Name | Description | Size | Catalog # | |
---|---|---|---|---|
(S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 1 mg | A-267 | More Info |
(S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 10 mg | A-267 | More Info |
(S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 25 mg | A-267 | More Info |
(S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 5 mg | A-267 | More Info |
(S)-AMPA | An active enantiomer of AMPA (EC50 = 3.5 µM)1. Synthetic. Purity >99… | 50 mg | A-267 | More Info |
Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 0.1 mg | SPE-160 | More Info |
Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 0.5 mg | SPE-160 | More Info |
Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 1 mg | SPE-160 | More Info |
Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 10 mg | SPE-160 | More Info |
Sarafotoxin S6b | Sarafotoxin S6b is an endothelin receptor agonist1,2. Synthetic peptide. P… | 5 mg | SPE-160 | More Info |
(S)-ATPO | An active enantiomer of ATPO, an antagonist of GluR1-4 and a partial agoni… | 25 mg | A-330 | More Info |
(S)-ATPO | An active enantiomer of ATPO, an antagonist of GluR1-4 and a partial agoni… | 5 mg | A-330 | More Info |
(S)-ATPO | An active enantiomer of ATPO, an antagonist of GluR1-4 and a partial agoni… | 10 mg | A-330 | More Info |
SB 203580 | SB 203580 is a specific inhibitor for the p38 MAP kinase homologues1-6. Sy… | 5 mg | S-370 | More Info |
SB 203580 | SB 203580 is a specific inhibitor for the p38 MAP kinase homologues1-6. Sy… | 5 x 1 mg | S-370 | More Info |
SB 203580 | SB 203580 is a specific inhibitor for the p38 MAP kinase homologues1-6. Sy… | 1 mg | S-370 | More Info |
SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 0.5 mg | S-205 | More Info |
SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 1 mg | S-205 | More Info |
SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 2.5 mg | S-205 | More Info |
SB209670 | SB209670 is a potent mixed antagonist of ET-A and ET-B Endothelin receptor… | 5 mg | S-205 | More Info |
SB-366791 | SB-366791 is a TRPV1 channel antagonist1. Synthetic. Purity >99%. MW: 287.7 | 10 mg | S-180 | More Info |
SB-366791 | SB-366791 is a TRPV1 channel antagonist1. Synthetic. Purity >99%. MW: 287.7 | 25 mg | S-180 | More Info |
SB-366791 | SB-366791 is a TRPV1 channel antagonist1. Synthetic. Purity >99%. MW: 287.7 | 50 mg | S-180 | More Info |
SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 10 mg | S-160 | More Info |
SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 100 mg | S-160 | More Info |
SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 25 mg | S-160 | More Info |
SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 5 mg | S-160 | More Info |
SB-705498 | SB-705498 is a potent orally active TRPV1 blocker1. Synthetic. Purity >99%… | 50 mg | S-160 | More Info |
(S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 1 mg | B-351 | More Info |
(S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 10 mg | B-351 | More Info |
(S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 100 mg | B-351 | More Info |
(S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 25 mg | B-351 | More Info |
(S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 5 mg | B-351 | More Info |
(S)(-)-Bay K8644 | (S)(-)-Bay K8644 is an L-type Ca2+-channel activator. It displays vasocons… | 50 mg | B-351 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 0.1 mg | STS-370 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 0.25 mg | STS-370 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 0.5 mg | STS-370 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 1 mg | STS-370 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 10 mg | STS-370 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 5 mg | STS-370 | More Info |
Scyllatoxin | Scyllatoxin inhibits small conductance Ca2+-activated K+ channels (SK)1-3.… | 50 µg | STS-370 | More Info |
(S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 100 mg | D-170 | More Info |
(S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 25 mg | D-170 | More Info |
(S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 250 mg | D-170 | More Info |
(S)-Duloxetine hydrochloride | (S)-Duloxetine hydrochloride blocks KV4.3 channels with an IC50 of 8.4 &mi… | 50 mg | D-170 | More Info |
SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 10 mg | S-145 | More Info |
SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 25 mg | S-145 | More Info |
SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 5 mg | S-145 | More Info |
SDZ 205-557 hydrochloride | SDZ 205-557 hydrochloride is a 5-HT3 and 5-HT4 receptor antagonist1. Synth… | 50 mg | S-145 | More Info |
SERCA Pump Inhibitor Explorer Kit | A Screening Package of SERCA Pump Inhibitors Economically Priced | 6 vials | EK-365 | More Info |
Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 1 g | S-165 | More Info |
Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 100 mg | S-165 | More Info |
Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 250 mg | S-165 | More Info |
Serotonin hydrochloride | Serotonin is an endogenous agonist at 5-HT receptors and endogenous substr… | 500 mg | S-165 | More Info |
(S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 10 mg | F-205 | More Info |
(S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 100 mg | F-205 | More Info |
(S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 25 mg | F-205 | More Info |
(S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 5 mg | F-205 | More Info |
(S)-(-)-5-Fluorowillardiine | (S)-(-)-5-Fluorowillardiine is a potent and selective AMPA receptor agonis… | 50 mg | F-205 | More Info |
sFTX-3.3 | sFTX-3.3, a synthetic funnel web spider toxin1-2, is a polyamine amide ana… | 5 x 1 mg | F-130 | More Info |
sFTX-3.3 | sFTX-3.3, a synthetic funnel web spider toxin1-2, is a polyamine amide ana… | 1 mg | F-130 | More Info |
Shaker (KV1) Channel Blocker Explorer Kit | A Screening Package of Shaker (KV1) Channel Blockers Economically Priced | 27 vials | EK-107 | More Info |
Shaker (KV)-Related Channel Blocker Explorer Kit | A Screening Package of Shaker (KV)-Related Channel Blockers Economically P… | 15 vials | EK-108 | More Info |
ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 0.1 mg | STS-390 | More Info |
ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 0.5 mg | STS-390 | More Info |
ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 1 mg | STS-390 | More Info |
ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 10 mg | STS-390 | More Info |
ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 5 mg | STS-390 | More Info |
ShK-186 | ShK-186 is a potent and selective blocker of Kv1.3 voltage-gated K+ channe… | 50 µg | STS-390 | More Info |
ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 0.1 mg | STS-400 | More Info |
ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 0.25 mg | STS-400 | More Info |
ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 0.5 mg | STS-400 | More Info |
ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 1 mg | STS-400 | More Info |
ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 10 mg | STS-400 | More Info |
ShK (Stichodactyla Toxin) | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 mg | STS-400 | More Info |
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