Name | Description | Size | Catalog # | |
---|---|---|---|---|
SsdTx3 | SsdTx3 inhibits hKATP channels with a Kd of <300 nM by blocking the hKi… | 5 mg | STS-670 | More Info |
SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 0.25 mg | STS-700 | More Info |
SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 0.5 mg | STS-700 | More Info |
SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 1 mg | STS-700 | More Info |
SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 10 mg | STS-700 | More Info |
SsTx Toxin | Blocks voltage-gated potassium channels KCNQ4, KCNQ1, KCNQ2 and KCNQ51 and… | 5 mg | STS-700 | More Info |
Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 0.1 mg | S-350 | More Info |
Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 0.47 mg | S-350 | More Info |
Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 1 mg | S-350 | More Info |
Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 5 x 50 µg | S-350 | More Info |
Staurosporine | Staurosporine potently inhibits a variety of kinases including PKC (IC50 =… | 50 µg | S-350 | More Info |
Stichodactyla Toxin-ATTO Fluor-590 | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 µg | STS-400-AR | More Info |
Stichodactyla Toxin-ATTO Fluor-590 | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 x 5 µg | STS-400-AR | More Info |
Stichodactyla Toxin-ATTO Fluor-590 | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 10 x 5 µg | STS-400-AR | More Info |
Stichodactyla Toxin-Biotin | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 µg | STS-400-B | More Info |
Stichodactyla Toxin-Biotin | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 5 x 5 µg | STS-400-B | More Info |
Stichodactyla Toxin-Biotin | Stichodactyla Toxin blocks KV1.3, KV1.1, KV1.4, and KV1.6 at subnanomolar… | 10 x 5 µg | STS-400-B | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 0.1 mg | STS-350 | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 0.25 mg | STS-350 | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 0.5 mg | STS-350 | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 1 mg | STS-350 | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 10 mg | STS-350 | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 5 mg | STS-350 | More Info |
Stromatoxin-1 | Stromatoxin-1 is a potent inhibitor of voltage-gated K+ channels. It inhib… | 50 µg | STS-350 | More Info |
Taipoxin | Taipoxin gradually and completely stops induced and spontaneous release of… | 5 x 0.5 mg | T-460 | More Info |
Taipoxin | Taipoxin gradually and completely stops induced and spontaneous release of… | 0.5 mg | T-460 | More Info |
TAK-044 | TAK-044 is a non-selective endothelin receptor antagonist1. Synthetic. Pur… | 10 mg | SPE-320 | More Info |
TAK-044 | TAK-044 is a non-selective endothelin receptor antagonist1. Synthetic. Pur… | 25 mg | SPE-320 | More Info |
TAK-044 | TAK-044 is a non-selective endothelin receptor antagonist1. Synthetic. Pur… | 5 mg | SPE-320 | More Info |
Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 10 mg | T-185 | More Info |
Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 25 mg | T-185 | More Info |
Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 5 mg | T-185 | More Info |
Talampanel | Talampanel is a potent non-competitive AMPA / kainate receptor antagonist.… | 50 mg | T-185 | More Info |
Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 10 mg | B-140 | More Info |
Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 25 mg | B-140 | More Info |
Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 5 mg | B-140 | More Info |
Talipexole dihydrochloride | B-HT 920 is a blocker of 5-HT3 channels1. It is also an agonist of D2 dopa… | 50 mg | B-140 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 0.1 mg | STT-400 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 0.25 mg | STT-400 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 0.5 mg | STT-400 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 1 mg | STT-400 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 10 mg | STT-400 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 5 mg | STT-400 | More Info |
Tamapin | Tamapin blocks KCa2 channels. Tamapin displays a remarkable selectivity fo… | 50 µg | STT-400 | More Info |
Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 10 mg | T-165 | More Info |
Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 25 mg | T-165 | More Info |
Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 5 mg | T-165 | More Info |
Tanshinone II-A sodium sulfonate | Tanshinone II-A sodium sulfonate is a KCa1.1 channel opener1. Synthetic. P… | 50 mg | T-165 | More Info |
Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 10 g | T-130 | More Info |
Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 100 g | T-130 | More Info |
Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 25 g | T-130 | More Info |
Taurine | Taurine is a Glycine receptor (GlyR) partial agonist (EC50=1.7 mM)1. It di… | 5 g | T-130 | More Info |
tBuBHQ | tBuBHQ is an inhibitor of the endoplasmic reticulum Ca2+-ATPase1. Syntheti… | 1 g | T-220 | More Info |
tBuBHQ | tBuBHQ is an inhibitor of the endoplasmic reticulum Ca2+-ATPase1. Syntheti… | 250 mg | T-220 | More Info |
tBuBHQ | tBuBHQ is an inhibitor of the endoplasmic reticulum Ca2+-ATPase1. Syntheti… | 5 g | T-220 | More Info |
TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 10 mg | T-200 | More Info |
TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 25 mg | T-200 | More Info |
TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 5 mg | T-200 | More Info |
TC-I 2014 | TC-I 2014 is a potent and selective TRPM8 blocker, inhibiting canine, rat,… | 50 mg | T-200 | More Info |
TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 10 mg | T-190 | More Info |
TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 100 mg | T-190 | More Info |
TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 25 mg | T-190 | More Info |
TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 5 mg | T-190 | More Info |
TCN 201 | TCN 201 blocks NR1 / NR2A NMDA receptors in an NR1 co-agonist dependent an… | 50 mg | T-190 | More Info |
TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 10 mg | T-215 | More Info |
TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 25 mg | T-215 | More Info |
TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 5 mg | T-215 | More Info |
TCN 213 | TCN 213 is a NMDA receptor antagonist, selective for NR2A- over NR2B-conta… | 50 mg | T-215 | More Info |
Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 1 g | T-170 | More Info |
Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 100 mg | T-170 | More Info |
Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 250 mg | T-170 | More Info |
Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 50 mg | T-170 | More Info |
Telmisartan | An antagonist of Angiotensin II type-1 receptor1. Synthetic. Purity ≥99… | 500 mg | T-170 | More Info |
Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 0.1 mg | STT-250 | More Info |
Tertiapin | Tertiapin blocks a range of inward rectifier K+ channels (Kir) in particul… | 0.25 mg | STT-250 | More Info |
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