Cat.No. | Name | Information |
---|---|---|
M6198 | Verucerfont | Verucerfont is a corticotropin-releasing factor receptor 1 (CRF1) antagonist with IC50s of ~6.1, >1000 and >1000 nM for CRF1, CRF2, and CRF-BP, respectively. |
M56170 | DMP 696 | DMP 696 is a selective corticotropin-releasing hormone receptor 1 (CRHR1) antagonist, used for the treatment of anxiety and depression. |
M54655 | K41498 TFA | K41498 TFA is an antisauvagine-30 (aSvg-30) analog and a strongly selective CRF2 receptor antagonist with Ki values of 0.66 nM, 0.62 nM, and 425 nM for human CRF2α, CRF2β, and CRF1 receptors, respectively.K41498 TFA inhibits sauvagine-stimulated cAMP accumulation in hCRF2α/hCRF2β expressing cells. K41498 TFA can be used in hypotension studies. |
M54646 | Astressin 2B TFA | Astressin 2B TFA is a potent and selective corticotropin-releasing factor receptor 2 (CRF2) antagonist with IC50 values of 1.3 and > 500 nM for CRF2 and CRF1, respectively. |
M21791 | Astressin | Astressin is a potent corticotropin releasing factor (CRF) antagonist. |
M10333 | CRF (bovine) TFA | CRF (bovine) TFA is a potent agonist of CRF receptor, and displaces [125I-Tyr]ovine CRF with a Ki of 3.52 nM. |
M9705 | CP-376395 | CP-376395 is a CRF1-selective antagonist. |
M8038 | CP-154526 hydrochloride | CP-154526 hydrochloride is a selective, non-peptide antagonist of corticotropin releasing factor receptors (CRF1) with a Ki of 2.7 nM. CP 154526 hydrochloride shows selective for CRF1 over CRF2 (Ki = >10 μM). |
M7611 | Antalarmin hydrochloride | Antalarmin hydrochloride is a non-peptide CRF1 corticotropin-releasing factor receptor antagonist with a Ki of 1 nM. |
M56169 | Antalarmin | Antalarmin is a selective nonpeptide corticotropin-releasing factor receptor 1 (CRHR1) antagonist with a Ki of 2.7 nM. |
M56168 | Antisauvagine-30 | Antisauvagine-30 (aSvg-30) is a potent, competitive and selective CRF2 receptor antagonist with Kd values of 1.4 nM and 153.6 nM for mouse CRF2β and rat CRF1 receptors, respectively. |
M56167 | NBI-27914 hydrochloride | NBI-27914 (hydrochloride) is a selective Corticotropin-Releasing Factor 1 (CRF1) receptor antagonist with a Ki value of 1.7 nM. |
M54394 | Urocortin, rat | Urocortin, rat (Urocortin (Rattus norvegicus)) is a neuropeptide and a potent endogenous CRFR agonist with Kis of 13 nM, 1.5 nM, and 0.97 nM for human CRF1, rat CRF2α and mouse CRF2β, respectively. |
M54287 | Urocortin, human | Urocortin, human, a 40-aa neuropeptide, acts as a selective agonist of endogenous CRF2 receptor, with Kis of 0.4, 0.3, and 0.5 nM for hCRF1, rCRF2α and mCRF2β, respectively. |
M54112 | CRF(6-33)(human) | CRF(6-33)(human) is a CRF binding protein (CRF-BP) ligand inhibitor. |
M54012 | α-Helical CRF(9-41) | α-Helical CRF(9-41) is a competitive CRF2 receptor antagonist with KB of ~100 nM. |
M53221 | (D-Phe12, Nle21, 38, α-Me-Leu37)-CRF (12-41) (human, rat) | (D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) is a CRF antagonist. |
M53220 | Urocortin III, mouse | Urocortin III, mouse is a corticotropin-releasing factor (CRF)-related peptide. |
M53219 | Sauvagine | Sauvagine, a 40-amino-acid neuropeptide from the skin of the frog, is a mammalian CRF agonist. |
M53218 | a-Helical Corticotropin Releasing Factor (9-41) | α-Helical Corticotropin Releasing Factor (9-41) is a corticotropin releasing factor (CRF) antagonist. |
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