cas 56341-41-4|| where to buy 5-Fluorooxindole

Nombre del producto:5-Fluorooxindole

IUPAC Name:5-fluoro-2,3-dihydro-1H-indol-2-one

Unidad de embalaje	Stock disponible	Precio($)
CM148054-100g	in stock	ŵȡǶ
CM148054-500g	in stock	ǜȡǊ

Sólo para uso en I+D..

Formulario de consulta

Nombre químico

Número CAS

Cantidad*

Especificaciones requeridas*
(% de ensayo, grado de material, etc.)

Nombre de contacto*

Correo electrónico de contacto*

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 56341-41-4 regularly via the above email.

Notas adicionales

Verification code*

refresh

: Núm. De CAS :56341-41-4; Fórmula molecular:C8H6FNO; Punto de fusión:-; Código de sonrisas:C1=C2C(=CC=C1F)NC(=O)C2; Densidad:

: Número de catálogo:CM148054; Peso molecular:151.14; Punto de ebullición:307.2°C at 760 mmHg; Nº Mdl:MFCD02179598; Almacenamiento:Keep in a tight container and store at ambient temperature

: Indolinones; Indolinone derivatives have in common the presence of a hydrogen bond between the C-2 carbonyl and a hydrogen donor in a side chain, generally a pyrrole ring. Indolinone displays very promising antitumor properties by inhibiting various kinase families.

: Vorolanib; EyePoint Pharmaceuticals announced on December 4th announced positive topline results of its Phase 2 DAVIO 2 trial of EYP-1901, an investigational sustained delivery maintenance treatment for wet age-related macular degeneration (wet AMD) combining vorolanib, a selective tyrosine kinase inhibitor with bioerodible Durasert E™. Vorolanib brings a new mechanistic approach to the treatment of VEGF-mediated retinal diseases as a pan-VEGF receptor blocker, blocking all VEGF isoforms. Vorolanib features reduced off-target binding and at clinically relevant doses does not inhibit Tie-2, a critical pathway associated with vascular stability, which may result in an improved efficacy. Further, in an in-vivo model of retinal detachment, vorolanib demonstrated neuroprotection, and potential antifibrotic benefits.