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首页-小分子抑制剂&激动剂-GPCR-Orexin Receptor

Request The Product List ofOrexin Receptor Orexin Receptor

Cat. No. Product Name Information
PC-60755

SB-649868

OX1R/OX2R antagonist

SB-649868 is a potent, selective, orally bioavailable, dual orexin OX1/OX2R antagonist with pKi of 9.4 and 9.5 respectively.
PC-60752

GSK-1059865

OX1R antagonist

GSK-1059865 is a highly potent, selective orexin-1 receptor (OX1R) antagonist with IC50 of 5.0 and 6.4 nM for hOX1R and rOX1R, respectively.
PC-60727

ACT-541468

Orexin receptor antagonist

ACT-541468 (Nemorexant) is a potent, selective, dual orexin receptor 1 and 2 (OX1 and OX2) antagonist with Kb of 0.52 and 0.78 nM, respectively.
PC-70015

JNJ-10397049

OX2R antagonist

JNJ-10397049 is a potent, selective, and bioavailable OX2 receptor (OX2R) antagonist with Kb of 4.5 nM.
PC-60062

Suvorexant

Orexin receptor antagonist

Suvorexant (MK-4305, MK4305) is a potent, CNS penetrant, orally available, dual orexin receptor antagonist with Ki of 0.55 and 0.35 nM for OX1R and OX2R, respectively.
PC-42731

SB-334867 free base

OX1R inhibitor

SB-334867 is the first selective Orexin-1 receptor (OX1R) antagonist with pKb of 7.4, displays 50-fold selectivity over OX2R (pKb 5.7).
PC-42730

SB-334867

OX1R inhibitor

SB-334867 (SB 334867A) is the first selective Orexin-1 receptor (OX1R) antagonist with pKb of 7.4.
PC-45062

Lemborexant

OX1R/OX2R antagonist

Lemborexant (E2006) is an orally active, potent, selective, dual Orexin receptor OX1/2 antagonist with binding Ki of 6/3 nM, respectively.
PC-45747

MK-1064

OX2R inhibitor

MK-1064 is a potent, selective, orally bioavailable Orexin 2 receptor (OX2R) antagonist with Ki/IC50 of 0.5/18 nM.
PC-45951

SB-408124

OX1R antagonist

SB-408124 is a potent, selective OX1 receptor (OX1R) antagonist with Ki of 57 nM (whole cell assay), and 27 nM (cell membrane-based SPA assay).
PC-42159

TCS-OX2-29

OX2R antagonist

TCS-OX2-29 is a potent, selective orexin-2 receptor (OX2R) antagonist with IC50 of 40 nM.
PC-42732

SB-674042

OX1R antagonist

SB-674042 is a potent, selective nonpeptide Orexin 1 receptor (OX1R) antagonist with Ki of 26.9 nM in the membrane SPA format, and Ki of 57 nM in the whole-cell assay.

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