Znn3bq.jpeg
±±¾©Ê¯ÓÍ»¯¹¤Ñ§Ôº2026ÄêÑо¿ÉúÕÐÉú½ÓÊÕµ÷¼Á¹«¸æ
²é¿´: 378  |  »Ø¸´: 3

ÒÀÁµË®µÄÊ÷

Í­³æ (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
»Ø¸´´ËÂ¥

» ²ÂÄãϲ»¶

ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangkaibo123

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

kerry

ÓÅÐã°æÖ÷

¡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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
2Â¥2013-08-28 20:18:07
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangkaibo123

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

kerry

ÓÅÐã°æÖ÷

¡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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
3Â¥2013-08-28 20:19:44
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

wangkaibo123

ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)

kerry

ÓÅÐã°æÖ÷

¡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
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
4Â¥2013-08-28 20:28:12
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
Ïà¹Ø°æ¿éÌø×ª ÎÒÒª¶©ÔÄÂ¥Ö÷ ÒÀÁµË®µÄÊ÷ µÄÖ÷Ìâ¸üÐÂ
×î¾ßÈËÆøÈÈÌûÍÆ¼ö [²é¿´È«²¿] ×÷Õß »Ø/¿´ ×îºó·¢±í
[¿¼ÑÐ] Çóµ÷¼Á +11 wwwwabcde 2026-04-07 11/550 2026-04-07 23:16 by JourneyLucky
[¿¼ÑÐ] ±¾¿ÆÖ£ÖÝ´óѧ£¬Ò»Ö¾Ô¸»ª¶«Ê¦·¶´óѧ282Çóµ÷¼Á +20 Ðܸçxtk 2026-04-07 23/1150 2026-04-07 22:51 by JourneyLucky
[¿¼ÑÐ] 338Çóµ÷¼Á +5 СÖíºìÉ« 678 2026-04-06 6/300 2026-04-07 21:18 by ÇÇßÕßÕßÕ
[¿¼ÑÐ] 277Çóµ÷¼Á ÊýÒ»104·Ö +9 Æ¿×ÓPZ 2026-04-05 14/700 2026-04-07 17:52 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 315Çóµ÷¼Á +3 TUZEIQAQ 2026-04-02 3/150 2026-04-07 17:32 by chenp123
[¿¼ÑÐ] »·¾³×¨Ë¶µ÷¼Á +12 »á˵»°µÄÖâ×Ó 2026-04-06 12/600 2026-04-07 17:23 by ¿É¿Ú¿ÉÀÖ²»¼Ó±ùØ
[¿¼ÑÐ] 264Çóµ÷¼Á +7 ÂóС¶£µ± 2026-04-07 7/350 2026-04-07 12:05 by Sammy2
[¿¼ÑÐ] 362Çóµ÷¼Á +7 ÎÒÒª¿¼´ó 2026-04-06 11/550 2026-04-07 09:32 by ÎÒÒª¿¼´ó
[¿¼ÑÐ] 327Çóµ÷¼Á +5 Xxjc1107. 2026-04-06 5/250 2026-04-06 21:43 by dongzh2009
[¿¼ÑÐ] 285Çóµ÷¼Á +5 mapmath 2026-04-06 6/300 2026-04-06 17:18 by À¶ÔÆË¼Óê
[¿¼ÑÐ] »¯Ñ§µ÷¼ÁÇóÖú +8 LULONG1 2026-04-03 8/400 2026-04-06 10:26 by dongzh2009
[¿¼ÑÐ] 311·Ö 22408 Çóµ÷¼Á +3 bing_bot 2026-04-03 3/150 2026-04-05 00:43 by chongya
[¿¼ÑÐ] 277Çóµ÷¼Á +4 12A3 2026-04-02 5/250 2026-04-04 20:28 by À¶ÔÆË¼Óê
[¿¼ÑÐ] 342Çóµ÷¼Á +3 Liang7111 2026-04-04 5/250 2026-04-04 19:47 by dongzh2009
[¿¼ÑÐ] 293Çóµ÷¼Á +5 ĩδmm 2026-04-02 6/300 2026-04-03 15:20 by Íõ±£½Ü33
[¿¼ÑÐ] ¸´ÊÔµ÷¼Á +3 bvzz 2026-04-01 3/150 2026-04-03 09:47 by À¶ÔÆË¼Óê
[¿¼ÑÐ] µ÷¼Á +3 osbbx 2026-04-02 3/150 2026-04-03 07:47 by cc8418
[¿¼ÑÐ] 298ÇóBÇøµ÷¼Á +4 zzz£¬£¬r 2026-04-02 5/250 2026-04-02 12:17 by ÍÁľ˶ʿÕÐÉú
[¿¼ÑÐ] °²È«¹¤³Ì 285 Çóµ÷¼Á +3 Xinyu56 2026-04-01 4/200 2026-04-01 21:50 by ¾²¾²¾²¾²¾²¾²¾²¾
[¿¼ÑÐ] 350Çóµ÷¼Á +7 °¢¼Ñ¡« 2026-03-31 7/350 2026-04-01 16:12 by yanflower7133
ÐÅÏ¢Ìáʾ
ÇëÌî´¦ÀíÒâ¼û