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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)

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²éѯ½á¹û£º¹²²éµ½206¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 6
    ÏàËÆ¶È:75%
Organic Magnetic Resonance          1984          22          127-128
13C and 15N NMR spectra of 4-substituted-1-dimethylphosphonopiperazines
G. W. Buchanan and S. H. Preusser
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     compound 6
    ÏàËÆ¶È:75%
Organic Magnetic Resonance          1984          22          127-128
13C and 15N NMR spectra of 4-substituted-1-dimethylphosphonopiperazines
G. W. Buchanan and S. H. Preusser
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     loliolide
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2009          34          2060-2062
Chemical constituents in the introduced Coleus forskohlii
ZHANG Weiwei, KONG Lingyi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     loliolide
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2008          33          1415-1417
Chemica constituents of aerial part of Acalypha australis
WANG Xiaolan , YU Kaibei, PENG Shulin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     loliolide
    ÏàËÆ¶È:63.6%
Chinese Traditional and Herbal Drugs          2010          41          1423-1425
Chemical constituents from Viola yedoensis
XU Jin-zhong; ZENG Shan-shan; QU Hai-bin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     loliolide
    ÏàËÆ¶È:63.6%
Journal of Shenyang Pharmaceutical University          2007          24          549-551
Chemical constituents of Ixeris sonchif olia (Bge.) Hance
ZHANG Nan, L-A-li, WANG Ding, CHEN Gang, DANG quan, PEI Yue-hu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Peruvianoxide
C19H24O3     ÏàËÆ¶È:63.6%
Food Chemistry          2009          116          462-469
New cytotoxic withanolides from Physalis peruviana
Yu-Hsuan Lan, Fang-Rong Chang, Mei-Jung Pan, Chin-Chung Wu, Shu-Jing Wu, Su-Li Chen, Shyh-Shyan Wang, Ming-Jung Wu, Yang-Chang Wu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     loliolide
    ÏàËÆ¶È:63.6%
Journal of Shenyang Pharmaceutical University          2012          29          758-764
Isolation and identification of chemical constituents from the whole plants of Ajuga decumbens
SUN Zhan-ping; GUI Li-ping; GUO Yuan-qiang; XU Jing; LI Yu-shan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     loliolide
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2013          38          1536-1538
Chemical constituents of Periploca forrestii
LI Yong, LIU Yun-bao, YU Shi-shan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     N,N-bis(2-chloroethyl)-hexahydro-[1,3,2]-diazaphospholo[1,5a]pyridine-1-amine 1-oxide
C10H20Cl2N3OP     ÏàËÆ¶È:62.5%
Archiv der Pharmazie          2011          344          765-770
Synthesis and Antioxidant Activity of Substituted-1,3,2-Diazaphosphole 1-Oxides (pages 765¨C770)
Kalla Reddi Mohan Naidu, Pasupuleti Visweswara Rao, Chamarthi Naga Raju and Kambam Srinivasulu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     compound 4h
C8H17N2O2SCl     ÏàËÆ¶È:62.5%
Chinese Chemical Letters          2012          23          297-300
Design, synthesis and primary activity of thiomorpholine derivatives as DPP-IV inhibitors
Bei Han, Jing Long Liu, Yi Huan, Peng Li, Qi Wu, Zi Yun Lin, Zhu Fang Shen, Da Li Yin, Hai Hong Huang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     1-methylspermidine trihydrochloride
C8H21N3     ÏàËÆ¶È:62.5%
Journal of Medicinal Chemistry          1992          35          724-734
alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines
John R. Lakanen, James K. Coward, Anthony E. Pegg
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     N-(cyclohexyl)-Glycine Ethylester,Hydrochloride
C10H19NO2     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          1999          7          543-564
The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity
James B Aggen, John M Humphrey, Carla-Maria Gauss, Hsien-Bin Huang, Angus C Nairn, A.Richard Chamberlin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     1,4-Dioxa-14-thiaspiro[4.17]docosane
    ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     Compound(¡À)-13
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry Letters          1997          7          811-816
Lipase-catalysed enantioselective hydrolysis of bicyclo[3.2.0]heptanol esters in supercritical carbon dioxide
Omar Parve, Imre Vallikivi, Lilja Lahe, Andrus Metsala, ¨¹lo Lille, Vello Tõugu, Heiki Vija, Tõnis Pehk
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     2-bromo-1-tricyclo[3.3.1.1(3,7)]decanemethyl bromide
C11H16Br2     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2009          17          1534-1541
Design and synthesis of 1,2-annulated adamantane piperidines with anti-influenza virus activity
Grigoris Zoidis, Nicolas Kolocouris, Lieve Naesens, Erik De Clercq
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     (8S)-3-(2-hydroxypropyl)cyclohexanone
C9H16O2     ÏàËÆ¶È:55.5%
The Journal of Antibiotics          1999          52          1124-1134
Biomolecular-chemical Screening: A Novel Screening Approach for the Discovery of Biologically Active Secondary Metabolites III. New DNA-binding Metabolites
CORINNA MAUL, ISABEL SATTLER, MARION ZERLIN, CLAUDIA HINZE, CORINNA KOCH, ARMIN MAIER, SUSANNE GRABLEY, RALF THIERICKE
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-12-31 11:13:52
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Éñҽѩѩ: ½ð±Ò+10 2015-02-02 18:18:07
²éѯ½á¹û£º¹²²éµ½206¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 6
    ÏàËÆ¶È:75%
Organic Magnetic Resonance          1984          22          127-128
13C and 15N NMR spectra of 4-substituted-1-dimethylphosphonopiperazines
G. W. Buchanan and S. H. Preusser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound 6
    ÏàËÆ¶È:75%
Organic Magnetic Resonance          1984          22          127-128
13C and 15N NMR spectra of 4-substituted-1-dimethylphosphonopiperazines
G. W. Buchanan and S. H. Preusser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     loliolide
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2009          34          2060-2062
Chemical constituents in the introduced Coleus forskohlii
ZHANG Weiwei, KONG Lingyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     loliolide
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2008          33          1415-1417
Chemica constituents of aerial part of Acalypha australis
WANG Xiaolan , YU Kaibei, PENG Shulin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     loliolide
    ÏàËÆ¶È:63.6%
Chinese Traditional and Herbal Drugs          2010          41          1423-1425
Chemical constituents from Viola yedoensis
XU Jin-zhong; ZENG Shan-shan; QU Hai-bin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     loliolide
    ÏàËÆ¶È:63.6%
Journal of Shenyang Pharmaceutical University          2007          24          549-551
Chemical constituents of Ixeris sonchif olia (Bge.) Hance
ZHANG Nan, L-A-li, WANG Ding, CHEN Gang, DANG quan, PEI Yue-hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     Peruvianoxide
C19H24O3     ÏàËÆ¶È:63.6%
Food Chemistry          2009          116          462-469
New cytotoxic withanolides from Physalis peruviana
Yu-Hsuan Lan, Fang-Rong Chang, Mei-Jung Pan, Chin-Chung Wu, Shu-Jing Wu, Su-Li Chen, Shyh-Shyan Wang, Ming-Jung Wu, Yang-Chang Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     loliolide
    ÏàËÆ¶È:63.6%
Journal of Shenyang Pharmaceutical University          2012          29          758-764
Isolation and identification of chemical constituents from the whole plants of Ajuga decumbens
SUN Zhan-ping; GUI Li-ping; GUO Yuan-qiang; XU Jing; LI Yu-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     loliolide
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2013          38          1536-1538
Chemical constituents of Periploca forrestii
LI Yong, LIU Yun-bao, YU Shi-shan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     N,N-bis(2-chloroethyl)-hexahydro-[1,3,2]-diazaphospholo[1,5a]pyridine-1-amine 1-oxide
C10H20Cl2N3OP     ÏàËÆ¶È:62.5%
Archiv der Pharmazie          2011          344          765-770
Synthesis and Antioxidant Activity of Substituted-1,3,2-Diazaphosphole 1-Oxides (pages 765¨C770)
Kalla Reddi Mohan Naidu, Pasupuleti Visweswara Rao, Chamarthi Naga Raju and Kambam Srinivasulu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 4h
C8H17N2O2SCl     ÏàËÆ¶È:62.5%
Chinese Chemical Letters          2012          23          297-300
Design, synthesis and primary activity of thiomorpholine derivatives as DPP-IV inhibitors
Bei Han, Jing Long Liu, Yi Huan, Peng Li, Qi Wu, Zi Yun Lin, Zhu Fang Shen, Da Li Yin, Hai Hong Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1-methylspermidine trihydrochloride
C8H21N3     ÏàËÆ¶È:62.5%
Journal of Medicinal Chemistry          1992          35          724-734
alpha.-Methyl polyamines: metabolically stable spermidine and spermine mimics capable of supporting growth in cells depleted of polyamines
John R. Lakanen, James K. Coward, Anthony E. Pegg
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     N-(cyclohexyl)-Glycine Ethylester,Hydrochloride
C10H19NO2     ÏàËÆ¶È:62.5%
Bioorganic & Medicinal Chemistry          1999          7          543-564
The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity
James B Aggen, John M Humphrey, Carla-Maria Gauss, Hsien-Bin Huang, Angus C Nairn, A.Richard Chamberlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     1,4-Dioxa-14-thiaspiro[4.17]docosane
    ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          2012          95          428-447
Exaltone (=Cyclopentadecanone) from Isomuscone (=Cyclohexadecanone), a One-C-Atom Ring-Contraction Methodology via a Stereospecific Favorskii Rearrangement: Regioselective Application to (-)-(R)-Muscone
Christian Chapuis, Fabrice Robvieux, Carole Cantatore, Christine Saint-L¨¦ger, and Laurent Maggi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Compound(¡À)-13
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry Letters          1997          7          811-816
Lipase-catalysed enantioselective hydrolysis of bicyclo[3.2.0]heptanol esters in supercritical carbon dioxide
Omar Parve, Imre Vallikivi, Lilja Lahe, Andrus Metsala, ¨¹lo Lille, Vello Tõugu, Heiki Vija, Tõnis Pehk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2-bromo-1-tricyclo[3.3.1.1(3,7)]decanemethyl bromide
C11H16Br2     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2009          17          1534-1541
Design and synthesis of 1,2-annulated adamantane piperidines with anti-influenza virus activity
Grigoris Zoidis, Nicolas Kolocouris, Lieve Naesens, Erik De Clercq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (8S)-3-(2-hydroxypropyl)cyclohexanone
C9H16O2     ÏàËÆ¶È:55.5%
The Journal of Antibiotics          1999          52          1124-1134
Biomolecular-chemical Screening: A Novel Screening Approach for the Discovery of Biologically Active Secondary Metabolites III. New DNA-binding Metabolites
CORINNA MAUL, ISABEL SATTLER, MARION ZERLIN, CLAUDIA HINZE, CORINNA KOCH, ARMIN MAIER, SUSANNE GRABLEY, RALF THIERICKE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     cyclohexanecarbonylalanine
C10H17NO3     ÏàËÆ¶È:55.5%
The Journal of Antibiotics          1982          35          1467-1473
STUDIES ON MYCOTRIENIN ANTIBIOTICS, A NOVEL CLASS OF ANSAMYCINS II. STRUCTURE ELUCIDATION AND BIOSYNTHESIS OF MYCOTRIENINS I AND II
MASANORI SUGITA, TETSUO SASAKI, KAZUO FURIHATA, HARUO SETO, NOBORU OTAKE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     molinate sulfone (S-ethyl-hexahydro-1Hazepine-1-carbothioate sulfone)
    ÏàËÆ¶È:55.5%
Chemical Research in Toxicology          2004          17          258-267
Characterization of S-(N,N-Dialkylaminocarbonyl)cysteine Adducts and Enzyme Inhibition Produced by Thiocarbamate Herbicides in the Rat
Lisa J. Zimmerman, Holly L. Valentine, and William M. Valentine
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 36
    ÏàËÆ¶È:55.5%
Magnetic Resonance in Chemistry          1992          30          1186-1195
Stereochemistry¨Cactivity relationships of ACE inhibitors. Conformational studies by 1H and 13C NMR of perindopril and selected stereoisomers
J. P. Bouchet, J. P. Volland, M. Laubie, M. Vincent, B. Marchand and N. Platzer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3Â¥2014-12-31 11:14:29
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