Weight | 254.414 g/mol |
---|---|
Formula | C16H30O2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 13 |
palmitoleic acid (2091-29-4, 373-49-9)
palmitoleate · palmitoleic acid, sodium salt, (Z)-isomer · C16:1n7
Score:
#1287 in Biochemistry
,
#3157 in Biology
,
#3952 in Chemistry
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- Sigma-Aldrich - palmitoleic acid74.80 - 983.00 USD
- Fisher Scientific - Search for palmitoleic acid
- TCI - palmitoleic acid34.00 - 153.00 USD
- The structure of the cytochrome p450BM-3 haem domain complexed with the fatty acid substrate, palmitoleic acid (Nature Structural & Molecular Biology, 1997)
- Differential effects of palmitate and palmitoleate on insulin action and glucose utilization in rat L6 skeletal muscle cells (Biochemical Journal, 2006)
- Trans-palmitoleic acid, metabolic risk factors, and new-onset diabetes in U.S. Adults: a cohort study. (Annals of Internal Medicine, 2010)
- Palmitoleic Acid Isomer (C16:16) in Human Skin Sebum Is Effective against Gram-Positive Bacteria (Skin Pharmacology and Applied Skin Physiology, 2003)
- Chronic administration of palmitoleic acid reduces insulin resistance and hepatic lipid accumulation in KK-Ay Mice with genetic type 2 diabetes. (Lipids in Health and Disease, 2011)
- Plasma palmitoleic acid content and obesity in children. (The American Journal of Clinical Nutrition, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - palmitoleate
- palmitoleic acid, sodium salt, (Z)-isomer
- C16:1n7
- palmitoleic acid, (E)-isomer
- palmitoleic acid, potassium salt, (Z)-isomer
- palmitelaidic acid
- palmitoleic acid, (Z)-isomer
- C16:1 trans-9
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SMILESCCCCCCC=CCCCCCCCC(=O)O
-
InChIKeySECPZKHBENQXJG-UHFFFAOYSA-N
- Pubchem - palmitoleic acid
- Wikipedia - palmitoleic acid
Palmitoleic acid, or (9Z)-hexadec-9-enoic acid, is an omega-7 monounsaturated fatty acid with the formula CH3(CH2)5CH=CH(CH2)7COOH that is a common constituent of the glycerides of human adipose tissue. It is present in all tissues but, in general, found in higher concentrations in the liver. It is biosynthesized from palmitic acid by the action of the enzyme Stearoyl-CoA desaturase-1.
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