
CAS 957476-07-2
:Formel:C20H24N2O8
InChl:InChI=1S/C20H24N2O8/c1-25-11-7-13(27-3)17(14(8-11)28-4)21-19(23)20(24)22-18-15(29-5)9-12(26-2)10-16(18)30-6/h7-10H,1-6H3,(H,21,23)(H,22,24)
InChI Key:NGVJMONAWAGMOA-UHFFFAOYSA-N
SMILES:COC1=CC(=C(C(=C1)OC)NC(=O)C(=O)NC2=C(C=C(C=C2OC)OC)OC)OC
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5 Produkte gefunden.
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N,N’-Bis(2,4,6-trimethoxyphenyl)oxalamide
CAS:Reinheit:95%Farbe und Form:SolidMolekulargewicht:420.42N,N'-Bis(2,4,6-trimethoxyphenyl)oxalamide
CAS:N,N'-Bis(2,4,6-trimethoxyphenyl)oxalamideFormel:C20H24N2O8Reinheit:97%Molekulargewicht:420.41N,N'-Bis(2,4,6-trimethoxyphenyl)oxalamide
CAS:Formel:C20H24N2O8Reinheit:98%Farbe und Form:SolidMolekulargewicht:420.4132N1,N2-Bis(2,4,6-trimethoxyphenyl)ethanediamide
CAS:N1,N2-Bis(2,4,6-trimethoxyphenyl)ethanediamideFormel:C20H24N2O8Reinheit:97% HPLCMolekulargewicht:420.41N1,N2-Bis(2,4,6-trimethoxyphenyl)ethanediamide
CAS:Adriamycin is a cytotoxic drug that inhibits the growth of cells by causing cross-linking in DNA. It is an analogue of the naturally occurring molecule bis(2,4,6-trimethoxyphenyl)ethanediamide. Adriamycin has been shown to inhibit cell proliferation in vitro and in vivo by interfering with DNA synthesis. This agent also inhibits the production of proteins and lipids needed for cellular division by binding to the purine base adenine. Adriamycin binds to the enzyme ribonucleotide reductase, which catalyzes the conversion of ribonucleosides into deoxyribonucleosides. Adriamycin has a relatively low activation energy and can be activated thermally or photolytically.
Formel:C20H24N2O8Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:420.41 g/molRef: 3D-FB171929
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