CAS 34450-16-3
:N1-Acetylspermidin-Dihydrochlorid
- Acetamide, N-[3-[(4-aminobutyl)amino]propyl]-, dihydrochloride
- Acetamide, N-[3-[(4-aminobutyl)amino]propyl]-, hydrochloride (1:2)
- N1-Acetylspermidine dihydrochloride
N(sup 1)-acetylspermidine dihydrochloride
CAS:Formel:C9H23Cl2N3OReinheit:95%Farbe und Form:SolidMolekulargewicht:260.2044N-(3-((4-Aminobutyl)Amino)Propyl)Acetamide Dihydrochloride
CAS:N-(3-((4-Aminobutyl)Amino)Propyl)Acetamide DihydrochlorideReinheit:95%Molekulargewicht:260.2g/molN1-Acetylspermidine hydrochloride
CAS:N1-Acetylspermidine hydrochlorideReinheit:≥98%Molekulargewicht:260.2g/molN1-Acetylspermidine-d3 Dihydrochloride
CAS:Kontrolliertes ProduktApplications N1-Acetylspermidine-d3 Dihydrochloride is the isotope labelled analog of N1-Acetylspermidine Dihydrochloride (A187845); an analog of Spermidine (S680400) which is an antineoplastic.
References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997)Formel:C9D3H18N3O·2HClFarbe und Form:NeatMolekulargewicht:263.223N1-Acetylspermidine hydrochloride
CAS:N1-Acetylspermidine HCl, an acetyl spermidine derivative, boosts polyamine oxidase levels in colorectal adenocarcinomas.Formel:C9H23Cl2N3OReinheit:99.76%Farbe und Form:SolidMolekulargewicht:260.2N1- Acetylspermidine Dihydrochloride
CAS:Applications Dihydrochloride salt of N1-Acetylspermidine which is an analog of Spermidine (S680400), an antineoplastic.
References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997);Formel:C9H21N3O·2ClHFarbe und Form:Off-WhiteMolekulargewicht:260.2N1-Acetylspermidine-d6 Dihydrochloride
CAS:Kontrolliertes ProduktApplications Labelled Dihydrochloride salt of N1-Acetylspermidine which is an analog of Spermidine (S680400), an antineoplastic.
References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997);Formel:C9H17D6Cl2N3OFarbe und Form:NeatMolekulargewicht:266.24N1-Acetylspermidine dihydrochloride
CAS:N-Acetylspermidine dihydrochloride is a polyamine oxidase inhibitor that has been shown to be useful in the treatment of cancer. It inhibits the synthesis of ornithine and N-acetylornithine, which are intermediates in polyamine biosynthesis. Inhibition of polyamine biosynthesis may lead to a decrease in cellular proliferation and an increase in apoptosis. The effect of this drug on human tissues has been studied using high performance liquid chromatography (HPLC). This drug also inhibits the activity of human urine decarboxylase, leading to a decrease in urinary excretion of ornithine and increased urinary excretion of putrescine.
Formel:C9H23Cl2N3OReinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:260.2 g/mol





