Name | Description | Size | Catalog # | |
---|---|---|---|---|
Isoguvacine hydrochloride | Isoguvacine hydrochloride is a specific agonist of the GABA(A) receptors,… | 25 mg | I-185 | More Info |
Isoguvacine hydrochloride | Isoguvacine hydrochloride is a specific agonist of the GABA(A) receptors,… | 250 mg | I-185 | More Info |
Isoguvacine hydrochloride | Isoguvacine hydrochloride is a specific agonist of the GABA(A) receptors,… | 50 mg | I-185 | More Info |
Isopimaric Acid | Isopimaric acid is a potent opener of large conductance Ca2+-activated K+… | 1 mg | I-370 | More Info |
Isopimaric Acid | Isopimaric acid is a potent opener of large conductance Ca2+-activated K+… | 10 mg | I-370 | More Info |
Isopimaric Acid | Isopimaric acid is a potent opener of large conductance Ca2+-activated K+… | 25 mg | I-370 | More Info |
Isopimaric Acid | Isopimaric acid is a potent opener of large conductance Ca2+-activated K+… | 5 mg | I-370 | More Info |
Isopimaric Acid | Isopimaric acid is a potent opener of large conductance Ca2+-activated K+… | 5 x 1 mg | I-370 | More Info |
Isradipine | Isradipine is a dihydropyridine that acts as an L-type, voltage-gated Ca2+… | 10 mg | I-100 | More Info |
Isradipine | Isradipine is a dihydropyridine that acts as an L-type, voltage-gated Ca2+… | 25 mg | I-100 | More Info |
Isradipine | Isradipine is a dihydropyridine that acts as an L-type, voltage-gated Ca2+… | 5 mg | I-100 | More Info |
Isradipine | Isradipine is a dihydropyridine that acts as an L-type, voltage-gated Ca2+… | 50 mg | I-100 | More Info |
Ivermectin | Ivermectin is a positive allosteric modulator of the α7 neuronal nic… | 1 g | I-110 | More Info |
Ivermectin | Ivermectin is a positive allosteric modulator of the α7 neuronal nic… | 250 mg | I-110 | More Info |
Jingzhaotoxin-34 | Potent and selective inhibitor of hNav1.7 and weak blocker of Nav1.3. JZTX… | 0.1 mg | STJ-500 | More Info |
Jingzhaotoxin-34 | Potent and selective inhibitor of hNav1.7 and weak blocker of Nav1.3. JZTX… | 0.5 mg | STJ-500 | More Info |
Jingzhaotoxin-34 | Potent and selective inhibitor of hNav1.7 and weak blocker of Nav1.3. JZTX… | 1 mg | STJ-500 | More Info |
Jingzhaotoxin-II | Jingzhaotoxin-II significantly slows rapid inactivation of TTX-resistant V… | 0.1 mg | STJ-150 | More Info |
Jingzhaotoxin-II | Jingzhaotoxin-II significantly slows rapid inactivation of TTX-resistant V… | 0.5 mg | STJ-150 | More Info |
Jingzhaotoxin-II | Jingzhaotoxin-II significantly slows rapid inactivation of TTX-resistant V… | 1 mg | STJ-150 | More Info |
Jingzhaotoxin-II | Jingzhaotoxin-II significantly slows rapid inactivation of TTX-resistant V… | 5 mg | STJ-150 | More Info |
Jingzhaotoxin-II | Jingzhaotoxin-II significantly slows rapid inactivation of TTX-resistant V… | 50 µg | STJ-150 | More Info |
Jingzhaotoxin-III | Inhibits NaV1.5 and KV2.1 channels1. Synthetic peptide. Purity >98% (HPLC)… | 0.1 mg | STJ-200 | More Info |
Jingzhaotoxin-III | Inhibits NaV1.5 and KV2.1 channels1. Synthetic peptide. Purity >98% (HPLC)… | 0.25 mg | STJ-200 | More Info |
Jingzhaotoxin-III | Inhibits NaV1.5 and KV2.1 channels1. Synthetic peptide. Purity >98% (HPLC)… | 0.5 mg | STJ-200 | More Info |
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