C24H32O7     ÏàËÆ¶È:73.0%
Natural Product Sciences          2005          11          248-252
Dibenzocyclooctene lignan compounds isolated from the fruits of Schisandra chinensis Baill
Piao, LongZhu; Lee, Yu-Joung; PhamPhu, ThanhTruc; Shin, Jae-Kyoon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     schizandrin
    ÏàËÆ¶È:73.0%
Natural Product Sciences          2006          12          134-137
Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis
An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     gomisin T
    ÏàËÆ¶È:73.0%
Tetrahedron Letters          2005          46          8467-8470
Regio- and stereoselective 12-O-demethylation of schizandrin into gomisin T, an important intermediate to gomisin A, by Mortierella sp. (TM-I1104)
Hirotoshi Kanatani, Susumu Terabayashi, Shuichi Takeda, Wei Li, Kazuo Koike, Tamotsu Nikaido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gomisin H
    ÏàËÆ¶È:69.2%
Chemical & Pharmaceutical Bulletin          1980          28          2414-2421
The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 12
    ÏàËÆ¶È:69.2%
Journal of Asian Natural products Research          2010          12          549-556
Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A
Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     methyl schisantherin F
    ÏàËÆ¶È:67.8%
Journal of Natural Products          2009          72          1133-1141
Lignans with Anti-HIV Activity from Schisandra propinqua var. sinensis
Xiao-Nian Li, Jian-Xin Pu, Xue Du, Liu-Meng Yang, Hui-Mei An, Chun Lei, Fei He, Xiao Luo, Yong-Tang Zheng,Yang Lu, Wei-Lie Xiao, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     met A-I
C22H26O7     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1988          36          2061-2069
Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix.
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 5a
C24H28O8     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1988          36          2061-2069
Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix.
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     schizandrin
C24H32O7     ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1988          36          3811-3815
Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II
FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 14
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1988          36          3811-3815
Strophanthidin Glycosides from the Roots of Apocynum venetum var. : basikurumon : Studies on Apocynum. II
FUMIKO ABE,YJIRO MORI,Tatsuo YAMAUCHI and YASUHISA SAIKI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     schizandrin
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1978          26          3257-3260
The Constituents of Schizandra chinensis BAILL. The Structures of Two New Lignans, Gomisin N and Tigloylgomisin P
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,ITIRO YOSIOKA and HIROSHI KOBAYASHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     schizandrin
    ÏàËÆ¶È:65.3%
Chemical & Pharmaceutical Bulletin          1980          28          2414-2421
The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     gomisin A
C23H28O7     ÏàËÆ¶È:65.3%
Natural Product Sciences          2005          11          248-252
Dibenzocyclooctene lignan compounds isolated from the fruits of Schisandra chinensis Baill
Piao, LongZhu; Lee, Yu-Joung; PhamPhu, ThanhTruc; Shin, Jae-Kyoon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     gomisin A
    ÏàËÆ¶È:65.3%
Natural Product Sciences          2006          12          134-137
Gomisin J with Protective Effect Against t-BHP-Induced Oxidative Damage in HT22 Cells from Schizandra chinensis
An, Ren-Bo; Oh, Seung-Hwan; Jeong, Gil-Saeng; Kim, Youn-Chul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     schizandrin
    ÏàËÆ¶È:65.3%
Phytochemistry          1988          27          569-573
A lignan from Schizandra chinensis
Yukinobu Ikeya,Heihachiro Taguchi,Hiroshi Mitsuhashi,Shigefumi Takeda,Yoshio Kase,Masaki Aburada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     schizandrin
    ÏàËÆ¶È:65.3%
Korean Journal of Pharmacognosy          2011          42          233-239
Quantitative Determination of Lignans from Schizandra chinensis by HPLC
Koo, Dong-Chil; Suh, Won-Se; Baek, So-Yoon; Shim, Sang-Hee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (+)-14-tigloylgomisin K3
C28H36O7     ÏàËÆ¶È:64.2%
Helvetica Chimica Acta          2008          Vol. 91          1053
Four New Dibenzocyclooctadiene Lignans from Schisandra rubriflora
Hong-Mei Li, Yong-Ming Luo, Jian-Xin Pu, Xiao-Nian Li, Chun Lei, Rui-Rui Wang, Yong-Tang Zheng, Han-Dong Sun and Rong-Tao Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Neglschisandrin D
C30H34O7     ÏàËÆ¶È:64.2%
Molecules          2008          13          1148-1155
Neglschisandrins C-D: Two New Dibenzocyclooctadiene Lignans from Schisandra neglecta
Min Chen, Zhihua Liao, Xiumei Xu, Yan Wen, Min Sun, Haoxiang Zhang and Wenhui Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     compound 20
C28H38O8     ÏàËÆ¶È:64.2%
Journal of Asian Natural products Research          2010          12          549-556
Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A
Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     tiegusanin C
C30H34O8     ÏàËÆ¶È:63.3%
Journal of Natural Products          2009          72          1133-1141
Lignans with Anti-HIV Activity from Schisandra propinqua var. sinensis
Xiao-Nian Li, Jian-Xin Pu, Xue Du, Liu-Meng Yang, Hui-Mei An, Chun Lei, Fei He, Xiao Luo, Yong-Tang Zheng,Yang Lu, Wei-Lie Xiao, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     compound 15
C27H36O8     ÏàËÆ¶È:62.9%
Journal of Asian Natural products Research          2010          12          549-556
Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A
Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     Kadsufolin A
C29H38O8     ÏàËÆ¶È:62.0%
Helvetica Chimica Acta          2011          94          519-527
Kadsufolins A ¨C D and Related Cytotoxic Lignans from Kadsura oblongifolia
Zehao Huang, Yan Lu, Yinan Liu, Kenneth F. Bastow, Kuohsiung Lee and Daofeng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     pyramidatin C
    ÏàËÆ¶È:61.5%
Phytochemistry          2000          55          653-661
Dibenzocyclooctadiene-type lignans from Magnolia pyramidata
Qi Song, Frank R. Fronczek, Nikolaus H. Fischer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     gomisin A
    ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          1990          38          136-141
Studies on the Metabolism of Gomisin A (TJN-101). II. : Structure Determination of Biliary and Urinary Metabolites in Rat
Yukinobu IKEYA,Hiroshi MITSUHASHI,Hiromi SASAKI,Yutaka MATSUZAKI,Tamae MATSUZAKI and Eikichi HOSOYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     gomisin A
    ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          1988          36          2061-2069
Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix.
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     met B
C22H28O7     ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          1988          36          2061-2069
Studies on the Metabolism of Gomisin A (TJN-101). I. : Oxidative Products of Gomisin A Formed by Rat Liver S9 Mix.
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI MITSUHASHI,HIROMI SASAKI,TAMAE MATSUZAKI,MASAKI ABURADA and EIKICHI HOSOYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     gomisin A
    ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          1980          28          2414-2421
The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     (-)-gomisin K1 acetate
    ÏàËÆ¶È:61.5%
Chemical & Pharmaceutical Bulletin          1980          28          2414-2421
The Constituents of Schizandra chinensis BAILL. VI. 13C Nuclear Magnetic Resonance Spectroscopy of Dibenzocyclooctadiene Lignans
YUKINOBU IKEYA,HEIHACHIRO TAGUCHI,HIROSHI SASAKI,KAORU NAKAJIMA and ITIRO YOSIOKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     isoschizandrin
C24H32O7     ÏàËÆ¶È:61.5%
Phytochemistry          1988          27          569-573
A lignan from Schizandra chinensis
Yukinobu Ikeya,Heihachiro Taguchi,Hiroshi Mitsuhashi,Shigefumi Takeda,Yoshio Kase,Masaki Aburada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     (Sa)-3',4,4',5,5'-pentamethoxy-3-hydroxypyramidatin
C23H28O7     ÏàËÆ¶È:61.5%
Phytochemistry          2010          71          1787-1795
Dibenzocyclooctadiene lignans from Magnolia and Talauma (Magnoliaceae): Their absolute configuration ascertained by circular dichroism and X-ray crystallography and re-evaluation of previously published pyramidatin structures
Wolfgang Sch¨¹hly, Barbara Gröblacher, Judith Neyer, Walter M.F. Fabian, Frank R. Fronczek, Olaf Kunert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 6
    ÏàËÆ¶È:61.5%
Journal of Asian Natural products Research          2010          12          549-556
Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A
Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     compound 10
    ÏàËÆ¶È:61.5%
Journal of Asian Natural products Research          2010          12          549-556
Synthesis and MDR inhibitory activity evaluation of derivatives of schizandrin A
Xiao-Xia Liang; Geng-Tao Liu; Qiao-Hong Chen; Hua Sun; Dong-Lin Chen; Feng-Peng Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     gomisin A
    ÏàËÆ¶È:61.5%
Chinese Traditional and Herbal Drugs          2009          40          1707-1710
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Ê·ÁÕ;ºÎÏþϼ;ÅËÓ¢;º«Áè;ÍõÖ¾³É;ÕÔÓàÇì
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     compound II
    ÏàËÆ¶È:61.5%
Archives of Pharmacal Research          1990          13          278-281
Lingans from Korean red ginseng
Bong Hee Huh, Ihn Ran Lee and Byung Hoon Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     Kadsufolin B
C26H34O8     ÏàËÆ¶È:61.5%
Helvetica Chimica Acta          2011          94          519-527
Kadsufolins A ¨C D and Related Cytotoxic Lignans from Kadsura oblongifolia
Zehao Huang, Yan Lu, Yinan Liu, Kenneth F. Bastow, Kuohsiung Lee and Daofeng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     gomisin A
    ÏàËÆ¶È:61.5%
Journal of Chinese Medicinal Materials          2009          32          1054-1056
Study on the Chemical Constituents of the Fruit Handles from Schizandra chinensis
SHI Lin, HE Xiao-xia, PAN Ying, HAN Ling, YANG Xiao-ou, ZHAO Yu-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

»¯ºÏÎï2
²éѯ½á¹û£º¹²²éµ½61¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     gliotoxin
C13H14N2O4S2     ÏàËÆ¶È:92.3%
Chinese Pharmaceutical Journal          2011          46          569-575
Antitumor Metabolites from Fungus Aspergillus sydowi D2-6
REN Hong, CAO Xue-li, WANG Qiao-e, XV Chun-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     gliotoxin
    ÏàËÆ¶È:92.3%
Marine Drugs          2014          12          69-87
Gliotoxin Isolated from Marine Fungus Aspergillus sp. Induces Apoptosis of Human Cervical Cancer and Chondrosarcoma Cells
Van-Tinh Nguyen, Jung Suck Lee, Zhong-Ji Qian, Yong-Xin Li, Kil-Nam Kim, Soo-Jin Heo, You-Jin Jeon, Won Sun Park, Il-Whan Choi, Jae-Young Je and Won-Kyo Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     gliotoxin
C13H14N2O4S2     ÏàËÆ¶È:84.6%
Journal of Natural Products          1990          Vol 53          717
Gliotoxin: Uncommon 1H Couplings and Revised 1H- and 13C-nmr Assignments
Mourad Kaouadji, Regine Steiman, Françoise Seigle-Murandi, Serge Krivobok, Lucile Sage
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     trans-4-propenylphenol (anol) glucoside
    ÏàËÆ¶È:58.3%
Phytochemistry          2006          67          1029-1033
Clerodanes and other constituents of Cleidion spiciflorum
Waree Naengchomnong, Paulo M. Pinho, Anake Kijjoa, Pichan Sawangwong,Maria Jos¨¦ Gonzalez, Artur M.S. Silva, Graham Eaton, Werner Herz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     tert-butyl [3-(ethoxycarbonyl)phenyl]carbamate
C10H11NO4     ÏàËÆ¶È:58.3%
European Journal of Organic Chemistry          2010                   3704-3710
Amination of Aryl Iodides Using a Fluorous-Tagged Ammonia Equivalent
Simon Dalsgaard Nielsen, Garrick Smith, Mikael Begtrup and Jesper Langgaard Kristensen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     A26771A
C14H16N2O3S2     ÏàËÆ¶È:58.3%
Marine Drugs          2012          10          2912-2935
Isolation, Structure Elucidation and Total Synthesis of Lajollamide A from the Marine Fungus Asteromyces cruciatus
Tobias A. M. Gulder, Hanna Hong, Jhonny Correa, Ekaterina Egereva, Jutta Wiese, Johannes F. Imhoff and Harald Gross
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     p-bromobenzoate of menisdaurilide
C15H11O4Br     ÏàËÆ¶È:53.8%
Phytochemistry          1993          33          389-392
Butenolides from Sinomenium acutum
Hideaki Otsuka, Aiko Ito, Naomi Fujioka, Ken' Ichiro Kawamata, Ryoji Kasai, Kazuo Yamasaki, Tomohiro Satoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 11
C21H18F3O9S     ÏàËÆ¶È:53.8%
Tetrahedron Letters          2001          42          1321-1324
1,6-Anhydro-¦Â-l-hexopyranoses as valuable building blocks toward the synthesis of l-gulosamine and l-altrose derivatives
Shang-Cheng Hung, Cheng-Chung Wang, Shu-Wen Chang, Chien-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 19
    ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          1996          4          1949-1961
Macromolecular recognition: Effect of multivalency in the inhibition of binding of yeast mannan to concanavalin A and pea lectins by mannosylated dendrimers
Daniel Pag¨¦, Diana Zanini, Ren¨¦ Roy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1D-1,4,5-Tri-O-benzoyl-2,3,6-trideoxy-myo-inositol
    ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          1993          115          4429-4434
Synthesis of 1D-3-deoxy-, 1D-2,3-dideoxy-, and 1D-2,3,6-trideoxy-myo-inositol 1,4,5-trisphosphate from quebrachitol, their binding affinities, and calcium release activity
A. P. Kozikowski, V. I. Ognyanov, A. H. Fauq, S. R. Nahorski, R. A. Wilcox
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     bisdethiobis(methylthio)gliotoxin
C15H20N2O4S2     ÏàËÆ¶È:53.3%
Chinese Journal of Marine Drugs          2008          27(4)          14-20
Bioactive alkaloids from sponge-derived actinomyces sh6004
FU Hai-chao, ZHAO Wen-ying, ZHONG Hui-min, HONG Kui, GU Qian-qun, ZHU Wei-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     2,2-dimethyl-6-vinylchromene
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2001          49(9)          1207-1209
Isolation and Structures of Two New Compounds from the Essential Oil of Brazilian Propolis
Toshihide KUSUMOTO,Tomofumi MIYAMOTO,Ryuichi HIGUCHI,Shima DOI,Hiroyuki SUGIMOTO,and Hideo YAMADA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     7-benzoyloxy-6-oxo-2,4Z-heptadiene-1,4-olide
C14H10O5     ÏàËÆ¶È:50%
Phytochemistry          2001          58          1311-1315
Oxidized heptenes from flowers of Melodorum fruticosum
Chaiyo Chaichantipyuth, Supachai Tiyaworanan, Somchai Mekaroonreung, Nattaya Ngamrojnavanich, Sophon Roengsumran, Songchan Puthong,Amorn Petsom, Tsutomu Ishikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     methyl 4-(1,1-dimethyl-2-propynyloxy)benzoate
    ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          169-176
Synthesis and Structure−Phytotoxicity Relationships of Acetylenic Phenols and Chromene Metabolites,and Their Analogues, from the Grapevine Pathogen Eutypa lata
Leverett R. Smith, Noreen Mahoney, and Russell J. Molyneux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     4-phenylaminobenzoate
C15H15NO2     ÏàËÆ¶È:50%
Molecules          2005          10          226-237
A Survey on the Reactivity of Phenyliodonium Ylide of 2-Hydroxy-1, 4-Naphthoquinone with Amino Compounds
Konstantina Spagou, Elizabeth Malamidou-Xenikaki and Spyros Spyroudis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3-(Oxiranecarbonyl-amino)-benzoic acid tert-butyl ester
C14H17NO4     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          145-155
Investigation of ¦Á-phenylnorstatine and ¦Á-benzylnorstatine as transition state isostere motifs in the search for new BACE-1 inhibitors
Fredrik Wångsell, Patrik Nordeman, Jonas Sävmarker, Rikard Emanuelsson, Katarina Jansson,Jimmy Lindberg, Åsa Rosenquist, Bertil Samuelsson, Mats Larhed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (2S,3R,4E)-2-N-(2'-hydroxytetracosanoyl) octadecasphinga-4-ene
    ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung B          2003          58b          1128-1132
A New Tetranortriterpenoid from Dysoxylum lenticellatum
Shu-Hua Qi, Da-Gang Wu, Si Zhang, and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 5
    ÏàËÆ¶È:50%
Tetrahedron Letters          2000          41          8311-8315
The cooperative effect of electrostatic and hydrophobic forces in the complexation of cationic molecules by a water-soluble resorcin[4]arene derivative
Seong Jin Park, Jong-In Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     methyl (Z)-5-(2-fluoro-5-nitrophenyl)-2-pentenoate
C12H12FNO4     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2010          47          1176-1182
Ester- and ketone-substituted (¡À)-1-alkyl-6-nitro-1,2,3,4-tetrahydroquinolines by a tandem SNAr-Michael reaction
Richard A. Bunce and Eric J. Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 11
C20H21NO2     ÏàËÆ¶È:50%
Heterocycles          2005          65          2871-2884
Stereoselective Functionalization of Alkenyl-¦Â-lactams
Luigino Troisi,* Emanuela Pindinelli, Luisella De Vitis, Catia Granito, and Ludovico Ronzini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (E)-4-(2-Ethoxycarbonylvinyl)benzoic acid ethyl ester
C14H16O4     ÏàËÆ¶È:50%
Molecules          2010          15          315-330
Palladium(II)/Cationic 2,2¡¯-Bipyridyl System as a Highly Efficient and Reusable Catalyst for the Mizoroki-Heck Reaction in Water
Shao-Hsien Huang, Jun-Rong Chen and Fu-Yu Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (2S,5S,6R)-6-(1,3-dioxoisoindolin-2-yl)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid
C16H14N2O5S     ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          2007          45          819-829
Comparison of various density functional methods for distinguishing stereoisomers based on computed 1H or 13C NMR chemical shifts using diastereomeric penam ¦Â-lactams as a test set (pages 819¨C829)
Keith W. Wiitala, Christopher J. Cramer and Thomas R. Hoye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     deoxyradicinol
    ÏàËÆ¶È:50%
Phytochemistry          1985          24          729-731
Phytotoxins from Alternaria helianthi: radicinin, and the structures of deoxyradicinol and radianthin
Beni Tal, David J. Robeson, Basil A. Burke, Arne J. Aasen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (2S,3R,4E)-2-N-(2'-hydroxy-tetracosanoyl)octadecasphinga-4-ene
    ÏàËÆ¶È:50%
Chinese Traditional and Herbal Drugs          2008          39          1606-1609
Chemical constituents of Amtipathes dichotoma
SU Guo-chen; ZHANG Si; QI Shu-hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound ent-7
C14H14NO4     ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          1209-1212
Synthesis of (2R,4R)- and (2S,4S)-4-hydroxypipecolic acid derivatives and (2S,4S)-(−-SS20846A
Mark Sabat, Carl R Johnson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     N,N',N''-tris(4-ethoxycarbonylphenyl)-1,3,5-benzenetricarboxamide
C36H33N3O9     ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          4717-4720
A new prearranged tripodant ligand N,N',N¡å-trimethyl-N,N',N¡å-tris(3-pyridyl)-1,3,5-benzene tricarboxamide is easily obtained via the N-methyl amide effect
Mikkel Jørgensen, Frederik C Krebs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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