CAS 34450-16-3
:N1-Acetylspermidine dihydrochloride
Description:
N1-Acetylspermidine dihydrochloride is a chemical compound that serves as a derivative of spermidine, an important polyamine involved in cellular functions such as growth and differentiation. This compound is characterized by the presence of an acetyl group attached to the nitrogen atom at the first position of the spermidine backbone, which enhances its solubility and biological activity. It typically appears as a white to off-white crystalline powder and is soluble in water due to the presence of dihydrochloride salts. N1-Acetylspermidine is of interest in biochemical research, particularly in studies related to cell proliferation, apoptosis, and the regulation of gene expression. Its role in cellular metabolism and potential implications in cancer research make it a subject of ongoing investigation. As with many chemical substances, proper handling and storage are essential to maintain its stability and efficacy, and safety data sheets should be consulted for information regarding toxicity and safe usage.
Formula:C9H21N3O·2ClH
InChI:InChI=1S/C9H21N3O.2ClH/c1-9(13)12-8-4-7-11-6-3-2-5-10;;/h11H,2-8,10H2,1H3,(H,12,13);2*1H
InChI key:InChIKey=IVLOLMVLUOGVCZ-UHFFFAOYSA-N
SMILES:C(NCCCCN)CCNC(C)=O.Cl
Synonyms:- Acetamide, N-[3-[(4-aminobutyl)amino]propyl]-, dihydrochloride
- Acetamide, N-[3-[(4-aminobutyl)amino]propyl]-, hydrochloride (1:2)
- N1-Acetylspermidine dihydrochloride
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Found 9 products.
N(sup 1)-acetylspermidine dihydrochloride
CAS:Formula:C9H23Cl2N3OPurity:95%Color and Shape:SolidMolecular weight:260.2044N-(3-((4-Aminobutyl)Amino)Propyl)Acetamide Dihydrochloride
CAS:<p>N-(3-((4-Aminobutyl)Amino)Propyl)Acetamide Dihydrochloride</p>Purity:95%Molecular weight:260.2g/molN1-Acetylspermidine hydrochloride
CAS:N1-Acetylspermidine hydrochloridePurity:≥98%Molecular weight:260.2g/molN1-Acetylspermidine-d6 Dihydrochloride
CAS:Controlled Product<p>Applications Labelled Dihydrochloride salt of N1-Acetylspermidine which is an analog of Spermidine (S680400), an antineoplastic.<br>References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997);<br></p>Formula:C9H17D6Cl2N3OColor and Shape:NeatMolecular weight:266.24N1-Acetylspermidine-d3 Dihydrochloride
CAS:Controlled Product<p>Applications N1-Acetylspermidine-d3 Dihydrochloride is the isotope labelled analog of N1-Acetylspermidine Dihydrochloride (A187845); an analog of Spermidine (S680400) which is an antineoplastic.<br>References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997)<br></p>Formula:C9D3H18N3O·2HClColor and Shape:NeatMolecular weight:263.223N1-Acetylspermidine hydrochloride
CAS:<p>N1-Acetylspermidine HCl, an acetyl spermidine derivative, boosts polyamine oxidase levels in colorectal adenocarcinomas.</p>Formula:C9H23Cl2N3OPurity:99.76%Color and Shape:SolidMolecular weight:260.2N1- Acetylspermidine Dihydrochloride
CAS:<p>Applications Dihydrochloride salt of N1-Acetylspermidine which is an analog of Spermidine (S680400), an antineoplastic.<br>References Bergeron, R. et al.: J. Med. Chem, 40, 1475 (1997);<br></p>Formula:C9H21N3O·2ClHColor and Shape:Off-WhiteMolecular weight:260.20N1-Acetylspermidine dihydrochloride
CAS:<p>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.</p>Formula:C9H23Cl2N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:260.2 g/mol





