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OD36

Catalog No. T35694   CAS 1638644-62-8
Synonyms: OD 36, OD 36 hydrochloride, OD-36

OD36 is a selective and potent RIPK2 inhibitor with an IC50 of 5.3 nM.OD36 inhibits ALK2 signaling and osteogenic differentiation (KD: 37 nM), and binds efficiently to the ALK2 kinase ATP pocket.

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OD36 Chemical Structure
OD36, CAS 1638644-62-8
Pack Size Availability Price/USD Quantity
1 mg In stock $ 177.00
5 mg In stock $ 437.00
10 mg In stock $ 646.00
25 mg In stock $ 987.00
50 mg In stock $ 1,380.00
100 mg In stock $ 1,860.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description OD36 is a selective and potent RIPK2 inhibitor with an IC50 of 5.3 nM.OD36 inhibits ALK2 signaling and osteogenic differentiation (KD: 37 nM), and binds efficiently to the ALK2 kinase ATP pocket.
Targets&IC50 ALK2:37 nM (Kd), ALK2:47 nM (IC50), RIPK2:5.3 nM (IC50), ALK2 (R206H):22 nM (IC50)
In vitro OD36 shows activity against ALK1 (KD=90 nM).[2]
OD36 potently antagonizes mutant ALK2 signaling and osteogenic differentiation.[2]
OD36 (0.1-1 μM; 24 h; KS483 cells) efficiently inhibits BMP-6 (50 ng/mL)-induced p-Smad1/5.[2]
OD36 (0.5 μM) completely prevents the activation of Smad1/5 and the gene targets ID-1 and ID-3 in response to activin A in preincubated fibrodysplasia ossificans progressiva (FOP) endothelial colony-forming cells (ECFCs).[2]
In vivo OD36 (6.25 mg/kg; i.p.; once; C57BL/6 mice, muramyl dipeptide (MDP)-induced model of peritonitis) inhibited the recruitment of inflammatory cells to the peritoneum, specifically that of neutrophils, and, to a lesser extent, lymphocytes. Decreased RIPK2-specific genes as well as inflammatory cytokine and chemokine gene expression. OD36 alleviates inflammation in an acute peritonitis mice model.[3]
Synonyms OD 36, OD 36 hydrochloride, OD-36
Molecular Weight 330.77
Formula C16H15ClN4O2
CAS No. 1638644-62-8

Storage

store at low temperature

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 25 mg/mL (75.58 mM), Sonication and heating are recommended.

TargetMolReferences and Literature

1. 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. 2. 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. 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.

Related compound libraries

This product is contained In the following compound libraries:
Kinase Inhibitor Library Inhibitor Library Membrane Protein-targeted Compound Library Bioactive Compound Library Bioactive Compounds Library Max

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Keywords

OD36 1638644-62-8 Angiogenesis Apoptosis NF-Κb Tyrosine Kinase/Adaptors ALK RIP kinase OD 36 OD36 Hydrochloride OD 36 Hydrochloride OD 36 hydrochloride OD-36 Hydrochloride OD-36 inhibitor inhibit

 

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