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µ-Conotoxin KIIIA
Item number: TGM-T80159-50mg
Description: µ-Conotoxin KIIIA, an analgesic compound derived from Conus kinoshitai, selectively inhibits mammalian neuronal voltage-gated sodium channels (VGSCs) (Nav1.2), offering potential utility in pain research [1] [2]. Target: Sodium Channel
| CAS | 884469-67-4 |
| MW: | 1884.16 D |
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omega-Hexatoxin-Hv1a
Item number: TGM-T80160-50mg
Description: omega-Hexatoxin-Hv1a, a neurotoxin extracted from the venom of the spider Hadronyche versuta, inhibits voltage-gated calcium channels [1] [2]. Target: Calcium Channel
| Keywords: | omega-Atracotoxin-HV1, omega-ACTX-Hv1 |
| CAS | 193981-10-1 |
| MW: | 4049.38 D |
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omega-Conotoxin SO3
Item number: TGM-T80161-50mg
Description: omega-Conotoxin SO3 is an analgesic peptide that functions as an antagonist to N-type voltage-sensitive calcium channels, and can be isolated from the venom of Conus striatus [1] [2]. Target: Calcium Channel
| CAS | 441284-32-8 |
| MW: | 2561 D |
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Aah II
Item number: TGM-T80162-50mg
Description: Aah II, a sodium channel modulator, is a toxin derived from the venom of the scorpion Androctonus australis [1] [2]. Target: Sodium Channel
| MW: | 7243.04 D |
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µ-Conotoxin PIIIA
Item number: TGM-T80163-50mg
Description: µ-Conotoxin PIIIA, isolated from Conus purpurascens [1] [2], is a blocker of the sodium channel NaV 1.4. Target: Sodium Channel
| CAS | 184840-20-8 |
| MW: | 2605.06 D |
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alpha-Conotoxin PeIA
Item number: TGM-T80164-50mg
Description: alpha-Conotoxin PeIA is an analgesic that inhibits nAChRs alpha6beta4, alpha9alpha10, and alpha3beta2, and potently inhibits the N-type calcium channel through GABAB receptor activation [1] [2] [3].
| CAS | 866876-88-2 |
| MW: | 1651.87 D |
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alpha-Conotoxin GID
Item number: TGM-T80165-50mg
Description: alpha-Conotoxin GID is a paralytic peptide neurotoxin that selectively antagonizes nAChR with IC50 values of 5 nM (alpha7), 3 nM (alpha3beta2), and 150 nM (alpha4beta2). This small, disulfide-rich peptide has potential for chronic pain inhibition. The presence of a C-terminal carboxylate is crucial, as...
| CAS | 547741-78-6 |
| MW: | 2186.39 D |
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alpha-Conotoxin BuIA
Item number: TGM-T80166-50mg
Description: alpha-Conotoxin BuIA is a paralytic peptide neurotoxin that acts as a competitive antagonist of nicotinic acetylcholine receptors (nAChR), with inhibitory concentration 50 (IC50) values of 0.258 nM for alpha6/alpha3beta2, 1.54 nM for alpha6/alpha3beta4, and 5.72 nM for alpha3beta2. It serves to...
| CAS | 846539-62-6 |
| MW: | 1311.57 D |
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alphaC-Conotoxin PrXA
Item number: TGM-T80167-50mg
Description: alphaC-Conotoxin PrXA is a neurotoxic paralytic peptide acting as a competitive antagonist of the nicotinic acetylcholine receptor (nAChR), exhibiting inhibitory constants (IC50) of 1.8 nM for the adult alpha1beta1epsilondelta subtype and 3.0 nM for the fetal alpha1beta1gammadelta subtype. The compound...
| Keywords: | alphaC-PrXA |
| MW: | 3541.06 D |
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Scorpion toxin Tf2
Item number: TGM-T80168-50mg
Description: Scorpion toxin Tf2, a beta-scorpion toxin first identified in the venom of the Brazilian scorpion Tityus fasciolatus, acts as an activator of the neuronal voltage-gated sodium (Nav) subtype Nav1.3, associated with epilepsy and nociception. It increases hNav1.3 activation voltage, prompting channel...
| MW: | 6953.86 D |
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ProTx-III
Item number: TGM-T80169-50mg
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...
| Keywords: | µ-TRTX-Tp1a |
| MW: | 3802.4 D |
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Tamapin
Item number: TGM-T80170-50mg
Description: Tamapin, a venom peptide isolated from the Indian red scorpion (Mesobuthus tamulus) [1], selectively targets and blocks small-conductance Ca(2+)-activated K(+) (SK) channels, particularily SK2 (Potassium Channel). It inhibits SK channel-mediated currents in the pyramidal neurons of the hippocampus....
| MW: | 3458.11 D |
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