Leconotide
Source: Wikipedia, the free encyclopedia.
Conotoxin peptide under investigation as an analgesic drug
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Formula | C107H179N35O36S7 |
Molar mass | 2756.24 g·mol−1 |
Leconotide (
It acts as an N-type voltage-gated calcium channel (Cav2.2) blocker and is highly selective for this channel over the related P/Q-type voltage-gated calcium channel (Cav2.1).[1][2]
Relative to
See also
- Ziconotide, an analgesic peptide derived from the toxin of the cone snail species Conus magus
- Lacosamide, an approved small molecule analgesic and anti-epileptic
- Ralfinamide, an investigational small molecule analgesic
References
- ^ ISBN 978-1-84973-645-9.
- ^ ISBN 978-94-007-6334-0.
- ISBN 978-1-4649-2221-3.
- PMID 20002322.
- PMID 21539704.
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VGKCsTooltip Voltage-gated potassium channels
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IRKsTooltip Inwardly rectifying potassium channel
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K2PsTooltip Tandem pore domain potassium channel
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VGSCsTooltip Voltage-gated sodium channels
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CaCCsTooltip Calcium-activated chloride channel
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TRPs Tooltip Transient receptor potential channels |
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LGICs Tooltip Ligand gated ion channels |
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