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S650153-1mg[8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity ( IC 50 =5 μM) and inhibits COX-2 ( IC 50 =17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells.Form:Liquid
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S650153-5mg[8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity ( IC 50 =5 μM) and inhibits COX-2 ( IC 50 =17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells.Form:Liquid
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S656152-1ml[8]-Shogaol, one of the pungent phenolic compounds in ginger, exhibits anti-platelet activity ( IC 50 =5 μM) and inhibits COX-2 ( IC 50 =17.5 μM). [8]-Shogaol induces apoptosis in human leukemia cells.
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A651443-1mgAbatacept (CTLA4lg) is a soluble fusion protein consisting of the extra-cellular domain of human CTLA4 and a fragment of the Fc portion of human IgG1 (hinge and CH2 and 3 domains). Abatacept is a selective T-cell co-stimulation modulator and a
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A651443-5mgAbatacept (CTLA4lg) is a soluble fusion protein consisting of the extra-cellular domain of human CTLA4 and a fragment of the Fc portion of human IgG1 (hinge and CH2 and 3 domains). Abatacept is a selective T-cell co-stimulation modulator and a
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A646153-10mgABR-238901 is an orally active and potent S100A8/A9 blocker and inhibits S100A8/A9 interaction with its receptors RAGE (receptor for advanced glycation endproducts) and TLR4 (toll-like receptor 4). ABR-238901 has the potential for myocardial
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A646153-25mgABR-238901 is an orally active and potent S100A8/A9 blocker and inhibits S100A8/A9 interaction with its receptors RAGE (receptor for advanced glycation endproducts) and TLR4 (toll-like receptor 4). ABR-238901 has the potential for myocardial
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A646153-50mgABR-238901 is an orally active and potent S100A8/A9 blocker and inhibits S100A8/A9 interaction with its receptors RAGE (receptor for advanced glycation endproducts) and TLR4 (toll-like receptor 4). ABR-238901 has the potential for myocardial
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A646153-5mgABR-238901 is an orally active and potent S100A8/A9 blocker and inhibits S100A8/A9 interaction with its receptors RAGE (receptor for advanced glycation endproducts) and TLR4 (toll-like receptor 4). ABR-238901 has the potential for myocardial
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A654467-1mlABR-238901 is an orally active and potent S100A8/A9 blocker and inhibits S100A8/A9 interaction with its receptors RAGE (receptor for advanced glycation endproducts) and TLR4 (toll-like receptor 4). ABR-238901 has the potential for myocardial
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A650587-1mgAc-Gly-BoroPro is a selective FAP inhibitor with a K i of 23 nM.In VitroFAP has been implicated in cancer however, its specific role remains elusive because inhibitors that distinguish FAP from other prolyl peptidases like dipeptidyl peptidase-4
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A650587-5mgAc-Gly-BoroPro is a selective FAP inhibitor with a K i of 23 nM.In VitroFAP has been implicated in cancer however, its specific role remains elusive because inhibitors that distinguish FAP from other prolyl peptidases like dipeptidyl peptidase-4