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1,2,3‐Triazole Tagged 3H‐Pyrano[2,3‐d]pyrimidine‐6‐carboxylate Derivatives: Synthesis, in Vitro Cytotoxicity, Molecular Docking and DNA Interaction Studies
1,2,3‐Triazole Tagged 3H‐Pyrano[2,3‐d]pyrimidine‐6‐carboxylate Derivatives: Synthesis, in Vitro Cytotoxicity, Molecular Docking and DNA Interaction Studies
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1,2,3‐Triazole Tagged 3H‐Pyrano[2,3‐d]pyrimidine‐6‐carboxylate Derivatives: Synthesis, in Vitro Cytotoxicity, Molecular Docking and DNA Interaction Studies

Boda, Sathish Kumar ; Pishka, Vasantha ; Lakshmi, P. V. Anantha ; Chinde, Srinivas ; Grover, Paramjit

Chemistry & biodiversity, 2018-06, Vol.15 (6), p.e18000101-n/a [Periódico revisado por pares]

Switzerland: Wiley Subscription Services, Inc

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2
1,3-Disubstituted-4-Aminopyrazolo [3, 4-d] Pyrimidines, a New Class of Potent Inhibitors for Phospholipase D
1,3-Disubstituted-4-Aminopyrazolo [3, 4-d] Pyrimidines, a New Class of Potent Inhibitors for Phospholipase D
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1,3-Disubstituted-4-Aminopyrazolo [3, 4-d] Pyrimidines, a New Class of Potent Inhibitors for Phospholipase D

Kulkarni, Aditya ; Quang, Phong ; Curry, Victoriana ; Keyes, Renee ; Zhou, Weihong ; Cho, Hyejin ; Baffoe, Jonathan ; Török, Béla ; Stieglitz, Kimberly

Chemical biology & drug design, 2014-09, Vol.84 (3), p.270-281 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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3
(1)H,(13)C and (19)F NMR data of N-substituted 6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amines in DMSO-d(6)
(1)H,(13)C and (19)F NMR data of N-substituted 6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amines in DMSO-d(6)
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(1)H,(13)C and (19)F NMR data of N-substituted 6-(4-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amines in DMSO-d(6)

Sørum, Christopher ; Simić, Nebojsa ; Sundby, Eirik ; Hoff, Bård Helge

Magnetic resonance in chemistry, 2010-03, Vol.48 (3), p.244-248 [Periódico revisado por pares]

England

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4
2-Sulfonyliminodihydropyrimidines: A Novel Class of Analgesic Compounds
2-Sulfonyliminodihydropyrimidines: A Novel Class of Analgesic Compounds
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2-Sulfonyliminodihydropyrimidines: A Novel Class of Analgesic Compounds

González-Rosende, M. Eugenia ; Olivar, Teresa ; Castillo, Encarna ; Sepúlveda-Arques, José

Archiv der Pharmazie (Weinheim), 2008-11, Vol.341 (11), p.690-695 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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5
2,2′‐Bipyrimidine as Efficient Sensitizer of the Solid‐State Luminescence of Lanthanide and Uranyl Ions from Visible to Near‐Infrared
2,2′‐Bipyrimidine as Efficient Sensitizer of the Solid‐State Luminescence of Lanthanide and Uranyl Ions from Visible to Near‐Infrared
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2,2′‐Bipyrimidine as Efficient Sensitizer of the Solid‐State Luminescence of Lanthanide and Uranyl Ions from Visible to Near‐Infrared

Zucchi, Gaël ; Maury, Olivier ; Thuéry, Pierre ; Gumy, Frédéric ; Bünzli, Jean‐Claude G. ; Ephritikhine, Michel

Chemistry : a European journal, 2009-09, Vol.15 (38), p.9686-9696 [Periódico revisado por pares]

Weinheim: WILEY‐VCH Verlag

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6
(2E)‐3‐(6‐Methoxynaphthalen‐2‐yl)‐1‐(pyridin‐3‐yl)prop‐2‐en‐1‐one and its cyclocondensation product with guanidine, (4RS)‐2‐amino‐4‐(6‐methoxynaphthalen‐2‐yl)‐6‐(pyridin‐3‐yl)‐3,4‐dihydropyrimidine monohydrate: two types of hydrogen‐bonded sheet
(2E)‐3‐(6‐Methoxynaphthalen‐2‐yl)‐1‐(pyridin‐3‐yl)prop‐2‐en‐1‐one and its cyclocondensation product with guanidine, (4RS)‐2‐amino‐4‐(6‐methoxynaphthalen‐2‐yl)‐6‐(pyridin‐3‐yl)‐3,4‐dihydropyrimidine monohydrate: two types of hydrogen‐bonded sheet
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(2E)‐3‐(6‐Methoxynaphthalen‐2‐yl)‐1‐(pyridin‐3‐yl)prop‐2‐en‐1‐one and its cyclocondensation product with guanidine, (4RS)‐2‐amino‐4‐(6‐methoxynaphthalen‐2‐yl)‐6‐(pyridin‐3‐yl)‐3,4‐dihydropyrimidine monohydrate: two types of hydrogen‐bonded sheet

Nayak, Prakash S. ; Narayana, Badiadka ; Yathirajan, Hemmige S. ; Hosten, Eric C. ; Betz, Richard ; Glidewell, Christopher

Acta crystallographica. Section C, Crystal structure communications, 2014-11, Vol.70 (11), p.1011-1016 [Periódico revisado por pares]

5 Abbey Square, Chester, Cheshire CH1 2HU, England: International Union of Crystallography

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7
2’,3’‐Protected Nucleotides as Building Blocks for Enzymatic de novo RNA Synthesis
2’,3’‐Protected Nucleotides as Building Blocks for Enzymatic de novo RNA Synthesis
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2’,3’‐Protected Nucleotides as Building Blocks for Enzymatic de novo RNA Synthesis

Pichon, Maëva ; Levi‐Acobas, Fabienne ; Kitoun, Camélia ; Hollenstein, Marcel

Chemistry : a European journal, 2024-04, Vol.30 (24), p.e202400137-n/a [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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8
3‐Aminopyrazolo[3,4‐b]pyridine: Effective Precursor for Barium Hydroxide‐Mediated Three Components Synthesis of New Mono‐ and Bis(pyrimidines) with Potential Cytotoxic Activity
3‐Aminopyrazolo[3,4‐b]pyridine: Effective Precursor for Barium Hydroxide‐Mediated Three Components Synthesis of New Mono‐ and Bis(pyrimidines) with Potential Cytotoxic Activity
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3‐Aminopyrazolo[3,4‐b]pyridine: Effective Precursor for Barium Hydroxide‐Mediated Three Components Synthesis of New Mono‐ and Bis(pyrimidines) with Potential Cytotoxic Activity

Sanad, Sherif M. H. ; Mekky, Ahmed E. M.

Chemistry & biodiversity, 2022-01, Vol.19 (1), p.e202100500-n/a [Periódico revisado por pares]

Switzerland

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9
3,3'-Dihydroxyisorenieratene, a Natural Carotenoid with Superior Antioxidant and Photoprotective Properties
3,3'-Dihydroxyisorenieratene, a Natural Carotenoid with Superior Antioxidant and Photoprotective Properties
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3,3'-Dihydroxyisorenieratene, a Natural Carotenoid with Superior Antioxidant and Photoprotective Properties

Martin, Hans-Dieter ; Kock, Sebastian ; Scherrers, Roger ; Lutter, Kaya ; Wagener, Tanja ; Hundsdörfer, Claas ; Frixel, Susanne ; Schaper, Klaus ; Ernst, Hansgeorg ; Schrader, Wolfgang ; Görner, Helmut ; Stahl, Wilhelm

Angewandte Chemie (International ed.), 2009-01, Vol.48 (2), p.400-403 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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10
3D-QSAR Studies on the Inhibitory Activity of Trimethoprim Analogues against Escherichia coli Dihydrofolate Reductase
3D-QSAR Studies on the Inhibitory Activity of Trimethoprim Analogues against Escherichia coli Dihydrofolate Reductase
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3D-QSAR Studies on the Inhibitory Activity of Trimethoprim Analogues against Escherichia coli Dihydrofolate Reductase

Vijayaraj, Ramadoss ; Lakshmi Vasavi Devi, Mekapothula ; Subramanian, Venkatesan ; Chattaraj, Pratim Kumar

Chemical biology & drug design, 2012-06, Vol.79 (6), p.935-942 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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