| Weight | 187.287 g/mol |
|---|---|
| Formula | C9H21N3O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 8 |
N1-Acetylspermidine (14278-49-0, 34450-16-3)
N(1)-acetylspermidine · 1-N-acetylspermidine · N-acetylspermidine
Score:
#61 in Molecular and cellular biology
,
#1906 in Biochemistry
,
#4072 in Biology
,
#5131 in Chemistry
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- Occurrence in high concentrations of N1-acetylspermidine and sym-homospermidine in the hamster epididymis (Biochemical and Biophysical Research Communications, 1982)
- Selective Elevation of the N1-Acetylspermidine Level in Human Colorectal Adenocarcinomas (Cancer Research, 1984)
- 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)
- Elevated N1-acetylspermidine levels in gerbil and rat brains after CNS injury (Journal of Neurochemistry, 2000)
- 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)
- Increased formation of N1-acetylspermidine in human breast cancer (Cancer Letters, 1989)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N(1)-acetylspermidine
- 1-N-acetylspermidine
- N-acetylspermidine
-
SMILESCC(=O)NCCCNCCCCN
-
InChIKeyMQTAVJHICJWXBR-UHFFFAOYSA-N
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Synthesis
acetamide
+
Reactant
(Alkylation of primary amines)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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