Dihydrocodeine/phenylephrine/phenylpropanolamine

UniPR129 is a potent Eph/ephrin antagonist. UniPR129 has the potential for the research of cancer disease.Form:Solid.

UniPR129 is a potent Eph/ephrin antagonist. UniPR129 has the potential for the research of cancer disease.Form:Solid.

Biochem/physiol Actions VUF 8430 dihydrobromide is a potent histamine H4 receptor agonist, with a 33-fold selectivity over the histamine H3 receptor and negligible affinity for the other histamine receptor. Features and Benefits This compound is

Androgen Receptor modulator.

gonadotropin-releasing hormone antagonists.

Wnt/β-catenin agonist 1 (compound 3f) is a Wnt/β-catenin signalling pathway agonist, with an EC 50 of 0.27 μM.In VitroEC50: 0.27 μM (Wnt/β-catenin). MCE has not independently confirmed the accuracy of these methods. They are for reference

Wnt/β-catenin agonist 1 (compound 3f) is a Wnt/β-catenin signalling pathway agonist, with an EC 50 of 0.27 μM.In VitroEC50: 0.27 μM (Wnt/β-catenin). MCE has not independently confirmed the accuracy of these methods. They are for reference

Wnt/β-catenin agonist 1 (compound 3f) is a Wnt/β-catenin signalling pathway agonist, with an EC 50 of 0.27 μM.In VitroEC50: 0.27 μM (Wnt/β-catenin). MCE has not independently confirmed the accuracy of these methods. They are for reference only.

YSFKPMPLaR.

YSFKPMPLaR.

Biochem/physiol Actions Z3670677764 is an inactive control for selective human melatonin MT2 receptor agonist UCSF4226 (ZINC128734226).

Biochem/physiol Actions Z3670677764 is an inactive control for selective human melatonin MT2 receptor agonist UCSF4226 (ZINC128734226).