LDN 193189 dihydrochloride

Modify Date: 2024-01-22 20:03:30

LDN 193189 dihydrochloride Structure
LDN 193189 dihydrochloride structure
Common Name LDN 193189 dihydrochloride
CAS Number 1435934-00-1 Molecular Weight 479.40
Density N/A Boiling Point N/A
Molecular Formula C25H24Cl2N6 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of LDN 193189 dihydrochloride


LDN-193189 (dihydrochloride) is a potent selective BMP type I receptor (BMP I) inhibitor. LDN-193189 efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 values of 5 nM and 30 nM, respectively. LDN-193189 can be used for the research of bone morphogenetic protein signalling, such as fibrodysplasia ossificans progressiva[1][2][3].

 Names

Name 4-{6-[4-(1-Piperazinyl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl}quinoline dihydrochloride
Synonym More Synonyms

 LDN 193189 dihydrochloride Biological Activity

Description LDN-193189 (dihydrochloride) is a potent selective BMP type I receptor (BMP I) inhibitor. LDN-193189 efficiently inhibits transcriptional activity of the BMP type I receptors ALK2 and ALK3 with IC50 values of 5 nM and 30 nM, respectively. LDN-193189 can be used for the research of bone morphogenetic protein signalling, such as fibrodysplasia ossificans progressiva[1][2][3].
Related Catalog
References

[1]. Yu PB, et al. BMP type I receptor inhibition reduces heterotopic [corrected] ossification. Nat Med, 2008, 14(12), 1363-1369.  

[2]. Daniel Horbelt, et al. Small molecules dorsomorphin and LDN-193189 inhibit myostatin/GDF8 signaling and promote functional myoblast differentiation. J Biol Chem. 2015 Feb 6;290(6):3390-404.  

[3]. Julien Vollaire, et al. The Bone Morphogenetic Protein Signaling Inhibitor LDN-193189 Enhances Metastasis Development in Mice. Front Pharmacol. 2019 Jun 19;10:667.  

 Chemical & Physical Properties

Molecular Formula C25H24Cl2N6
Molecular Weight 479.40
Exact Mass 478.143951
Storage condition -20℃

 Synonyms

Quinoline, 4-[6-[4-(1-piperazinyl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]-, hydrochloride (1:2)
4-{6-[4-(1-Piperazinyl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl}quinoline dihydrochloride