Sitagliptin phosphate

&beta-Sitosterol is a common plant steroid that possesses anticholesteremic properties. &beta-Sitosterol has recently been shown to induce G2/M arrest, endoreduplication, and apoptosis through the Bcl-2 and PI3K/Akt signaling pathways.

&beta-Sitosterol is a common plant steroid that possesses anticholesteremic properties. &beta-Sitosterol has recently been shown to induce G2/M arrest, endoreduplication, and apoptosis through the Bcl-2 and PI3K/Akt signaling pathways.

13(S)-HODE is the LO metabolite of linoleic acid. 13(S)-HODE modulates the PAF, LTB4, and fMLP-induced calcium influx in human PMNL.

15(S)-HETE is a major arachidonic acid metabolite produced by the 15-LO pathway. It has been characterized as a potent inhibitor of 5-LO.

15(S)-HETE is a major arachidonic acid metabolite produced by the 15-LO pathway. It has been characterized as a potent inhibitor of 5-LO.

15(S)-HETE is a major arachidonic acid metabolite produced by the 15-LO pathway. It has been characterized as a potent inhibitor of 5-LO.

3,4-Dephostatin is a PTP (protein tyrosine phosphatase) inhibitor that enhances growth factor-induced differentiation in PC12 cells possibly by sustaining MAP kinase activity. 3,4-Dephostatin can also be used as a protein S-nitrosylating agent and

MPB is a versatile thiol-specific biotinylating reagent. It is specific for sulfhydryl groups or reduced disulfide bonds and will not label proteins lacking a free sulfhydryl group at a pH between 6.

MPB is a versatile thiol-specific biotinylating reagent. It is specific for sulfhydryl groups or reduced disulfide bonds and will not label proteins lacking a free sulfhydryl group at a pH between 6.

MPB is a versatile thiol-specific biotinylating reagent. It is specific for sulfhydryl groups or reduced disulfide bonds and will not label proteins lacking a free sulfhydryl group at a pH between 6.

Information3PO 3PO (3-(3-pyridinyl)-1-(4-pyridinyl)-2-propen-1-one) is a small-molecule inhibitor of PFKFB3 with an IC50 of 22.9 μM for recombinant human PFKFB3 protein and does not inhibit PFK-1 activity. It suppresses glucose uptake, and decreases

Information3PO 3PO (3-(3-pyridinyl)-1-(4-pyridinyl)-2-propen-1-one) is a small-molecule inhibitor of PFKFB3 with an IC50 of 22.9 μM for recombinant human PFKFB3 protein and does not inhibit PFK-1 activity. It suppresses glucose uptake, and decreases