| Weight | 335.326 g/mol |
|---|---|
| Formula | C16H31BrO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 14 |
2-Bromohexadecanoic acid (18263-25-7)
2-bromopalmitate · alpha-bromopalmitate · 2-bromopalmitate, potassium salt
Score:
#2645 in Biochemistry
,
#6579 in Chemistry
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- Inhibition of Protein Palmitoylation, Raft Localization, and T Cell Signaling by 2-Bromopalmitate and Polyunsaturated Fatty Acids (Journal of Biological Chemistry, 2000)
- Specific inhibition of mitochondrial fatty acid oxidation by 2-bromopalmitate and its co-enzyme A and carnitine esters (Biochemical Journal, 1972)
- 2-Bromopalmitate and 2-(2-hydroxy-5-nitro-benzylidene)-benzo[b]thiophen-3-one inhibit DHHC-mediated palmitoylation in vitro (Journal of Lipid Research, 2009)
- 2-Bromopalmitoyl-CoA and 2-bromopalmitate: promiscuous inhibitors of membrane-bound enzymes. (Biochimica et Biophysica Acta, 1992)
- Downregulation of leptin by free fatty acids in rat adipocytes: effects of triacsin C, palmitate, and 2-bromopalmitate. (Metabolism-clinical and Experimental, 2000)
- Profiling targets of the irreversible palmitoylation inhibitor 2-bromopalmitate (ACS Chemical Biology, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-bromopalmitate
- alpha-bromopalmitate
- 2-bromopalmitate, potassium salt
- 2-bromopalmitate, (+-)-isomer
- 2-bromopalmitate, 77Br-labeled
-
SMILESCCCCCCCCCCCCCCC(C(=O)O)Br
-
InChIKeyDPRAYRYQQAXQPE-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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