| Weight | 187.287 g/mol |
|---|---|
| Formula | C9H21N3O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 8 |
N8-Acetylspermidine (13431-24-8, 34450-15-2)
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- Association constants for the interaction of double-stranded and single-stranded DNA with spermine, spermidine, putrescine, diaminopropane, N1- and N8-acetylspermidine, and magnesium: determination from analysis of the broadening of thermal denaturation curves (Archives of Biochemistry and Biophysics, 1986)
- Deacetylation of N8-acetylspermidine by subcellular fractions of rat tissue. (Archives of Biochemistry and Biophysics, 1978)
- Separation of N1- and N8-acetylspermidine isomers by reversed-phase column liquid chromatography after derivatization with dansyl chloride (Journal of Chromatography B: Biomedical Sciences and Applications, 1986)
- The chemistry of naturally occurring polyamines. 6. Efficient syntheses of N1- and N8-acetylspermidine (Journal of Organic Chemistry, 1983)
- A selective inhibitor of N8-acetylspermidine deacetylation in mice and HeLa cells without effects on histone deacetylation (Archives of Biochemistry and Biophysics, 1989)
- Design and synthesis of inhibitors of N8-acetylspermidine deacetylase. (Journal of Medicinal Chemistry, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(=O)NCCCCNCCCN
-
InChIKeyFONIWJIDLJEJTL-UHFFFAOYSA-N
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Synthesis
acetamide
+
Reactant
(Alkylation of primary amines)
acetamide
+
Reactant
(Amide N-alkylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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