Pyrrolidines
Medchemexpress LLC HY-15298A 10mg Medchemexpress, Grazoprevir potassium salt CAS:1206524-86-8 Purity:>98%
Medchemexpress, HY-15298A 10mg Grazoprevir potassium salt CAS:1206524-86-8 Grazoprevir potassium salt (MK-5172 potassium salt) is a selective inhibitor of Hepatitis C virus NS3/4a protease with broad activity across genotypes and resistant variants, with Kis of 0.01 nM (gt1b), 0.01 nM (gt1a), 0.08 nM (gt2a), 0.15 nM (gt2b), 0.90 nM (gt3a), respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
eMolecules Medchem Express / Grazoprevir potassium salt / 5mg / 446265389 / HY-15298A / / 1206524-86-8 / MFCD25976701 / 805.000 / C38H49KN6O9S
Medchem Express / Grazoprevir potassium salt / 5mg / 446265389 / HY-15298A / / 1206524-86-8 / MFCD25976701 / 805.000 / C38H49KN6O9S
AdipoGen Bisindolylmaleimide I (5 mg)
Chemical. CAS: 133052-90-1. Formula: C25H24N4O2. MW: 412.5. Cell permeable kinase inhibitor with improved selectivity for protein kinase C (PKC) (Ki = 10 nM). Competetive inhibitor for the ATP-binding site of PKC. Anti-inflammatory. Binds to P-glycoprotein. Telomerase activity inhibitor. Potent glycogen synthase kinase-3 (GSK-3) inhibitor. Necrosis inhibitor. Blocks hERG potassium channels. Promotes osteoblastogenesis in human mesenchymal stem cells.
AdipoGen Bisindolylmaleimide I HCl
Chemical. CAS 176504-36-2. Formula C25H24N4O2 . HCl. MW 412.5 . 36.5. Cell permeable kinase inhibitor with improved selectivity for protein kinase C PKC Ki = 10 nM. Competitive inhibitor for the ATP-binding site of PKC. Anti-inflammatory. Binds to P-glycoprotein. Telomerase activity inhibitor. Potent glycogen synthase kinase-3 GSK-3 inhibitor. Necrosis inhibitor. Blocks hERG potassium channels. Promotes osteoblastogenesis in human mesenchymal stem cells.
AdipoGen Bisindolylmaleimide I free b
Chemical. CAS 133052-90-1. Formula C25H24N4O2. MW 412.5. Cell permeable kinase inhibitor with improved selectivity for protein kinase C PKC Ki = 10 nM. Competetive inhibitor for the ATP-binding site of PKC. Anti-inflammatory. Binds to P-glycoprotein. Telomerase activity inhibitor. Potent glycogen synthase kinase-3 GSK-3 inhibitor. Necrosis inhibitor. Blocks hERG potassium channels. Promotes osteoblastogenesis in human mesenchymal stem cells.