Powder: -20°C for 3 years | In solvent: -80°C for 1 year
1. Pulegone ((+)-Pulegone) has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the opening of L-type calcium channels. 3. Pulegone has negative reinforcing properties and seems to possess anxiolytic-like actions unrelated to the benzodiazepine site of the γ-aminobutyric acid type A (GABAA) receptor.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
5 mg | In stock | $ 39.00 | |
10 mg | In stock | $ 55.00 | |
25 mg | In stock | $ 91.00 | |
50 mg | In stock | $ 133.00 | |
100 mg | In stock | $ 198.00 | |
500 mg | In stock | $ 492.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 43.00 |
Description | 1. Pulegone ((+)-Pulegone) has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the opening of L-type calcium channels. 3. Pulegone has negative reinforcing properties and seems to possess anxiolytic-like actions unrelated to the benzodiazepine site of the γ-aminobutyric acid type A (GABAA) receptor. |
Source |
Synonyms | (+)-Pulegone |
Molecular Weight | 152.23 |
Formula | C10H16O |
CAS No. | 89-82-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 50 mg/mL (328.44 mM)
You can also refer to dose conversion for different animals. More
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Pulegone 89-82-7 Membrane transporter/Ion channel Metabolism Endogenous Metabolite Calcium Channel TRP/TRPV Channel Transient receptor potential channels TRP Channel (+)-Pulegone Inhibitor inhibit inhibitor