Dicarboxylic acids and derivatives
Selleck Chemical LLC MZ-101-E1913-25MG
MZ-101 (GYS1-IN-2) is a potent small molecule inhibitor of Glycogen synthase 1(GYS1) with an IC50 value of 0 041 M By depleting muscle glycogen MZ-101 treatment normalizes glycogen levels and corrects transcriptional and metabolic abnormalities in Pompe mice
Selleck Chemical LLC MZ-101-E1913-100MG
MZ-101 (GYS1-IN-2) is a potent small molecule inhibitor of Glycogen synthase 1(GYS1) with an IC50 value of 0 041 M By depleting muscle glycogen MZ-101 treatment normalizes glycogen levels and corrects transcriptional and metabolic abnormalities in Pompe mice
Medchemexpress LLC Uk-101 | 1000313-40-5 | 99.6% | 484.74 | C25H48N2O5Si | 10 MG
UK-101 is a potent, selective inhibitor of the immunoproteasome β1i (LMP2) subunit used as a biochemical probe to study immunoproteasome activity and apoptosis-related pathways.
- Potent LMP2 inhibition (IC50 ≈ 104 nM).
- High selectivity versus β1c and β5 subunits.
- High purity suitable for research use (≈99.6%).
- Soluble in DMSO (≈7.3 mg/mL); may require warming or sonication.
- Supplied in small quantities appropriate for laboratory assays.
- Commonly used in biochemical assays and apoptosis research.
Selleck Chemical LLC GlyH-101
GlyH-101 is a selective and reversible CFTR inhibitor with Ki of 4 3 M
Medchemexpress LLC Sulforhodamine 101 DHPE | 187099-99-6 | >95.0% | 1381.84 | C74H117N4O14PS2 | 1MG
Sulforhodamine 101 DHPE is a red fluorescent phospholipid probe created by conjugating dipalmitoyl phosphoethanolamine to sulforhodamine 101. It readily incorporates into lipid bilayers and is used for membrane imaging, monitoring probe colocalization in liposomes, and detecting protein-ligand interactions on supported bilayers. The dye exhibits excitation/emission peaks near 586/605 nm and is supplied as a powder with recommended cold storage.
Medchemexpress LLC ULK-101 50mg | 2443816-45-1 | 460.45 g/mol | C22H16F4N4OS | 50 MG
ULK-101 is a potent, selective small-molecule inhibitor of Unc-51-like autophagy-activating kinase 1 (ULK1) that suppresses autophagy and sensitizes cancer cells to nutrient stress. It is characterized in vitro with low-nanomolar activity against ULK1 and shows activity versus ULK2. Supplied as a powder for laboratory research use only.