| ²é¿´: 378 | »Ø¸´: 3 | ||||
ÒÀÁµË®µÄÊ÷ͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
|
Ò»¡¢26.1,29.7,50.9,134.3,191.1 ¶þ¡¢13.1,17.8,18.2,18.3,20.5,20.7,23.9,25.7,25.9,27.5,28.3,28.6,40.4,40.7,41.7, 47.2,49.4,73.4,73.8,122.8,127.9,130.2,132.9,147.7,157.2,168.9,170.1,172.7, 201.3,208.7 Èý¡¢12.0,16.3,17.6,19.6,19.9,21.1,23.0,28.3,29.7,32.0,33.1,37.0,38.4,39.1,40.4,40.8,42.8,46.2,54.6,55.7,70.5,116.3,119.6,132.0,135.6,139.8 |
» ²ÂÄãϲ»¶
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ39È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸211µç×ÓÐÅÏ¢347Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
323Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
1 ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½24¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,6-bis(bromoacetyl)cyclohepta-1,3,5-triene C11H10O2Br2 ÏàËÆ¶È:66.6% Heterocycles 2001 54 159-170 Synthesis and Properties of anti-6,15-Epithia-8,13-methanobenzo[e][14]annulene-7,14-dione, anti-5,14-Epithia-7,12-methanofuro[3,4-e][14]annulene-5,13-diones, and Their Ionic Species Shengli Zuo, Shigeyasu Kuroda,* Mitsunori Oda,* Shin-ya Kuramoto, Yoshihiro Mizukami, Atsushi Fukuta, Yukiyasu Hirano, Teruhiko Nishikawa, Shinji Furuta, Ryuta Miyatake, Sha. I. Shaheen, Takanori Kajioka, and Mayumi Kyogoku Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . capaurine ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1977 25 1426-1435 Studies on the Alkaloids of Papaveraceous Plants. XXIX. Conformational Analysis of Tetrahydroprotoberberines by Carbon-13 Magnetic Resonance Spectroscopy NARAO TAKAO,KINUKO IWASA,MIYOKO KAMIGAUCHI and MAKIKO SUGIURA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . O-methylcapaurine ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1977 25 1426-1435 Studies on the Alkaloids of Papaveraceous Plants. XXIX. Conformational Analysis of Tetrahydroprotoberberines by Carbon-13 Magnetic Resonance Spectroscopy NARAO TAKAO,KINUKO IWASA,MIYOKO KAMIGAUCHI and MAKIKO SUGIURA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (R)-(-)-(1,5-diaminopentyl)phosphonic acid C5H15N2O3P ÏàËÆ¶È:60% European Journal of Organic Chemistry 2011 1870-1879 Chemoenzymatic Synthesis of Phosphonic Acid Analogues of L-Lysine, L-Proline, L-Ornithine, and L-Pipecolic Acid of 99 % ee ¨C Assignment of Absolute Configuration to (¨C)-Proline Frank Wuggenig, Anna Schweifer, Kurt Mereiter and Friedrich Hammerschmidt Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . dimethyl azelate ÏàËÆ¶È:60% Australian Journal of Chemistry 1995 48 1893-1897 A Synthesis of (Z)-Octadec-9-enedioic Acid G Brunow, RV Stick, K Syrjanen, DMG Tilbrook and SJ Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . [(dien)Pt(NH2(CH2)8NH2)Pt(dien)]Cl4 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2005 83 2091-2097 ¦Á- and ¦Â-Cyclodextrin [2]rotaxanes with (diethylenetriamine)platinum(II) stoppers Victor X. Jin, Donal H. Macartney, and Erwin Buncel Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . N,N'-tetramethylenebis(3-oxobutanamide) C12H20N2O4 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 1337-1344 A Facile synthesis of n,n'-oligomethylenebis(4,5-dihydrofuran-3-carboxamide)s using manganese(III)-based radical cyclization of n,n'-oligomethylenebis(3-oxobutanamide)s with 1,1-diarylethenes Firoz Alam Chowdhury and Hiroshi Nishino Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . N-(5-Bromo-1,3,4-thiadiazol-2-yl)acetoacetamide C6H6BrN3O2S ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 1105-1109 Preparation of 2-amino-5-methyl-7H-1,3,4-thiadiazolo[3,2-]pyrimidin-7-ones Saifidin Safarov,Muhamacho Ahmadovich Kukaniev,Heinz Kolshorn and Herbert Meier Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2b ÏàËÆ¶È:50% Heterocycles 2003 60 2685-2705 Nuclear Magnetic Resonance Spectroscopical Studies of 2-Carbonyl Derivatives of Five-membered Monoheterocycles and Determination of Aromaticity Indices Kyu Ok Jeon, Ji Sook Yu, and Chang Kiu Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 2b ÏàËÆ¶È:50% Heterocycles 2003 60 2685-2705 Nuclear Magnetic Resonance Spectroscopical Studies of 2-Carbonyl Derivatives of Five-membered Monoheterocycles and Determination of Aromaticity Indices Kyu Ok Jeon, Ji Sook Yu, and Chang Kiu Lee* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . anti-7-Bromo-2-azabicyclo[2.2.1]heptane C6H10NBr ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2006 16 5493-5497 Epibatidine isomers and analogues: Structure¨Cactivity relationships Richard White, John R. Malpass, Sandeep Handa, S. Richard Baker, Lisa M. Broad, Liz Folly, Adrian Mogg Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-Cyclohexyl-1,3-isoindolinedione ÏàËÆ¶È:50% Archives of Pharmacal Research 2004 27 495-501 Synthesis and anticonvulsant evaluation of N -substituted-isoindolinedione derivatives Atef Abdel-Monem Abdel-Hafez Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 33 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 2487-2490 ¦Ð-Facial selectivities in nucleophilic additions to 4-hetero-tricyclo[5.2.1.02,6]decan-10-ones and 4-hetero-tricyclo[5.2.1.02,6]dec-8-en-10-ones: an experimental and computational study Goverdhan Mehta, Vanessa Gagliardini, U.Deva Priyakumar, G.Narahari Sastry Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2,6-bis(tert-butyldimethylsilyl)-4H-thiopyran C17H34SSi2 ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 87-90 Synthesis of new silylated sulfur-containing heterocycles through thionation of bis(acylsilanes) Jean-Philippe Bouillon, Antonella Capperucci, Charles Portella, Alessandro Degl¡¯Innocenti Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (1R,2R)-N1,N2-Tert-butyl-3-methylenecyclopropane-1,2-dicarboxamide C14H24N2O2 ÏàËÆ¶È:50% Molecules 2012 17 5550-5563 Synthesis and Characterization of Some New C2 Symmetric Chiral Bisamide Ligands Derived from Chiral Feist¡¯s Acid Abdullah M. A. Al Majid, Mohammad Shahidul Islam, Zeid Abdullah Al-Othman, Ahlam F. Al-Salhoob and Assem Barakat Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (1S,2S)-N1,N2-tert-Butyl-3-methylenecyclopropane-1,2-dicarboxamide C14H24N2O2 ÏàËÆ¶È:50% Molecules 2012 17 5550-5563 Synthesis and Characterization of Some New C2 Symmetric Chiral Bisamide Ligands Derived from Chiral Feist¡¯s Acid Abdullah M. A. Al Majid, Mohammad Shahidul Islam, Zeid Abdullah Al-Othman, Ahlam F. Al-Salhoob and Assem Barakat Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-Phenylphospholane-Borane C10H13OP ÏàËÆ¶È:50% European Journal of Organic Chemistry 2012 2521-2534 In Situ Dearomatisation/Alkylation of Arylphosphane Derivatives Marek Stankevič, Karolina W¨®jcik, Magdalena Jakli¨½ska and K. Michał Pietrusiewicz Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 2-cyclohexylisoindole-1,3-dione ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 6719-6724 Carbon Monoxide-Free One-Step Synthesis of Isoindole-1,3-diones by Cycloaminocarbonylation of o-Haloarenes Using Formamides Dinesh N. Sawant, Yogesh S. Wagh, Kushal D. Bhatte and Bhalchandra M. Bhanage Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-28 20:18:07
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
|
2 ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½994¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . CS-E ÏàËÆ¶È:87.8% Chemical & Pharmaceutical Bulletin 1996 44 1834-1848 Isolation of New Tremorgenic Metabolites from an Ascomycete, Corynascus setosus Haruhiro FUJIMOTO,Etsuko NEGISHI,Kentaro YAMAGUCHI,Nahoko NISHI and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Helvolic acid C33H44O8 ÏàËÆ¶È:87.8% Chinese Journal of Applied & Environmental Biology 2007 13 66-68 Chemical Study on Aspergillus sp.136 QIN Ling; LI Bogang; GUAN Jiafa & ZHANG Guolin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Helvolic acid C33H44O8 ÏàËÆ¶È:83.8% Chinese Journal of Applied & Environmental Biology 2010 16 76-78 Isolation and Anti-phytopathogenic Activity of Secondary Metabolites from Alternaria sp. FL25,an Endophytic Fungus in Ficus carica FENG Chengliang & MA Yangmin Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (4S,5S,6S,8S,9S,10R,13R,14S,16S,17Z)-6,16-diacetoxy-25-hydroxy-3,7-dioxy-29-nordammara-1,17(20)-dien-21-oic acid C33H46O9 ÏàËÆ¶È:78.7% Journal of Natural Products 2008 71(6) 985-989 Cytotoxic Alkaloids and Antibiotic Nordammarane Triterpenoids from the Marine-Derived Fungus Aspergillus sydowi Min Zhang, Wen-Liang Wang, Yu-Chun Fang, Tian-Jiao Zhu, Qian-Qun Gu, and Wei-Ming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . helvolic acid ÏàËÆ¶È:73.3% Chinese Pharmaceutical Journal 2011 46 1154-1158 Metabolites of Aspergillus sp. HT-2 ZHANG, Li-min, LI, Zhan-lina, BAI, Jiao, Wu, Xinc, WANG, Yu, HUA, Hui-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl cecropioate C35H54O8 ÏàËÆ¶È:60% Phytochemistry 1998 48 171-174 Cecropioic acid, a pentacyclic triterpene from Musanga cecropioides D. Lontsi, B. L. Sondengam, M. T. Martin, B. Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . rotundic acid C30H48O5 ÏàËÆ¶È:60% Phytochemistry 1993 32 417-420 Triterpenoid saponins from Ilex integra Issei Yano, Chikage Nishiizumi, Kazuko Yoshikawa, Shigenobu Arihara Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Klysimplexin sulfoxide C C30H48O10S ÏàËÆ¶È:60% Organic & Biomolecular Chemistry 2010 8 2363-2366 Anti-inflammatory eunicellin-based diterpenoids from the cultured soft coral Klyxum simplex Bo-Wei Chen, Chih-Hua Chao, Jui-Hsin Su, Zhi-Hong Wen, Ping-Jyun Sung and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . kalimantacin A C30H48N2O7 ÏàËÆ¶È:60% The Journal of Antibiotics 1996 49 140-144 Kalimantacin A, B, and C, Novel Antibiotics Produced by Alcaligenes sp. YL-02632S II. Physico-chemical Properties and Structure Elucidation TATSUHIRO TOKUNAGA, KAZUMA KAMIGIRI, MASAYA ORITA, TOSHIAKI NISHIKAWA, MINORU SHIMIZU, HIDETOSHI KANIWA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 12-O-[(2R)-N,N-Dimethyl-3-methylbutanoyl]-20-p-bromobenzoyl-4-deoxyphorbol 13-acetate C36H46O8NBr ÏàËÆ¶È:57.5% Journal of Natural Products 2006 69(6) 887-890 Nitrogen-Containing Phorbol Esters from Croton ciliatoglandulifer and Their Effects on Cyclooxygenases-1 and -2 Mara Yolanda Rios, and A. Berenice Aguilar-Guadarrama Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (2S,1'''R,2'''R,4'''S)-Fenchyl-3,4-dihydro-5-hydroxy-2,7-dimethyl-8-(3''-methyl-2''-butenyl)-2-(4'-methyl-1',3'-pentadienyl)-2H-1-benzopyran-6-carboxylate C33H46O4 ÏàËÆ¶È:57.5% The Journal of Organic Chemistry 2011 76 2603-2612 Structure Elucidation and Absolute Stereochemistry of Isomeric Monoterpene Chromane Esters João M. Batista, Jr., Andrea N. L. Batista, Jonas S. Mota, Quezia B. Cass, Massuo J. Kato,Vanderlan S. Bolzani, Teresa B. Freedman,Silvia N. L opez, Maysa Furlan,and Laurence A. Nafie Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (3¦Â,5¦Á)-20-hydroxy-6-oxocevan-3-yl acetate C29H45NO4 ÏàËÆ¶È:56.6% Chemistry & Biodiversity 2008 Vol. 5 259 Cytotoxic Alkaloids from the Bulbs of Fritillaria hupehensis Yong-Hui Zhang, Xi-Liang Yang, Peng Zhang, Xue-Feng Zhou, Han-Li Ruan, Hui-Fang Pi, Ji-Zhou Wu, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ilexhainanin B C30H46O6 ÏàËÆ¶È:56.6% Helvetica Chimica Acta 2007 Vol. 90 121 Triterpenoids from the Leaves of Ilex hainanensis Si-Xiang Zhou, Jun-Shan Yang, Fu-Cheng Liu, and Peng-Fei Tu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . myrioside A C46H78O18 ÏàËÆ¶È:56.6% Chemical & Pharmaceutical Bulletin 2002 50(8) 1097-1099 Five Triterpene Glycosides from Oxytropis myriophylla Masafumi OKAWA,Rie YAMAGUCHI, Hurlad DELGER,Ryota TSUCHIHASHI, Toshihiro NOHARA,Junei KINJO, Susumu ISODA, and Yoshiteru IDA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . cycloartan-24-ene-1¦Á,3¦Â-diol C30H50O2 ÏàËÆ¶È:56.6% Journal of Natural Products 2008 71(1) 81-86 Cycloartane-Type Triterpenoids from the Resinous Exudates of Commiphora opobalsamum Tao Shen, Hui-Qing Yuan, Wen-Zhu Wan, Xiao-Ling Wang, Xiao-Ning Wang, Mei Ji, and Hong-Xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . garcinielliptone L C30H44O5 ÏàËÆ¶È:56.6% Journal of Natural Products 2004 67 1796-1799 Anti-inflammatory Phloroglucinols and Terpenoids from Garcinia subelliptica Jing-Ru Weng, Lo-Ti Tsao, Jih-Pyang Wang, Ru-Rong Wu, and Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . garcinielliptone M C30H44O5 ÏàËÆ¶È:56.6% Journal of Natural Products 2004 67 1796-1799 Anti-inflammatory Phloroglucinols and Terpenoids from Garcinia subelliptica Jing-Ru Weng, Lo-Ti Tsao, Jih-Pyang Wang, Ru-Rong Wu, and Chun-Nan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 29- or 30-hydroxylated hederagenin ÏàËÆ¶È:56.6% Journal of Natural Products 1999 62 445-448 Triterpenoid Saponins of Acanthopanax nipponicus Leaves Masazumi Miyakoshi, Katsuya Shirasuna, Yasuaki Hirai, Kazushi Shingu, Susumu Isoda, Junzo Shoji, Yoshiteru Ida, and Torao Shimizu Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . rotundic acid ÏàËÆ¶È:56.6% Journal of Natural Products 1999 62 1379-1384 Activity of Triterpenoid Glycosides from the Root Bark of Mussaenda macrophylla against Two Oral Pathogens Nam-Cheol Kim, Anne E. Desjardins, Christine D. Wu, and A. Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 8 ÏàËÆ¶È:56.6% Journal of Natural Products 1996 59 304-307 Triterpenoids from Adina rubella Shi-yue Fang, Zhi-sheng He, and Gao-jun Fan, Hou-ming Wu and Jing-fei Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . bis(Stigmasta-5,22t-dien)-3¦Â-yl oxalate C60H95O4 ÏàËÆ¶È:56.6% Chemistry of Natural Compounds 2006 42 549-552 FACILE SYNTHESIS OF NEW OXALATE DIMERS OF NATURALLY OCCURRING 3-HYDROXYSTEROIDS L. Nahar, S. D. Sarker, and A. B. Turner Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 1,3-Dioxoolean-12-en-20-oic acid ÏàËÆ¶È:56.6% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (20S)-3¦Á-acetoxy-20-cyano-5¦Â-pregnan-16 ¦Â-yl (3'R)-(4'-chloro-3'-methyl)-pentanoate C29H44ClNO4 ÏàËÆ¶È:56.6% Steroids 2009 74 112-120 Beckmann reactions of steroidal spirocyclic oximes derived from the 16¦Â,23:23,26-diepoxy-22-oxo moiety Mariana Mac¨ªas-Alonso, Marcos Flores-Alamo, Mart¨ªn A. Iglesias-Arteaga Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â,6¦Â,19¦Á,-23-tetrahydroxy-urs-12-ene C30H50O4 ÏàËÆ¶È:56.6% Natural Product Research 2001 15 177-185 Triterpenes from Mimusops elengi Nusrat Jahan; Abdul Malik; Ghulam Mustafa; Zaheer Ahmad; Saeed Ahmad; Erum Anis; Shahid Malik; Shahida Shujaat; Night Afza; Atta-ur-rahman Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-08-28 20:19:44
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
ÒÀÁµË®µÄÊ÷: ½ð±Ò+50, ¡ï¡ï¡ïºÜÓаïÖú, лл ºÏ×÷Óä¿ì 2013-08-29 21:08:49
ÒÀÁµË®µÄÊ÷: ½ð±Ò+50, ¡ï¡ï¡ïºÜÓаïÖú, лл ºÏ×÷Óä¿ì 2013-08-29 21:08:49
|
3 ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½8054¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ergosta-5,7,---triene-3¦Â-ol ÏàËÆ¶È:96.1% Chinese Journal of Marine Drugs 2006 25(1) 6-10 Studies on the chemical constituents of the fermentation liquid from marine actinomyces Micromonos por a sp. and bacteria Ocea nos pi rillum sp. SHI Ying, TIAN Li, WANG Jing, PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ergosta-5,7,22-t riene-3¦Â-ol ÏàËÆ¶È:96.1% Chinese Journal of Marine Drugs 2004 23(1) 14-16 Study on the chemical constituents of the fermentation liquid from marine fungus Aspergillus versicolor ZHANG Hai-long, MA Li, TIAN Li Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ergosterol derived ÏàËÆ¶È:96.1% Tetrahedron Letters 2000 41 2791-2795 Stereochemistry of hydrogen introduction at C-25 in ergosterol synthesized by the mevalonate-independent pathway Wen-xu Zhou, W. David Nes Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Ergosterol ÏàËÆ¶È:96.1% Archives of Pharmacal Research 2002 25 851-855 Cytotoxic ergosterols from paecilomyces sp. J300 Hak Cheol Kwon, Sang Deuk Zee, Sae Yun Cho, Sang Un Choi and Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ergosterol ÏàËÆ¶È:96.1% Natural Product Research 2012 26 2008-2012 A new phenol compound from endophytic Phomopsis sp. DC01 Jun-Tian Li, Qian-Qian Chen, Ying Zeng, Qi Wang & Pei-Ji Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ergostatrien-3¦Â-ol ÏàËÆ¶È:96.1% Journal of Agricultural and Food Chemistry 2010 58 7445-7452 Analgesic Effects and the Mechanisms of Anti-inflammation of Ergostatrien-3¦Â-ol from Antrodia camphorata Submerged Whole Broth in Mice Guan-Jhong Huang, Shyh-Shyun Huang, Shiang-Shiou Lin, Yi-Yuan Shao, Chin-Chu Chen, Wen-Chi Hou and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ergosterol ÏàËÆ¶È:96.1% Journal of Agricultural and Food Chemistry 2002 50 7581-7585 Cyclooxygenase Inhibitory and Antioxidant Compounds from the Mycelia of the Edible Mushroom Grifola frondosa Yanjun Zhang, Gary L. Mills, and Muraleedharan G. Nair Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (22E,24R)-Ergosta-5,7,22E-trien-3¦Â-ol ÏàËÆ¶È:96.1% Chemistry of Natural Compounds 2012 48 771-773 A new sulfo-xanthone from the marine-derived fungus Penicillium sacculum Tao Liu, Limin Zhang, Zhanlin Li, Yu Wang, Li Tian, Yuehu Pei, Huiming Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Ergosta-5,7,22-trien-3¦Â-ol ÏàËÆ¶È:92.5% Helvetica Chimica Acta 2004 Vol. 87 1912 Vibratilicin: a Novel Compound from the Basidiomycete Cortinarius vibratilis Fei Wang, Jian-Wen Tan, and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ergosterol ÏàËÆ¶È:92.5% Chinese Pharmaceutical Journal 2013 48 17-21 Secondary Metabolites from Endophyte Fungus Fusariums sp. LC £1 HU Xiao-lan, XU Wen-feng, LU Xuan, WU Xin, BAI Jiao, , PEI Yue-hu, Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ergosterol ÏàËÆ¶È:92.3% China Journal of Chinese Materia Medica 2002 27 674-676 Studies on the Chemical Constituents of Shiraia bambusicola SHEN Yuxiu, RONG Xianguo, GAO Zonghua Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Âó½ÇçÞ´¼ C28H44O ÏàËÆ¶È:92.3% Chinese Traditional and Herbal Drugs 2004 35 493-495 È˹¤Ó¼³æ²Ý»¯Ñ§³É·ÖÑо¿ Íõ¸Õ,Âé±ø¼Ì,Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ergosterol ÏàËÆ¶È:89.2% Phytochemistry 1997 45 1669-1671 Ergosta-4, 6, 8, 22-tetraen-3-one from the edible fungus, Pleurotus ostreatus (oyster fungus) Vladimir Chobot, Lubom¨ªr Opletal, Ludk J¨¢hod¨¢, Asmita V. Patel, Christopher G. Dacke, Gerald Blunden Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ergosterol C28H44O ÏàËÆ¶È:89.2% Natural Product Sciences 2009 15 173-179 Steroids and Triterpenoid from the Fruit Bodies of Ganoderma lucidum and Their Cytotoxic Activity Lee, Joon-Seok; Lee, Mi-Kyoung; Hung, Tran-Manh; Lee, Ik-Soo; Min, Byung-Sun; Bae, Ki-Hwan Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ergosterol ÏàËÆ¶È:89.2% Phytochemistry 1996 41 1301-1308 Sterol analysis of DMI-resistant and -sensitive strains of Venturia inaequalis Noboru Shirane, Hideyuki Takenaka, Kazuo Ueda, Yutaka Hashimoto, Kenji Katoh, Hideo Ishii Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (3¦Â,22E)-Ergosta-5,7,22-trien-3-ol ÏàËÆ¶È:89.2% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 541-544 BIOACTIVE METABOLITES FROM Penicillium sp. P-1,A FUNGAL ENDOPHYTE IN Huperzia serrata You-Min Ying, Zha-Jun Zhan, Zhi-Shan Ding,and Wei-Guang Shan Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-08-28 20:28:12














»Ø¸´´ËÂ¥