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ProTx-III, a spider venom peptide derived from the Peruvian green velvet tarantula, functions as a selective and potent inhibitor of the voltage-gated sodium channel Na v 1.7, exhibiting an IC 50 of 2.1 nM. Characterized by its inhibitor cystine knot motif (ICK), ProTx-III can attenuate the pain response and is applicable in research on chronic pain, epilepsy, and arrhythmia [1].
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Description | ProTx-III, a spider venom peptide derived from the Peruvian green velvet tarantula, functions as a selective and potent inhibitor of the voltage-gated sodium channel Na v 1.7, exhibiting an IC 50 of 2.1 nM. Characterized by its inhibitor cystine knot motif (ICK), ProTx-III can attenuate the pain response and is applicable in research on chronic pain, epilepsy, and arrhythmia [1]. |
Targets&IC50 | Nav1.7:2.1 nM |
In vitro | Natural, recombinant, and synthetic C-terminal (acid and amide) forms of ProTx-III exhibit IC50 values for the inhibition of hNav1.7 at 2.1, 9.5, 11.5, and 2.5 nM, respectively [1]. ProTx-III suppresses hNav1.7 without significantly altering the voltage dependency of its activation or inactivation [1]. |
In vivo | ProTx-III (0.01-1 μM; intraplantar injection) reversibly mitigated spontaneous pain in a mouse model induced by intraplantar OD1 injection, demonstrating its analgesic properties [1]. |
Alias | μ-TRTX-Tp1a |
Molecular Weight | 3802.4 |
Formula | C162H246N52O43S6 |
Sequence | Asp-Cys-Leu-Lys-Phe-Gly-Trp-Lys-Cys-Asn-Pro-Arg-Asn-Asp-Lys-Cys-Cys-Ser-Gly-Leu-Lys-Cys-Gly-Ser-Asn-His-Asn-Trp-Cys-Lys-Leu-His-Ile-NH2 (Disulfide bonds: Cys2-Cys17, Cys9-Cys22, Cys16-Cys29) |
Sequence Short | DCLKFGWKCNPRNDKCCSGLKCGSNHNWCKLHI (Disulfide bonds: Cys2-Cys17, Cys9-Cys22, Cys16-Cys29) |
Storage | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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