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Umbellulone is a natural product isolated from Umbellularia californica, and stimulates the TRPA1 channel in a subset of peptidergic, nociceptive neurons, activating the trigeminovascular system via this mechanism.


| Description | Umbellulone is a natural product isolated from Umbellularia californica, and stimulates the TRPA1 channel in a subset of peptidergic, nociceptive neurons, activating the trigeminovascular system via this mechanism. |
| In vitro | Umbellulone selectively stimulates transient receptor potential ankyrin 1-expressing HEK293 cells. |
| In vivo | In Trpa1+/+ mice, Umbellulone (50–250?nM/5ul) causes an acute nocioceptive response in a dose-dependent manner . Umbellulone (30-150 μg/kg; i.v.) increases meningeal blood flow in a dose-dependent manner. |
| Molecular Weight | 150.22 |
| Formula | C10H14O |
| Cas No. | 546-78-1 |
| Smiles | [H][C@@]12C[C@]1(C(C)C)C(=O)C=C2C |
| Relative Density. | no data available |
| 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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