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Refinado por: materia: Structure Activity Relationship eliminar
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1
The steric factor in medicinal chemistry dissymmetric probes of pharmacological receptors
The steric factor in medicinal chemistry dissymmetric probes of pharmacological receptors
Material Type:
Libro 		Añadir a Mi Portal

The steric factor in medicinal chemistry dissymmetric probes of pharmacological receptors

Alan F. Casy George H Dewar

New York Plenum Press c1993

Disponible en FCFRP - Fac. Ciên. Farm. Ribeirão Preto    (541.63 C356s )(Obténgalo)

2
Chirality and the biological activity of drugs
Chirality and the biological activity of drugs
Material Type:
Libro 		Añadir a Mi Portal

Chirality and the biological activity of drugs

Roger Crossley 1947-

Boca Raton CRC Press c1995

Disponible en CQ - Conjunto das Químicas    (615.19 C951c ) y otras localizaciones(Obténgalo)

3
Models for the modern power grid
Models for the modern power grid
Material Type:
Artículo 		Añadir a Mi Portal

Models for the modern power grid

Cardieri, Paulo, 1964- Universidade Estadual de Campinas (Unicamp); Universidade Estadual De Campinas

https://repositorio.unicamp.br/acervo/detalhe/1191204

2014

Acceso en línea

4
Non-covalent NRF2 Activation Confers Greater Cellular Protection than Covalent Activation
Non-covalent NRF2 Activation Confers Greater Cellular Protection than Covalent Activation
Material Type:
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Non-covalent NRF2 Activation Confers Greater Cellular Protection than Covalent Activation

Liu, Pengfei ; Tian, Wang ; Tao, Shasha ; Tillotson, Joseph ; Wijeratne, E.M. Kithsiri ; Gunatilaka, A.A. Leslie ; Zhang, Donna D. ; Chapman, Eli

Cell chemical biology, 2019-10, Vol.26 (10), p.1427-1435.e5 [Revista revisada por pares]

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5
Impact of the structure-activity relationship of AHL analogues on quorum sensing in Gram-negative bacteria
Impact of the structure-activity relationship of AHL analogues on quorum sensing in Gram-negative bacteria
Material Type:
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Impact of the structure-activity relationship of AHL analogues on quorum sensing in Gram-negative bacteria

Chbib, Christiane

Bioorganic & medicinal chemistry, 2020-02, Vol.28 (3), p.115282-115282, Article 115282 [Revista revisada por pares]

England: Elsevier Ltd

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6
Further Insights on Structural Modifications of Muramyl Dipeptides to Study the Human NOD2 Stimulating Activity
Further Insights on Structural Modifications of Muramyl Dipeptides to Study the Human NOD2 Stimulating Activity
Material Type:
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Further Insights on Structural Modifications of Muramyl Dipeptides to Study the Human NOD2 Stimulating Activity

Cheng, Wei‐Chieh ; You, Ting‐Yun ; Teo, Zhen‐Zhuo ; Sayyad, Ashik A. ; Maharana, Jitendra ; Guo, Chih‐Wei ; Liang, Pi‐Hui ; Lin, Chung‐Shun ; Meng, Fan‐Chun

Chemistry, an Asian journal, 2020-11, Vol.15 (22), p.3836-3844 [Revista revisada por pares]

Germany: Wiley Subscription Services, Inc

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7
Discovery of new nanomolar inhibitors of GPa: Extension of 2-oxo-1,2-dihydropyridinyl-3-yl amide-based GPa inhibitors
Discovery of new nanomolar inhibitors of GPa: Extension of 2-oxo-1,2-dihydropyridinyl-3-yl amide-based GPa inhibitors
Material Type:
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Discovery of new nanomolar inhibitors of GPa: Extension of 2-oxo-1,2-dihydropyridinyl-3-yl amide-based GPa inhibitors

Loughlin, Wendy A. ; Jenkins, Ian D. ; Karis, N. David ; Healy, Peter C.

European journal of medicinal chemistry, 2017-02, Vol.127, p.341-356 [Revista revisada por pares]

France: Elsevier Masson SAS

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8
P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellular localization and drug efficiency
P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellular localization and drug efficiency
Material Type:
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P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellular localization and drug efficiency

Barz, Matthias ; Armiñán, Ana ; Canal, Fabiana ; Wolf, Florian ; Koynov, Kaloian ; Frey, Holger ; Zentel, Rudolf ; Vicent, María J.

Journal of controlled release, 2012-10, Vol.163 (1), p.63-74 [Revista revisada por pares]

Kidlington: Elsevier B.V

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9
Three-Dimensional Quantitative Structure–Activity Relationship Analysis for Human Pregnane X Receptor for the Prediction of CYP3A4 Induction in Human Hepatocytes: Structure-Based Comparative Molecular Field Analysis
Three-Dimensional Quantitative Structure–Activity Relationship Analysis for Human Pregnane X Receptor for the Prediction of CYP3A4 Induction in Human Hepatocytes: Structure-Based Comparative Molecular Field Analysis
Material Type:
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Three-Dimensional Quantitative Structure–Activity Relationship Analysis for Human Pregnane X Receptor for the Prediction of CYP3A4 Induction in Human Hepatocytes: Structure-Based Comparative Molecular Field Analysis

Handa, Koichi ; Nakagome, Izumi ; Yamaotsu, Noriyuki ; Gouda, Hiroaki ; Hirono, Shuichi

Journal of pharmaceutical sciences, 2015-01, Vol.104 (1), p.223-232 [Revista revisada por pares]

United States: Elsevier Inc

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10
New insight into adenosine receptors selectivity derived from a novel series of [5-substituted-4-phenyl-1,3-thiazol-2-yl] benzamides and furamides
New insight into adenosine receptors selectivity derived from a novel series of [5-substituted-4-phenyl-1,3-thiazol-2-yl] benzamides and furamides
Material Type:
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New insight into adenosine receptors selectivity derived from a novel series of [5-substituted-4-phenyl-1,3-thiazol-2-yl] benzamides and furamides

Inamdar, Gajanan S. ; Pandya, Amit N. ; Thakar, Hardik M. ; Sudarsanam, Vasudevan ; Kachler, Sonja ; Sabbadin, Davide ; Moro, Stefano ; Klotz, Karl-Norbert ; Vasu, Kamala K.

European journal of medicinal chemistry, 2013-05, Vol.63, p.924-934 [Revista revisada por pares]

France: Elsevier Masson SAS

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por este autor/creador:

  1. Okoshi, M
  2. Bandarra, E
  3. Okoshi, K
  4. Corrêa, L
  5. Nobrega, M

con este tema:

  1. Molecular Conformation
  2. Structure Activity Relationship
  3. Structure Activity Relationship
  4. Science & Technology
  5. Life Sciences & Biomedicine

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