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E414173-100mgInformationEvobrutinib (M-2951) Evobrutinib (M-2951, MSC-2364447C) is a highly selective BTK inhibitor with an IC50 of 37.9 nM. It has potential anti-neoplastic activity.TargetsBTK (Cell-free assay) 37.9 nMIn vitroEvobrutinib can inhibit the
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E414173-10mgInformationEvobrutinib (M-2951) Evobrutinib (M-2951, MSC-2364447C) is a highly selective BTK inhibitor with an IC50 of 37.9 nM. It has potential anti-neoplastic activity.TargetsBTK (Cell-free assay) 37.9 nMIn vitroEvobrutinib can inhibit the
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E414173-25mgInformationEvobrutinib (M-2951) Evobrutinib (M-2951, MSC-2364447C) is a highly selective BTK inhibitor with an IC50 of 37.9 nM. It has potential anti-neoplastic activity.TargetsBTK (Cell-free assay) 37.9 nMIn vitroEvobrutinib can inhibit the
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E414173-50mgInformationEvobrutinib (M-2951) Evobrutinib (M-2951, MSC-2364447C) is a highly selective BTK inhibitor with an IC50 of 37.9 nM. It has potential anti-neoplastic activity.TargetsBTK (Cell-free assay) 37.9 nMIn vitroEvobrutinib can inhibit the
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E414173-5mgInformationEvobrutinib (M-2951) Evobrutinib (M-2951, MSC-2364447C) is a highly selective BTK inhibitor with an IC50 of 37.9 nM. It has potential anti-neoplastic activity.TargetsBTK (Cell-free assay) 37.9 nMIn vitroEvobrutinib can inhibit the
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