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A classic L-type Ca2+ channel blocker (IC50=75nM) which can also inhibit T-type Ca2+ channels (IC50=244nM). It is a novel inhibitor of drug transport by p-glycoprotein (both stereoisomers are equipotent at inhibition of p-glycoprotein).
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| Regulatory Status |
RUO – Research Use Only |
|---|
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| Alternative Name | 6-(6-Methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-6,8-dihydrofuro[3,4-E][1,3]benzodioxol-8-ol, (+)-Decumbensine |
|---|---|
| CAS | 6883-44-9 |
| Purity | ≥98% (HPLC) |
| Alternative Name | (3S,3aR,4R,4aS,8aR,9aS)-4-[(1E)-2-[(2R,6S)-1,6-Dimethyl-2-piperdinyl]ethenyl]decahydro-3-methyl-naphtho[2,3-c]furan-1(3H)-one |
|---|---|
| CAS | 6879-74-9 |
| Couple Type | Inhibitor |
| Purity | ≥98% |
| Alternative Name | (±)-Anatoxin A fumarate, (±)-2-Acetyl-9-aza bicyclo[4,2,1]non-2-ene fumarate |
|---|---|
| CAS | 1219922-30-1 |
| Couple Type | Ligand |
| Purity | ≥96% (HPLC) |