Base de dados : MEDLINE
Pesquisa : D03.132.206 [Categoria DeCS]
Referências encontradas : 495 [refinar]
Mostrando: 1 .. 10   no formato [Detalhado]

página 1 de 50 ir para página                         

  1 / 495 MEDLINE  
              next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27889556
[Au] Autor:Wang H; Wang D; Yang L; Wang Y; Jia J; Na D; Chen H; Luo Y; Liu C
[Ad] Endereço:Modern College of Arts and Science, or School of Life Science, Shanxi Normal University, Linfen, China. Electronic address: shilvshe@163.com.
[Ti] Título:Compact bone-derived mesenchymal stem cells attenuate nonalcoholic steatohepatitis in a mouse model by modulation of CD4 cells differentiation.
[So] Source:Int Immunopharmacol;42:67-73, 2017 Jan.
[Is] ISSN:1878-1705
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Increasing evidence has accrued which indicates that mesenchymal stem cells (MSCs) have a potential clinical value in the treatment of certain diseases. Globally, nonalcoholic steatohepatitis (NASH) is a widespread disorder. In the present study, MSCs were isolated successfully from compact bone and a mouse model of NASH was established as achieved with use of a methionine-choline deficient (MCD) diet. Compact bone-derived MSCs transplantation reduced MCD diet-induced weight loss, hepatic lipid peroxidation, steatosis, ballooning, lobular inflammation and fibrogenesis. It was shown that MSCs treatment hampered MCD diet-induced proliferation of CD4 IFN-γ and CD4 IL-6 T spleen cells. In addition, CD4 IL-17 lymphocytes that associated with anti-inflammation show little change in MCD as well as in MCD+MSCs splenocytes. We conclude that MSCs may have a potential clinical value upon NASH, through their capacity to suppress activation of CD4 IFN-γ and CD4 IL-6 lymphocytes.
[Mh] Termos MeSH primário: Linfócitos T CD4-Positivos/imunologia
Fígado/patologia
Transplante de Células-Tronco Mesenquimais
Células Mesenquimais Estromais/imunologia
Hepatopatia Gordurosa não Alcoólica/terapia
[Mh] Termos MeSH secundário: Animais
Diferenciação Celular
Alcaloides de Cinchona
Osso Cortical/patologia
Dieta
Modelos Animais de Doenças
Fibrose
Seres Humanos
Interferon gama/metabolismo
Interleucina-6/metabolismo
Peroxidação de Lipídeos
Camundongos
Camundongos Endogâmicos C57BL
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Cinchona Alkaloids); 0 (Interleukin-6); 0 (N,N'-dimethylcinchoninium); 82115-62-6 (Interferon-gamma)
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170414
[Lr] Data última revisão:
170414
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161128
[St] Status:MEDLINE


  2 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27126793
[Au] Autor:Lajkó G; Orosz T; Grecsó N; Fekete B; Palkó M; Fülöp F; Lindner W; Péter A; Ilisz I
[Ad] Endereço:Department of Inorganic and Analytical Chemistry, University of Szeged, H-6720 Szeged, Dóm tér 7, Hungary; Institute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Eötvös u. 6, Hungary.
[Ti] Título:High-performance liquid chromatographic enantioseparation of cyclic ß-aminohydroxamic acids on zwitterionic chiral stationary phases based on Cinchona alkaloids.
[So] Source:Anal Chim Acta;921:84-94, 2016 05 19.
[Is] ISSN:1873-4324
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Cyclic ß-aminohydroxamic acid enantiomer pairs were stereoselectively separated by high-performance liquid chromatography on the recently developed Cinchona alkaloid-based zwitterionic chiral stationary phases Chiralpak ZWIX(+)™, ZWIX(-)™, ZWIX(+A) and ZWIX(-A). The results of variation of the applied chromatographic conditions, such as the bulk solvent composition, the concentrations and ratio of the acid and base additives, the presence of water as mobile phase additive and the counter-ion concentration furnished a better understanding of the retention mechanism. A thermodynamic study in the temperature range 5-50 °C revealed enthalpy-controlled enantiodiscrimination in all cases. The structure-selectivity relationships clearly indicated the importance of the strereochemistry of the functional groups. From an enantiorecognition aspect, the diexo position of the functional groups always proved more favorable than the diendo position. The elution sequence was determined in all cases and was found to reversed when ZWIX(+)™ was changed to ZWIX(-)™ or ZWIX(+A) to ZWIX(-A).
[Mh] Termos MeSH primário: Cromatografia Líquida de Alta Pressão/métodos
Alcaloides de Cinchona/química
Ácidos Hidroxâmicos/isolamento & purificação
[Mh] Termos MeSH secundário: Aminação
Ciclização
Ácidos Hidroxâmicos/química
Estereoisomerismo
Temperatura Ambiente
Termodinâmica
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Cinchona Alkaloids); 0 (Hydroxamic Acids)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171012
[Lr] Data última revisão:
171012
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160430
[St] Status:MEDLINE


  3 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26955754
[Au] Autor:Grecsó N; Kohout M; Carotti A; Sardella R; Natalini B; Fülöp F; Lindner W; Péter A; Ilisz I
[Ad] Endereço:Department of Inorganic and Analytical Chemistry, University of Szeged, H-6720 Szeged, Dóm tér 7, Hungary; Institute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Eötvös u. 6, Hungary.
[Ti] Título:Mechanistic considerations of enantiorecognition on novel Cinchona alkaloid-based zwitterionic chiral stationary phases from the aspect of the separation of trans-paroxetine enantiomers as model compounds.
[So] Source:J Pharm Biomed Anal;124:164-73, 2016 May 30.
[Is] ISSN:1873-264X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The enantiomers of trans-paroxetine were separated on four chiral stationary phases (CSPs) based on chiral zwitterionic Cinchona alkaloids fused with (R,R)- or (S,S)-trans-2-aminocyclohexanesulfonic acid. The enantioseparations were carried out in polar-ionic or in hydro-organic mobile phases with MeOH/THF, MeCN/THF, MeCN/THF/H2O and MeOH/MeCN/THF containing organic acid and base additives, in the temperature range 0-50°C. The effects of the mobile phase composition, the natures and concentrations of the additives and temperature on the separations were investigated. Thermodynamic parameters were calculated from plots of ln α vs 1/T. Δ(ΔH°) ranged between -3.0 and +1.5 kJ mol(-1), and Δ(ΔS°) between -8.8 and +5.9 J mol(-1)K(-1). The enantioseparation was generally enthalpically controlled, the retention factor and separation factor decreasing with increasing temperature, but entropically controlled separation was also observed. The elution sequences of the paroxetine enantiomers on the two pairs of pseudo-enantiomeric CSPs were investigated, and an attempt was made to explain the observed anomalies in silico in order to gain an insight into the underlying molecular recognition events between the four chiral selectors and the analyte enantiomers.
[Mh] Termos MeSH primário: Alcaloides de Cinchona/química
Modelos Químicos
Paroxetina/química
[Mh] Termos MeSH secundário: Estereoisomerismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Cinchona Alkaloids); 41VRH5220H (Paroxetine)
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170110
[Lr] Data última revisão:
170110
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160310
[St] Status:MEDLINE


  4 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26914694
[Au] Autor:Schettini R; De Riccardis F; Della Sala G; Izzo I
[Ad] Endereço:Dipartimento di Chimica e Biologia "A. Zambelli", Università degli Studi di Salerno , Via Giovanni Paolo II 132, 84084 Fisciano, SA, Italy.
[Ti] Título:Enantioselective Alkylation of Amino Acid Derivatives Promoted by Cyclic Peptoids under Phase-Transfer Conditions.
[So] Source:J Org Chem;81(6):2494-505, 2016 Mar 18.
[Is] ISSN:1520-6904
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The effects of substituents and cavity size on catalytic efficiency of proline-rich cyclopeptoids under phase-transfer conditions were studied. High affinity constants (Ka) for the sodium and potassium cations, comparable to those reported for crown ethers, were observed for an alternated N-benzylglycine/L-proline hexameric cyclopeptoid. This compound was found to catalyze the alkylation of N-(diphenylmethylene)glycine cumyl ester in values of enantioselectivities comparable with those reported for the Cinchona alkaloid ammonium salts derivatives (83-96% ee), and with lower catalyst loading (1-2.5% mol), in the presence of a broad range of benzyl, allyl and alkyl halides.
[Mh] Termos MeSH primário: Arginina/química
Derivados de Benzeno/química
Alcaloides de Cinchona/química
Glicina/análogos & derivados
Peptídeos Cíclicos/química
Prolina/química
[Mh] Termos MeSH secundário: Alquilação
Glicina/química
Estrutura Molecular
Prolina/análogos & derivados
Estereoisomerismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Benzene Derivatives); 0 (Cinchona Alkaloids); 0 (N-(diphenylmethylene)glycine cumyl ester); 0 (N-benzylglycine); 0 (Peptides, Cyclic); 94ZLA3W45F (Arginine); 9DLQ4CIU6V (Proline); TE7660XO1C (Glycine)
[Em] Mês de entrada:1609
[Cu] Atualização por classe:160318
[Lr] Data última revisão:
160318
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160226
[St] Status:MEDLINE
[do] DOI:10.1021/acs.joc.6b00065


  5 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26902149
[Au] Autor:Poudel PP; Arimitsu K; Yamamoto K
[Ad] Endereço:Department of Chemistry and Biochemistry, University of Toledo, 2801 W. Bancroft St., Toledo, OH 43606, USA. kana.yamamoto@utoledo.edu.
[Ti] Título:Self-assembled ion-pair organocatalysis--asymmetric Baeyer-Villiger oxidation mediated by flavinium-cinchona alkaloid dimer.
[So] Source:Chem Commun (Camb);52(22):4163-6, 2016 Mar 18.
[Is] ISSN:1364-548X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:An ion-pair catalyst generated by assembly of a chiral flavinium and a cinchona alkaloid dimer for use in asymmetric Baeyer-Villiger oxidation is presented. Ion-pair formation is essential for enhancing the catalytic activity and stereoselectivity. The catalyst is applicable to structurally diverse 3-substituted cyclobutanones, providing good to excellent enantioselectivities (up to 98 : 2 e.r.). This study provides the first example of self-assembly of a flavin derivative and a base to form a chiral reaction site that enables a highly stereoselective reaction to occur.
[Mh] Termos MeSH primário: Alcaloides de Cinchona/química
Flavonas/química
[Mh] Termos MeSH secundário: Catálise
Dimerização
Íons
Oxirredução
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Cinchona Alkaloids); 0 (Flavones); 0 (Ions)
[Em] Mês de entrada:1611
[Cu] Atualização por classe:161230
[Lr] Data última revisão:
161230
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160224
[St] Status:MEDLINE
[do] DOI:10.1039/c6cc00663a


  6 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:26895817
[Au] Autor:Klein W; Pieters T
[Ti] Título:The Hidden History of a Famous Drug: Tracing the Medical and Public Acculturation of Peruvian Bark in Early Modern Western Europe (c. 1650-1720).
[So] Source:J Hist Med Allied Sci;71(4):400-421, 2016 Oct.
[Is] ISSN:1468-4373
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:The history of the introduction of exotic therapeutic drugs in early modern Europe is usually rife with legend and obscurity and Peruvian bark is a case in point. The famous antimalarial drug entered the European medical market around 1640, yet it took decades before the bark was firmly established in pharmaceutical practice. This article argues that the history of Peruvian bark can only be understood as the interplay of its trajectories in science, commerce, and society. Modern research has mostly focused on the first of these, largely due to the abundance of medico-historical data. While appreciating these findings, this article proposes to integrate the medical trajectory in a richer narrative, by drawing particular attention to the acculturation of the bark in commerce and society. Although the evidence we have for these two trajectories is still sketchy and disproportionate, it can nevertheless help us to make sense of sources that have not yet been an obvious focus of research. Starting from an apparently isolated occurrence of the drug in a letter, this article focuses on Paris as the location where medical and public appreciation of the bark took shape, by exploring several contexts of knowledge circulation and medical practice there. These contexts provide a new window on the early circulation of knowledge of the bark, at a time when its eventual acceptance was by no means certain.
[Mh] Termos MeSH primário: Antimaláricos/história
Antimaláricos/uso terapêutico
Alcaloides de Cinchona/história
Alcaloides de Cinchona/uso terapêutico
Malária/tratamento farmacológico
Fitoterapia/história
[Mh] Termos MeSH secundário: Cinchona/química
Europa (Continente)
História do Século XVII
História do Século XVIII
Seres Humanos
[Pt] Tipo de publicação:HISTORICAL ARTICLE; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antimalarials); 0 (Cinchona Alkaloids)
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170713
[Lr] Data última revisão:
170713
[Sb] Subgrupo de revista:IM; QIS
[Da] Data de entrada para processamento:160221
[St] Status:MEDLINE


  7 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26881828
[Au] Autor:Li X; Su J; Liu Z; Zhu Y; Dong Z; Qiu S; Wang J; Lin L; Shen Z; Yan W; Wang K; Wang R
[Ad] Endereço:Institute of Pharmacology, Key Laboratory of Preclinical Study for New Drugs of Gansu Province, School of Basic, Medical Sciences, Lanzhou University , Lanzhou 730000, China.
[Ti] Título:Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block".
[So] Source:Org Lett;18(5):956-9, 2016 Mar 04.
[Is] ISSN:1523-7052
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:The ß-isocupreidine, a cinchonine derived alkaloid, catalyzed asymmetric SN2'-SN2' reaction between N-2,2,2-trifluoroethylisatin ketimines and MBH type carbonates was realized in a simple and efficient way. A series of chiral α-trifluoromethylamines were prepared with excellent yields and stereoselectivities. A subsequent and easy process of deprotection gave γ-trifluoromethyl-α-methylenelactam in a stereoselective manner.
[Mh] Termos MeSH primário: Etilaminas/síntese química
Hidroxiquinolinas/química
Quinuclidinas/química
[Mh] Termos MeSH secundário: Carbonatos/química
Catálise
Alcaloides de Cinchona/química
Etilaminas/química
Iminas/química
Estrutura Molecular
Nitrilos/química
Estereoisomerismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Carbonates); 0 (Cinchona Alkaloids); 0 (Ethylamines); 0 (Hydroxyquinolines); 0 (Imines); 0 (Nitriles); 0 (Quinuclidines); 0 (beta-isocupreidine); 0 (ketimine); 29010-16-0 (trifluoroethylamine); V43X79NZCD (cinchonine)
[Em] Mês de entrada:1608
[Cu] Atualização por classe:160304
[Lr] Data última revisão:
160304
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160217
[St] Status:MEDLINE
[do] DOI:10.1021/acs.orglett.5b03566


  8 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26785222
[Au] Autor:Grayson MN; Houk KN
[Ad] Endereço:Department of Chemistry and Biochemistry, University of California , Los Angeles, California 90095-1569, United States.
[Ti] Título:Cinchona Alkaloid-Catalyzed Asymmetric Conjugate Additions: The Bifunctional Brønsted Acid-Hydrogen Bonding Model.
[So] Source:J Am Chem Soc;138(4):1170-3, 2016 Feb 03.
[Is] ISSN:1520-5126
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Wynberg's report from 1977 that natural cinchona alkaloids catalyze the asymmetric conjugate addition of aromatic thiols to cycloalkenones is a landmark discovery in hydrogen bonding organocatalysis. Wynberg proposed that this reaction proceeded via the formation of a thiolate-alkylammonium tight ion pair and activation of the enone electrophile by a hydrogen bond from the catalyst's hydroxyl group. This reaction model provided the mechanistic basis for understanding Wynberg's reaction and many other asymmetric transformations since. Our quantum mechanical calculations reveal a different model should be used to explain the results: the alkylammonium ion activates the enone by Brønsted acid catalysis, and the catalyst's hydroxyl group orients the thiolate nucleophile. The new model rationalizes the stereoselective outcome of Wynberg's reaction and provides a new, general model for asymmetric cinchona organocatalysis.
[Mh] Termos MeSH primário: Alcaloides de Cinchona/metabolismo
Cinchona/química
Modelos Químicos
[Mh] Termos MeSH secundário: Catálise
Alcaloides de Cinchona/química
Ligações de Hidrogênio
Estrutura Molecular
Estereoisomerismo
Compostos de Sulfidrila
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T; RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.
[Nm] Nome de substância:
0 (Cinchona Alkaloids); 0 (Sulfhydryl Compounds)
[Em] Mês de entrada:1612
[Cu] Atualização por classe:161217
[Lr] Data última revisão:
161217
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160120
[St] Status:MEDLINE
[do] DOI:10.1021/jacs.5b13275


  9 / 495 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26645397
[Au] Autor:Maehara S; Agusta A; Kitamura C; Ohashi K; Shibuya H
[Ad] Endereço:Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Sanzo 1, Gakuen-cho, Fukuyama, Hiroshima, 729-0292, Japan. maehara@fupharm.fukuyama-u.ac.jp.
[Ti] Título:Composition of the endophytic filamentous fungi associated with Cinchona ledgeriana seeds and production of Cinchona alkaloids.
[So] Source:J Nat Med;70(2):271-5, 2016 Apr.
[Is] ISSN:1861-0293
[Cp] País de publicação:Japan
[La] Idioma:eng
[Ab] Resumo:Four kinds of endophytic filamentous fungi (code names: CLS-1, CLS-2, CLS-3, and CLS-4) associated with the seeds of Cinchona ledgeriana (Rubiaceae) from West Java, Indonesia, were isolated. All of the isolates were classified into Diaporthe spp. based on phylogenetic analysis of the nucleotide sequences of the internal transcribed spacers (ITS1 and ITS2) including the 5.8S ribosomal DNA region. All four of these endophytic fungi produce Cinchona alkaloids, mainly quinine and quinidine, in synthetic liquid medium.
[Mh] Termos MeSH primário: Ascomicetos/metabolismo
Alcaloides de Cinchona/metabolismo
Cinchona/microbiologia
Endófitos/metabolismo
Filogenia
Sementes/microbiologia
[Mh] Termos MeSH secundário: Ascomicetos/classificação
Ascomicetos/isolamento & purificação
Sequência de Bases
Cinchona/química
Endófitos/classificação
Endófitos/isolamento & purificação
Indonésia
Quinidina/metabolismo
Quinina/metabolismo
Sementes/química
Especificidade da Espécie
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Cinchona Alkaloids); A7V27PHC7A (Quinine); ITX08688JL (Quinidine)
[Em] Mês de entrada:1610
[Cu] Atualização por classe:171104
[Lr] Data última revisão:
171104
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151210
[St] Status:MEDLINE
[do] DOI:10.1007/s11418-015-0954-0


  10 / 495 MEDLINE  
              first record previous record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:26579982
[Au] Autor:Deka J; Satyanarayana L; Karunakar GV; Bhattacharyya PK; Bania KK
[Ad] Endereço:Department of Chemical Tezpur University, Assam, 784028, India. kusum@tezu.ernet.in.
[Ti] Título:Chiral modification of copper exchanged zeolite-Y with cinchonidine and its application in the asymmetric Henry reaction.
[So] Source:Dalton Trans;44(48):20949-63, 2015 Dec 28.
[Is] ISSN:1477-9234
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Chirally modified Cu(2+) exchanged zeolite-Y was synthesized by direct adsorption of cinchonidine under ambient conditions. The chirally modified materials were characterized using various spectrochemical and physicochemical techniques viz. BET, FTIR, MAS ((1)H and (13)C NMR), XPS, SEM, cyclic voltammetry and PXRD. Characteristic peaks of cinchonidine observed in the supported materials confirmed the adsorption of cinchonidine and its coordination with the Cu(2+) active site on copper exchanged zeolite-Y. (13)C SSNMR and XPS analysis however confirmed for the half encapsulation process, only the quinoline ring of cinchonidine gets coordinated to the internal metal sites via the N atom while the quinuclidine moiety extends out of the host surface. Cinchonidine supported Cu(2+)-Y zeolites were found to exhibit good catalytic performance in the asymmetric Henry reaction. (1)H SSNMR studies also confirmed the protonation of the N atom of the quinuclidine ring during the course of the Henry reaction. Heterogeneous chiral catalysts were effective for up to two consecutive cycles. Leaching of cinchonidine after the second cycle was found to have a negative result in the catalytic performance.
[Mh] Termos MeSH primário: Alcaloides de Cinchona/química
Cobre/química
Zeolitas/química
[Mh] Termos MeSH secundário: Técnicas Eletroquímicas
Espectroscopia de Ressonância Magnética
Modelos Moleculares
Espectroscopia Fotoeletrônica
Teoria Quântica
Espectroscopia de Infravermelho com Transformada de Fourier
Estereoisomerismo
[Pt] Tipo de publicação:JOURNAL ARTICLE; RESEARCH SUPPORT, NON-U.S. GOV'T
[Nm] Nome de substância:
0 (Cinchona Alkaloids); 1318-02-1 (Zeolites); 1U622LRA8Z (cinchonidine); 789U1901C5 (Copper)
[Em] Mês de entrada:1609
[Cu] Atualização por classe:151202
[Lr] Data última revisão:
151202
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151119
[St] Status:MEDLINE
[do] DOI:10.1039/c5dt03630e



página 1 de 50 ir para página                         
   


Refinar a pesquisa
  Base de dados : MEDLINE Formulário avançado   

    Pesquisar no campo  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde