Name | Description | Size | Catalog # | |
---|---|---|---|---|
m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 0.1 mg | STH-102 | More Info |
m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 0.5 mg | STH-102 | More Info |
m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 1 mg | STH-102 | More Info |
m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 10 mg | STH-102 | More Info |
m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 5 mg | STH-102 | More Info |
m3-Huwentoxin IV | m3-Huwentoxin IV is a mutated form of the Huwentoxin IV with significant i… | 50 µg | STH-102 | More Info |
mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 0.1 mg | STH-101 | More Info |
mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 0.5 mg | STH-101 | More Info |
mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 5 x 50 µg | STH-101 | More Info |
mHuwentoxin-IV | mHWTX-IV inhibits tetrodotoxin-sensitive NaV channels of dorsal root gangl… | 50 µg | STH-101 | More Info |
Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 1 mg | M-150 | More Info |
Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 10 mg | M-150 | More Info |
Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 25 mg | M-150 | More Info |
Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 5 mg | M-150 | More Info |
Mibefradil dihydrochloride hydrate | Mibefradil blocks T-type Ca2+ channels with an IC50 of ~1 µM. Orai1-… | 50 mg | M-150 | More Info |
Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 1 g | M-206 | More Info |
Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 10 g | M-206 | More Info |
Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 25 g | M-206 | More Info |
Miconazole nitrate | Miconazole blocks hERG in HEK transfected cells as well as KV1.3 and KV1.5… | 5 g | M-206 | More Info |
Mirtazapine | Mirtazipine is an antidepressant agent; potent 5-HT2, 5-HT3 and histamine… | 100 mg | M-130 | More Info |
Mirtazapine | Mirtazipine is an antidepressant agent; potent 5-HT2, 5-HT3 and histamine… | 25 mg | M-130 | More Info |
Mirtazapine | Mirtazipine is an antidepressant agent; potent 5-HT2, 5-HT3 and histamine… | 50 mg | M-130 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 0.1 mg | M-100 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 0.25 mg | M-100 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 0.5 mg | M-100 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 10 µg | M-100 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 20 µg | M-100 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 5 µg | M-100 | More Info |
MitTx Toxin | MitTx toxin activates ASIC1-containing channels1,2. Natural protein isolat… | 50 µg | M-100 | More Info |
MK-5435 | MK-5435 is a potent and selective allosteric mGluR1 antagonist, inhibiting… | 10 mg | M-265 | More Info |
MK-5435 | MK-5435 is a potent and selective allosteric mGluR1 antagonist, inhibiting… | 25 mg | M-265 | More Info |
MK-5435 | MK-5435 is a potent and selective allosteric mGluR1 antagonist, inhibiting… | 5 mg | M-265 | More Info |
MK-5435 | MK-5435 is a potent and selective allosteric mGluR1 antagonist, inhibiting… | 50 mg | M-265 | More Info |
(+)-MK 801 maleate | (+)-MK 801 maleate is a potent, selective and non-competitive NMDA recepto… | 10 mg | M-230 | More Info |
(+)-MK 801 maleate | (+)-MK 801 maleate is a potent, selective and non-competitive NMDA recepto… | 100 mg | M-230 | More Info |
(+)-MK 801 maleate | (+)-MK 801 maleate is a potent, selective and non-competitive NMDA recepto… | 25 mg | M-230 | More Info |
(+)-MK 801 maleate | (+)-MK 801 maleate is a potent, selective and non-competitive NMDA recepto… | 250 mg | M-230 | More Info |
(+)-MK 801 maleate | (+)-MK 801 maleate is a potent, selective and non-competitive NMDA recepto… | 5 mg | M-230 | More Info |
(+)-MK 801 maleate | (+)-MK 801 maleate is a potent, selective and non-competitive NMDA recepto… | 50 mg | M-230 | More Info |
ML 218 | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 10 mg | M-165 | More Info |
ML 218 | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 25 mg | M-165 | More Info |
ML 218 | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 5 mg | M-165 | More Info |
ML-301 | ML-301 is a selective agonist of NTR1 receptors, shown to stimulate NTR1-m… | 10 mg | M-315 | More Info |
ML-301 | ML-301 is a selective agonist of NTR1 receptors, shown to stimulate NTR1-m… | 25 mg | M-315 | More Info |
ML-301 | ML-301 is a selective agonist of NTR1 receptors, shown to stimulate NTR1-m… | 5 mg | M-315 | More Info |
ML-301 | ML-301 is a selective agonist of NTR1 receptors, shown to stimulate NTR1-m… | 50 mg | M-315 | More Info |
ML 218 hydrochloride | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 10 mg | M-166 | More Info |
ML 218 hydrochloride | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 25 mg | M-166 | More Info |
ML 218 hydrochloride | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 5 mg | M-166 | More Info |
ML 218 hydrochloride | ML 218 is a blocker of T-type Ca2+ channels (IC50 values are 270 and 310 n… | 50 mg | M-166 | More Info |
ML133 hydrochloride | ML133 hydrochloride selectively inhibits Kir2 inward-rectifier potassium c… | 10 mg | M-275 | More Info |
ML133 hydrochloride | ML133 hydrochloride selectively inhibits Kir2 inward-rectifier potassium c… | 100 mg | M-275 | More Info |
ML133 hydrochloride | ML133 hydrochloride selectively inhibits Kir2 inward-rectifier potassium c… | 25 mg | M-275 | More Info |
ML133 hydrochloride | ML133 hydrochloride selectively inhibits Kir2 inward-rectifier potassium c… | 5 mg | M-275 | More Info |
ML133 hydrochloride | ML133 hydrochloride selectively inhibits Kir2 inward-rectifier potassium c… | 50 mg | M-275 | More Info |
ML297 (VU0456810) | ML297 is a potent and selective activator of GIRK1 / 2 channels (EC50=160-… | 10 mg | M-215 | More Info |
ML297 (VU0456810) | ML297 is a potent and selective activator of GIRK1 / 2 channels (EC50=160-… | 25 mg | M-215 | More Info |
ML297 (VU0456810) | ML297 is a potent and selective activator of GIRK1 / 2 channels (EC50=160-… | 5 mg | M-215 | More Info |
ML297 (VU0456810) | ML297 is a potent and selective activator of GIRK1 / 2 channels (EC50=160-… | 50 mg | M-215 | More Info |
MMK1 | MMK1 is a selective and potent agonist of the formyl peptide receptor (FPR… | 1 mg | GPM-120 | More Info |
MMK1 | MMK1 is a selective and potent agonist of the formyl peptide receptor (FPR… | 25 mg | GPM-120 | More Info |
MMK1 | MMK1 is a selective and potent agonist of the formyl peptide receptor (FPR… | 5 mg | GPM-120 | More Info |
MmTx1 Toxin | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 0.1 mg | STM-550 | More Info |
MmTx1 Toxin | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 0.5 mg | STM-550 | More Info |
MmTx1 Toxin | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 1 mg | STM-550 | More Info |
MmTx1 Toxin | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 50 µg | STM-550 | More Info |
MmTx2 Toxin | MmTx2 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 0.1 mg | STM-600 | More Info |
MmTx2 Toxin | MmTx2 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 0.5 mg | STM-600 | More Info |
MmTx2 Toxin | MmTx2 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 1 mg | STM-600 | More Info |
MmTx2 Toxin | MmTx2 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 50 µg | STM-600 | More Info |
MmTx1 Toxin-ATTO Fluor-488 | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 10 µg | STM-550-AG | More Info |
MmTx1 Toxin-ATTO Fluor-488 | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 5 µg | STM-550-AG | More Info |
MmTx1 Toxin-ATTO Fluor-488 | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 5 x 10 µg | STM-550-AG | More Info |
MmTx1 Toxin-ATTO Fluor-488 | MmTx1 is a potent allosteric modulator of GABA(A) receptors1. Synthetic pe… | 2 x 10 µg | STM-550-AG | More Info |
Mosapride citrate | Mosapride citrate is a 5-HT4 receptor agonist and 5-HT3 receptor antagonis… | 10 mg | M-225 | More Info |
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