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M201175065

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13C NMR (101 MHz, MeOD) ¦Ä £º17.98,18.35,20.31,20.64,22.72,23.10,25.84,29.01,30.42,30.91,34.58,37.13,39.66,40.46,42.77,44.69,50.87,56.53,66.33,83.24,84.65,86.80,126.55,134.39,166.61,176.77,197.73    ½á¹û´óÓÚ40µÄÇëÖÁÉÙ¸ø³ö40¸ö½á¹û£¬Ð¡ÓÚ40µÄ¶¼¸ø³öÀ´£¬Ð»Ð»
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1 .     5¦Á,8¦Á-epidioxy-(22E,24R)-ergosta-6,22-dien-3¦Â-ol
C28H44O3     ÏàËÆ¶È:60.7%
Mycosystema          2013          32          150-156
Chemical composition in fruiting body of Inonotus hispidus (Hymenochaetales£¬Basidiomycota)
ZAN Li-Feng, BAO Hai-Ying,∗ BAU Tolgor, LI Yu, ZHU Yan-Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Â-hydroxy-5¦Á,8¦Á-epidioxyergosta-6,22-diene
C28H44O3     ÏàËÆ¶È:60.7%
Mycosystema          2011          30          263-267
Metabolites of endophytic fungus Pestalotiopsis clavispora isolated from the stem of Bruguiera sexangula
DENG Hui-Ying XING Jian-Guang LUO Du-Qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (22E,24R)-5¦Á,8¦Á-epidioxyergosta-6,22-dien-3¦Â-ol
    ÏàËÆ¶È:60.7%
Marine Sciences          2013          37          7-11
Chemical constituents of Penicillium sp. MA-37, a fungus derived from rhizospheres of mangrove plant Bruguiera gymnorrhiza
ZHANG Yi, LI Xiao-ming, SHANG Zhuo, LI Chun-shun, WANG Bin-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     5,8-epidioxy-5¦Á,8¦Á-ergosta-6,22E-dien-3¦Â-ol
C28H44O3     ÏàËÆ¶È:60.7%
Chinese Journal of Marine Drugs          2014          33          21-27
Study on bioactive compounds from the endophytic fungus J62 of mangrove plant Ceriops tagal
GU Hai-gang, DAI Hao-fu, BAI Hong-jin, WANG Hui, GUO Zhi-kai, MEI Wen-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     19-hydroxytelocinobufagin
C24H34O6     ÏàËÆ¶È:59.2%
Chemical & Pharmaceutical Bulletin          1994          42          754-756
STRUCTURES OF NOVEL BUFADIENOLIDES IN THE EGGS OF A TOAD, Bufo marinus
Toshifumi AKIZAWA,Tsutomu MUKAI,Motomi MATSUKAWA,Masanori YOSHIOKA,Jennifer F. MORRIS and Vincent P. BUTLER
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     ent-15¦Â-Isovaleryloxykaur-16(17)-en-19-oic acid
    ÏàËÆ¶È:59.2%
Biochemical Systematics and Ecology          1996          24          585-587
Constituents of Viguiera aspillioides and V. robusta
Fernando B. Da Costa, Walter Vichnewski, Werner Herz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     5¦Á,6¦Â-dihydroxysitosterol
C29H52O3     ÏàËÆ¶È:59.2%
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
8 .     polypodine B
    ÏàËÆ¶È:59.2%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     ajugasterone C
    ÏàËÆ¶È:59.2%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (24R,6E)-24-ethyl-5¦Á-cholestan-6-hydroximino-3¦Â,5-diol
    ÏàËÆ¶È:58.6%
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
11 .     (24R,6E)-24-Ethyl-5¦Á-eholestan-6-hydroximino-3¦Â,5-diol
    ÏàËÆ¶È:58.6%
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
12 .     2¦Á,3¦Â,11¦Á,23-tetrahydroxyurs-12-en-28-oic acid
C30H48O6     ÏàËÆ¶È:58.6%
Journal of Natural Products          2011          74          163-168
Triterpenoid Saponins from Symplocos lancifolia
Ivone Lucia Acebey-Castellon, Laurence Voutquenne-Nazabadioko, Huong Doan Thi Mai, Nathalie Roseau, Naima Bouthagane, Dima Muhammad, Elisabeth Le Magrex Debar, Sophie C. Gangloff, Marc Litaudon, Thierry Sevenet, Nguyen Van Hung, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     topsentisterol B4
C28H44O3     ÏàËÆ¶È:57.1%
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
14 .     3,4-seco-ursan-4-hydroxy-12-en-3,28-dioic acid
C30H48O5     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2009          17          7265-7274
Ursolic acid derivatives induce cell cycle arrest and apoptosis in NTUB1 cells associated with reactive oxygen species
Huang-Yao Tu, A-Mei Huang, Bai-Luh Wei, Kim-Hong Gan, Tzyh-Chyuan Hour, Shyh-Chyun Yang, Yeong-Shiau Pu, Chun-Nan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     9¦Á,11¦Á-dihydroxyergosta-4,6,8(14),22-tetraen-3-one
C28H40O3     ÏàËÆ¶È:57.1%
Journal of Natural Products          2011          74          1281-1283
A Highly Conjugated Dihydroxylated C28 Steroid from a Myxobacterium
Dnyaneshwar Gawas, Ronald Garcia, Volker Huch, and Rolf M¨¹ller
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Polypodine B 20,22-acetonide
C30H48O8     ÏàËÆ¶È:56.6%
Phytochemistry          1994          37          707-711
Ecdysteroids from the roots of Leuzea carthamoides
Jaroslav P¨ªš, Miloš Bud¨§š¨ªnsky̌, Karel Vok¨¢č, V¨§ra Laudov¨¢, Juraj Harmatha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Topsentinol K trisulfate
C30H49O12S3Na3     ÏàËÆ¶È:56.6%
Journal of Natural Products          2010          73          1597-1600
Topsentinols, 24-Isopropyl Steroids from the Marine Sponge Topsentia sp.
Jingqiu Dai, Analia Sorribas, Wesley Y. Yoshida, Michelle Kelly, and Philip G. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3¦Â,7¦Â,24-Trihydroxy-urs-12-en-28-oic acid
C30H48O5     ÏàËÆ¶È:56.6%
Phytochemistry Letters          2011          4          287-291
Ursolic acid derivatives from Bangladeshi medicinal plant, Saurauja roxburghii:Isolation and cytotoxic activity against A431 and C6 glioma cell lines
Kishor Mazumder, Eric R.O. Siwu, Satoshi Nozaki, Yasuyoshi Watanabe, Katsunori Tanaka, Koichi Fukase
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     urmiensolide
C30H46O5     ÏàËÆ¶È:56.6%
Journal of Natural Products          2013          76          1806-1809
Antitrypanosomal Triterpenoid with an ¦Å-Lactone E-Ring from Salvia urmiensis
Mahdi Moridi Farimani, Samad Nejad Ebrahimi, Peyman Salehi, Mir Babak Bahadori, Ali Sonboli, Hamid Reza Khavasi, Stefanie Zimmermann, Marcel Kaiser, and Matthias Hamburger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     polypodine B 20,22-acetonide
C30H48O8     ÏàËÆ¶È:56.6%
Chinese Traditional and Herbal Drugs          2014          45          906-912
Chemical constituents from roots tubers of Serratula chinensis
TANG Hai-jiao, FAN Chun-lin, WANG Gui-yang, WEI Wei, WANG Ying, YE Wen-cai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ivorengenin A
C30H46O6     ÏàËÆ¶È:56.6%
Chemistry & Biodiversity          2011          8          1301-1309
Novel 3-Oxo- and 3,24-Dinor-2,4-secooleanane-Type Triterpenes from Terminalia ivorensis A. Chev.
Beaudelaire Kemvoufo Ponou, R¨¦my Bertrand Teponno, Massimo Ricciutelli, T¨¦lesphore B¨¦noit Nguelefack, Luana Quassinti, Massimo Bramucci, Giulio Lupidi, Luciano Barboni*, and L¨¦on Azefack Tapondjou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     sericic acid
    ÏàËÆ¶È:56.6%
Chemistry & Biodiversity          2011          8          1301-1309
Novel 3-Oxo- and 3,24-Dinor-2,4-secooleanane-Type Triterpenes from Terminalia ivorensis A. Chev.
Beaudelaire Kemvoufo Ponou, R¨¦my Bertrand Teponno, Massimo Ricciutelli, T¨¦lesphore B¨¦noit Nguelefack, Luana Quassinti, Massimo Bramucci, Giulio Lupidi, Luciano Barboni*, and L¨¦on Azefack Tapondjou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     2¦Â,24-dihydroxyurs-12-en-27-oic acid
C30H48O4     ÏàËÆ¶È:56.6%
Acta Crystallographica Section E          2007          63          o2375-o2377
2¦Â,24-Dihydroxyurs-12-en-27-oic acid methanol solvate from the rhizome of Astilbe chinensis
Jun-Yi Hu, Zhi Yao, Ying-Qian Xu, Pu Liu and Hong-Quan Duan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     corosolic acid
    ÏàËÆ¶È:56.6%
Journal of Chinese Medicinal Materials          2008          31          1669-1671
Triterpenoids and Steroids of Root of Rubus biflorus
KANG Shu-he, SHI Yong-qing, YANG Cai-xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     2¦Á,3¦Á,24-trihydroxyurs-12-en-28-oic acid
    ÏàËÆ¶È:56.6%
China Journal of Chinese Materia Medica          2014          39          2024-2028
Chemical of Vitex trifolia
Liu Quanyu, Chen Yongsheng, Wang Fei, Chen Shiwu, Zhang Yonghong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     topsentisterol A3
C27H40O3     ÏàËÆ¶È:55.5%
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
27 .     thorectandrol B
C27H40O5     ÏàËÆ¶È:55.5%
Journal of Natural Products          2001          64          661-663
Thorectandrols A and B, New Cytotoxic Sesterterpenes from the Marine Sponge Thorectandra Species
Romila D. Charan, Tawnya C. McKee, and Michael R. Boyd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     2¦Â,3¦Â,11¦Á,14¦Á,20¦Â,23-hexahydroxy-5-cholest-7-en-6-one
    ÏàËÆ¶È:55.5%
Acta Botanica Boreali-Occidentalia Sinica          2002          22          1457-1459
A new ecdysterone from Rhaponticumuni florum
CHENG Jie kai, HUANG Ming hua, ZHANG Zi yi, CHENG Dong liang, ZHANG Guo lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3¦Â-Hydroxy-24-norchol-5-en-23-oic acid
    ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
30 .     nodososide
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1986          Vol 49          67
Starfish Saponins, Part 23. Steroidal Glycosides from the Starfish Halityle regularis
Maria Iorizzi, Luigi Minale, Raffaele Riccio, Maurice Debray, Jean Luis Menou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (25S)-5¦Â-cholestane-3¦Â,6¦Â,15¦Á,16¦Â-tetraol
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1995          Vol 58          653-671
Chemical and Biological Investigation of the Polar Constituents of the Starfish Luidia clathrata, Collected in the Gulf of Mexico
Maria Iorizzi, Patrick Bryan, James McClintock, Luigi Minale, Elio Palagiano, Stefano Maurelli, Raffaele Riccio, Franco Zollo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     stenophlline B
C27H45O2N     ÏàËÆ¶È:55.5%
Acta Pharmaceutica Sinica          1988          Vol 23          584-487
THE STRUCTURE AND ABSOLUTE CONFIGURATION OF VERTALINE B ISOLATED FROM VERATRUM TALIENSE LOSE. F.
ZD Min; RX Tan; QT Zheng and CH He
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     3¦Â-hydroxy-24-methylcholesta-5,8-dien-7-one
C27H42O2     ÏàËÆ¶È:55.5%
Natural Product Sciences          2005          11          253-256
A New 5¦Á,8¦Á-epidioxy Sterol from a Marine Sponge Psammocinia Species
Park, Hye-Jin; Luo, Xuan; Hong, Jong-Ki; Kim, Dong-Kyoo; Im, Kwang-Sik; Jung, Jee-H.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     sodium (E)-((1R,4aS,4bS,8aS,10aS)-1-(2-((2S,3S,4R,5R)-3,4-dihydroxy-2,5-dimethoxy-tetrahydrofuran-3-yl)ethyl)-4b,8,8,10a-tetramethyl-decahydrophenanthren-2(1H,3H,4bH)-ylidene)methyl sulfate
C27H45O9SNa     ÏàËÆ¶È:55.5%
Journal of Natural Products          2011          74          1805-1811
Sesterterpenes from the Tropical Sponge Coscinoderma sp.
Jaemin Bae, Ju-eun Jeon, Yeon-Ju Lee, Hyi-Seung Lee, Chung J. Sim, Ki-Bong Oh, and Jongheon Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     tauroselocholic acid
C26H45NO7S     ÏàËÆ¶È:55.5%
Chemical & Pharmaceutical Bulletin          2009          57          528-531
Novel Bile Acids from Bear Bile Powder and Bile of Geese
Dan Bi, Xing-Yun Chai, Yue-Lin Song, Yu Lei and Peng-Fei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     Corosolic acid
    ÏàËÆ¶È:55.5%
Archives of Pharmacal Research          2005          28          1135-1141
Inhibitory effect on TNF-¦Á-induced IL-8 production in the HT29 cell of constituents from the leaf and stem ofWeigela subsessilis
Phuong Thien Thuong, WenYi Jin, JongPill Lee, RackSeon Seong and Young-Mi Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     5¦Â-steroid disulphate
    ÏàËÆ¶È:55.5%
Tetrahedron Letters          1992          33          4641-4644
Isolation, structure characterization and conformational analysis of a unique 4¦Á, 9¦Á-epoxysteroid sulphate from the okinawan ophiuroid Ophiomastix annulosa
M.Valeria D'Auria, Luigi Gomez Paloma, Luigi Minale, Raffaele Riccio, Angela Zampella, Jun-ichi Tanaka, Tatsuo Higa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     compound 1a
    ÏàËÆ¶È:55.5%
Tetrahedron Letters          1992          33          4641-4644
Isolation, structure characterization and conformational analysis of a unique 4¦Á, 9¦Á-epoxysteroid sulphate from the okinawan ophiuroid Ophiomastix annulosa
M.Valeria D'Auria, Luigi Gomez Paloma, Luigi Minale, Raffaele Riccio, Angela Zampella, Jun-ichi Tanaka, Tatsuo Higa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     2,3-dihydroxy-9(11)-fernen-23-oic acid
    ÏàËÆ¶È:55.5%
Natural Product Research and Development          2010          22          940-944
Chemical Constituents from Melastoma dodecandrum
YANG Dan;MA Qing-yun; LIU Yu-qing; DING Zhong-tao; ZHOU Jun; ZHAO You-xing;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     polypodingB
    ÏàËÆ¶È:55.5%
Natural Product Research and Development          2002          14(1)          9-12
STUDY ON THE CHEMICAL CONSTITUENTS OF LYCHNIS CORONARIA
DAI Hao-fu; LIU Yu-qing; DENG Shi-ming; TAN Ning-hua; ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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