CAS 1779796-38-1

Formel: C21H19Cl2F3N4

InChl: InChI=1S/C21H17F3N4.2ClH/c22-21(23,24)17-6-3-14(4-7-17)11-26-19-8-5-15(12-27-19)10-16-13-28-20-18(16)2-1-9-25-20;;/h1-9,12-13H,10-11H2,(H,25,28)(H,26,27);2*1H

InChI Key: MVMKWLRKACAUTB-UHFFFAOYSA-N

SMILES: C1=CC2=C(NC=C2CC3=CN=C(C=C3)NCC4=CC=C(C=C4)C(F)(F)F)N=C1.Cl.Cl

PLX647 dihydrochloride

CAS: 1779796-38-1

PLX647 dihydrochloride: potent FMS/KIT inhibitor (IC50: 28/16 nM), highly selective, limited FLT3/KDR activity, oral use.

Formel: C₂₁H₁₉Cl₂F₃N₄

Farbe und Form: Solid

Molekulargewicht: 455.31

Ref: TM-T39194

5-((1H-Pyrrolo[2,3-b]pyridin-3-yl)methyl)-N-(4-(trifluoromethyl)benzyl)pyridin-2-amine dihydrochloride

CAS: 1779796-38-1

Formel: C₂₁H₁₉Cl₂F₃N₄

Reinheit: 98%

Molekulargewicht: 455.3

Ref: IN-DG01205609

PLX 647 dihydrochloride

CAS: 1779796-38-1

PLX 647 is a high purity, synthetic peptide that can be used as a research tool to study protein interactions. It can be used to inhibit the activity of ion channels and receptor ligands. PLX 647 has been shown to inhibit the activity of ion channels such as NMDA receptors, GABA receptors, and angiotensin II AT1 receptors in rat hippocampal neurons. This drug also inhibits the binding of ligands to their corresponding receptors, such as acetylcholine at nicotinic acetylcholine receptors and serotonin at 5-HT2A serotonin receptors.

Formel: C₂₁H₁₉Cl₂F₃N₄

Reinheit: Min. 95%

Molekulargewicht: 455.3 g/mol

Ref: 3D-EWC79638