Product Name | Minoxidil |
Description |
K+ channel activator |
Purity | >98% |
CAS No. | 38304-91-5 |
Molecular Formula | C9H15N5O |
Molecular Weight | 209.25 |
Field of Use | Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only. |
Storage Temperature | -20ºC |
Shipping Temperature | Shipped Ambient |
Product Type | Activator |
Solubility | Soluble to 25 mM in ethanol and to 25 mM in DMSO |
Source | Synthetic |
Appearance | White solid |
SMILES | C1CCN(CC1)C2=NC(=[N+](C(=C2)N)[O-])N |
InChI | InChI=1S/C9H15N5O/c10-7-6-8(12-9(11)14(7)15)13-4-2-1-3-5-13/h6,11,15H,1-5,10H2 |
InChIKey | ZIMGGGWCDYVHOY-UHFFFAOYSA-N |
Safety Phrases |
Classification: Harmful. May be harmful if inhaled, swallowed, or absorbed through the skin. Safety Phrases: S22 - Do not breathe dust S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection S24/25- Avoid contact with shin and eyes Risk Phrases: R62 - Possible risk of impaired fertility Hazard Phrases: H302-H315-H319-H335 Precautionary Phrases: P261-P305 + P351 + P338 |
Cite This Product | Minoxidil (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-318) |
Alternative Names | 3-hydroxy-2-imino-6-piperidin-1-ylpyrimidin-4-amine |
Research Areas | Ion Channels, Neuroscience |
PubChem ID | 4201 |
Scientific Background | Minoxidil is a vasodilator that opens potassium channels, leading to hyperpolarization of cell membranes. In neurodegenerative research, its nitric oxide moiety and ion channel modulation properties have been explored for neurovascular regulation. Minoxidil may influence cerebral blood flow and neuroprotection through vascular mechanisms, although its primary applications remain in cardiovascular and dermatological domains. |
References |
1. www.medicinenet.com/minoxidiloral/article.htm 2. Olsen E.A., et al. (2007) J Am Acad Dermatol. 57(5): 767. |
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