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13C NMR (126 MHz, MeOD) ¦Ä 11.98,12.03,12.59,18.71,19.01,19.84,21.68,23.05,24.03,26.08,28.07,29.10,33.82,36.07,37.02,37.42,38.06,38.11,39.37,45.78,46.65,53.47,56.00,56.61,57.53,64.58,129.30,137.47,208.90,211.69
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×ÔÓɵÄÌì¿Õ: ½ð±Ò+50, ¡ï¡ï¡ïºÜÓаïÖú, лл 2013-05-27 19:57:47
1 .     7¦Á-hydrositosterol
    ÏàËÆ¶È:66.6%
Journal of China Pharmaceutical University          2007          38          315-319
Chemical constituents of the aerial parts of Euphorbia sororia
ZHANG Wei-ku; ZHANG Xiao-qi; YE Wen-cai;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     stigmast-4-en-3-one
C29H48O     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          2012          47          1179-1182
A new monoterpenoid glucoside from the twigs of Chamaecyparis obtusa var.breviramea f.crippsii
XU Jian; ZHANG Yu-mei; CHEN Ke-li; TAN Ning-hua; LIU Yi-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ophirapstanol trisulfate
C31H53O12S3Na3     ÏàËÆ¶È:64.5%
Journal of Natural Products          1994          Vol 57          1751
Ophirapstanol Trisulfate, a New Biologically Active Steroid Sulfate from the Deep Water Marine Sponge Topsentia ophiraphidites
Sarath P. Gunasekera, Susan H. Sennett, Michelle Kelly-Borges, Robert W. Bryant
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     ¦Â-Sitosteryl acetate
    ÏàËÆ¶È:64.5%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3¦Â-hydroxyolean-12-en-27- oic acid
C30H48O3     ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2003          Vol. 86          2414
Cytotoxic Pentacyclic Triterpenoids from the Rhizome of Astilbe chinensis
Hongxiang Sun, Jianxin Zhang, Yiping Ye, Yuanjiang Pan, and Yueao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     topsentisterol A1
C29H46O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     topsentisterol B2
C29H46O3     ÏàËÆ¶È:63.3%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (24R,6E)-24-ethyl-5¦Á-cholestan-6-hydroximino-3¦Â,5-diol
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          2001          37          351-355
13C NMR SPECTRA OF 6-HYDROXIMINOSTEROIDS OF THE STIGMASTANE SERIES
N. V. Kovganko and Yu. G. Chernov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (24R,6E)-24-Ethyl-5¦Á-eholestan-6-hydroximino-3¦Â,5-diol
    ÏàËÆ¶È:63.3%
Chemistry of Natural Compounds          2000          36          189-191
NOVEL SYNTHESIS OF (24R,6E)-24-ETHYLCHOLEST-6-HYDROXYIMINO-4-EN-3-ONE, A STEROIDAL OXIME FROM Cinachyrella spp. SPONGES
N. B. Kovganko and Yu. G. Chernov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (22R,23R)-2¦Á-Fluoro-3¦Â,22,23-trihydroxy-5¦Á-stigmastan-6-one
C29H49FO4     ÏàËÆ¶È:63.3%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 1
    ÏàËÆ¶È:63.3%
Phytochemistry          1998          49          195-198
Triterpenoid saponins from the seeds of amaranthus cruentus
MARTA JUNKUSZEW,WIESLAW OLESZEK MARIAN JURZYST¦Á,SONIA PIANCHENTE,COSIMO PIZZA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ¿üÂåάËá
    ÏàËÆ¶È:63.3%
Chinese Traditional and Herbal Drugs          2009          40          1369-1372
ÂæÍÕÌã°ê¾¥ÖÐÈýÝÆÀà³É·ÖÑо¿
·ëÓýÁÖ;ÎâÝí;ºÎÃ÷Õä;ÕÅС¾ê;ÐìÀöÕä;ÑîÊÀÁÖ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ¦Â-sitosterol
    ÏàËÆ¶È:63.3%
Natural Product Research and Development          2004          16          131-132
STUDIES ON CHEMICAL CONSTITUENTS OF GENDARUSSA VENTRICOSA
ZHANG Xiao-li;YU Zheng-wen;GUO Fang-qin; YANG Xiao-sheng *; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ¦Â-Sitosterol
    ÏàËÆ¶È:63.3%
Journal of Agricultural and Food Chemistry          2011          59          7743-7751
Evaluation of the Potential Hypoglycemic and Beta-Cell Protective Constituents Isolated from Corni Fructus To Tackle Insulin-Dependent Diabetes Mellitus
Mei-Hsiang Lin, Hui-Kang Liu, Wei-Jan Huang, Chu-Chun Huang, Tzu-Hua Wu, and Fen-Lin Hsu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     ¦Â-Sitosterol
    ÏàËÆ¶È:63.3%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     ¦Â-sitosterol
C29H50O     ÏàËÆ¶È:63.3%
Chinese Journal of Applied & Environmental Biology          1999          5          501-506
NEW MONOTERPENOID GLYCOSIDES FROM LIGUSTRUM ROBUSTUM
TIAN Jun, & SUN Handong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     ¦Â-¹ÈçÞ´¼
    ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2012          37          1963-1967
Chemical constituents contained in Aeschynanthus moningeriae
LIU Huixin; LIAO Haibing; YUAN Ke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     daucosterol
    ÏàËÆ¶È:60.6%
Natural Product Research          2012          26          2107-2111
Main constituents from the seeds of Vietnamese Cnidium monnieri and cytotoxic activity
Pham Huu Dien, Nguyen Thi Nhan, Hoang Thi Le Thuy & Dang Ngoc Quang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     7¦Â,15¦Â-dihydroxynigranoic acid
C30H46O6     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2007          Vol. 4          112
Hydroxylation of the Triterpenoid Nigranoic Acid by the Fungus Gliocladium roseum YMF1.00133
Jin-Yan Dong, Ye-Gao Chen, Hong-Chuan Song, Yan-Hui Zhu, Yong-Ping Zhou, Lei Li, Yan-Ping H, Jie Cao, and Ke-Qin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     3¦Â-hydroxyurs-12-en-27-oic acid
C30H48O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2003          Vol. 86          2414
Cytotoxic Pentacyclic Triterpenoids from the Rhizome of Astilbe chinensis
Hongxiang Sun, Jianxin Zhang, Yiping Ye, Yuanjiang Pan, and Yueao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ursolic acid
    ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          1624-1626
DNA Polymerase ¦Â Inhibitors from Baeckea gunniana
Jing-Zhen Deng, Shelley R. Starck, and Sidney M. Hecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     musambin B
C30H48O6     ÏàËÆ¶È:60%
Phytochemistry          2009          70          1239-1245
Hydroperoxy-cycloartane triterpenoids from the leaves of Markhamia lutea,a plant ingested by wild chimpanzees
Damien Lacroix, Soizic Prado, Alexandre Deville, Sabrina Krief, Vincent Dumontet, John Kasenene, Elisabeth Mouray, Christian Bories, Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     5¦Á,6¦Â-dihydroxysitosterol
C29H52O3     ÏàËÆ¶È:60%
Steroids          2005          70          886-895
Gram-scale chromatographic purification of ¦Â-sitosterol: Synthesis and characterization of ¦Â-sitosterol oxides
Xin Zhang, Philippe Geoffroy, Michel Miesch, Diane Julien-David, Francis Raul, Dalal Aoud¨¦-Werner, Eric Marchioni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (22R,23R)-2¦Á-Fluoro-3¦Á,22,23-trihydroxy-5¦Á-stigmastan-6-one
C29H49FO4     ÏàËÆ¶È:60%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol
C29H52O3     ÏàËÆ¶È:60%
Journal of Natural Products          1993          Vol 56          2210
Studies on Marine Chemicals, Part VI. A New Clionasterol Derivative from the Marine Sponge Spirastrella inconstans
B. Das, S. Padma Rao, K. V. N. S. Srinivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     halistanol sulfate F
    ÏàËÆ¶È:60%
Journal of Natural Products          1994          Vol 57          164
Novel HIV-Inhibitory Halistanol Sulfates F-H from a Marine Sponge, Pseudoaxinissa digitata
G. Bifulco, I. Bruno, L. Minale, R. Riccio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     donellanic acid A
C29H42O4     ÏàËÆ¶È:60%
Tetrahedron          2012          68          4621-4627
Donellanic acids A¨CC: new cyclopropanic oleanane derivatives from Donella ubanguiensis (Sapotaceae)
Aurelie V.B. Djoumessi, Louis P. Sandjo, Johannes C. Liermann, Dieter Schollmeyer, Victor Kuete, Vincent Rincheval, Abegaz M. Berhanu, Samuel O. Yeboah, Pascal Wafo, Bonaventure T. Ngadjui, Till Opatz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol
    ÏàËÆ¶È:60%
Chinese Journal of Applied & Environmental Biology          2009          15          615-620
Chemical Constituents from Polygonum perfoliatum
LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     (22E)-3-Acetoxy-5¦Á-stigmasta-2,22-dien-6-one
C31H48O3     ÏàËÆ¶È:58.0%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     ophirapstanol
C31H56O3     ÏàËÆ¶È:58.0%
Journal of Natural Products          1994          Vol 57          1751
Ophirapstanol Trisulfate, a New Biologically Active Steroid Sulfate from the Deep Water Marine Sponge Topsentia ophiraphidites
Sarath P. Gunasekera, Susan H. Sennett, Michelle Kelly-Borges, Robert W. Bryant
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     3¦Â-[N-((N',N',N'-trimethyl)-2'-aminoethyl)-N-(2-amino-ethyl)carbamoyl]cholesterol
    ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          2010          18          330-342
Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery
Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     3¦Â-[N-(N'-guanidinyl-2'-aminoethyl)-N-(N-glycine(N-(3-aminopropyl)amide)) carbamoyl]cholesterol
    ÏàËÆ¶È:58.0%
Bioorganic & Medicinal Chemistry          2010          18          330-342
Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery
Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     Euphonerin F
C31H50O4     ÏàËÆ¶È:58.0%
Planta medica          2012          78          1370-1377
Cycloartane Triterpenes and Ingol Diterpenes Isolated from Euphorbia neriifolia in a Screening Program for Death-Receptor Expression-Enhancing Activity
Toume, Kazufumi; Nakazawa, Takafumi; Hoque, Tahmina; Ohtsuki, Takashi; Arai, Midori A.; Koyano, Takashi; Kowithayakorn, Thaworn; Ishibashi, Masami:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     daucosterol
    ÏàËÆ¶È:57.5%
China Journal of Chinese Materia Medica          2007          32          605-608
Studies on chemical constituents from Serissa serissoides
LI Yaolan, WANG Guan, XUE Junyi, CEN Yingzhou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     7¦Á-hydroxysitosterol-3-O-¦Â-D-glucoside
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1987          Vol 50          881
Sterols and Steryl Glycosides from Urtica dioica
Neera Chaurasia, Max Wichtl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     ¦Â-sitosteryl-D-glucoside
    ÏàËÆ¶È:57.1%
Journal of the Brazilian Chemical Society          2001          12          467-472
Alkamides and Phemethyl Derivatives from Aristolochia gehrtii.
Hosana M. D. Navickiene and Lucia M. X. Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     6¦Á,15¦Â-dihydroxynigranoic acid
C30H46O6     ÏàËÆ¶È:56.6%
Chemistry & Biodiversity          2007          Vol. 4          112
Hydroxylation of the Triterpenoid Nigranoic Acid by the Fungus Gliocladium roseum YMF1.00133
Jin-Yan Dong, Ye-Gao Chen, Hong-Chuan Song, Yan-Hui Zhu, Yong-Ping Zhou, Lei Li, Yan-Ping H, Jie Cao, and Ke-Qin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     fetisinine
C27H39NO3     ÏàËÆ¶È:56.6%
Phytochemistry          2003                   115-122
New class of steroidal alkaloids from Fritillaria imperialis
M. Nadeem Akhtar, Atta-ur-Rahman, M. Iqbal Choudhary, Bilge Sener, Ilkay Erdogan, Yoshisuke Tsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     topsentisterol C1
C29H46O4     ÏàËÆ¶È:56.6%
Journal of Natural Products          2006          69          1760-1768
26,27-Cyclosterols and Other Polyoxygenated Sterols from a Marine Sponge Topsentia sp.
Xuan Luo, Famei Li, Pramod B. Shinde, Jongki Hong, Chong-O. Lee, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     plakinamine E
C31H50N2O2     ÏàËÆ¶È:56.6%
Journal of Natural Products          2001          64          1474-1476
New Steroidal Alkaloids from an Undescribed Sponge of the Genus Corticium
Hyi-Seung Lee,Youngwan Seo,Jung-Rae Rho, Jongheon Shin,and Valerie J. Paul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     Metatrichosin B
C30H44O6     ÏàËÆ¶È:56.6%
Acta Botanica Yunnanica          2006          28(6)          673-675
Two New Triterpenes from Metadina trichotoma ( Rubiaceae)
ZHANG Yu-Mei,TAN Ning-Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     (22E)-2¦Á-Fluoro-5¦Á-stigmasta-22-en-3,6-dione
C29H45O2F     ÏàËÆ¶È:56.6%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     (22E)-2¦Á-Fluoro-3¦Á-hydroxy-5¦Á-stigmast-22-en-6-one
C29H47O2F     ÏàËÆ¶È:56.6%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     (22E)-2¦Á-fluoro-3¦Â-hydroxy-5¦Á-stigmast-22-en-6-one
C29H47O2F     ÏàËÆ¶È:56.6%
Steroids          2009          74          435-440
Synthesis and biological activity of brassinosteroids fluorinated at C-2
Sof¨ªa L. Acebedo, Javier A. Ram¨ªrez, Lydia R. Galagovsky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     3¦Â, 19¦Á-dihydroxy-30-norurs-12-ene
C29H48O2     ÏàËÆ¶È:56.6%
Fitoterapia          2001          72          382-385
Ursene type nortriterpene from Debregeasia salicifolia
Erum Akbar, Muhammad Riaz, Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     3,5,6-trihydroxysitostane
    ÏàËÆ¶È:56.6%
Phytochemistry          1998          47          789-797
On the cytotoxity of oxidized phytosterols isolated from photoautotrophic cell cultures of Chenopodium rubrum tested on meal-worms Tenebrio molitor
Werner Meyer, Harald Jungnickel, Markus Jandke, Konrad Dettner, Gerhard Spiteller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     plakinamine A
    ÏàËÆ¶È:56.6%
Journal of Natural Products          1994          Vol 57          1004
Two Steroidal Alkaloids from a Sponge, Corticium Sp.
Jaroslaw Jurek, Paul J. Scheuer, Michelle Kelly-Borges
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3¦Â-[N-((N'-guanidinyl)-2'-aminoethyl)-N-(2-aminoethyl)-carbamoyl]cholesterol
    ÏàËÆ¶È:56.6%
Bioorganic & Medicinal Chemistry          2010          18          330-342
Solid phase synthesis of novel asymmetric hydrophilic head cholesterol-based cationic lipids with potential DNA delivery
Widchaya Radchatawedchakoon, Ramida Watanapokasin, Aungkana Krajarng, Boon-ek Yingyongnarongkul
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     saikogenin F
    ÏàËÆ¶È:56.6%
Natural Product Research and Development          2008          20          833-835
Study on the Chemical Constituents of Bupleurum bicaule Helm
ZHU Zhan-jun; PAN Rui-le; SI Jian-yong; FU Ying; HUANG Qian-qian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     pomolic acid
C30H48O4     ÏàËÆ¶È:56.6%
Natural Product Research and Development          2001          13(2)          11-13
THE STUDIES OF CHEMICAL COMPONENTS OF CLAUSENA DUNNIANA
CUI Shu ya;CHENG Dong liang; TIAN Jun; WU Feng e
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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