207463-28-3Relevant articles and documents
Synthesis and BK channel-opening activity of 2-amino-1,3-thiazole derivatives
Cui, Yong-Mei,Ji, Tong-Tong,Jo, Heeji,Lin, Hai-Xia,Park, Chul-Seung,Qi, Xiao-Lei,Wang, Xue-Ying
supporting information, (2021/05/19)
A series of 2-amino-5-arylmethyl- or 5-heteroarylmethyl-1,3-thiazole derivatives were synthesized and evaluated for BK channel-opening activities in cell-based fluorescence assay and electrophysiological recording. The assay results indicated that the activities of the investigated compounds were influenced by the physicochemical properties of the substituent at benzene ring.
MODULATORS OF ATP-BINDING CASSETTE TRANSPORTERS
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Page/Page column 236; 243-244, (2010/02/11)
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Heterocyclic Syntheses on the Basis of Anionarylation Products of Unsaturated Compounds. I. 2-Amino-5-arylmethyl-1,3-thiazoles
Obushak,Matiichuk,Ganushchak
, p. 1010 - 1013 (2007/10/03)
3-Aryl-2-chloropropionaldehydes have been prepared by reactions of arenediazonium chlorides with acrolein in the presence of CuCl2. Reactions of these aldehydes with thiourea provide a convenient route to difficultly accessible 2-amino-5-arylme