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FEBS Journal, ISSN 1742-464X, 06/2009, Volume 276, Issue 12, pp. 3256 - 3268
Thiamine and its three phosphorylated derivatives (mono-, di- and triphosphate) occur naturally in most cells. Recently, we reported the presence of a fourth... 
Adenosine hiamine riphosphate | Nucleotides | Metabolism | Adenosine thiamine diphosphate | Cofactor | adenosine thiamine diphosphate | DIPHOSPHATE | BIOCHEMISTRY & MOLECULAR BIOLOGY | cofactor | PHOSPHATE-ESTERS | ESCHERICHIA-COLI | CYTOSOLIC ADENYLATE KINASE | PERFORMANCE LIQUID-CHROMATOGRAPHY | adenosine thiamine triphosphate | TRIPHOSPHATE | OLIGOPHOSPHATES | metabolism | TISSUES | STRESS | nucleotides | Thiamine Pyrophosphate - analysis | Adenine - chemical synthesis | Myocardium - chemistry | Thiamine Pyrophosphate - chemistry | Adenosine Diphosphate - chemical synthesis | Humans | Adenine - analysis | Adenosine Diphosphate - chemistry | Thiamine Triphosphate - chemistry | Chromatography, High Pressure Liquid | Adenine - chemistry | Thiamine Triphosphate - analysis | Spectrometry, Mass, Electrospray Ionization | Adenosine Triphosphate - chemical synthesis | Muscle, Skeletal - chemistry | Thiamine Triphosphate - chemical synthesis | Molecular Structure | Fibroblasts - chemistry | Adenine - analogs & derivatives | Magnetic Resonance Spectroscopy | Adenosine Triphosphate - analysis | Models, Molecular | Spectrometry, Fluorescence | Thiamine Pyrophosphate - chemical synthesis | Escherichia coli - chemistry | Quail | Adenosine Diphosphate - analysis | Liver - chemistry | Animals | Cell Line, Tumor | Kidney - chemistry | Brain Chemistry | Mice | Adenosine Triphosphate - chemistry | 3T3 Cells | Purines | Pyrimidines | Analysis | Escherichia coli | Water quality | Chemical properties | Chemical synthesis | Enzymes | Biochemistry | Cellular biology | Molecular biology | Index Medicus
Journal Article
ChemMedChem, ISSN 1860-7179, 04/2017, Volume 12, Issue 7, pp. 487 - 501
Sulfoximines have gained considerable recognition as an important structural motif in drug discovery of late. In particular, the clinical kinase inhibitors for... 
kinase inhibitors | pharmacophores | sulfoximines | drug design | medicinal chemistry | PHOSPHODIESTERASE-5 INHIBITORS | CHEMISTRY, MEDICINAL | ASYMMETRIC-SYNTHESIS | DIELS-ALDER REACTIONS | DEPENDENT KINASE INHIBITOR | BREAST-CANCER | POTENT INHIBITOR | STRUCTURAL BASIS | CDK4/6 INHIBITOR | PHARMACOLOGY & PHARMACY | ERECTILE DYSFUNCTION | Estradiol - analogs & derivatives | Sulfoxides - chemical synthesis | Cyclin-Dependent Kinases - metabolism | Ataxia Telangiectasia Mutated Proteins - metabolism | Imatinib Mesylate - chemical synthesis | Pyrazoles - chemical synthesis | Pyridines - chemistry | Imatinib Mesylate - metabolism | Piperazines - metabolism | Piperazines - chemistry | Aminopyridines - metabolism | Fulvestrant | Aminopyridines - chemistry | Protein Kinase Inhibitors - chemistry | Pyrazoles - chemistry | Vardenafil Dihydrochloride - chemistry | Drug Design | Ataxia Telangiectasia Mutated Proteins - antagonists & inhibitors | Cyclin-Dependent Kinases - antagonists & inhibitors | Purines - chemical synthesis | Estradiol - metabolism | Protein Kinase Inhibitors - chemical synthesis | Piperidines - chemistry | Piperidines - metabolism | Purines - metabolism | Pyridines - chemical synthesis | Pyrazoles - metabolism | Piperidines - chemical synthesis | Imatinib Mesylate - chemistry | Vardenafil Dihydrochloride - metabolism | Aminopyridines - chemical synthesis | Sulfoxides - chemistry | Estradiol - chemistry | Purines - chemistry | Pyridines - metabolism | Vardenafil Dihydrochloride - chemical synthesis | Sulfoxides - metabolism | Piperazines - chemical synthesis | Estradiol - chemical synthesis | Protein Kinase Inhibitors - metabolism | Drug discovery | Chemical properties | Pharmaceutical industry | Index Medicus | Full Paper | Full Papers
Journal Article
Journal Article
Current Protocols in Nucleic Acid Chemistry, ISSN 1934-9270, 06/2012, Volume Chapter 13, Issue 49, p. Unit13.10
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 2005, Volume 33, Issue 18, pp. 5771 - 5780
Oxanine (Oxa, O), one of the major damaged bases from guanine generated by NO- or HNO2-induced nitrosative deamination, has been considered as a mutagen-potent... 
BIOCHEMISTRY & MOLECULAR BIOLOGY | Thermodynamics | Purine Nucleosides - chemical synthesis | Base Pairing | Oligodeoxyribonucleotides - chemical synthesis | Oligodeoxyribonucleotides - chemistry | Purine Nucleosides - chemistry | Index Medicus
Journal Article
Journal Article
Organic Letters, ISSN 1523-7060, 02/2000, Volume 2, Issue 3, pp. 293 - 295
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 03/2009, Volume 52, Issue 5, pp. 1486 - 1490
Journal Article
Current Medicinal Chemistry, ISSN 0929-8673, 03/2006, Volume 13, Issue 5, pp. 539 - 545
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 04/2017, Volume 82, Issue 7, pp. 3552 - 3560
Arylated nucleobases were synthesized by visible light photocatalysis using rhodamine 6G as photoredox catalyst and N,N-diisopropylethylamine as sacrificial... 
H BOND ACTIVATION | ORGANIC-SYNTHESIS | HETEROARENES | BASES | PURINE | ARENES | PYRIMIDINE NUCLEOSIDES | CHEMISTRY, ORGANIC | RADICALS | URACIL | DERIVATIVES | Arylation | Oxidation-reduction reaction | Usage | Catalysis | Chemical synthesis
Journal Article
Journal Article
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 02/2014, Volume 57, Issue 3, pp. 1097 - 1110
Journal Article