Deucravacitinib - BMS986165

Based on 101 reference(s) in Google Scholar 8 10 101

Axon 4091

CAS [1609392-27-9]

MF C20H19D3N8O3
MW 425.46

  • Purity: 98%
  • Soluble in DMSO

Deucravacitinib

Description

Deucravacitinib is a potent, highly selective, allosteric and orally bioavailable inhibitor of tyrosine kinase 2 (TYK2) with an IC50 value of 0.20 nM. Deucravacitinib shows excellent pharmacokinetic properties with minimal profiling liabilities and is efficacious in several murine models of autoimmune disease.

KEYWORDS: Deucravacitinib | Supplier | TYK2 inhibitor | BMS986165 | BMS 986165 | BMS-986165 | CAS [1609392-27-9] | [1609392-28-0] | JAK-STAT Pathway | JAK | Inhibitor | Enzymes | Autoimmune disease | JH2 ligand | TYK2 pseudokinase (JH2) domain

Potent, highly selective, allosteric and orally bioavailable TYK2 inhibitor

Chemical name

6-(Cyclopropanecarbonylamino)-4-[2-methoxy-3-(1-methyl-1,2,4-triazol-3-yl)anilino]-N-(trideuteriomethyl)pyridazine-3-carboxamide

Parent CAS No.

[1609392-27-9]

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The purity of Axon Ligands™ is confirmed by HPLC-MS, 1H-NMR and/or microanalysis. Analytical data are available upon request.

Caution: Axon Ligands™ are not fully tested. They are for research purposes only! Not for human consumption!

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