2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)-

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2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- Suppliers list
Company Name: Suzhou Haiben Pharmaceutical Co., Ltd  
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2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- manufacturers

  • XT2
  • XT2 pictures
  • $2800.00
  • 2026-05-26
  • CAS:2582816-37-1
  • Purity:
  • Supply Ability: 10g
2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- Basic information
Product Name:2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)-
Synonyms:2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)-
CAS:2582816-37-1
MF:C19H14FN5OS
MW:379.41
EINECS:
Product Categories:
Mol File:2582816-37-1.mol
2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- Structure
2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- Chemical Properties
Boiling point 672.1±65.0 °C(Predicted)
density 1.54±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
form Solid
pka10.81±0.29(Predicted)
color Light yellow to yellow
Safety Information
MSDS Information
2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- Usage And Synthesis
UsesXT2 is a potent, orally active, and selective inhibitor of NF-κB-inducing kinase (NIK) with an IC50 of 9.1 nM. XT2 suppresses CCl4-induced upregulation of ALT, a key biomarker of acute liver injury. XT2 also decreases immune cell infiltration into the injured liver tissue. XT2 has the potential for the research of liver inflammatory diseases[1]. XT2 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Biological ActivityXT2 is a potent, orally active, and selective inhibitor of NF-κB-inducing kinase (NIK) with an IC50 of 9.1 nM. XT2 suppresses CCl4-induced upregulation of ALT, a key biomarker of acute liver injury. XT2 also decreases immune cell infiltration into the injured liver tissue. XT2 has the potential for the research of liver inflammatory diseases[1].
References[1]. Li Z, et al. Discovery of a Potent and Selective NF-κB-Inducing Kinase (NIK) Inhibitor That Has Anti-inflammatory Effects in Vitro and in Vivo. J Med Chem. 2020;63(8):4388-4407.
2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)- Preparation Products And Raw materials
Tag:2-Thiazolemethanol, α-[2-[3-(2-amino-5H-pyrrolo[3,2-d]pyrimidin-7-yl)-4-fluorophenyl]ethynyl]-α-methyl-, (αR)-(2582816-37-1) Related Product Information
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