
D-156844
CAS No. 1005501-84-7
D-156844( —— )
Catalog No. M10049 CAS No. 1005501-84-7
D156844 is a potent SMN2 inducer and DcpS inhibitor; highly potent at activating SMN2 promoter activity with EC50 of 4 nM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
100MG | Get Quote | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameD-156844
-
NoteResearch use only, not for human use.
-
Brief DescriptionD156844 is a potent SMN2 inducer and DcpS inhibitor; highly potent at activating SMN2 promoter activity with EC50 of 4 nM.
-
DescriptionD156844 is a potent SMN2 inducer and DcpS inhibitor; highly potent at activating SMN2 promoter activity with EC50 of 4 nM; increases SMN expression in neonatal mouse neural tissues, delays motor neuron loss at PND11 and ameliorates the motor phenotype of SMNDelta7 SMA mice; orally active.Spinal Muscular Atrophy (SMA)Preclinical.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayOthers
-
TargetSMN2
-
RecptorSMN2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1005501-84-7
-
Formula Weight381.455
-
Molecular FormulaC21H24FN5O
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical Name5-((1-(2-fluorobenzyl)piperidin-4-yl)methoxy)quinazoline-2,4-diamine
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Butchbach ME, et al. Hum Mol Genet. 2010 Feb 1;19(3):454-67.
2. Butchbach ME, et al. Exp Neurol. 2014 Jun;256:1-6.
molnova catalog



related products
-
RG7800
RG7800 (RG-7800, RG 7800) is a potent, orally available, small molecule SMN2 splicing modifier with EC1.5X of 23 nM and 87 nM for SMN2 splicing and SMN2 protein, respectively.
-
D-156844
D156844 is a potent SMN2 inducer and DcpS inhibitor; highly potent at activating SMN2 promoter activity with EC50 of 4 nM.
-
Risdiplam
Risdiplam (RG7916, RG-7916, RO7034067) is a highly potent, selective, orally active?SMN2 splicing modifier for treatment of?spinal muscular atrophy (SMA).