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B659183-5mgBio-AMS (TFA) is a potent bacterial biotin protein ligase inhibitor. Bio-AMS (TFA) possesses selective activity against Mycobacterium tuberculosis ( Mtb ) and arrests fatty acid and lipid biosynthesis.Appearance:SolidIC50&: Target:Biotin protein
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B647017-10mgbio-THZ1 is a biotinylated version of THZ1 and binds irreversibly to CDK7 . THZ1 is a selective and potent covalent CDK7 inhibitor with an IC 50 of 3.2 nMForm:SolidIC50&: Target:CDK7.
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B647017-25mgbio-THZ1 is a biotinylated version of THZ1 and binds irreversibly to CDK7 . THZ1 is a selective and potent covalent CDK7 inhibitor with an IC 50 of 3.2 nMForm:SolidIC50&: Target:CDK7.
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B647017-5mgbio-THZ1 is a biotinylated version of THZ1 and binds irreversibly to CDK7 . THZ1 is a selective and potent covalent CDK7 inhibitor with an IC 50 of 3.2 nMForm:SolidIC50&: Target:CDK7.
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B649735-5mgBitopertin R enantiomer (RG1678 R enantiomer: RO4917838 R enantiomer) is the R-enantiomer of Bitopertin. Bitopertin is a potent, noncompetitive glycine reuptake inhibitor, inhibits glycine uptake at human GlyT1 with a concentration exhibiting IC50
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B152550-100mgBIX-01294 trihydrochloride.
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B152550-250mgBIX-01294 trihydrochloride.
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B152550-25mgBIX-01294 trihydrochloride.
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B152550-5mgBIX-01294 trihydrochloride.
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B651566-10mgBIX-01338 hydrate is a histone lysine methyltransferase inhibitor.Form:SolidIC50&: Target:Histone lysine methyltransferase.
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B651566-5mgBIX-01338 hydrate is a histone lysine methyltransferase inhibitor.Form:SolidIC50&: Target:Histone lysine methyltransferase.
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B646794-100mgBJE6-106 (B106) is a potent, selective 3 rd generation PKCδ inhibitor with an IC 50 of 0.05 μM and targets selectivity over classical PKC isozyme PKCα (IC 50 =50 μM). BJE6-106 (B106) induces caspase-dependent apoptosis . BJE6-106 (B106) possesses