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Corrigendum: Design of Aminobenzothiazole Inhibitors of Rho Kinases 1 and 2 by Using Protein Kinase a as a Structure Surrogate
ChemBioChem
Organic Chemistry
Biochemistry
Molecular Medicine
Molecular Biology
Synthesis and SAR Studies of 5-(Pyridin-4-Yl)-1,3,4-Thiadiazol-2-Amine Derivatives as Potent Inhibitors of Bloom Helicase
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
N-{(Z)-3-Oxo-3-[(E)-(Pyridin-2-Ylmethyl)diazenyl]-1-(Thiophen-2-Yl)prop-1-En-2-Yl}benzamide
IUCrData
[2-(Piperidin-1-Yl)ethylamine]dithiocyanatozinc(II)
Acta Crystallographica Section E Structure Reports Online
Palladium-Catalyzed Regioselective 2-Carbethoxyethylation of 1H– Indoles by C-H Activation: One-Step Synthesis of Ethyl 2-(1h-Indol-2-Yl) Acetates
Organic Chemistry: Current Research
(Z)-3-(Anthracen-9-Yl)-1-(2-Ethoxyphenyl)prop-2-En-1-One
Acta Crystallographica Section E Structure Reports Online
Design and Synthesis of Redox Stable Analogues of Sunflower Trypsin Inhibitors (SFTI-1) on Solid Support, Potent Inhibitors of Matriptase
(2,7-Dimethoxynaphthalen-1-Yl)(naphthalen-1-Yl)methanone
Acta Crystallographica Section E Structure Reports Online
Discovery and Metabolic Stabilization of Potent and Selective 2-Amino-N-(Adamant-2-Yl) Acetamide 11b-Hydroxysteroid Dehydrogenase Type 1 Inhibitors
Synthesis of 3-Hydroxy-6-Oxo[1, 2, 4]triazin-1-Yl Alaninamides, a New Class of Cyclic Dipeptidyl Ureas
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