Paxilline
Tocris Bioscience, part of Bio-Techne | Catalog # 2006
SERCA ATPase blocker. Also potent BKCa channel blocker
Key Product Details
Description
SERCA ATPase blocker. Also potent BKCa channel blocker
Product Description
Paxilline is a potent blocker of high-conductance Ca2+-activated K+ (BKCa, KCa1.1) channels. Binds to the α-subunit of BKCa (Ki = 1.9 nM for block of currents in α-subunit-expressing oocytes) and enhances binding of charybdotoxin to BKCa channels in vascular smooth muscle. Also inhibits sarco/endoplasmic reticulum Ca2+-ATPase (IC50 = 5 - 50 μM).Product Specifications
Molecular Weight
435.56
Formula
C27H33NO4
Storage
Store at -20°C
Purity
≥98% (HPLC)
Chemical Name
(2R,4bS,6aS,12bS,12cR,14aS)-5,6,6a,7,12,12b,12c,13,14,14a-Decahydro-4b-hydroxy-2-(1-hydroxy-1-methylethyl)-12b,12c-dimethyl-2H-pyranobenzindeno[1,2-b]indol-3(4bH)-one
CAS Number
57186-25-1
PubChem ID
105008
InChI Key
ACNHBCIZLNNLRS-UBGQALKQSA-N
SMILES
[H][C@@]4([C@](C)3[C@]5(C)[C@@](C([C@]6([H])CC5)=CC([C@@H]([C@](O)(C)C)O6)=O)(O)CC4)CC2=C3NC1=CC=CC=C12
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 43.56 | 100 |
Preparing Stock Solutions
for Paxilline
The following data is based on the product molecular weight 435.56
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.30 mL | 11.48 mL | 22.96 mL |
| 5 mM | 0.46 mL | 2.30 mL | 4.59 mL |
| 10 mM | 0.23 mL | 1.15 mL | 2.30 mL |
| 50 mM | 0.05 mL | 0.23 mL | 0.46 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Sanchez and McManus Paxilline inhibition of the alpha-subunit of the high-conductance calcium-activated potassium channel. Neuropharmacology 1996 PMID: 8938726
- Bilmen The mechanism of inhibition of the sarco/endoplasmic reticulum Ca2+ ATPase by paxilline. Arch.Biochem.Biophys. 2002 PMID: 12234490
- Knaus Tremorgenic indole alkaloids potently inhibit smooth muscle high-conductance calcium-activated potassium channels. Biochemistry 1994 PMID: 7514038
Product Specific Notices for Paxilline
For research use only
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