| Cat. No. |
Product Name |
Information |
| PC-45535 |
Azoramide
|
A small-molecule compound that improves ER protein-folding ability and activates ER chaperone capacity to protect cells against ER stress in multiple systems. |
| PC-42675 |
Neuropathiazol
|
A small molecule that induces selective neuronal differentiation and competitively suppresses astrocyte differentiation. |
| PC-42098 |
Madrasin
|
A small molecule inhibitor of pre-mRNA splicing that interferes with the early stages of spliceosome assembly and stalls spliceosome assembly at the A complex. |
| PC-45395 |
Olumacostat glasaretil
|
A small molecule inhibitor of acetyl coenzyme A (CoA) carboxylase (ACC). |
| PC-45557 |
RR6
|
A selective, reversible, and competitive Vanin inhibitor with IC50 of 0.54 uM for hVVN1 pantetheinase. |
| PC-45331 |
Bromethalin
|
A rodenticide that poisons the central nervous system by uncoupling mitochondrial oxidative phosphorylation, which causes a decrease in adenosine triphosphate (ATP) synthesis.. |
| PC-42291 |
Conduritol B epoxide
|
A potent, specific, irreversible glucocerebrosidase (acid β-glucosidase) inhibitor with Ki of 53 uM. |
| PC-42268 |
TN1
|
A potent, small molecule fetal hemoglobin (HbF) inducer with EC50 of 100 nM. |
| PC-45669 |
GSK-2256294A
|
A potent, selective soluble epoxide hydrolase (sEH, EPHX2) inhibitor with IC50 of 27/61/189 pM for recombinant human/rat/mouse sEH, respectively. |
| PC-45486 |
DZ-2002
|
A potent, reversible type III inhibitor of SAHH (S-adenosyl-L-homocysteine hydrolase) with Ki of 17.9 nM. |
| PC-45053 |
CH-5450
|
A potent, peptide-inhibitor of human chymase with Ki of 1 nM. |
| PC-42141 |
FCCP
|
A potent ionophore and uncoupler of oxidative phosphorylation in mitochondria that disrupts ATP synthesis by transporting protons across cell membranes. |
