scholarly journals Effect of pyrrolo[3,4-d]pyridazinone derivatives in neuroinflammation induced by preincubation with lipopolysaccharide or coculturing with microglia-like cells

2021 ◽  
Vol 141 ◽  
pp. 111878
Author(s):  
Katarzyna Potyrak ◽  
Benita Wiatrak ◽  
Edward Krzyżak ◽  
Łukasz Szczukowski ◽  
Piotr Świątek ◽  
...  
2019 ◽  
Author(s):  
Chem Int

A series of heterocyclic compounds incorporating pyridazine moiety were for diverse biological activities. Pyridazines and pyridazinones derivatives showed wide spectrum of biological activities such as vasodialator, cardiotonic, anticonvulsant, antihypertensive, antimicrobial, anti-inflammatory, analgesic, anti-feedant, herbicidal, and various other biological, agrochemical and industrial chemical activities. The results illustrated that the synthesized pyridazine/pyridazine compounds have diverse and significant biological activities. Mechanistic insights into the biological properties of pyridazinone derivatives and various synthetic techniques used for their synthesis are also described.


2008 ◽  
Vol 16 (1) ◽  
pp. 382-389 ◽  
Author(s):  
Khaled Abouzid ◽  
Maha Abdel Hakeem ◽  
Omnya Khalil ◽  
Yosria Maklad

ChemInform ◽  
2010 ◽  
Vol 28 (52) ◽  
pp. no-no
Author(s):  
G. TOTH ◽  
S. MOLNAR ◽  
T. TAMAS ◽  
I. BORBELY

1968 ◽  
Vol 88 (6) ◽  
pp. 784-787 ◽  
Author(s):  
TORIZO TAKAHASHI ◽  
YOSHIFUMI MAKI ◽  
MASAHIRO TAKAYA ◽  
HIROKO KIZU

2011 ◽  
Vol 66 (6) ◽  
pp. 597-602
Author(s):  
Elham S. Darwish ◽  
Mahmoud A. Abdelrahman ◽  
Abdellatif M. Salaheldin

An efficient and easy preparation of enamine derivatives, via active methyl and methylene compounds by in situ-generated 1-(diethoxymethyl)piperidine, produced from the mixture of triethyl orthoformate/piperidine/DMF, are described. Some new pyridazinone derivatives have been synthesized from the reaction of enamines with hydrazine hydrate and cyanoacid hydrazide.


Chemistry ◽  
2020 ◽  
Vol 2 (4) ◽  
pp. 837-848
Author(s):  
Csilla Sepsey Für ◽  
Hedvig Bölcskei

The large originator pharmaceutical companies need more and more new compounds for their molecule banks, because high throughput screening (HTS) is still a widely used method to find new hits in the course of the lead discovery. In the design and synthesis of a new compound library, important points are in focus nowadays: Lipinski’s rule of five (RO5); the high Fsp3 character; the use of bioisosteric heterocycles instead of aromatic rings. With said aim in mind, we have synthesized a small compound library of new spiro[cycloalkane-pyridazinones] with 36 members. The compounds with this new scaffold may be useful in various drug discovery projects.


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