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ION CHANNEL and RECEPTOR LIGANDS TOXINS & ALKALOIDS

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| | L9035 Q Me
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a rigid bicyclic analog of TMA and TEA. Molecular probe for calibration of the size of ion channels or receptors sites. Nicotinic AChR blocker. Acetylcholinesterase inhibitor. Lipid layers modifier.
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Quaternary quinuclidine derivative, C8H16IN, synthetic.
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| PRICES |
| Quantity | US Dollars | EURO |
2 mg | 96.60 | 69.00 |
5 x 2 mg | 386.40 | 276.00 |
- Molecular Weight : 253.13 Da.
- Melting Point : > 269-273 °C.
- Solubility in : very soluble in water, ethanol.
- Purity min. : min. 98%. (NMR (D2O))
- Physical Form : yellowish crystal powder.
- Chemical Name : 1-methyl quinicludinium iodide, N-methyl quinuclidinium iodide.
- Biological Activity : Nicotinic AChR: less active than Tetraethylammonium (TEA) and Tetramethylammonium (TMA).
Acetylcholinesterase: Ki TMA=1.87 mM, Ki TEA=1.04 mM, Ki QMe=0.12 mM [2].
- Toxicity (LD50) : mice (orally): 200 mg/kg
- Storage recommendations : store at room temperature in a dark place, in a dessicator (extremely hygroscopic). Solution for use: dissolve in water: 10-3M (2 mg in 7.91 ml), stable for 1-2 days at 20°C.
- Safety recommendations : Do not swallow or inhale; avoid eye and skin contact.
- CAS Reg. No. : 45651-41-0
- Bibliography :
- Lukec R. et al., Chem. Listy (1955). 49: 510-508
- Kellet Jr., J. Pharm. Sci. (1965). 54 (3): 883-887
- Kellet Jr., J. Pharm. Sci. (1966). 55 (3): 414-417
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Revised : 26/04/2007 10:27 - Copyright © Latoxan |
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