Nombre del producto:2-(6-Chloro-3-pyridazinyl)-2-(2,6-dichlorophenyl)-acetonitrile

IUPAC Name:2-(6-chloropyridazin-3-yl)-2-(2,6-dichlorophenyl)acetonitrile

CAS:209412-06-6
Fórmula molecular:C12H6Cl3N3
Pureza:95%
Número de catálogo:CM164362
Peso molecular:298.55

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CM164362-5g in stock ƻȌƱ

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Detalles del producto

Núm. De CAS :209412-06-6
Fórmula molecular:C12H6Cl3N3
Punto de fusión:-
Código de sonrisas:N#CC(C1=NN=C(Cl)C=C1)C2=C(Cl)C=CC=C2Cl
Densidad:
Número de catálogo:CM164362
Peso molecular:298.55
Punto de ebullición:
Nº Mdl:MFCD00202119
Almacenamiento:Store at 2-8°C.

Category Infos

Pyridazines
Pyridazine, also known as o-diazobenzene, is a six-membered heterocyclic compound containing two nitrogen heteroatoms in the 1 and 2 positions with a special structure and a wide biological activity. Pyridazine is more and more popular in drug development, and a variety of pyridazine drugs have been developed and marketed. From the perspective of the therapeutic field, pyridazine drug molecules are mainly used for tumor treatment, but also involve in many therapeutic fields such as inflammation, hypertension and cardiovascular disease. With the increase and in-depth of research, pyridazine drugs will play more roles in the treatment of diseases.

Column Infos

Neflamapimod
Dementia with Lewy Bodies (DLB) is a rapidly progressive neurodegenerative disorder with a significant aging population and unmet health need. Alterations in p38 mitogen-activated protein kinases (MAPKs) are found to contribute to the neurodegenerative process in Alzheimer's disease (AD) and related dementias.
CervoMed’s Neflamapimod (VX-745) is an oral, brain penetrant, small molecule inhibitor of the protein kinase p38α. It is designed to specifically target the mechanisms that cause dysfunction and degeneration of neurons in the basal forebrain cholinergic system. Neflamapimod has the potential of reversing synaptic dysfunction in the basal forebrain. The positive phase 2a data was published in Nature Communications, Neurology, and JPAD. Neflamapimod was granted Fast Track Designation by the FDA for DLB, and phase 2b enrollment was completed in June, 2024.