Synthesis of 1,4-dihydro-4-oxopyrrolo[1,2-b]pyridazine-3-carboxylic acids and 1,4-dihydro-4-oxoimidazo[1,5-b]pyridazine-3-carboxylic acids as potential antibacterial agents-Reference-Cited by-同舟云学术

Synthesis of 1,4-dihydro-4-oxopyrrolo[1,2-b]pyridazine-3-carboxylic acids and 1,4-dihydro-4-oxoimidazo[1,5-b]pyridazine-3-carboxylic acids as potential antibacterial agents

Published:1994-03 Issue:2 Volume:31 Page:409-417
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Ruxer J. M.,Lachoux C.,Ousset J. B.,Torregrosa J. L.,Mattioda G.

Publisher

Wiley

Subject

Organic Chemistry

Reference36 articles.

1. 1,8-Naphthyridine Derivatives. A New Class of Chemotherapeutic Agents

2. Structure-activity relationships of antibacterial 6,7- and 7,8-disubstituted 1-alkyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acids

3. Pefloxacin Mesylate

4. 1,4-Dihydro-4-oxopyridinecarboxylic acids as antibacterial agents. 2. Synthesis and structure-activity relationships of 1,6,7-trisubstituted 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids, including enoxacin, a new antibacterial agent

5. I. Hayakawa, Y. Tanaka and T. Hiramitsu, European Patent Appl. 47,005 (1982);

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Naphthoquinone-Quinolone Hybrids with Antitumor Effects on Breast Cancer Cell Lines—From the Synthesis to 3D-Cell Culture Effects;International Journal of Molecular Sciences;2024-06-12

2. Synthesis of novel pyridazino[1,6-a]indole-2,4(1H,3H)-dione and pyridazino[1,6-a]indol-2(1H)-one via intramolecular electrophilic aromatic substitution;Results in Chemistry;2022-01

3. Selective AMPK activator leads to unfolded protein response downregulation and induces breast cancer cell death and autophagy;Life Sciences;2021-07

4. Phthalazinone Scaffold: Emerging Tool in the Development of Target Based Novel Anticancer Agents;Anti-Cancer Agents in Medicinal Chemistry;2020-11-23

5. Synthesis and photodynamic effects of new porphyrin/4-oxoquinoline derivatives in the inactivation of S. aureus;Photochemical & Photobiological Sciences;2019