Activin and Inhibin

L-826266 is a selective and competitive EP3 receptor antagonist. L-826266 can be used for convulsive disorders researchIn VitroIn adult rat hippocampal slices, L-826266 (1 μM) prevents the PGE2-induced decrease of Na+,K+-ATPase activity. MCE has not

L-873724 is a potent, orally bioavailable, selective and reversible non-basic cathepsin K inhibitor , with IC 50 s of 0.2, 178, 264, and 5239 nM for cathepsin K , cathepsin S , cathepsin L , cathepsin B , respectively L-873724 also exhibits an IC

L-Ascorbic Acid 2-Phosphate Sesquimagnesium Salt Hydrate.

L-Ascorbic Acid 2-Phosphate Sesquimagnesium Salt Hydrate.

L-Ascorbic Acid 2-Phosphate Sesquimagnesium Salt Hydrate.

L-Ascorbic Acid 2-Phosphate Sesquimagnesium Salt Hydrate.

L-Ascorbic Acid 2-Phosphate Sesquimagnesium Salt Hydrate.

L-Buthionine-(S,R)-sulfoximine hydrochloride is a cell-permeable, potent, fast acting, orally active and irreversible inhibitor of g-glutamylcysteine synthetase and depletes cellular glutathione levels. The IC 50 value of

L-Buthionine-(S,R)-sulfoximine hydrochloride is a cell-permeable, potent, fast acting, orally active and irreversible inhibitor of g-glutamylcysteine synthetase and depletes cellular glutathione levels. The IC 50 value of

L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) is an enantiomer of Eflornithine. L-Eflornithine is an irreversible ornithine decarboxylase ( ODC ) inhibitor with a K D of 1.3±0.3 µM, and a K inact of 0.15±0.03 min -1In VitroEflornithine

L-Eflornithine monohydrochloride (L-DFMO monohydrochloride) is an enantiomer of Eflornithine. L-Eflornithine is an irreversible ornithine decarboxylase ( ODC ) inhibitor with a K D of 1.3±0.3 µM, and a K inact of 0.15±0.03 min -1In VitroEflornithine

L-JNKI-1 is a cell-permeable peptide inhibitor specific for JNK .Appearance:SolidIC50&amp: Target:JNKIn Vivo:L-JNKI-1 has been shown to effectively inhibit JNK activity in in vivo studies. It is shown that Ang II induces a dose-dependent pressor