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Villocarine A, an indole alkaloid with natural vasorelaxant properties [1], is a chemical compound known for its ability to relax blood vessels.

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|---|---|---|---|---|
| 5 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | Villocarine A, an indole alkaloid with natural vasorelaxant properties [1], is a chemical compound known for its ability to relax blood vessels. |
| In vitro | Villocarine A demonstrated significant efficacy shortly after administration, showing potent vasorelaxant properties at a concentration of 30 μM in counteracting PE-induced contraction in rat aortic tissue within 10-30 minutes post-injection. Additionally, at the same concentration, Villocarine A presented a moderate inhibitory effect on contractions incited by PE and 1 μM in aortic rings under the conditions of a Ca2+-free medium and in the presence of nicardipine (1 μM) [2]. |
| Molecular Weight | 366.45 |
| Formula | C22H26N2O3 |
| Cas No. | 1319743-81-1 |
| Smiles | C(\C(OC)=O)(=C/OC)/[C@H]/1C[C@@]2(C3=C(C=4C(N3)=CC=CC4)CCN2C\C1=C\C)[H] |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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