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D651775-10mgDazcapistat is a potent calpain inhibitor, with IC 50 s of <:3 μM for calpain 1, calpain 2 and calpain 9, respectively (patent WO2018064119A1, compound 405).Form:Solid.
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D651775-25mgDazcapistat is a potent calpain inhibitor, with IC 50 s of <:3 μM for calpain 1, calpain 2 and calpain 9, respectively (patent WO2018064119A1, compound 405).Form:Solid.
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D651775-5mgDazcapistat is a potent calpain inhibitor, with IC 50 s of <:3 μM for calpain 1, calpain 2 and calpain 9, respectively (patent WO2018064119A1, compound 405).Form:Solid.
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D656819-1mlDazcapistat is a potent calpain inhibitor, with IC 50 s of <:3 μM for calpain 1, calpain 2 and calpain 9, respectively (patent WO2018064119A1, compound 405).
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D659286-10mgDB008 is potent and selective PARP16 inhibitor with an IC 50 value of 0.27 μM, containing an acrylamide electrophilic reagent. DB008 is membrane-permeable and marks PARP16 selectively.Appearance:SolidIC50&: Target:PARP16 0.27 μM (IC 50 )In
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D659286-1mgDB008 is potent and selective PARP16 inhibitor with an IC 50 value of 0.27 μM, containing an acrylamide electrophilic reagent. DB008 is membrane-permeable and marks PARP16 selectively.Appearance:SolidIC50&: Target:PARP16 0.27 μM (IC 50 )In
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D659286-5mgDB008 is potent and selective PARP16 inhibitor with an IC 50 value of 0.27 μM, containing an acrylamide electrophilic reagent. DB008 is membrane-permeable and marks PARP16 selectively.Appearance:SolidIC50&: Target:PARP16 0.27 μM (IC 50 )In
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D651610-10mgDBPR108 is a potent, selective, and orally bioavailable dipeptide-derived inhibitor of DPP4 with IC50 of 15 nM: no inhibition on DDP8 and DPP9.IC50 value: 15 nM Target: DPP4 inhibitorDBPR108 is an IC50=15 nM DPP IV inhibitor displays a more than
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D651610-50mgDBPR108 is a potent, selective, and orally bioavailable dipeptide-derived inhibitor of DPP4 with IC50 of 15 nM: no inhibition on DDP8 and DPP9.IC50 value: 15 nM Target: DPP4 inhibitorDBPR108 is an IC50=15 nM DPP IV inhibitor displays a more than
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D651610-5mgDBPR108 is a potent, selective, and orally bioavailable dipeptide-derived inhibitor of DPP4 with IC50 of 15 nM: no inhibition on DDP8 and DPP9.IC50 value: 15 nM Target: DPP4 inhibitorDBPR108 is an IC50=15 nM DPP IV inhibitor displays a more than
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D656743-1mlDBPR108 is a potent, selective, and orally bioavailable dipeptide-derived inhibitor of DPP4 with IC50 of 15 nM: no inhibition on DDP8 and DPP9.IC50 value: 15 nM Target: DPP4 inhibitorDBPR108 is an IC50=15 nM DPP IV inhibitor displays a more than
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D658771-10mgDC-BPi-11 hydrochloride is an inhibitor of bromodomain PHD finger transcription factor (BPTF), with an IC 50 value of 698 nM. DC-BPi-11 hydrochloride shows remarkable inhibition against leukemia cell proliferation.Appearance:SolidIC50&: