Sitagliptin phosphate hydrate

Biochem/physiol Actions PPTN is a very potent (IC 50 = 1 nM) P2Y14 receptor antagonist that does not interact with any other P2Y receptor at concentrations up to 10 &#956:M. PPTN blocks UDP-glucose inhibition of forskolin-induced cAMP

Biochem/physiol Actions PPTN is a very potent (IC 50 = 1 nM) P2Y14 receptor antagonist that does not interact with any other P2Y receptor at concentrations up to 10 &#956:M. PPTN blocks UDP-glucose inhibition of forskolin-induced cAMP

General description Pyridoxal 5&#8242:-phosphate (PLP) is synthesized in a multiple-step process. The two pathways inlcude pyridoxal phosphate biosynthetic protein (PdxA)- pyridoxine-5&#8242:-phosphate synthase (PdxJ) pathway and the pyridoxal

General description Pyridoxal 5&#8242:-phosphate (PLP) is synthesized in a multiple-step process. The two pathways inlcude pyridoxal phosphate biosynthetic protein (PdxA)- pyridoxine-5&#8242:-phosphate synthase (PdxJ) pathway and the pyridoxal

General description Pyridoxal 5&#8242:-phosphate (PLP) is synthesized in a multiple-step process. The two pathways inlcude pyridoxal phosphate biosynthetic protein (PdxA)- pyridoxine-5&#8242:-phosphate synthase (PdxJ) pathway and the pyridoxal

General description Pyridoxal-phosphate (PLP, pyridoxal-5&#8242:-phosphate, P5P) is a prosthetic group of some enzymes. It is the active form of vitamin B6, which comprises three natural organic compounds, pyridoxal, pyridoxamine and pyridoxine.

General description Cell signaling hormone that is prominent in the prostate, and belongs to the insulin superfamily Biochem/physiol Actions Relaxin 1 may function in regulating blood pressure, controlling heart rate, and releasing oxytocin and

SAR247799 (S1P1 agonist 3) is an oral activity, selective G-protein-biased sphingosine-1 phosphate receptor-1 (S1P1 ) agonist, with EC 50 s rang from 12.6 to 493 nM in S1P1-overexpressing cells and HUVECs. SAR247799 can be used for the research of

SAR247799 (S1P1 agonist 3) is an oral activity, selective G-protein-biased sphingosine-1 phosphate receptor-1 (S1P1 ) agonist, with EC 50 s rang from 12.6 to 493 nM in S1P1-overexpressing cells and HUVECs. SAR247799 can be used for the research of

Amino Acid Sequence Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe Biochem/physiol Actions Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe has contractile effects on vascular and gastric smooth muscle. It stimulates the

Amino Acid Sequence Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe Biochem/physiol Actions Ser-Phe-Leu-Leu-Arg-Asn-Pro-Asn-Asp-Lys-Tyr-Glu-Pro-Phe has contractile effects on vascular and gastric smooth muscle. It stimulates the

InformationSetipiprant (ACT-129968) Setipiprant (ACT-129968, KYTH-105) is a selective, orally available antagonist of the prostaglandin D2 receptor 2 (DP2) that that has been shown to have greater specificity for DP2 (CRTH2) than for DP1.