1310726-60-3

  • Product Name:Upadacitinib
  • Molecular Formula:C17H19F3N6O
  • Purity:99%
  • Molecular Weight:380.373
Inquiry

Product Details:

CasNo: 1310726-60-3

Molecular Formula: C17H19F3N6O

Buy Reliable Quality Upadacitinib 1310726-60-3 On Stock

  • Molecular Formula:C17H19F3N6O
  • Molecular Weight:380.373
  • PKA:11.89±0.60(Predicted) 
  • PSA:78.32000 
  • Density:1.56±0.1 g/cm3(Predicted) 
  • LogP:3.23670 

Upadacitinib 1310726-60-3 Usage

Description

Upadacitinib, sold under the brand name Rinvoq, is an immunosuppressant medication approved by the FDA for treating various conditions. As a second-generation Janus kinase (JAK) inhibitor specifically targeting the JAK1 enzyme, Upadacitinib works by reducing the activity of the immune system.

Uses

It is used to treat the following conditions:

Moderate to severe rheumatoid arthritis
Active psoriatic arthritis
Ankylosing spondylitis
Non-radiographic axial spondyloarthritis
Moderate to severe ulcerative colitis
Moderate to severe Crohn's disease
Atopic dermatitis
Upadacitinib's mechanism of action involves blocking the activity of Janus kinases, which play a role in immune system signaling. It is specifically indicated for cases of moderate to severe rheumatoid arthritis that do not respond to first-line therapy.

1310726-60-3 Relevant articles

Safety and efficacy of upadacitinib in patients with rheumatoid arthritis and inadequate response to conventional synthetic disease-modifying anti-rheumatic drugs (SELECT-NEXT): a randomised, double-blind, placebo-controlled phase 3 trial

Prof Gerd R Burmester, MD Prof Joel M Kremer, MD Prof Filip Van den Bosch, MD Alan Kivitz, MD Prof Louis Bessette, MD Yihan Li, PhD

The Lancet, VOLUME 391, ISSUE 10139, P2503-2512, JUNE 23, 2018

Using interactive response technology, we randomly assigned patients receiving stable background csDMARDs (2:2:1:1) to receive a once-daily extended-release formulation of upadacitinib 15 mg or 30 mg, or placebo, for 12 weeks. Patients, investigators, and the funder were masked to allocation.

Development of a Scalable Enantioselective Synthesis of JAK Inhibitor Upadacitinib

Bhagavatula, Lakshmi,Christesen, Alan,Dunn, Travis B.,Ickes, Andrew,Kotecki, Brian J.,Marek, James C.,Morrill, Westin H.,Moschetta, Eric,Mulhern, Mathew,Rasmussen, Michael,Reynolds, Troy,Rozema, Michael J.,Yu, Su

, (2021/10/21)

Process development of a six-stage synth...

PYRROLIDINE COMPOUNDS, ITS SALT AND USE IN THE PREPARATION OF UPADACITINIB THEREOF

-

, (2021/01/29)

The present invention relates to process...

1310726-60-3 Upstream products

  • 753-90-2
    753-90-2

    trifluoroethylamine

  • 530-62-1
    530-62-1

    1,1'-carbonyldiimidazole

  • 1428243-26-8
    1428243-26-8

    (3R,4S)-benzyl 3-(2-bromoacetyl)-4-ethylpyrrolidine-1-carboxylate

  • 1201186-54-0
    1201186-54-0

    2-bromo-5-(p-toluenesulfonyl)-5H-pyrrolo[2,3-b]pyrazine

Relevant Products