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Cat. No. Product Name Information
PC-60345

PB28

Sigma 2 receptor agonist, Sigma 1 inhibitor

PB 28 is a potent, mixed sigma2 agonist and sigma1 antagonist with Ki of 0.28 and 13.0 nM, respectively.
PC-60289

NE-100 hydrochloride

Sigma 1 receptor antagonist

NE-100 hydrochloride is a potent, selective, and orally active sigma-1 receptor antagonist with Ki of 1.03 nM.
PC-60288

NE-100

Sigma 1 receptor antagonist

NE-100 is a potent, selective, and orally active sigma-1 receptor antagonist with Ki of 1.03 nM.
PC-60076

IPAG

Sigma 1 inhibitor

IPAG is a prototypic selective inhibitor of sigma1 receptor that engages the unfolded protein response and induces autophagy in cancer cells.
PC-45420

BD-1063 dhydrochloride

Sigma 1 receptor antagonist

BD-1063 dhydrochloride (BD1063) is a potent, selective sigma-1 receptor antagonist with binding Ki of 9 nM.
PC-45418

S1RA hydrochloride

Sigma 1 receptor antagonist

S1RA hydrochloride (E52862) is a potent and selective sigma-1 receptor (S1R) antagonist with Ki of 17 nM.
PC-45417

S1RA

Sigma 1 receptor antagonist

S1RA (E-52862) is a potent and selective sigma-1 receptor (S1R) antagonist with Ki of 17 nM.
PC-45419

PRE-084 hydrochloride

Sigma 1 receptor agonist

PRE-084 is a highly potent, selective sigma-1 receptor agonist with Ki of 2.2 nM, IC50 of 44 nM.
PC-42070

4-IBP

Sigma receptor agonist

4-IBP is a highly potent sigma receptor agonist with Ki of 1.7 nM and 25.2 nM for σ1 and σ2, respectively.
PC-26651

RC-106

Sigma receptor modulator

RC-106 is a high affinity, brain-penetrant, pan-sigma receptor modulator with Ki of 12.0 nM and 22.0 nM for S1R and S2R respectively.
PC-25927

SKF83959 hydrobromide

Sigma-1 receptor PAM

SKF83959 hydrobromide is a potent and selective dopamine D1-like receptor partial agonist with binding Ki of 1.18, 7.56, 920 and 399 nM for rat D1, D5, D2 and D3 receptors respectively, also is a potent allosteric modulator of Sigma 1 receptor (S1R), shows anti-seizure activities.
PC-25926

SKF83959

Sigma-1 receptor PAM

SKF83959 is a potent and selective dopamine D1-like receptor partial agonist with binding Ki of 1.18, 7.56, 920 and 399 nM for rat D1, D5, D2 and D3 receptors respectively, also is a potent allosteric modulator of Sigma 1 receptor (S1R), shows anti-seizure activities.

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