OD36
OD36 is a RIPK2 inhibitor with an IC50 of 5.3 nM. OD36 is a macrocyclic inhibitor with potent binding to the ALK2 kinase ATP pocket. OD36 shows ALK2-directed activity with KDs of 37 nM[1][2].
Product Specifications
CAS Number
1638644-62-8
UNSPSC
12352005
Target
RIP kinase; TGF-β Receptor
Type
Reference compound
Related Pathways
Apoptosis; TGF-beta/Smad
Applications
COVID-19-immunoregulation
Field of Research
Inflammation/Immunology
Assay Protocol
https://www.medchemexpress.com/od36.html
Purity
99.33
Solubility
DMSO : 33.33 mg/mL (ultrasonic)
Smiles
ClC1=CC(C2=C3N/C(C=CN3N=C2)=N/CCOCCO4)=CC4=C1
Molecular Formula
C16H15ClN4O2
Molecular Weight
330.77
References & Citations
[1]Gonzalo Sánchez-Duffhues, et al. Development of Macrocycle Kinase Inhibitors for ALK2 Using Fibrodysplasia Ossificans Progressiva-Derived Endothelial Cells. JBMR Plus. 2019 Oct 7;3 (11) :e10230.|[2]Justine T Tigno-Aranjuez, et al. In vivo inhibition of RIPK2 kinase alleviates inflammatory disease. J Biol Chem. 2014 Oct 24;289 (43) :29651-64.|[3]Tigno-Aranjuez JT, et al. In vivo inhibition of RIPK2 kinase alleviates inflammatory disease. J Biol Chem. 2014 Oct 24;289 (43) :29651-64.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
ALK2; RIPK2
Available Sizes
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
A00175-HRP 100 µg/Vial
Anti-Mannose Phosphate Isomerase/MPI Antibody Picoband® (HRP Conjugate)
Sign In for Pricing
View Details 