Cyclophosphamide anhydrous

Chemical structure: epipolythiodioxopiperazine Gliotoxin is the mycotoxin produced by Aspergillus fumigatus (AF). It is a hydrophobic metabolite of 326 Da.

Humulone (α-Lupulic acid), a prenylated phloroglucinol derivative, is a potent cyclooxygenase-2 (COX-2) inhibitor. Humulone acts as a positive modulator of GABA A receptor at low micromolar concentrations. Humulone is an inhibitor of bone

Humulone (α-Lupulic acid), a prenylated phloroglucinol derivative, is a potent cyclooxygenase-2 (COX-2) inhibitor. Humulone acts as a positive modulator of GABA A receptor at low micromolar concentrations. Humulone is an inhibitor of bone

Hypophyllanthin is a major lignan in Phyllanthus spp , with strong anti-inflammatory activity. Hypophyllanthin directly inhibits P-glycoprotein (P-gp) activity and did not interfere with multidrug resistance protein 2 (MRP2) activityIn

Hypophyllanthin is a major lignan in Phyllanthus spp , with strong anti-inflammatory activity. Hypophyllanthin directly inhibits P-glycoprotein (P-gp) activity and did not interfere with multidrug resistance protein 2 (MRP2) activityIn

Application Has been discovered and used as a reagent to propagate some organic reactions, such as cyclization and cleavage of diselenide or disulfide. Can also be used to prepare In-containing complexes.

Immunogen Fusion protein amino acids 1-1881 (full-length) of human Ankyrin-R Physical form PBS pH 7.4, 50% glyercol, 0.

PrEST Antigen ANKS6 ankyrin repeat and sterile alpha motif d

PyOxim [1] is a novel reagent which mediates coupling reactions with efficiencies superior to HATU and PyBOP and comparable to COMU. It is has excellent solubility in DMF and is stable in solution under an inert atmosphere for two days.

InformationRITA (NSC 652287) RITA (NSC 652287) induces both DNA-protein and DNA-DNA cross-links with no detectable DNA single-strand breaks, and also inhibits MDM2-p53 interaction by targeting p53.In vitroRITA shows a highly selective pattern of

InformationSalinosporamide A (NPI-0052, ML858, Marizomib, MRZ) is a novel marine derived proteasome inhibitor which inhibitsCT-L β5,C-L β1, andT-L β2proteasome activities in human erythrocyte-derived 20S proteasomes with IC50 of 3.5 nM, 430 nM, 28

TETRADECYLSUCCINIC ANHYDRIDE-