Passa al contenuto
Merck
Tutte le immagini(1)

Key Documents

View All Documentation

238422

Sigma-Aldrich

2-Bromohexadecanoic acid

~97%

Sinonimo/i:

2-Bromopalmitic acid

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula condensata:
CH3(CH2)13CH(Br)CO2H
Numero CAS:
18263-25-7
Peso molecolare:
335.32
Beilstein:
1726517
Numero CE:
242-137-0
Numero MDL:
MFCD00004215
Codice UNSPSC:
12352203
ID PubChem:
57648040
NACRES:
NA.77

Saggio

~97%

Forma fisica

solid

Stringa SMILE

CCCCCCCCCCCCCCC(Br)C(O)=O

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)
DPRAYRYQQAXQPE-UHFFFAOYSA-N

Informazioni sul gene

human ... PPARD(5467)

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

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. 2-Bromohexadecanoic acid has also been used in studies of fatty acid oxidation, palmitoylation, and glucose uptake.

Azioni biochim/fisiol

2-Bromohexadecanoic acid is a PPARδ agonist. It has also been shown to inhibit fatty acid oxidation, inhibit DHHC-mediated palmitoylation, and promote glucose uptake in rat cardiac cells and the insulin-sensitive murine fibroblast line A31-IS.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 8

1 of 8

Atglistatin ≥98% (HPLC)

Sigma-Aldrich

SML1075

Atglistatin

Cerulenin ≥98% (HPLC), from Cephalosporium caerulens

Sigma-Aldrich

C2389

Cerulenin

Esomeprazole ≥98% (HPLC)

Sigma-Aldrich

E7906

Esomeprazole

Sodium palmitate ≥98.5%

Sigma-Aldrich

P9767

Sodium palmitate

Palmitic acid for synthesis

Sigma-Aldrich

8.00508

Palmitic acid

Palmitic acid BioXtra, ≥99%

Sigma-Aldrich

P5585

Palmitic acid

N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine

Sigma-Aldrich

P4413

N,N,N′,N′-Tetrakis(2-pyridylmethyl)ethylenediamine

Tunicamycin Ready Made Solution 5 mg/mL in DMSO, from Streptomyces sp.

Sigma-Aldrich

SML1287

Tunicamycin Ready Made Solution

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
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
Benjamin C Jennings et al.
Journal of lipid research, 50(2), 233-242 (2008-10-02)
Pharmacologic approaches to studying palmitoylation are limited by the lack of specific inhibitors. Recently, screens have revealed five chemical classes of small molecules that inhibit cellular processes associated with palmitoylation (Ducker, C. E., L. K. Griffel, R. A. Smith, S.
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.