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Purmorphamine (GMP)

Purmorphamine (GMP-grade), a hedgehog pathway activator, has been shown to promote differentiation of motor neurons from human pluripotent stem cells and human and mesenchymal stem cells. This product is manufactured under cGMP and is ideal for cell therapy applications.

Grouped product items
SKUSIZEPRICE QTY
SML28BG10 mg
$1,375.00
- +
SML28KG50 mg
$4,250.00
- +
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Description
Specifications
More Information
SKUSML28-GMP
FormPowder
GradeGMP-grade
Chemical Name9-Cyclohexyl-N-[4-(4-morpholinyl)phenyl]-2-(1-naphthalenyloxy)-9H-purin-6-amine
Chemical FormulaC31H32N6O2
Molecular Weight520.62
CAS Number483367-10-8
SMILESN1(C2=CC=C(NC3=NC(OC4=CC=CC5=C4C=CC=C5) =NC6=C3N=CN6C7CCCCC7)C=C2)CCOCC1
Purity≥98% (HPLC)
Physical AppearanceOff-white to pale purple

Captivate Bio offers a portfolio of GMP-grade small molecules. GMP-grade small molecules are produced under well establish, controlled cGMP guidelines and are used as ancillary reagents in the generation of stem cells and in reprogramming, self-and differentiation workflows for cell therapy applications.

Purmorphamine is a small molecule that activates the hedgehog signaling pathway by directly binding to and activating the Smoothened (Smo) receptor. It is used in stem cell research to promote osteogenesis (bone formation) and neural differentiation, and has also been studied for its neuroprotective effects.

Accelerating Cell Therapy Research Programs

As your research program advances into therapeutic applications, making the transition from research-grade to GMP-grade reagents is critical to the success of your project. Captivate Bio can facilitate this transition easier with the availability of both RUO and GMP-grade small molecules that are designed with enhanced quality testing and are suitable for use as ancillary reagents.

GMP Features
  • Enhanced quality testing and documentation
  • High purity and consistent activity
  • Reduce risk of unwanted genetic material
  • Easily scalable, available in large volumes
  • Manufactured following ICH Q7 guidelines
Quality Assurance
  • QC tests include: purity, water content, residual solvents, bioburden, endotoxin, elemental impurities, and solubility
  • Documentation includes: Certificate of Analysis (CoA), Safety Data Sheet (SDS), Certificate of Origin (CoO), TSE/BSE Statement, Technical Data Sheet, and Declaration of GMP Compliance

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