cas 946323-73-5|| where to buy N-(3-{6-methoxyimidazo[1,2-b]pyridazin-2-yl}phenyl)-2,3-dihydro-1,4-benzodioxine-6-sulfonamide

Produktname:N-(3-{6-methoxyimidazo[1,2-b]pyridazin-2-yl}phenyl)-2,3-dihydro-1,4-benzodioxine-6-sulfonamide

IUPAC Name:N-(3-{6-methoxyimidazo[1,2-b]pyridazin-2-yl}phenyl)-2,3-dihydro-1,4-benzodioxine-6-sulfonamide

Packungseinheit	Verfügbarer Vorrat	Preis($)	Menge

Nur für den Einsatz in Forschung und Entwicklung..

Anfrage-Formular

Chemische Bezeichnung

CAS-Nummer

Menge*

Erforderliche Spezifikationen*
(Gehalt %, Materialqualität etc.)

Name des Ansprechpartners*

E-Mail des Ansprechpartners*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 946323-73-5 regularly via the above email.

Zusätzliche Hinweise

Verification code*

refresh

: CAS-Nr.:946323-73-5; Molekulare Formel:C21H18N4O5S; Schmelzpunkt:-; SMILES-Code:COC1=NN2C=C(N=C2C=C1)C1=CC=CC(NS(=O)(=O)C2=CC=C3OCCOC3=C2)=C1; Dichte:

: Katalognummer:CM645376; Molekulargewicht:438.46; Siedepunkt:; Mdl-Nr.:; Lagerung:

: Benzodioxanes; Benzodioxanes are a class of isomeric compounds with the molecular formula C8H8O2. The three isomers of benzodioxane are 1,2-benzodioxane, 1,3-benzodioxane and 1,4-benzodioxane. 1,4-Benzodioxane has long been a versatile template widely used to design molecules with diverse biological activities. Its use spans past decades in medicinal chemistry to today, involving many drug discovery strategies, not excluding the most advanced ones. 1,4-Benzodioxane derivatives have been described as agonists and antagonists of nicotinic, alpha-adrenergic and 5-HT receptor subtypes. 1,4-Benzodioxane derivatives have been also reported as antitumor and antibacterial agents.

: Imidazopyridazines; Potent IRAK-4 inhibitors have been reported by several groups including some structurally related benzimidazoles as well as alternative fused heterocycles such as the imidazopyridine and imidazopyridazine. Such compounds are reported to have IRAK-1 and IRAK-4 activity with varying degrees of selectivity.