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A649787-100mgAZ5576 is a potent and highly selective CDK9 inhibitor (IC 50 : <:5 nM). AZ5576 can be used for hematological Malignancy researchForm:SolidIC50&: Target:CDK9 <:5 nM ().
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A649787-10mgAZ5576 is a potent and highly selective CDK9 inhibitor (IC 50 : <:5 nM). AZ5576 can be used for hematological Malignancy researchForm:SolidIC50&: Target:CDK9 <:5 nM ().
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A649787-25mgAZ5576 is a potent and highly selective CDK9 inhibitor (IC 50 : <:5 nM). AZ5576 can be used for hematological Malignancy researchForm:SolidIC50&: Target:CDK9 <:5 nM ().
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A649787-50mgAZ5576 is a potent and highly selective CDK9 inhibitor (IC 50 : <:5 nM). AZ5576 can be used for hematological Malignancy researchForm:SolidIC50&: Target:CDK9 <:5 nM ().
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A649787-5mgAZ5576 is a potent and highly selective CDK9 inhibitor (IC 50 : <:5 nM). AZ5576 can be used for hematological Malignancy researchForm:SolidIC50&: Target:CDK9 <:5 nM ().
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A655995-1mlAZ5576 is a potent and highly selective CDK9 inhibitor (IC 50 : <:5 nM). AZ5576 can be used for hematological Malignancy researchIC50&: Target:CDK9 <:5 nM ().
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A648582-10mgAZ82 is a selective kinesin-like protein KIFC1 (HSET/KIFC1) inhibitor, with a K i of 43 nM and an IC 50 of 300 nM for KIFC1.In VitroAZ82 is shown to specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal
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A648582-25mgAZ82 is a selective kinesin-like protein KIFC1 (HSET/KIFC1) inhibitor, with a K i of 43 nM and an IC 50 of 300 nM for KIFC1.In VitroAZ82 is shown to specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal
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A648582-50mgAZ82 is a selective kinesin-like protein KIFC1 (HSET/KIFC1) inhibitor, with a K i of 43 nM and an IC 50 of 300 nM for KIFC1.In VitroAZ82 is shown to specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal
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A648582-5mgAZ82 is a selective kinesin-like protein KIFC1 (HSET/KIFC1) inhibitor, with a K i of 43 nM and an IC 50 of 300 nM for KIFC1.In VitroAZ82 is shown to specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal
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A655482-1mlAZ82 is a selective kinesin-like protein KIFC1 (HSET/KIFC1) inhibitor, with a K i of 43 nM and an IC 50 of 300 nM for KIFC1.In VitroAZ82 is shown to specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal
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A648755-100mgPipofezine(Azafen or Azaphen) is a potent inhibitor of the reuptake of serotonin.IC50 Value:Target: SSRIsPipofezine is a tricyclic antidepressant (TCA) approved in Russia for the treatment ofdepression.Form:Solid.