CAS 34450-16-3
:N1-Acetylspermidine dihydrochloride
- 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:Formula:C9H23Cl2N3OPurity:95%Color and Shape:SolidMolecular weight:260.2044N-(3-((4-Aminobutyl)Amino)Propyl)Acetamide Dihydrochloride
CAS:N-(3-((4-Aminobutyl)Amino)Propyl)Acetamide DihydrochloridePurity:95%Molecular weight:260.2g/molN1-Acetylspermidine hydrochloride
CAS:N1-Acetylspermidine hydrochloridePurity:≥98%Molecular weight:260.2g/molN1-Acetylspermidine-d6 Dihydrochloride
CAS:Controlled ProductApplications 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);Formula:C9H17D6Cl2N3OColor and Shape:NeatMolecular weight:266.24N1-Acetylspermidine-d3 Dihydrochloride
CAS:Controlled ProductApplications 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)Formula:C9D3H18N3O·2HClColor and Shape:NeatMolecular weight:263.223N1-Acetylspermidine hydrochloride
CAS:N1-Acetylspermidine HCl, an acetyl spermidine derivative, boosts polyamine oxidase levels in colorectal adenocarcinomas.Formula:C9H23Cl2N3OPurity:99.76%Color and Shape:SolidMolecular weight: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);Formula:C9H21N3O·2ClHColor and Shape:Off-WhiteMolecular weight:260.20N1-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.
Formula:C9H23Cl2N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:260.2 g/mol





