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M201175065½ð³æ (ÕýʽдÊÖ)
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[ÇóÖú]
35-15άÆ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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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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M201175065: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-10-08 16:23:26
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²éѯ½á¹û£º¹²²éµ½5055¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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