Name | Description | Size | Catalog # | |
---|---|---|---|---|
A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 5 mg | A-195 | More Info |
A-889425 | A-889425 blocks TRPV1 channels with an IC50 of 335 nM (rat) and 34 nM (hum… | 50 mg | A-195 | More Info |
AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 10 mg | A-370 | More Info |
AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 25 mg | A-370 | More Info |
AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 5 mg | A-370 | More Info |
AA 29504 | AA 29504 is a positive allosteric modulator of GABA(A) receptors, reducing… | 50 mg | A-370 | More Info |
AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 10 mg | A-410 | More Info |
AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 25 mg | A-410 | More Info |
AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 5 mg | A-410 | More Info |
AACBA hydrochloride | AACBA hydrochloride is a potent and selective antagonist of P2X7 receptors… | 50 mg | A-410 | More Info |
17-AAG | 17-AAG is a less toxic and more stable derivative of the antibiotic Geldan… | 0.1 mg | A-580 | More Info |
17-AAG | 17-AAG is a less toxic and more stable derivative of the antibiotic Geldan… | 5 x 0.1 mg | A-580 | More Info |
AaH1 Toxin | AaH1 Toxin is a NaV channel activator. It blocks the fast inactivation of… | 0.1 mg | STA-155 | More Info |
AaH1 Toxin | AaH1 Toxin is a NaV channel activator. It blocks the fast inactivation of… | 0.5 mg | STA-155 | More Info |
AaH1 Toxin | AaH1 Toxin is a NaV channel activator. It blocks the fast inactivation of… | 1 mg | STA-155 | More Info |
Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 0.1 mg | STA-110 | More Info |
Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 0.5 mg | STA-110 | More Info |
Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 1 mg | STA-110 | More Info |
Aam-KTX | Aam-KTX is a KV1.3 channel blocker1. Synthetic peptide. Purity >99% (HPLC)… | 50 µg | STA-110 | More Info |
Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 0.1 mg | RTA-400 | More Info |
Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 10 µg | RTA-400 | More Info |
Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 5 µg | RTA-400 | More Info |
Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 5 x 10 µg | RTA-400 | More Info |
Aa1 Toxin | Aa1 Toxin is a blocker of A-type voltage-gated transient K+ channels of ce… | 5 x 5 µg | RTA-400 | More Info |
Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 100 mg | A-150 | More Info |
Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 25 mg | A-150 | More Info |
Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 250 mg | A-150 | More Info |
Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 5 mg | A-150 | More Info |
Aconitine | Aconitine modulates voltage-dependent sodium channels in a complex way1. I… | 50 mg | A-150 | More Info |
ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 10 mg | A-350 | More Info |
ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 25 mg | A-350 | More Info |
ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 5 mg | A-350 | More Info |
ACT-132577 | ACT-132577, a metabolite of macitentan, is a dual antagonist of ET-A and E… | 50 mg | A-350 | More Info |
ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 10 mg | A-450 | More Info |
ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 25 mg | A-450 | More Info |
ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 5 mg | A-450 | More Info |
ACT-462206 | ACT-462206 is a potent and selective dual orexin receptor antagonist (IC50… | 50 mg | A-450 | More Info |
ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 0.1 mg | STW-100 | More Info |
ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 0.25 mg | STW-100 | More Info |
ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 0.5 mg | STW-100 | More Info |
ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 1 mg | STW-100 | More Info |
ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 10 mg | STW-100 | More Info |
ADWX-1 | Selective potent KV1.3 blocker1-3. Synthetic peptide. Purity >98% (HPLC).… | 5 mg | STW-100 | More Info |
AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 10 mg | A-375 | More Info |
AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 25 mg | A-375 | More Info |
AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 5 mg | A-375 | More Info |
AF-353 | AF-353 is a highly potent and selective P2X3 and P2X2 / 3 receptor antagon… | 50 mg | A-375 | More Info |
Agitoxin-1 | Agitoxin-1 is a blocker of Shaker voltage-gated K+ channels as well as the… | 0.1 mg | STA-150 | More Info |
Agitoxin-1 | Agitoxin-1 is a blocker of Shaker voltage-gated K+ channels as well as the… | 0.5 mg | STA-150 | More Info |
Agitoxin-1 | Agitoxin-1 is a blocker of Shaker voltage-gated K+ channels as well as the… | 1 mg | STA-150 | More Info |
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