There is no indication that this product is light sensitive in solution. It is recommended that solutions be stored in aliquots at - 20 deg C for up to 1 month. Keep containers tightly sealed. Avoid repeated freeze/thaw cycles.
238422
2-Bromohexadecanoic acid
~97%, PPARδ agonist, solid
Synonim(y):
2-Bromopalmitic acid
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Informacje o tej pozycji
Wzór liniowy:
CH3(CH2)13CH(Br)CO2H
Numer CAS:
Masa cząsteczkowa:
335.32
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352203
EC Number:
242-137-0
MDL number:
Beilstein/REAXYS Number:
1726517
Przejdź do
Pomoc techniczna
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Pozwól nam pomócNazwa produktu
2-Bromohexadecanoic acid, ~97%
InChI
1S/C16H31BrO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15H,2-14H2,1H3,(H,18,19)
SMILES string
CCCCCCCCCCCCCCC(Br)C(O)=O
InChI key
DPRAYRYQQAXQPE-UHFFFAOYSA-N
assay
~97%
form
solid
Quality Level
Gene Information
human ... PPARD(5467)
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Ta pozycja | |||
|---|---|---|---|
| form solid | form solid | form - | form solid |
| assay ~97% | assay ≥99.0% (GC) | assay ≥98.5% (GC) | assay ≥98% (HPLC) |
| Quality Level 100 | Quality Level - | Quality Level 100 | Quality Level 100 |
| Gene Information human ... PPARD(5467) | Gene Information human ... PPARD(5467) | Gene Information - | Gene Information - |
General description
PPARδ (peroxisome proliferator-activated receptor, delta isoform) acts as a transcription factor for gene expression as well as playing a role in lipid metabolism regulation; activity of this receptor is ligand-regulated. 2-Bromohexadecanoic acid is a metabolically stable analoge of the fatty acid palmitic acid that has been shown to be a natural ligand for the PPARδ receptor.[1] 2-Bromohexadecanoic acid has also been used in studies of fatty acid oxidation, palmitoylation, and glucose uptake.
Biochem/physiol Actions
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Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Joel Berger et al.
Annual review of medicine, 53, 409-435 (2002-01-31)
The peroxisome proliferator-activated receptors (PPARs) are a group of three nuclear receptor isoforms, PPAR gamma, PPAR alpha, and PPAR delta, encoded by different genes. PPARs are ligand-regulated transcription factors that control gene expression by binding to specific response elements (PPREs)
Abiy M Mohammed et al.
Biochemical pharmacology, 85(1), 109-114 (2012-10-25)
Phagocyte-like NADPH oxidase (Nox2) has been shown to play regulatory roles in the metabolic dysfunction of the islet β-cell under the duress of glucolipotoxic conditions and exposure to proinflammatory cytokines. However, the precise mechanisms underlying Nox2 activation by these stimuli
Aaron C Baldwin et al.
American journal of physiology. Endocrinology and metabolism, 302(11), E1390-E1398 (2012-03-23)
Exposure of insulin-producing cells to elevated levels of the free fatty acid (FFA) palmitate results in the loss of β-cell function and induction of apoptosis. The induction of endoplasmic reticulum (ER) stress is one mechanism proposed to be responsible for
Priyanka Tripathi et al.
Journal of lipid research, 62, 100021-100021 (2021-01-01)
Microtubules are polymers composed of αβ-tubulin subunits that provide structure to cells and play a crucial role in in the development and function of neuronal processes and cilia, microtubule-driven extensions of the plasma membrane that have sensory (primary cilia) or
Kenji Hayata et al.
Journal of pharmacological sciences, 108(3), 348-354 (2008-11-15)
To obtain compounds that promote glucose uptake in muscle cells, the novel cell lines A31-IS derived from Balb/c 3T3 A31 and C2C12-IS from mouse myoblast C2C12 were established. In both cell lines, glucose consumption was induced by insulin and suppressed
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