Category: 88511-47-1

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Application In Synthesis of Pyridazine-4-carboxamide, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 88511-47-1, name is Pyridazine-4-carboxamide. In an article，Which mentioned a new discovery about 88511-47-1

The present application relates to novel substituted indazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N450 – PubChem

 

Reference of 88511-47-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.88511-47-1, Name is Pyridazine-4-carboxamide, molecular formula is C5H5N3O. In a Patent，once mentioned of 88511-47-1

The invention relates to 1,2,4 oxadiazole compounds and analogs thereof, represented by formula (II), and compositions and methods of use thereof.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N451 – PubChem

 

Electric Literature of 88511-47-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.88511-47-1, Name is Pyridazine-4-carboxamide, molecular formula is C5H5N3O. In a Article，once mentioned of 88511-47-1

The modulation of bacterial communication to potentiate the effect of existing antimicrobial drugs is a promising alternative to the development of novel antibiotics. In the present study, we synthesized 58 analogues of hamamelitannin (HAM), a quorum sensing inhibitor and antimicrobial potentiator. These efforts resulted in the identification of an analogue that increases the susceptibility of Staphylococcus aureus towards antibiotics in vitro, in Caenorhabditis elegans, and in a mouse mammary gland infection model, without showing cytotoxicity. Don’t let the bad bugs bite: Staphylococcus aureus (blue) is notorious for causing antibiotic (yellow) resistant biofilm-related infections. The discovery of hamamelitannin as an antimicrobial potentiator led to an investigation of its structure-activity relationship. A potent and metabolically stable analogue (see structure, green) was identified that shows improved activity and drug-like properties.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N456 – PubChem

 

Electric Literature of 88511-47-1, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 88511-47-1, Pyridazine-4-carboxamide, introducing its new discovery.

Compounds of the formula (I) wherein the substituents are as defined in claim 1, useful as pesticides, especially as herbicides.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N452 – PubChem

 

88511-47-1, Name is Pyridazine-4-carboxamide, belongs to pyridazine compound, is a common compound. COA of Formula: C5H5N3OIn an article, once mentioned the new application about 88511-47-1.

On the synthesis of pyridazomycin congeners – Part 23,4: L-alpha-amino acids bearing a terminal azinium or diazinium system

The synthesis of a variety of novel compounds structurally related to the antimicrobial natural product pyridazomycin via alkylation of appropriate azine and diazine derivatives is reported. Based on the results of preliminary antimicrobial tests the dependence of antimicrobial activity from several structural features of pyridazomycin is discussed.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N454 – PubChem

 

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On the synthesis of azinium and diazinium compounds structurally related to pyridazomycin

Preparation of series of pyridine-, pyridazine-, and pyrazine-derived carboxamides bearing at the ring N-alom an alkyl side-chain with a terminal carboxylic group (7-11) or with a terminal acetylamino malonic ester moiety (13-17,19-23) is described. Two desaza-pyridazomycin derivatives (24, 26) and homologs thereof (25, 27) were synthesised. The novel compounds which are structurally related to the antifungal antibiotic pyridazomycin were screened for antifungal activity: preliminary in vitro tests showed no activity.

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Pyridazine – Wikipedia,
Pyridazine | C4H4N453 – PubChem