Juranic Ivan (23 results)

Condition: New.

PAP. Condition: New. New Book. Shipped from UK. Established seller since 2000.

Condition: New.

Condition: New.

Taschenbuch. Condition: Neu. Synthesis and QSAR of thia-Derivatives of Aroylacrylic Acids | Medicinal Chemistry Modeling of Protein-Ligand Interactions | Ivan Juranic (u. a.) | Taschenbuch | 292 S. | Englisch | 2017 | Scholars' Press | EAN 9783330653610 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

Taschenbuch. Condition: Neu. Synthesis and QSAR of thia-Derivatives of Aroylacrylic Acids | Medicinal Chemistry Modeling of Protein-Ligand Interactions2nd Edition | Ivan Juranic (u. a.) | Taschenbuch | Englisch | 2025 | Scholars' Press | EAN 9786209088827 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.

Paperback. Condition: Brand New. 292 pages. 8.66x5.91x0.66 inches. In Stock.

Condition: New. Print on Demand.

Condition: New. PRINT ON DEMAND.

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Dilber SandaSanda Dilber (maid. Jovanovic), is born 1953. in Novi Becej, by father Paja and mother Nevenka Jovanovic. Since 1983. is employed at Faculty of Pharmacy, University of Belgrade, starting as a teaching associate, now is th.

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Syntheses of thirty-one aroylacrylic acids, twenty-seven 2-[(carboxymethyl)sulfanyl]-4-oxo-4-arylbutanoic acids (CSAB), three 2-[(2-carboxyethyl)sulfanyl]-4-oxo-4-arylbutanoic acids, one 2-[(1-carboxyethylsulfanyl]-4-oxo-4-arylbutanoic acid, one 2-[(2-methoxy-2-oxoethyl)sulfanyl]-4-oxo-4-arylbutanoic acid and one 2-ethoxycarbonylmethylsulfanyl]-4-oxo-4-arylbutanoic acid, are described. Conformational preferences of CSAB in polar and non-polar solvents, DMSO and chloroform, are examined. Analysis of conformational preferences in solution (NAMFIS analysis) is performed, using 1H NMR, NOESY, J-HMBC spectra, and conformational assemblies of compound obtained by CS in Macro Model and OMEGA. Most abound conformers in non-polar chloroform have an extended shape - largest part of apolar surface area of molecules are exposed to solvent. Advantages of methods based on 3D structure of compounds for the estimation of n-octanol/water partition coefficients (logP values) are briefly outlined. In 'extended' conformations divalent S atom could form non-covalent intermolecular interactions with other heteroatoms (O, N) in closest proximity. 292 pp. Englisch.

Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Juranic IvanIvan Juranic is retired professor of the Faculty of Chemistry, University of Belgrade, Serbia. He is still active in research and in coaching of PhD students. He has over 150 published research papers, and several patents.

Condition: New. Print on Demand.

Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 292 pp. Englisch.

Condition: New. PRINT ON DEMAND.

Paperback. Condition: new. Paperback. Syntheses of thirty-one aroylacrylic acids, twenty-seven 2-[(carboxymethyl)sulfanyl]-4-oxo-4-arylbutanoic acids (CSAB), three 2-[(2-carboxyethyl)sulfanyl]-4-oxo-4-arylbutanoic acids, one 2-[(1-carboxyethylsulfanyl]-4-oxo-4-arylbutanoic acid, one 2-[(2-methoxy-2-oxoethyl)sulfanyl]-4-oxo-4-arylbutanoic acid and one 2-ethoxycarbonylmethylsulfanyl]-4-oxo-4-arylbutanoic acid, are described. Conformational preferences of CSAB in polar and non-polar solvents, DMSO and chloroform, are examined. Analysis of conformational preferences in solution (NAMFIS analysis) is performed, using 1H NMR, NOESY, J-HMBC spectra, and conformational assemblies of compound obtained by CS in Macro Model and OMEGA. Most abound conformers in non-polar chloroform have an extended shape - largest part of apolar surface area of molecules are exposed to solvent. Advantages of methods based on 3D structure of compounds for the estimation of n-octanol/water partition coefficients (logP values) are briefly outlined. In 'extended' conformations divalent S atom could form non-covalent intermolecular interactions with other heteroatoms (O, N) in closest proximity. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Syntheses of thirty-one aroylacrylic acids, twenty-seven 2-[(carboxymethyl)sulfanyl]-4-oxo-4-arylbutanoic acids (CSAB), three 2-[(2-carboxyethyl)sulfanyl]-4-oxo-4-arylbutanoic acids, one 2-[(1-carboxyethylsulfanyl]-4-oxo-4-arylbutanoic acid, one 2-[(2-methoxy-2-oxoethyl)sulfanyl]-4-oxo-4-arylbutanoic acid and one 2-ethoxycarbonylmethylsulfanyl]-4-oxo-4-arylbutanoic acid, are described. Conformational preferences of CSAB in polar and non-polar solvents, DMSO and chloroform, are examined. Analysis of conformational preferences in solution (NAMFIS analysis) is performed, using 1H NMR, NOESY, J-HMBC spectra, and conformational assemblies of compound obtained by CS in Macro Model and OMEGA. Most abound conformers in non-polar chloroform have an extended shape - largest part of apolar surface area of molecules are exposed to solvent. Advantages of methods based on 3D structure of compounds for the estimation of n-octanol/water partition coefficients (logP values) are briefly outlined. In 'extended' conformations divalent S atom could form non-covalent intermolecular interactions with other heteroatoms (O, N) in closest proximity.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 292 pp. Englisch.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Syntheses of thirty-one aroylacrylic acids, twenty-seven 2-[(carboxymethyl)sulfanyl]-4-oxo-4-arylbutanoic acids (CSAB), three 2-[(2-carboxyethyl)sulfanyl]-4-oxo-4-arylbutanoic acids, one 2-[(1-carboxyethylsulfanyl]-4-oxo-4-arylbutanoic acid, one 2-[(2-methoxy-2-oxoethyl)sulfanyl]-4-oxo-4-arylbutanoic acid and one 2-ethoxycarbonylmethylsulfanyl]-4-oxo-4-arylbutanoic acid, are described. Conformational preferences of CSAB in polar and non-polar solvents, DMSO and chloroform, are examined. Analysis of conformational preferences in solution (NAMFIS analysis) is performed, using 1H NMR, NOESY, J-HMBC spectra, and conformational assemblies of compound obtained by CS in Macro Model and OMEGA. Most abound conformers in non-polar chloroform have an extended shape - largest part of apolar surface area of molecules are exposed to solvent. Advantages of methods based on 3D structure of compounds for the estimation of n-octanol/water partition coefficients (logP values) are briefly outlined. In 'extended' conformations divalent S atom could form non-covalent intermolecular interactions with other heteroatoms (O, N) in closest proximity.

Taschenbuch. Condition: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Syntheses of thirty-one aroylacrylic acids, twenty-seven 2-[(carboxymethyl)sulfanyl]-4-oxo-4-arylbutanoic acids (CSAB), three 2-[(2-carboxyethyl)sulfanyl]-4-oxo-4-arylbutanoic acids, one 2-[(1-carboxyethylsulfanyl]-4-oxo-4-arylbutanoic acid, one 2-[(2-methoxy-2-oxoethyl)sulfanyl]-4-oxo-4-arylbutanoic acid and one 2-ethoxycarbonylmethylsulfanyl]-4-oxo-4-arylbutanoic acid, are described. Conformational preferences of CSAB in polar and non-polar solvents, DMSO and chloroform, are examined. Analysis of conformational preferences in solution (NAMFIS analysis) is performed, using 1H NMR, NOESY, J-HMBC spectra, and conformational assemblies of compound obtained by CS in Macro Model and OMEGA. Most abound conformers in non-polar chloroform have an extended shape - largest part of apolar surface area of molecules are exposed to solvent. Advantages of methods based on 3D structure of compounds for the estimation of n-octanol/water partition coefficients (logP values) are briefly outlined. In 'extended' conformations divalent S atom could form non-covalent intermolecular interactions with other heteroatoms (O, N) in closest proximity.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 292 pp. Englisch.

Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering.

Condition: New. Print on Demand.

Condition: New. Print on Demand.

Condition: New. PRINT ON DEMAND.