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SMN-C3 Inhibitor

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS5753930

SMN-C3 is an orally active modulator of SMN2 splicing, and has the potential to treat spinal muscular atrophy (SMA). More details

Product Documentation
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Sample Manual Insert View PDF
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Testing Data View PDF
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Certificate of Analysis (COA) View PDF
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QC Report View PDF
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Material Safety Data Sheet View PDF
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Technical Datasheet View PDF
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Protocol View PDF

Product Overview

Online Datasheet in PDF
Product Name
SMN-C3, Inhibitor
Full Product Name
SMN-C3
Product Gene Name
Form/Format
Solid. Powder
Purity/Purification
98.00%
Preparation and Storage
Store at -20 degree C for 3 years powder
-80 degree C for 2 years in solvent
Molecular Weight
416.52
Solubility
DMSO: 5mg/mL (12.00mM) Need ultrasonic
H2O: <0.1mg/mL (insoluble)
(<1mg/ml refers to the product slightly soluble or insoluble)
Formula
C24H28N6O
SMILES
O=C1C=C(C2=NN3C(C(C)=NC(C)=C3)=C2)N=C4N1C=C(C5CCN(CC)CC5)C=C4C
CAS Number
1449597-34-5
Target & IC50
SMN
In Vitro
At P16, the vehicle-treated D7 mice were much smaller than the control group of heterozygous litter pups and were dying. In contrast, D7 mice treated with high doses of SMN-C3 showed a phenotype similar to the heterozygous control. In the D7 mice, SMN-C3 treatment,induces a dose-dependent bodyweight gain, with some animals showing a body weight that is ~80% that of heterozygous controls. SMN-C3 normalizes the motor behavior of D7 mice, illustrated by the ability of the mice to right themselves as quickly as heterozygous controls and by their level of locomotor activity. Most importantly, whereas vehicle-treated mice die within 3 weeks after birth with a median survival of 18 days, SMN-C3 treatment,increases survival in a dose-dependent manner to a median survival time of 28 days in the low-dose (0.3mg/kg per day) group. In the two higher-dose groups (1 and 3mg/kg per day), ~90% of animals survive beyond P65 when the study is completed.

Structure of SMN-C3, inhibitor

SMN-C3 Inhibitor – Cat# MBS5753930

Product References and Citations for SMN-C3, inhibitor

Naryshkin NA, et al. Motor neuron disease. SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy. Science. 2014 Aug 8;345(6197):688-93.

Other Notes

Small volumes of SMN-C3, inhibitor vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Searchable Terms for SMN-C3 purchase

MBS5753930 is an inhibitor targeting SMN-C3.
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