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²éѯ½á¹û£º¹²²éµ½1669¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (17¦Â,20R,22E,24R)-19-norergosta-1,3,5,7,9,14,22-heptaene C27H34 ÏàËÆ¶È:67.8% Journal of Natural Products 2004 67 2133-2135 Natural Aromatic Steroids as Potential Molecular Fossils from the Fruiting Bodies of the Ascomycete Daldinia concentrica Xiang-Dong Qin, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (17¦Â,20R,22E,24R)-1-methyl-19-norergosta-1,3,5,7,9,14,22-heptaene C28H36 ÏàËÆ¶È:67.8% Journal of Natural Products 2004 67 2133-2135 Natural Aromatic Steroids as Potential Molecular Fossils from the Fruiting Bodies of the Ascomycete Daldinia concentrica Xiang-Dong Qin, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ganodermaside A C28H40O2 ÏàËÆ¶È:67.8% Bioorganic & Medicinal Chemistry 2010 18 999-1002 Ganodermasides A and B, two novel anti-aging ergosterols from spores of a medicinal mushroom Ganoderma lucidum on yeast via UTH1 gene Yufang Weng, Lan Xiang, Akira Matsuura, Yang Zhang, Qianming Huang, Jianhua Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 19-norergosta-1,3,5,7,9,14,22-heptaene ÏàËÆ¶È:67.8% Tetrahedron 2012 68 6485-6491 Oxidation with selenium dioxide: the first report of solvent-selective steroidal aromatization, efficient access to 4¦Â,7¦Á-dihydroxy steroids, and syntheses of natural diaromatic ergosterols Pranab Ghosh, Jayanta Das, Antara Sarkar, Seik Weng Ng, Edward R.T. Tiekink Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 15¦Â-methoxy-(22E,24R)-ergosta-4,6,8(14),22-tetraen-3-one C29H42O2 ÏàËÆ¶È:65.5% Natural Products and Bioprospecting 2012 2 240-244 Six novel steroids from culture of basidiomycete Polyporus ellisii Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (22E)-5a,8a-epidioxyergosta-6,9(11),22-trien-3b-ol ÏàËÆ¶È:64.2% Chemistry & Biodiversity 2008 Vol. 5 743 Chemical Constituents of Stereum subtomentosum and Two Other Birch-Associated Basidiomycetes: An Interspecies Comparative Study Simona Hybelbauerov¨¢, Jan Sejbal, Martin Drač¨ªnský , Alice Hahnov¨¢, and Bohum¨ªr Koutek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . gymnasterone D C28H38O3 ÏàËÆ¶È:64.2% Journal of Natural Products 2007 70 1731-1740 Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Crinosterol C28H46O ÏàËÆ¶È:64.2% Chinese Journal of Marine Drugs 2006 25(4) 22-25 Studies on the chemical constituents of the sea pen Cavernularia sp. DUAN Lin, FAN G Yu-chuan, ZHU Wei-ming, GU Qian-qun, GUAN Hua-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol ÏàËÆ¶È:64.2% Chinese Journal of Medicinal Chemistry 2008 18 452-456 Secondary metabolites produced by Fusarium sp. 2TnP1-2, an endophytic fungus from Trewia nudif lora DU Zhi-zhi, SONG Cheng-zhi, YU Bu-zhu, LUO Xiao-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . ganodermaside B C28H40O2 ÏàËÆ¶È:64.2% Bioorganic & Medicinal Chemistry 2010 18 999-1002 Ganodermasides A and B, two novel anti-aging ergosterols from spores of a medicinal mushroom Ganoderma lucidum on yeast via UTH1 gene Yufang Weng, Lan Xiang, Akira Matsuura, Yang Zhang, Qianming Huang, Jianhua Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . trans-4-(1'-methoxymethyloxybutyl)-6,8-dimethyl-1,6,7,8-tetrahydrocyclopent[g]indole-2-methanol C20H29NO3 ÏàËÆ¶È:64.2% Australian Journal of Chemistry 1998 51 177-187 Total Synthesis of (¡À)-Iso-trans-trikentrin B John K. MacLeod, Annemarie Ward and Anthony C. Willis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . gymnasterone ÏàËÆ¶È:64.2% Natural Products and Bioprospecting 2012 2 240-244 Six novel steroids from culture of basidiomycete Polyporus ellisii Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 22E-3,7-epoxy-5,10:8,9-disecoergosta-9(10),22-diene-5,8-dione C28H44O3 ÏàËÆ¶È:64.2% Journal of Shenyang Pharmaceutical University 2012 29 678-684 A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1) LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . gymnasterone C C28H40O3 ÏàËÆ¶È:60.7% Journal of Natural Products 2007 70 1731-1740 Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . comnostin B C27H38O4 ÏàËÆ¶È:60.7% Journal of Natural Products 2000 63 339-343 Novel Extracellular Diterpenoids with Biological Activity from the Cyanobacterium Nostoc commune B. Jaki, J. Orjala, J. Heilmann, A. Linden, B. Vogler, and O. Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ergosta-5,8(14),22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:60.7% Journal of Natural Products 1998 61 1491-1496 Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (22E)-3¦Â-Hydroxy-5¦Á-ergosta-8(14),22-dien-15-one ÏàËÆ¶È:60.7% Steroids 2007 72 305-312 Novel side chain modified ¦¤8(14)-15-ketosterols Alexander Yu. Misharin, Vitali S. Ivanov, Arif R. Mehtiev, Galina E. Morozevich, Yaroslav V. Tkachev, Vladimir P. Timofeev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 3¦Â-Hydroxyl-(22E,24R)-ergosta-5,8,22-trien-7,15-dione C28H40O3 ÏàËÆ¶È:60.7% Steroids 2008 73 19-26 Six new ergosterols from the marine-derived fungus Rhizopus sp. Fazuo Wang, Yuchun Fang, Min Zhang, Aiqun Lin, Tianjiao Zhu, Qianqun Gu, Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . ergosta-8(14),22-diene-3,5,6,7-tetraol(3¦Â,5¦Á,6¦Â,7¦Á,22E) C28H46O4 ÏàËÆ¶È:60.7% Natural Product Research 2006 20 381-384 Cytotoxic sterols from marine-derived fungus Pennicillium sp. Yi Sun; Li Tian; Jian Huang; Wen Li; Yue-hu Pei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . ergosta-4,6,8(14),22-tetraen-3-one ÏàËÆ¶È:60.7% China Journal of Chinese Materia Medica 2005 30 193-195 Studies on chemical constituents in the mycelia from fermented culture of Flammulian velutipes KANG Jie, CHEN Ruoyun Structure 13C NMR ̼Æ×Ä£Äâͼ |
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lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
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- ºì»¨: 208
- Ìû×Ó: 4735
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ycg999888: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Thank you! 2013-10-09 16:52:19
ycg999888: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Thank you! 2013-10-09 16:52:19
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²éѯ½á¹û£º¹²²éµ½1319¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (17¦Â,20R,22E,24R)-19-norergosta-1,3,5,7,9,14,22-heptaene C27H34 ÏàËÆ¶È:65.5% Journal of Natural Products 2004 67 2133-2135 Natural Aromatic Steroids as Potential Molecular Fossils from the Fruiting Bodies of the Ascomycete Daldinia concentrica Xiang-Dong Qin, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (17¦Â,20R,22E,24R)-1-methyl-19-norergosta-1,3,5,7,9,14,22-heptaene C28H36 ÏàËÆ¶È:65.5% Journal of Natural Products 2004 67 2133-2135 Natural Aromatic Steroids as Potential Molecular Fossils from the Fruiting Bodies of the Ascomycete Daldinia concentrica Xiang-Dong Qin, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ganodermaside A C28H40O2 ÏàËÆ¶È:65.5% Bioorganic & Medicinal Chemistry 2010 18 999-1002 Ganodermasides A and B, two novel anti-aging ergosterols from spores of a medicinal mushroom Ganoderma lucidum on yeast via UTH1 gene Yufang Weng, Lan Xiang, Akira Matsuura, Yang Zhang, Qianming Huang, Jianhua Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 19-norergosta-1,3,5,7,9,14,22-heptaene ÏàËÆ¶È:65.5% Tetrahedron 2012 68 6485-6491 Oxidation with selenium dioxide: the first report of solvent-selective steroidal aromatization, efficient access to 4¦Â,7¦Á-dihydroxy steroids, and syntheses of natural diaromatic ergosterols Pranab Ghosh, Jayanta Das, Antara Sarkar, Seik Weng Ng, Edward R.T. Tiekink Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 15¦Â-methoxy-(22E,24R)-ergosta-4,6,8(14),22-tetraen-3-one C29H42O2 ÏàËÆ¶È:65.5% Natural Products and Bioprospecting 2012 2 240-244 Six novel steroids from culture of basidiomycete Polyporus ellisii Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 15¦Á-acetoxy-(22E,24R)-ergosta-4,6,8(14),22-tetraen-3-one C30H42O3 ÏàËÆ¶È:63.3% Natural Products and Bioprospecting 2012 2 240-244 Six novel steroids from culture of basidiomycete Polyporus ellisii Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (22E)-5a,8a-epidioxyergosta-6,9(11),22-trien-3b-ol ÏàËÆ¶È:62.0% Chemistry & Biodiversity 2008 Vol. 5 743 Chemical Constituents of Stereum subtomentosum and Two Other Birch-Associated Basidiomycetes: An Interspecies Comparative Study Simona Hybelbauerov¨¢, Jan Sejbal, Martin Drač¨ªnský , Alice Hahnov¨¢, and Bohum¨ªr Koutek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . gymnasterone D C28H38O3 ÏàËÆ¶È:62.0% Journal of Natural Products 2007 70 1731-1740 Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Crinosterol C28H46O ÏàËÆ¶È:62.0% Chinese Journal of Marine Drugs 2006 25(4) 22-25 Studies on the chemical constituents of the sea pen Cavernularia sp. DUAN Lin, FAN G Yu-chuan, ZHU Wei-ming, GU Qian-qun, GUAN Hua-shi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 5¦Á,6¦Á-epoxy-24(R)-methylcholesta-7,22-dien-3¦Â-ol ÏàËÆ¶È:62.0% Chinese Journal of Medicinal Chemistry 2008 18 452-456 Secondary metabolites produced by Fusarium sp. 2TnP1-2, an endophytic fungus from Trewia nudif lora DU Zhi-zhi, SONG Cheng-zhi, YU Bu-zhu, LUO Xiao-dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . ganodermaside B C28H40O2 ÏàËÆ¶È:62.0% Bioorganic & Medicinal Chemistry 2010 18 999-1002 Ganodermasides A and B, two novel anti-aging ergosterols from spores of a medicinal mushroom Ganoderma lucidum on yeast via UTH1 gene Yufang Weng, Lan Xiang, Akira Matsuura, Yang Zhang, Qianming Huang, Jianhua Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . trans-4-(1'-methoxymethyloxybutyl)-6,8-dimethyl-1,6,7,8-tetrahydrocyclopent[g]indole-2-methanol C20H29NO3 ÏàËÆ¶È:62.0% Australian Journal of Chemistry 1998 51 177-187 Total Synthesis of (¡À)-Iso-trans-trikentrin B John K. MacLeod, Annemarie Ward and Anthony C. Willis Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . gymnasterone ÏàËÆ¶È:62.0% Natural Products and Bioprospecting 2012 2 240-244 Six novel steroids from culture of basidiomycete Polyporus ellisii Shuang Wang, Ling Zhang, Liang-Yan Liu, Ze-Jun Dong, Zheng-Hui Li, Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 22E-3,7-epoxy-5,10:8,9-disecoergosta-9(10),22-diene-5,8-dione C28H44O3 ÏàËÆ¶È:62.0% Journal of Shenyang Pharmaceutical University 2012 29 678-684 A new disecosteroid from an endolichenic fungal stain Sporormiella irregularis(No.71-11-4-1) LI Yan-jun; LI Xiao-xia; CHEN Guo-dong; GAO Hao; GUO Liang-dong; YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . helianol C30H52O ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1996 44 1255-1257 Helianol [3, 4-seco-19(10¡ú9)abeo-8¦Á, 9¦Â, 10¦Á-eupha-4, 24-dien-3-ol], a Novel Triterpene Alcohol from the Tabular Flowers of Helianthus annuus L. Toshihiro AKIHISA,Hirotoshi OINUMA,Ken YASUKAWA,Yoshimasa KASAHARA,Yumiko KIMURA,Sei-ichi TAKASE,Sakae YAMANOUCHI,Michio TAKIDO,Kunio KUMAKI and Toshitake TAMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 5-Hydroxy-5¦Á-ergosta-6,8(14)-22-trien-3¦Â-ylacetate C30H46O3 ÏàËÆ¶È:60% Steroids 2006 71 565-577 Regio and stereoselective oxidations of unsaturated steroidal compounds with H2O2 mediated by CH3ReO3 Francesco P. Ballistreri, Rosa Chillemi, Sebastiano Sciuto, Gaetano A. Tomaselli, Rosa M. Toscano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . sasanquol C30H52O ÏàËÆ¶È:60% Phytochemistry 1998 48 301-305 Sasanquol, A 3,4-seco-triterpene alcohol from sasanqua oil, and its anti-inflammatory effect Toshihiro Akihisa, Kem Yasukawa, Yumiko Kimura, Sakae Yamanouchi, Toshitake Tamura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . rgosterimide C32H45NO3 ÏàËÆ¶È:59.3% Steroids 2007 72 723-727 Ergosterimide, a new natural Diels¨CAlder adduct of a steroid and maleimide in the fungus Aspergillus niger Yi Zhang, Xiao-Ming Li, Peter Proksch, Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . sasanquyl acetate C32H54O2 ÏàËÆ¶È:59.3% Phytochemistry 1998 48 301-305 Sasanquol, A 3,4-seco-triterpene alcohol from sasanqua oil, and its anti-inflammatory effect Toshihiro Akihisa, Kem Yasukawa, Yumiko Kimura, Sakae Yamanouchi, Toshitake Tamura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (22E,24R)-3¦Á-ureido-ergosta-4,6,8(14),22-tetraene C29H44N2O ÏàËÆ¶È:58.6% Chemical & Pharmaceutical Bulletin 2001 49(8) 1030-1032 Two New Steroidal Derivatives from the Fruit Body of Chlorophyllum molybdites Kazuko YOSHIKAWA,Mizuho IKUTA, Shigenobu ARIHARA,Eiko MATSUMURA,and Satoshi KATAYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . gymnasterone C C28H40O3 ÏàËÆ¶È:58.6% Journal of Natural Products 2007 70 1731-1740 Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source Taro Amagata,Makoto Tanaka,Takeshi Yamada, Mitsunobu Doi, Katsuhiko Minoura, Hirofumi Ohishi,Takao Yamori, and Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . comnostin B C27H38O4 ÏàËÆ¶È:58.6% Journal of Natural Products 2000 63 339-343 Novel Extracellular Diterpenoids with Biological Activity from the Cyanobacterium Nostoc commune B. Jaki, J. Orjala, J. Heilmann, A. Linden, B. Vogler, and O. Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . ergosta-5,8(14),22-trien-3¦Â-ol C28H44O ÏàËÆ¶È:58.6% Journal of Natural Products 1998 61 1491-1496 Phycomysterols and Other Sterols from the Fungus Phycomyces blakesleeanus Alejandro F. Barrero, J. Enrique Oltra, Juan A. Poyatos, David Jim¨¦nez, and Eulalia Oliver Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 4-Methyl-ergosta-6,8(14),22E-triene-3-ol ÏàËÆ¶È:58.6% Molecules 2009 14 3360-3366 A New 4¦Á-Methylated Sterol from a Nephthea sp. (Nephtheidae) Bornean Soft Coral Takahiro Ishii, Hiroshi Matsuura, Zhan Zhaoqi and Charles S. Vairappan Structure 13C NMR ̼Æ×Ä£Äâͼ |
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