Chemical
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- Catálogos PDF
Chemical Hay 28543 productos.
Bendamustine
Bendamustine (SDX-105 free base), a purine analogue, is a DNA cross-linking agent. Bendamustine activates DNA-damage stress response and apoptosis. Bendamustine has potent alkylating, anticancer and antimetabolite properties.
Thiethylperazine dimaleate
Thiethylperazine dimaleate, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine dimaleate is also a selective ABCC1activator that reduces amyloid-β (Aβ) load in mice. Thiethylperazine dimaleate has anti-emetic, antipsychotic and antimicrobial effects.
GPR39-C3
GPR39-C3 is a potent and orally available GPR39 agonist with EC50 values of 0.4 and 0.8 nM for rat and human receptors respectively.
Molidustat (BAY 85-3934)
Molidustat (BAY 85-3934) is a potent hypoxia-inducible factor prolyl hydroxylase (HIF-PH) inhibitor with IC50 of 480 nM, 280 nM, and 450 nM for PHD1, PHD2, and PHD, respectively.
IEM 1754 dihydrobromide
IEM 1754 dihydrobroMide is a selective AMPA/kainate receptor blockers for GluR1 and GluR3 with IC50 of 6 μM.
Fosciclopirox
Fosciclopirox suppresses growth of urothelial cancer by targeting the γ-secretase complex. Fosciclopirox selectively delivers the active metabolite, Ciclopirox (CPX), to the entire urinary tract. Ciclopirox has anticancer activity in a number of solid and hematologic malignancies.
Rebaudioside-D
Rebaudioside D is a glycoside found in stevia leaf and used as a sweetener.
SKL2001
SKL2001 is a novel agonist of Wnt/β-catenin pathway with anti-cancer activity.
D-Glucose 6-phosphate disodium salt
D-Glucose 6-phosphate disodium salt is a molecule produced when glucose is phosphorylated (at carbon 6). It is a common molecule in living cells and is involved in biochemical pathways such as the pentose phosphate pathway and glycolysis.
Dipotassium hydrogen phosphate trihydrate
Dipotassium Hydrogen Phosphate Trihydrate is commonly used as a buffering agent.
AZ304
AZ304 is a potent dual BRAF inhibitor targeting the kinase domains of wild type BRAF, V600E mutant BRAF with IC50 values of 79 nM and 38 nM respectively.
Bendazac L-Lysine
Bendazac L-Lysine is an aldose reductase (AR) inhibitor, which can be used to inhibit the activity of AR in the eye to prevent cataracts.