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A650647-5mgAdrenomedullin (16-31), human is amino acid residues 16-31 fragment of human adrenomedullin (hADM). Adrenomedullin has appreciable affinity for the CGRP1 receptor. Adrenomedullin (16-31), human possesses pressor activity in the systemic vascular bed
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A650641-100mgAdriforant hydrochloride (PF-3893787 hydrochloride) is a novel histamine H4 receptor antagonist binding affinity ( K i =2.4 nM) and is also a functional ( K i =1.56 nM) antagonist.In VitroAdriforant is tested and observed binding K i =2.4 nM and
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A650641-10mgAdriforant hydrochloride (PF-3893787 hydrochloride) is a novel histamine H4 receptor antagonist binding affinity ( K i =2.4 nM) and is also a functional ( K i =1.56 nM) antagonist.In VitroAdriforant is tested and observed binding K i =2.4 nM and
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A650641-50mgAdriforant hydrochloride (PF-3893787 hydrochloride) is a novel histamine H4 receptor antagonist binding affinity ( K i =2.4 nM) and is also a functional ( K i =1.56 nM) antagonist.In VitroAdriforant is tested and observed binding K i =2.4 nM and
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A650641-5mgAdriforant hydrochloride (PF-3893787 hydrochloride) is a novel histamine H4 receptor antagonist binding affinity ( K i =2.4 nM) and is also a functional ( K i =1.56 nM) antagonist.In VitroAdriforant is tested and observed binding K i =2.4 nM and
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A656356-1mlAdriforant hydrochloride (PF-3893787 hydrochloride) is a novel histamine H4 receptor antagonist binding affinity ( K i =2.4 nM) and is also a functional ( K i =1.56 nM) antagonist.In VitroAdriforant is tested and observed binding K i =2.4 nM and
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A651980-5mgAE-3763 is a peptide-based human neutrophil elastase inhibitor with an IC 50 of 29 nM.In VitroAE-3763 exhibits potent in vitro inhibitory activity against human neutrophil elastase as well as extremely high solubility and stability in water. MCE has
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A649710-100mgAER-271 is an inhibitor of aquaporin-4.In Vivo:Treatment with AER-271 ameliorated early cerebral edema measured at 3 h after CA vs vehicle treated rats. This treatment also attenuated early NDS. In contrast to rats treated with vehicle after CA,
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A649710-10mgAER-271 is an inhibitor of aquaporin-4.In Vivo:Treatment with AER-271 ameliorated early cerebral edema measured at 3 h after CA vs vehicle treated rats. This treatment also attenuated early NDS. In contrast to rats treated with vehicle after CA,
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A649710-25mgAER-271 is an inhibitor of aquaporin-4.In Vivo:Treatment with AER-271 ameliorated early cerebral edema measured at 3 h after CA vs vehicle treated rats. This treatment also attenuated early NDS. In contrast to rats treated with vehicle after CA,
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A649710-50mgAER-271 is an inhibitor of aquaporin-4.In Vivo:Treatment with AER-271 ameliorated early cerebral edema measured at 3 h after CA vs vehicle treated rats. This treatment also attenuated early NDS. In contrast to rats treated with vehicle after CA,
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A649710-5mgAER-271 is an inhibitor of aquaporin-4.In Vivo:Treatment with AER-271 ameliorated early cerebral edema measured at 3 h after CA vs vehicle treated rats. This treatment also attenuated early NDS. In contrast to rats treated with vehicle after CA,