²é¿´: 289  |  »Ø¸´: 1

listentome

гæ (³õÈëÎÄ̳)

[ÇóÖú] 2014-10.17΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë

»¯ºÏÎï70-1
13C NMR (101 MHz, Acetone) ¦Ä 217.91, 213.58, 185.19, 170.22, 150.90, 137.28, 132.75, 108.16, 80.51, 78.32, 71.96, 71.82, 69.41, 55.16, 49.26, 47.86, 46.45, 40.43, 39.26, 36.92, 34.80, 33.77, 33.46, 33.13, 30.33,  27.27, 26.77, 25.95, 24.71, 24.01, 23.11, 19.86, 19.70, 19.52, 17.64

»¯ºÏÎï1-4-1
13C NMR (101 MHz, Acetone) ¦Ä 159.44, 141.48, 120.66, 70.83, 56.78, 56.05, 50.34, 45.85, 44.24, 42.46, 39.78, 37.36, 36.43, 36.04, 33.83, 31.91, 31.74, 31.65,  28.05, 24.05, 20.91, 19.18, 18.90, 18.45, 11.33

»¯ºÏÎï80-6
13C NMR (101 MHz, MeOD) ¦Ä 171.32, 171.02, 169.06, 138.18, 134.93, 134.67, 124.82, 79.57, 78.25, 72.52, 72.05, 71.45, 69.10, 68.47, 56.88, 49.21, 40.59, 40.39, 39.81, 37.95, 36.79, 33.98, 33.64, 33.26, 30.59, 30.24, 28.82, 28.46, 28.04, 25.85, 25.38, 25.27, 24.60, 23.02, 22.91, 22.31, 22.05, 20.00, 19.66, 19.37, 19.16, 19.08, 19.03.
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:

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

zhou_biao

ľ³æ (ÕýʽдÊÖ)

¡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
listentome: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú, Ê®·Ö¸Ðл 2014-10-17 12:07:02
»¯ºÏÎï70-1
1 .     alisol F 24-acetate
    ÏàËÆ¶È:74.2%
Chinese Traditional and Herbal Drugs          2012          43          841-843
A new triterpene in rhizome of Alisma orientale
XU Nan; ZHANG Hong-da; XIE Xue
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     16,23-oxidoalisol B
C30H46O4     ÏàËÆ¶È:71.4%
Phytochemistry          1994          36          119-127
Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma
Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     alisol F 24-acetate
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2001          13(4)          1-4
TERPENOIDS OF ALISMA ORIENTALIS JUZEP.
PENG Guo ping; LOU Feng chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     alisol F
C30H48O5     ÏàËÆ¶È:65.7%
Chemical & Pharmaceutical Bulletin          1993          41          1948-1954
Crude Drugs from Aquatic Plants. I. On the Constituents of Alismatis Rhizoma. (1). Absolute Stereostructures of Alisols E 23-Acetate, F, and G, Three New Protostane-Type Triterpenes from Chinese Alismatis Rhizoma
Masayuki YOSHIKAWA,Shoko HATAKEYAMA,Nobumitsu TANAKA,Youichi FUKUDA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     alisol F
    ÏàËÆ¶È:65.7%
Chinese Chemical Letters          2008          19          438-440
A new triterpenoid from Alisma orientalis
Xue Yan Hu, Yuan Qiang Guo, Wen Yuan Gao, Hai Xia Chen, Tie Jun Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     Alisol F
    ÏàËÆ¶È:65.7%
Journal of Asian Natural Products Research          2008          10          487-490
Two new triterpenes from the rhizomes of Alisma orientalis
Xue-Yan Hu, Yuan-Qiang Guo, Wen-Yuan Gao, Tie-Jun Zhang and Hai-Xia Chen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     16,23-oxidoalisol B
C30H46O4     ÏàËÆ¶È:65.7%
China Journal of Chinese Materia Medica          2005          30          1263-1265
Studies on triterpenes chemical constituents in rhizome of Alixma gramineum
WO Lianqun, LUO Guangming, WANG Baoxiu, ZHU Weifeng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     alisol F
C30H48O5     ÏàËÆ¶È:65.7%
China Journal of Chinese Materia Medica          2005          30          1263-1265
Studies on triterpenes chemical constituents in rhizome of Alixma gramineum
WO Lianqun, LUO Guangming, WANG Baoxiu, ZHU Weifeng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     Alisol A Triacetate
    ÏàËÆ¶È:63.8%
Phytochemistry          1994          36          119-127
Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma
Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     alizexol A
    ÏàËÆ¶È:62.8%
Chinese Chemical Letters          1995          6          675-678
ALIZEXOL A.A NOVEL PROTOSTANE TYPE OF TRTTERPENE FROM ALISMA ORIENTALIS JUZEP
LU ZENG,XIAN PEN AND RU YI ZHANG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     alismalactone-A 23-acetate
C32H50O6     ÏàËÆ¶È:62.8%
Chemical & Pharmaceutical Bulletin          1997          45          756-758
ABSOLUTE STEREOSTRUCTURES OF ALISMALACTONE 23-ACETATE AND ALISMAKETONE-A 23-ACETATE, NEW SECO-PROTOSTANE AND PROTOSTANE-TYPE TRITERPENES WITH VASORELAXANT EFFECTS FROM CHINESE ALISMATIS RHIZOMA
Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Akira IKEBATA,Atsushi ISHIKADO,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     16,23-oxidoalisol B
C30H46O4     ÏàËÆ¶È:62.8%
Chinese Traditional and Herbal Drugs          2008          39          1788-1790
Ôóк»¯Ñ§³É·ÖµÄÑо¿
ºúÑ©ÑÞ;³Âº£Ï¼;¸ßÎÄÔ¶;ÁõÐÂÇÅ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     dihydrocucurbitacin E
    ÏàËÆ¶È:62.8%
Archives of Pharmacal Research          1994          17          348-353
Antitumor activity of Trichosanthes kirilowii
Shi Yong Ryu, Seung Ho Lee, Sang Un Choi, Chong Ock Lee and Zaesung No, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     compound 39
C32H46O7     ÏàËÆ¶È:62.8%
Bioorganic & Medicinal Chemistry          2012          20          3016-3030
Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives
Karen Luise Lang, Izabella Tha¨ªs Silva, Lara Almida Zimmermann, Vanessa Rocha Machado, Marina Rodrigues Teixeira, Mar¨ªa Ivana Lapuh, Mariana Alejandra Galetti, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, L¨ªlian Sibelle Campos Bernardes, Cl¨¢udia Mari
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     alisol F
    ÏàËÆ¶È:62.8%
Natural Product Research and Development          2001          13(4)          1-4
TERPENOIDS OF ALISMA ORIENTALIS JUZEP.
PENG Guo ping; LOU Feng chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     alisol B 23-acetate
    ÏàËÆ¶È:62.8%
Natural Product Sciences          2012          18          121-129
Protective Effects of Methanol Extract and Alisol B 23-acetate of Alisma orientale on Acetaminophen-Induced Hepatotoxicity in Rats
Yang, Ki-Ho; Choi, Seong-Hee; Park, Jong-Cheol
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     alisol F
    ÏàËÆ¶È:62.8%
Chinese Traditional and Herbal Drugs          2012          43          841-843
A new triterpene in rhizome of Alisma orientale
XU Nan; ZHANG Hong-da; XIE Xue
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3-O-(3'-O-Acetyl)-¦Á-L-arabinopyranosyloleanolic acid
C37H58O8     ÏàËÆ¶È:62.1%
Journal of Asian Natural Products Research          2014          16          20-28
Four new triterpenoids isolated from the resin of Garcinia hanburyi
Hong-Min Wang, Qun-Fang Liu, Yi-Wu Zhao, Shuang-Zhu Liu, Zhen-Hua Chen, Ru-Jun Zhang, Zhen-Zhong Wang, Wei Xiao & Wei-Min Zhao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     fasciculic acid B
C36H60O9     ÏàËÆ¶È:61.1%
Chemical & Pharmaceutical Bulletin          1989          37          3247-3250
Fasciculic Acids A, B and C as Calmodulin Antagonists from the Mushroom Naematoloma fasciculare
Akira TAKAHASHI,Genjiro KUSANO,Tomihisa OHTA,Yasushi OHIZUMI and Shigeo NOZOE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     ¦Á-L-Rhamnopyranosyl oleanolate
C36H58O7     ÏàËÆ¶È:61.1%
Molecules          2008          13          1472-1486
Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides
Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     compound 15
C38H52O7S     ÏàËÆ¶È:61.1%
Bioorganic & Medicinal Chemistry          2012          20          3016-3030
Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives
Karen Luise Lang, Izabella Tha¨ªs Silva, Lara Almida Zimmermann, Vanessa Rocha Machado, Marina Rodrigues Teixeira, Mar¨ªa Ivana Lapuh, Mariana Alejandra Galetti, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, L¨ªlian Sibelle Campos Bernardes, Cl¨¢udia Mari
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     25-O-acetylbryoamaride
C36H52O10     ÏàËÆ¶È:60.5%
Chemical & Pharmaceutical Bulletin          2002          50(5)          645-648
A New Pentacyclic Cucurbitane Glucoside and a New Triterpene from the Fruits of Gymnopetalum integrifolium
Toshikazu SEKINE,Hiroshi KURIHARA, Mayumi WAKU,Fumio IKEGAMI,a and Nijsiri RUANGRUNGSI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     3¦Â-acetyl-16-oxo-13¦Â, 28-epoxyoleanane
C32H50O4     ÏàËÆ¶È:60%
Phytochemistry          2006          67          2641-2650
Oleanane-type triterpenes of Embelia schimperi leaves
Lawrence Onyango Arot Manguro, Steve Onyango Okwiri, Peter Lemmen
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     N-[3-oxolup-20(29)-en-28-oyl]cyclopentylamine
C35H55NO2     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2008          44          327-333
SYNTHESIS OF BETULONIC ACID AMIDES
A. N. Antimonova, N. V. Uzenkova, N. I. Petrenko,M. M. Shakirov, E. E. Shul¡äts, and G. A. Tolstikov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
»¯ºÏÎï1-4-1
13C NMR (101 MHz, Acetone) ¦Ä 159.44, 141.48, 120.66, 70.83, 56.78, 56.05, 50.34, 45.85, 44.24, 42.46, 39.78, 37.36, 36.43, 36.04, 33.83, 31.91, 31.74, 31.65,  28.05, 24.05, 20.91, 19.18, 18.90, 18.45, 11.33

1 .     ¦Â-sitosterol
    ÏàËÆ¶È:82.1%
Chinese Joumal of Experimental Traditional Medical Fomulae          2014          20          82-85
Chemical Constituents of Gonostegia hirta
HAN He-dong, HU Hai-qing, LIN Yan, LI Rong-jiao, WANG Xiao-ling
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-sitosterol
    ÏàËÆ¶È:80.7%
Korean Journal of Pharmacognosy          2004          35(1)          80-87
The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii
Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Â,20S)-3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]chol-5-en-24-ol
    ÏàËÆ¶È:80%
Steroids          2003          68          159-166
First synthesis of ent-desmosterol and its conversion to ent-deuterocholesterol
Emily J. Westover, Douglas F. Covey
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     3¦Â-Hydroxy-24-norchol-5-en-23-oic acid
    ÏàËÆ¶È:80%
Steroids          2005          70          873-878
Isolation and absolute configuration of new bioactive marine steroids from Euryspongia n. sp.
Anne Mandeau, Cecile Debitus, Marie-Françoise Ari¨¨s, Bruno David
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-Chol-5-en-24-oic acid,methyl ester
    ÏàËÆ¶È:80%
Steroids          2006          71          484-488
Synthesis of ent-25-hydroxycholesterol
Emily J. Westover, Douglas F. Covey
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-27-Norcholest-5-en-25-one
C26H42O2     ÏàËÆ¶È:80%
Steroids          2006          71          484-488
Synthesis of ent-25-hydroxycholesterol
Emily J. Westover, Douglas F. Covey
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     (20R)-25-thia-27-norcholest-5-en-3¦Â-ol
C28H50OSiS     ÏàËÆ¶È:80%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     compound 6
    ÏàËÆ¶È:80%
Magnetic Resonance in Chemistry          1993          31          421-424
Carbon-13 NMR spectra of bile acid derivatives. Part III. Unsaturated 5¦Â-cholanoic acids
Takashi Iida, Junichi Goto and Toshio Nambara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     ¦Â-sitosterol
    ÏàËÆ¶È:79.3%
Natural Product Research and Development          2011          23          1017-1020
Chemical Constituents of Phyllanthus niruri L.
ZHU, Hong-lin, WEI, Wan-xing, ZHOU, Min, YANG, Dan, FAN, Xi-wang, LIU, Jian-xiong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol
    ÏàËÆ¶È:79.3%
South African Journal of Botany          2013          88          341-351
Phytotoxic activity of Cleome arabica L. and its principal discovered active compounds
Afef Ladhari, Faten Omezzine, Marina DellaGreca, Armando Zarrelli, Simona Zuppolini, Rabiaa Haouala
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     campesterol
C28H48O     ÏàËÆ¶È:78.5%
Natural Product Research          2014          28          1134-1141
Dragmacidoside: a new nucleoside from the Red Sea sponge Dragmacidon coccinea
Dina R. Abou-Hussein, Jihan M. Badr & Diaa T.A. Youssef
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     (20S)-verazine
    ÏàËÆ¶È:77.7%
Planta Medica          1992          58          449-453
Epimeric (20R,20S)-Verazine Isolated from Veratrum maackii: Two-Dimensional NMR Studies and Total Assignment of 1H- and 13C-Resonances
Xiuwen Han and heinz Ruegger
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
»¯ºÏÎï80-6
13C NMR (101 MHz, MeOD) ¦Ä 171.32, 171.02, 169.06, 138.18, 134.93, 134.67, 124.82, 79.57, 78.25, 72.52, 72.05, 71.45, 69.10, 68.47, 56.88, 49.21, 40.59, 40.39, 39.81, 37.95, 36.79, 33.98, 33.64, 33.26, 30.59, 30.24, 28.82, 28.46, 28.04, 25.85, 25.38, 25.27, 24.60, 23.02, 22.91, 22.31, 22.05, 20.00, 19.66, 19.37, 19.16, 19.08, 19.03.

1 .     fomitoside H
C42H66O11     ÏàËÆ¶È:60.4%
Journal of Natural Products          2005          68          69-73
Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2
Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     spinasteryl glucosyl peracetate
    ÏàËÆ¶È:60.4%
Planta Medica          1985          51          322-325
Isolation of Spinasterol and its Glucoside from Cell Suspension Cultures of Saponaria officinalis: 13CNMR Spectral Data and Batch Culture Production
Max Henry and Isabelle Chantalat-Dublanche
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     betulamaximoside B
C40H66O12     ÏàËÆ¶È:60.4%
Chemical & Pharmaceutical Bulletin          1996          44          1748-1753
Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     22-dihydro-¦Á-spinasterol ¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:60.4%
Phytochemistry          1990          29          2539-2543
Caffeine and theanine from cultured cells of Camellia sinensis
Tsutomu Furuya,Yutaka Orihara,Yumiko Tsuda
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     catalyrique de A
C56H82O17     ÏàËÆ¶È:59.0%
Phytochemistry          1980          19          615-622
Triterpenoïdes nouveaux de Napoleonaea imperialis
Mpuza Kapundu, Roger Warin, Clement Delaude, Robert Huls
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     3¦Á-acetoxy-12¦Â-O-(2',3',4',6'-tetra-O-acetyl-¦Â-D-glucopyranosyloxy)-20S,24R-epoxydammarane
C46H72O14     ÏàËÆ¶È:58.6%
Chemistry of Natural Compounds          2014          49          1076-1081
Structures of Side Products from Helferich Reaction Synthesis of 3¦Á,12¦Â,25-Trihydroxy-20S,24R-Epoxydammarane Glucosides
L. N. Atopkina, V. A. Denisenko
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     fomitoside G
C38H60O8     ÏàËÆ¶È:58.1%
Journal of Natural Products          2005          68          69-73
Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2
Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     betulamaximoside A
C38H64O11     ÏàËÆ¶È:58.1%
Chemical & Pharmaceutical Bulletin          1996          44          1748-1753
Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana
Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     3-isobutyryl-7-deacetylglabretal
    ÏàËÆ¶È:58.1%
Phytochemistry          1992          31          4163-4166
Limonoids from Australian members of the meliaceae
Dulcie A. Mulholland, David A.H. Taylor
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ¦Â-sitosterol-¦Â-D-ghcopyranoside
    ÏàËÆ¶È:58.1%
Phytochemistry          1991          30          1026-1029
A butyrolactone lignan disaccharide from Flacourtia ramontchi  
V. Satyanarayana, G.L.David Krupadanam, G. Srimannarayana
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     stigmasta-3¦Á,5¦Á-diol-3-O-¦Â-D-glucopyranoside tetraacetate
    ÏàËÆ¶È:58.1%
Phytochemistry          1991          30          3383-3387
Steroids and triterpenoids from Rosa laevigata
Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     compound 6a
    ÏàËÆ¶È:58.1%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 6b
    ÏàËÆ¶È:58.1%
Phytochemistry          1990          29          2351-2355
Sterol glucosides from Prunella vulgaris
Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     compound 5a
C30H52O3     ÏàËÆ¶È:58.1%
Phytochemistry          1985          24          2359-2367
Triterpenoids from Mangifera indica
V. Anjaneyulu, K. Harischandra Prasad, K. Ravi, J.D. Connolly
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     3¦Â-[(¦Á-L-arabinopyranosyl)oxy]-urs-12,18-dien-28-oic acid-¦Â-D-glucopyranosyl ester
    ÏàËÆ¶È:58.1%
Chinese Journal of Medicinal Chemistry          2008          18          138-141
Triterpenoid saponins of Sanguisorba off icinalis and their anti-inflammatory activity
LUO Yan, WANG Han, YUAN Zhong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     3¦Â,24(S),25-trihydroxycycloartane and 3¦Â,24(R),25-trihydroxycycloartane
    ÏàËÆ¶È:58.1%
Zeitschrift f¨¹r Naturforschung C          2004          59          15-18
Chemical Constituents of Euphorbia marschalliana Boiss.
A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     rivaloside A
C44H68O16     ÏàËÆ¶È:56.8%
Journal of Natural Products          2000          63          1012-1014
Rivalosides A and B, Two 19-Oxo Triterpenoid Saponins from Galium rivale
Salvatore De Rosa,Maya Mitova, Nedyalka Handjieva, Simeon Popov, and Mincho Anchev
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     artemisterol B
C44H72O4     ÏàËÆ¶È:56.8%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     amphiphilic hexasubstituted [60]fullerene
C412H576O38     ÏàËÆ¶È:56.8%
Tetrahedron Letters          2005          46          6507-6510
Interfacial behavior and film-forming properties of an amphiphilic hexasubstituted [60]fullerene
Delphine Felder-Flesch, Cyril Bourgogne, Jean-Louis Gallani, Daniel Guillon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     Didemnaketal A
C44H72O14     ÏàËÆ¶È:56.8%
Journal of the American Chemical Society          1991          113          6321-6322
Didemnaketals A and B, HIV-1 protease inhibitors from the ascidian Didemnum sp
Barbara C. M. Potts, D. John Faulkner, James A. Chan, Gerald C. Simolike, Priscilla Offen, Mark E. Hemling, Terry A. Francis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-10-17 11:59:13
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ listentome µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] 0703»¯Ñ§µ÷¼Á£¬Çóµ¼Ê¦ÊÕ +7 ÌìÌìºÃÔËÀ´Éϰ¶° 2026-03-24 7/350 2026-03-24 20:26 by peike
[¿¼ÑÐ] µ÷¼Á +4 13853210211 2026-03-24 4/200 2026-03-24 19:44 by ms629
[¿¼ÑÐ] »¯¹¤×¨Ë¶Çóµ÷¼Á +3 questionÍì·ç 2026-03-24 3/150 2026-03-24 18:48 by jhhcooi
[¿¼²©] É격26Äê +4 °Ë6°Ë68 2026-03-19 4/200 2026-03-24 15:49 by СBenºÇºÇ
[¿¼ÑÐ] 307Çóµ÷¼Á +3 ÓàÒâÇä 2026-03-21 6/300 2026-03-24 15:03 by ÓàÒâÇä
[¿¼ÑÐ] 293Çóµ÷¼Á +6 ¼ÓÒ»Ò»¾Å 2026-03-24 6/300 2026-03-24 14:29 by JourneyLucky
[¿¼ÑÐ] 305·ÖÇóµ÷¼Á£¨Ê³Æ·¹¤³Ì£© +5 Sxy112 2026-03-21 7/350 2026-03-24 12:27 by 544594351
[¿¼ÑÐ] Ò»Ö¾Ô¸¼ª´ó»¯Ñ§322Çóµ÷¼Á +4 17501029541 2026-03-23 6/300 2026-03-24 10:21 by ´÷Χ²±µÄСÎÃ×Ó
[¿¼ÑÐ] ²ÄÁÏר˶ӢһÊý¶þ306 +8 z1z2z3879 2026-03-18 8/400 2026-03-23 20:49 by baobaoye
[¿¼ÑÐ] 316Çóµ÷¼Á +7 ÁºÜçö© 2026-03-19 7/350 2026-03-23 16:21 by lingjue
[¿¼ÑÐ] ½ÓÊÕ2026˶ʿµ÷¼Á(ѧ˶+ר˶) +4 allen-yin 2026-03-23 6/300 2026-03-23 15:04 by Íô£¡£¿£¡
[¿¼ÑÐ] 323Çóµ÷¼Á +6 ÍÝСͰ 2026-03-18 6/300 2026-03-23 00:29 by king123£¡
[¿¼ÑÐ] 352Çóµ÷¼Á +3 ´óÃ×·¹£¡ 2026-03-22 3/150 2026-03-22 23:28 by king123£¡
[¿¼ÑÐ] 289²ÄÁÏÓ뻯¹¤£¨085600£©BÇøÇóµ÷¼Á +3 ÕâôÃû×ÖÕ¦Ñù 2026-03-22 4/200 2026-03-22 17:56 by ÔÆÃñ´óÀîÀÏʦ
[¿¼ÑÐ] 265Çóµ÷¼Á +12 ÁºÁºÐ£Ð£ 2026-03-19 14/700 2026-03-21 13:38 by lature00
[¿¼ÑÐ] Ò»Ö¾Ô¸ÖØÇì´óѧ085700×ÊÔ´Óë»·¾³×¨Ë¶£¬×Ü·Ö308Çóµ÷¼Á +3 īīĮ 2026-03-18 3/150 2026-03-21 00:39 by JourneyLucky
[¿¼ÑÐ] 304Çóµ÷¼Á +6 ÂüÊâ2266 2026-03-18 6/300 2026-03-21 00:32 by JourneyLucky
[¿¼ÑÐ] ÖÐÄÏ´óѧ»¯Ñ§Ñ§Ë¶337Çóµ÷¼Á +3 niko- 2026-03-19 6/300 2026-03-20 21:58 by luoyongfeng
[¿¼ÑÐ] ²ÄÁÏѧ˶318Çóµ÷¼Á +5 February_Feb 2026-03-19 5/250 2026-03-19 23:51 by 23Postgrad
[¿¼ÑÐ] 320Çóµ÷¼Á0856 +3 ²»ÏëÆðÃû×Ö112 2026-03-19 3/150 2026-03-19 22:53 by ѧԱ8dgXkO
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û