
CAS 1800505-64-9
:Fórmula:C26H26N6O2
InChI:InChI=1S/C26H26N6O2/c1-26(2,3)23-13-24(30-34-23)29-25(33)11-17-5-8-20(9-6-17)32-16-27-21-12-18(7-10-22(21)32)19-14-28-31(4)15-19/h5-10,12-16H,11H2,1-4H3,(H,29,30,33)
Clave InChI:NJLMIILZNLZZFW-UHFFFAOYSA-N
SMILES:CC(C)(C)C1=CC(=NO1)NC(=O)CC2=CC=C(C=C2)N3C=NC4=C3C=CC(=C4)C5=CN(N=C5)C
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Pz-1
CAS:N-(5-(tert-Butyl)isoxazol-3-yl)-2-(4-(5-(1-methyl-1H-pyrazol-4-yl)-1H-benzo[d]imidazol-1-yl)phenyl)acetamideFórmula:C26H26N6O2Pureza:99%Peso molecular:454.52N-(5-tert-Butyl-1,2-oxazol-3-yl)-2-{4-[5-(1-methyl-1H-pyrazol-4-yl)-1H-1,3-benzodiazol-1-yl]phenyl}acetamide
CAS:N-(5-tert-Butyl-1,2-oxazol-3-yl)-2-[4-(5-(1-methyl-1H-pyrazol-4-yl)-1H-1,3-benzodiazol-1-yl)phenyl]acetamide (TPOXX) is a new potent and broad spectrum antifungal agent with photochemical properties. It has been shown to be active against opportunistic fungal pathogens, such as Candida glabrata and bacterial strains, including Pseudomonas aeruginosa. TPOXX is also effective against Gram positive bacteria, including methicillin resistant Staphylococcus aureus (MRSA). TPOXX inhibits the enzyme DNA polymerase and is a competitive inhibitor of topoisomerase I. The reaction mechanism of TPOXX involves the formation of adducts that are stabilized by hydrogen bonds between the carbonyl group of theFórmula:C26H26N6O2Pureza:Min. 95%Peso molecular:454.52 g/molPz-1
CAS:Pz-1 is an inhibitor of VEGFR2 and RET (rearranged during transfection) tyrosine kinase that blocks the blood supply required for RET-stimulated growth.Fórmula:C26H26N6O2Pureza:99.89%Forma y color:White SolidPeso molecular:454.5236




