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Literature DB >> 5654216

Antimalarials. 3. Benzothiazole amino alcohols.

A Burger, S N Sawhney.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 1968 PMID： 5654216 DOI： 10.1021/jm00308a018

Source DB: PubMed Journal: J Med Chem ISSN： 0022-2623 Impact factor: 7.446

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8 in total

1. DNA Binding, Cleavage and Antibacterial Activity of Mononuclear Cu(II), Ni(II) and Co(II) Complexes Derived from Novel Benzothiazole Schiff Bases.

Authors: Narendrula Vamsikrishna; Marri Pradeep Kumar; Somapangu Tejaswi; Aveli Rambabu
Journal: J Fluoresc Date: 2016-05-11 Impact factor: 2.217

Review 2. An epigrammatic status of the 'azole'-based antimalarial drugs.

Authors: Mousmee Sharma; Parteek Prasher
Journal: RSC Med Chem Date: 2019-12-23

3. Development of novel apoferritin formulations for antitumour benzothiazoles.

Authors: Alastair F Breen; Geoffrey Wells; Lyudmila Turyanska; Tracey D Bradshaw
Journal: Cancer Rep (Hoboken) Date: 2019-01-16

4. 2-(4-Amino-phen-yl)-1,3-benzothia-zole.

Authors: Yong Zhang; Zhen-Hong Su; Qing-Zhi Wang; Lei Teng
Journal: Acta Crystallogr Sect E Struct Rep Online Date: 2008-10-04

5. Synthesis of benzo[d]thiazole-hydrazone analogues: molecular docking and SAR studies of potential H⁺/K⁺ ATPase inhibitors and anti-inflammatory agents.

Authors: Shi-Meng Wang; Gao-Feng Zha; K P Rakesh; N Darshini; T Shubhavathi; H K Vivek; N Mallesha; Hua-Li Qin
Journal: Medchemcomm Date: 2017-04-26 Impact factor: 3.597

Antimalarials. 3. Benzothiazole amino alcohols.

1. DNA Binding, Cleavage and Antibacterial Activity of Mononuclear Cu(II), Ni(II) and Co(II) Complexes Derived from Novel Benzothiazole Schiff Bases.

Review 2. An epigrammatic status of the 'azole'-based antimalarial drugs.

3. Development of novel apoferritin formulations for antitumour benzothiazoles.

4. 2-(4-Amino-phen-yl)-1,3-benzothia-zole.

5. Synthesis of benzo[d]thiazole-hydrazone analogues: molecular docking and SAR studies of potential H⁺/K⁺ ATPase inhibitors and anti-inflammatory agents.

6. 5-Chloro-2-(3,4,5-trimeth-oxy-phen-yl)-1,3-benzothia-zole.

7. 5-Chloro-2-(4-meth-oxy-phen-yl)-1,3-benzo-thia-zole.

8. Synthesis, Antifungal Activities and Molecular Docking Studies of Benzoxazole and Benzothiazole Derivatives.