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M201175065

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13C NMR (101 MHz, MeOD) ¦Ä£º 16.41,16.78,18.74,19.07,21.15,21.53,24.27,27.44,28.85,29.34,33.01,35.56,38.09,38.89,41.20,43.12,49.30,54.96,64.76,81.67,83.08,85.23,124.98,132.82,134.35,165.04,175.20,196.16
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1 .     Larreagenin A
    ÏàËÆ¶È:65.5%
Planta Medica          1989          55          303-306
Yemuoside YM7, YM11, YM13, and YM14:Four Nortriterpenoid Saponins from Stauntonia chinensis
Huai-Bin Wang,De-Quan Yu,Xiao-Tian Liang, Naoharu Watanabe, Masaharu Tamai, and Sadafumi Omura
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     30-nor,larreagenin A
    ÏàËÆ¶È:65.5%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     modified fusidic acid
C29H44O4     ÏàËÆ¶È:65.5%
The Journal of Antibiotics          1991          44          785-792
INACTIVATION OF FUSIDIC ACID BY RESISTANT Streptomyces STRAINS
BEATE VON DER HAAR, DOUWE ROSENBERG, WERNER DITTRICH, HILDGUND SCHREMPF
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     FAIP-1
    ÏàËÆ¶È:65.5%
The Journal of Antibiotics          1999          52          335-339
Inactivation of Fusidic Acid by Pathogenic Nocardia
KEN-ICHI HARADA, KOJI TOMITA, KIYONAGA FUJII, NORIKO SATO, HIDEAKI UCHIDA, KATSUKIYO YAZAWA, YUZURU MIKAMI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ergosterol 5¦Á,8¦Â-peroside
C28H44O3     ÏàËÆ¶È:64.2%
Chinese Traditional and Herbal Drugs          2009          40          1211-1214
Ó¡¶È¿é¾úµÄ»¯Ñ§³É·ÖÑо¿
ÎâÉÙ»ª;³ÂÓÐΪ;ÑîÀöÔ´;ÀîÉÜÀ¼;ÀîÖÎäÞ
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     (22E,24R)-ergosta-5,22-dien-3¦Â-hydroxyl-7-one
    ÏàËÆ¶È:64.2%
Natural Product Research and Development          2007          19          605-609
Study on the Chemical Constitutes of Hydnellum concrescens
YANG Xiao-long;WANG Fei; SHAO Hong-jun; DONG Ze-jun; DING Zhi-hui; YANG Wan-qiu; LIU Ji-kai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     (24S)-ergost-5-ene-3¦Â,7¦Á-diol
C28H48O2     ÏàËÆ¶È:64.2%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2003          42(2)          56-58
Sterols from the Soft Coral Sinularia depressa Tixier-Durivault
ZHANG Guang-wen, MA Xiang-quan, SU Jing-yu, ZENG Long-mei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3¦Â,5¦Á-dihydroxy-ergosta-7,22-dien-7-one
C28H44O3     ÏàËÆ¶È:64.2%
Tropic Oceanology          2013          32          55-59
Steroids from South China Sea sponge Halichondria sp.
SUN Jian-fan, LI Yun-qiu, YANG Bin, HU Jing, DONG Guang, LIU Yong-hong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     ilexolic acid
    ÏàËÆ¶È:63.3%
Journal of Guangdong Phamaceutical University          2011          27          468-470
Studies on the chemical constituents from Ilex asprella
WEN Jin-lian, CHEN Xiao-li, MO Rui-yi, GUO Li-bing
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (24R)-3¦Â-Methoxy-24-methyl-5¦Á-cholest-8,14-diene
C29H48O2     ÏàËÆ¶È:62.0%
Journal of Natural Products          1992          Vol 55          311
Unique 3¦Â-O-Methylsterols from the Pacific Sponge Jereicopsis graphidiophora
M. Valeria D'Auria, Luigi Gomez Paloma, Luigi Minale, Raffaele Riccio, Cecil Debitus, Claudi L¨¦vi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     (22R,23R)-22,23-oxidostigmast-4-en-3-one
C29H44O2     ÏàËÆ¶È:62.0%
Bioorganic & Medicinal Chemistry          2008          16          1460-1473
Synthesis and cytotoxicity evaluation of 22,23-oxygenated stigmastane derivatives
Alexander Yu. Misharin, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     lanost-25-en-3¦Â-ol acetyl derivative
    ÏàËÆ¶È:61.2%
Planta Medica          1999          65          478-479
A New Lanostane-Type Triterpenoid from Chamaesyce prostrata
Susana Rojas, Martha Maclas, Perla Castañeda,Robert Bye, Edelmira Linares, and Rachel Mata
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     3,27-diacetoxy-28-desmethylolean-12-ene
C33H52O4     ÏàËÆ¶È:61.2%
Chemical & Pharmaceutical Bulletin          1996          44          343-351
Endothelin Receptor Antagonist Triterpenoid, Myriceric Acid A, Isolated from Myrica cerifera, and Structure Activity Relationships of Its Derivatives
Kensuke SAKURAWI,Fumio YASUDA,Takehiko TOZYO,Miharu NAKAMURA,Tomohiro SATO,Junko KIKUCHI,Yoshihiro TERUI,Yuji IKENISHI,Tsuyoshi IWATA,Kazuhiro TAKAHASHI,Toshiro KONOIKE,Shin-ichi MIHARA and Masafumi FUJIMOTO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     30-nor-taraxaster-20en-3¦Â-yl acetate
C31H50O2     ÏàËÆ¶È:61.2%
Phytochemistry          1983          22          1457-1459
Sesquiterpene alcohols and triterpenoids from Liatris microcephala
Werner Herz, Kinzo Watanabe
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     hyrtiosin D
C27H42O5     ÏàËÆ¶È:60.7%
Helvetica Chimica Acta          2005          Vol. 88          1004
Hyrtiosins A-E, Five New Scalarane Sesterterpenes from the South China Sea Sponge Hyrtios erecta
Zhi-Guo Yu, Kai-Shun Bi, Yue-Wei Guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     24(S),25-Epoxycholest-5-en-3¦Â-ol-7-one,3¦Â-Acetate
C29H44O4     ÏàËÆ¶È:60.7%
Steroids          2000          65          529-535
Synthesis of 7¦Á-hydroxy derivatives of regulatory oxysterols
Dansu Li, Thomas A. Spencer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     5¦Á,6¦Á-epoxy-(22E,24R)-ergosta-8,22-diene-3¦Â,7¦Â,14¦Á-triol
C28H42O3     ÏàËÆ¶È:60.7%
Chemical & Pharmaceutical Bulletin          1998          46          944-950
Sterol Constituents from Five Edible Mushrooms
Yasunori YAOITA,Keiko AMEMIYA,Hiroyuki OHNUMA,Katsuyuki FURUMURA,Akihiro MASAKI,Toshihiko MATSUKI and Masao KIKUCHI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     3¦Â,5¦Á,6¦Â,8¦Â,14¦Á-pentahydroxy-(22E,24R)-ergost-22-en-7-one
C28H46O6     ÏàËÆ¶È:60.7%
Natural Product Research          2011          Vol. 25, No. 14          1304-1311
Polyoxygenated ergostane-type sterols from the liquid culture of Ganoderma applanatum
So Young Lee, Ju Sun Kim, Sanghyun Lee and Sam Sik Kang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     2¦Á,3¦Á-dihydroxyolean-13(18)-ene
C30H50O2     ÏàËÆ¶È:60.7%
Phytochemistry          1987          26          793-794
Hirsudiol a triterpenoid from cocculus hirsutus
Viqar Uddin Ahmad,Faryal Vali Mohammad,Tahir Rasheed
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     melithasterol B
    ÏàËÆ¶È:60.7%
Chinese Journal of Natural Medicines          2008          6          348-353
Chemical Constituents of Marine Sponge Biemna fortis Topsent
HUANG Xiao-Chun; LIU Hai-Li; GUO Yue-Wei
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     22-diene-3¦Â,5¦Á,6¦Â,7¦Á-tetraol
    ÏàËÆ¶È:60.7%
Chinese Journal of Medicinal Chemistry          2005          15          221-223
The chemical constituents from the mycel ia of marine fungus Rhizopus sp.
SHI Ying, TIAN Li, PEI Yue-hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     3¦Â-hyohoxy-ergosta-5,22-dien-7-one
C28H44O2     ÏàËÆ¶È:60.7%
Natural Product Research and Development          2004          16          204-206
THE CHEMICAL CONSTITUENTS OF BASIDIOMYCETE CALODON SUAVEOLENS
WANG Fei; LIU Ji-kai *
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     Gargalol A
C28H44O3     ÏàËÆ¶È:60.7%
Tetrahedron          2011          67          6576-6581
Osteoclast-forming suppressing compounds, gargalols A, B, and C, from the edible mushroom Grifola gargal
Jing Wu, Jae-Hoon Choi, Miyuki Yoshida, Hirofumi Hirai, Etsuko Harada, Kikuko Masuda, Tomoyuki Koyama, Kazunaga Yazawa, Keiichi Noguchi, Kazuo Nagasawa, Hirokazu Kawagishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     Gargalol C
C28H42O4     ÏàËÆ¶È:60.7%
Tetrahedron          2011          67          6576-6581
Osteoclast-forming suppressing compounds, gargalols A, B, and C, from the edible mushroom Grifola gargal
Jing Wu, Jae-Hoon Choi, Miyuki Yoshida, Hirofumi Hirai, Etsuko Harada, Kikuko Masuda, Tomoyuki Koyama, Kazunaga Yazawa, Keiichi Noguchi, Kazuo Nagasawa, Hirokazu Kawagishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     chaxine C
C28H40O4     ÏàËÆ¶È:60.7%
Tetrahedron          2009          65          9850-9853
Chaxines B, C, D, and E from the edible mushroom Agrocybe chaxingu
Jae-Hoon Choi, Akihiro Ogawa, Nobuo Abe, Kikuko Masuda, Tomoyuki Koyama, Kazunaga Yazawa, Hirokazu Kawagishi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-10-08 11:53:51
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