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ycg999888

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14.8,17.4,19.1,19.6,19.8,19.9,20.8,23.1,33.1,33.4,36.6,37.1,37.9,39.0,42.6,42.8,44.5,59.5,121.6,125.6,128.2,129.4,132.3,132.9,134.8,135.6,143.3,143.9¿ÉÄÜ»¹ÓÐ150.1
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-09 12:40:10
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

lifeliuyan

ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

¡¾´ð°¸¡¿Ó¦Öú»ØÌû

¡ï ¡ï ¡ï ¡ï ¡ï
ycg999888: ½ð±Ò+5, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, Thank you! 2013-10-09 16:52:19
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
3Â¥2013-10-09 12:41:20
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