SMN-C3

SMN-C3 Suppliers list
Company Name: WUHAN SUN-SHINE BIO-TECHNOLOGY Co., Ltd.  
Tel: 17702719238
Email: sales@sun-shinechem.com
Company Name: SHANGHAI FORTUNE CHEMICAL TECHNOLOGY CO., LTD  
Tel: 13816107857
Email: sales@fortunechem-sh.com
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 177-54423994 17754423994
Email: 2853530910@QQ.com
Company Name: Shanghai Changyu Medical Technology Co. Ltd.  
Tel: +86-13301875428
Email: sales@changyuhe.com
Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com

SMN-C3 manufacturers

  • SMN-C3
  • SMN-C3 pictures
  • $179.00
  • 2026-05-11
  • CAS:1449597-34-5
  • Purity: 99.31%
  • Supply Ability: 10g
  • SMN-C3
  • SMN-C3 pictures
  • $179.00
  • 2026-05-11
  • CAS:1449597-34-5
  • Purity: 99.31%
  • Supply Ability: 10g
SMN-C3 Basic information
Product Name:SMN-C3
Synonyms:SMN-C3;4H-Pyrido[1,2-a]pyrimidin-4-one, 2-(4,6-dimethylpyrazolo[1,5-a]pyrazin-2-yl)-7-(1-ethyl-4-piperidinyl)-9-methyl-
CAS:1449597-34-5
MF:C24H28N6O
MW:416.52
EINECS:
Product Categories:APIS
Mol File:1449597-34-5.mol
SMN-C3 Structure
SMN-C3 Chemical Properties
density 1.31±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 5 mg/mL (12.00 mM);Water : < 0.1 mg/mL (insoluble)
form Solid
pka9.27±0.10(Predicted)
color Light yellow to yellow
Safety Information
MSDS Information
SMN-C3 Usage And Synthesis
UsesSMN-C3 is an orally active SMN2 splicing modulator and has the potential to treat spinal muscular atrophy (SMA).
in vivo

At P16, vehicle treated D7 mice are much smaller than heterozygous littermate controls and appear moribund. In contrast, D7 mice treated with the high dose of SMN-C3 show a phenotype similar to that of heterozygous controls. SMN-C3 treatment induces a dose-dependent bodyweight gain in the D7 mice, 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 (0.3 mg/kg per day) group. In the two higher-dose groups (1 and 3 mg/kg per day), ~90% of animals survive beyond P65 when the study is completed[1].

References[1] 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. DOI:10.1126/science.1250127
SMN-C3 Preparation Products And Raw materials
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