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A412452-25mgInformationACT-389949 is a potent, selective agonist of formyl peptide receptor type 2 (FPR2)/Lipoxin A4 receptor (ALX) with EC50 of 3 nM for FPR2/ALX internalization into monocytes. ACT-389949 has potential for inflammatory disorders.
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A412452-50mgInformationACT-389949 is a potent, selective agonist of formyl peptide receptor type 2 (FPR2)/Lipoxin A4 receptor (ALX) with EC50 of 3 nM for FPR2/ALX internalization into monocytes. ACT-389949 has potential for inflammatory disorders.
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A412452-5mgInformationACT-389949 is a potent, selective agonist of formyl peptide receptor type 2 (FPR2)/Lipoxin A4 receptor (ALX) with EC50 of 3 nM for FPR2/ALX internalization into monocytes. ACT-389949 has potential for inflammatory disorders.
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A414096-100mgInformationACY-738 inhibitsHDAC6with low nanomolar potency (IC50=1.7 nM) and a selectivity of 60- to 1500-fold over class I HDACs.TargetsHDAC6 (Cell-free) 1.7 nMIn vivoACY-738 induces dramatic increases in α-tubulin acetylation in brain and
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A414096-10mgInformationACY-738 inhibitsHDAC6with low nanomolar potency (IC50=1.7 nM) and a selectivity of 60- to 1500-fold over class I HDACs.TargetsHDAC6 (Cell-free) 1.7 nMIn vivoACY-738 induces dramatic increases in α-tubulin acetylation in brain and
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A414096-2mgInformationACY-738 inhibitsHDAC6with low nanomolar potency (IC50=1.7 nM) and a selectivity of 60- to 1500-fold over class I HDACs.TargetsHDAC6 (Cell-free) 1.7 nMIn vivoACY-738 induces dramatic increases in α-tubulin acetylation in brain and