Metformin/pioglitazone

Biochem/physiol Actions 3-AP-Me is a dimethyl derivative of the ribonucleotide reductase inhibitor 3-AP (SML0568). 3-AP-Me is a potent inducer of ER stress and the unfolded protein response in cancer cell lines, incuding IRE1, PERK and ATF6

3-methoxy PGF1&alpha is a novel analog of PGF1&alpha with a methoxy group in the 3-position of the upper side chain. There are no published reports describing the pharmacology of 3-methoxy PGF1&alpha at this time.

3-methoxy PGF1&alpha is a novel analog of PGF1&alpha with a methoxy group in the 3-position of the upper side chain. There are no published reports describing the pharmacology of 3-methoxy PGF1&alpha at this time.

3-methoxy PGF1&alpha is a novel analog of PGF1&alpha with a methoxy group in the 3-position of the upper side chain. There are no published reports describing the pharmacology of 3-methoxy PGF1&alpha at this time.

A novel analog of PGF1α with a methoxy group in the 3-position of the upper side chain. No published reports describing the pharmacology of this compound.

A novel analog of PGF1α with a methoxy group in the 3-position of the upper side chain. No published reports describing the pharmacology of this compound.

3BETA 17ALPHA-DIACETOXYPREGN-5-EN-20-ONE

A metabolite of PGI2 enhances intracellular cAMP and cholesterol catabolism in bovine arterial smooth muscle cells.

7-Methoxyisoflavone 7-Methoxyisoflavone (MIF) is a potent activator of adenosine monophosphate-activated protein kinase (AMPK) .TargetsAMPK

Product Describtion:8-M-PDOT (AH-002) is a selective melatonin MT2 receptor agonist. 8-M-PDOT is 5.2-fold selective for MT2 over MT1 receptors. 8-M-PDOT binds human recombinant MT2 and MT2 receptors with pKi values of 8.23 and 8.95 respectively.

Product Describtion:8-M-PDOT (AH-002) is a selective melatonin MT2 receptor agonist. 8-M-PDOT is 5.2-fold selective for MT2 over MT1 receptors. 8-M-PDOT binds human recombinant MT2 and MT2 receptors with pKi values of 8.23 and 8.95 respectively.

Product Describtion:8-M-PDOT (AH-002) is a selective melatonin MT2 receptor agonist. 8-M-PDOT is 5.2-fold selective for MT2 over MT1 receptors. 8-M-PDOT binds human recombinant MT2 and MT2 receptors with pKi values of 8.23 and 8.95 respectively.