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The invention provides compounds of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treating immunological conditions.

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Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2199 – PubChem

 

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A compound of formula (I), or a pharmaceutically acceptable salt thereof and a pharmaceutical composition comprising the compound. The compound is an inhibitor of interactions between S100A9 and interaction partners such as RAGE, TLR4 and EMMPRIN and as such is useful in the treatment of disorders such as cancer, autoimmune disorders, inflammatory disorders and neurodegenerative disorders.

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Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2207 – PubChem

 

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Imidazopyridazines of formula (I) a process for their production and the use thereof

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2201 – PubChem

 

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no abstract published

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2204 – PubChem

 

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A compound of formula (I), or a pharmaceutically acceptable salt thereof and a pharmaceutical composition comprising the compound. The compound is an inhibitor of interactions between S100A9 and interaction partners such as RAGE, TLR4 and EMMPRIN and as such is useful in the treatment of disorders such as cancer, autoimmune disorders, inflammatory disorders and neurodegenerative disorders.

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Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2207 – PubChem

 

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The present invention relates to compounds that are fast dissociating dopamine 2 receptor antagonists, processes for preparing these compounds, pharmaceutical compositions comprising these compounds as an active ingredient. The compounds find utility as medicines for treating or preventing central nervous system disorders, for example schizophrenia, by exerting an antipsychotic effect without motor side effects.

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Pyridazine – Wikipedia,
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The invention provides named compounds of formula (I), wherein R4 is a N- sustituted quinuclidine (I) pharmaceutical compositions containing them and a process for preparing the pharmaceutical compositions. Their use in therapy for’ the treatment of conditions mediated by M3 muscarinic receptors, such as chronic obstructive pulmonary disease is also disclosed

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Pyridazine – Wikipedia,
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COMPOUNDS USEFUL AS CSF1 MODULATORS

This invention relates to novel compounds and to pharmaceutical compositions comprising the novel compounds. More specifically, the invention relates to compounds useful as Colony Stimulating Factor 1 Receptor (cFMS) modulators (e.g. cFMS inhibitors). This invention also relates to processes for preparing the compounds, uses of the compounds in treatment and methods of treatment employing the compounds. Specifically, the invention relates to the use of the compounds for the treatment of cancer and autoimmune diseases.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2200 – PubChem

 

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Intramolecular Metal-Free N?N Bond Formation with Heteroaromatic Amines: Mild Access to Fused-Triazapentalene Derivatives

Formation of N?N bonds may offer an original approach to various nitrogen-containing heterocycles with numerous applications. For this purpose, we found that readily available heteroaromatic amines are appropriate substrates for providing an efficient and innovative approach for the formation of N?N bonds in the presence of iodine (III) reagent in very mild conditions. This method makes it possible to synthesize nitrogen rich triazapentalene derivatives exhibiting fluorescent properties, inaccessible with existing approaches.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N2209 – PubChem

 

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IMIDAZOPYRIDAZINES AS AKT KINASE INHIBITORS

Imidazopyridazines of formula (I) a process for their production and the use thereof

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Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2201 – PubChem