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791056P

Avanti

2-OHOA

2-hydroxyoleic acid (sodium salt), powder

Szinonimák:

Minerval; NaCHOleate; 2OHOA

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

Tapasztalati képlet (Hill-képlet):
C18H33NaO3
CAS-szám:
Molekulatömeg:
320.44
MDL-szám:
UNSPSC kód:
12352211
NACRES:
NA.25

Teszt

>99% (TLC)

Forma

powder

kiszerelés

pkg of 1 × 1 g (791056P-1g)

gyártó/kereskedő neve

Avanti Research - A Croda Brand 791056P

lipidtípus

neutral lipids
neutral glycerides

kiszállítva

dry ice

tárolási hőmérséklet

−20°C

Általános leírás

2-hydroxyoleic acid (2-OHOA) is a synthetic and non-β oxidation-metabolizable oleic acid derivative. It contains 18 carbon atoms in its fatty acid chain length.

Alkalmazás

2-hydroxyoleic acid (2-OHOA) is suitable for use:
  • to study its antihypertensive action in adult spontaneously hypertensive rats (SHRs)
  • to study the chemical structure-effect relation of 2-OHOA in the reduction of body weight in rats
  • as an antitumor compound, to study its effect on xenografts lipidome based on imaging mass spectrometry (IMS)

Biokémiai/fiziológiai hatások

2-Hydroxy Oleic Acid is an inducer of cell cycle arrest and apoptosis in several cancer cell lines, including glioma, leukemia, breast and colon cancer lines. 2-Hydroxy Oleic Acid increases sphingomyelin (SM) levels in the membranes of tumor cells, which typically display decreased SM membrane content, and remodeled membranes, compared with normal cells. The compound has no effect on SM levels in non-cancer cells.
2-hydroxyoleic acid (2-OHOA) acts as a potential antihypertensive agent. Oral administration of 2-OHOA is used to reduce body weight.

Kiszerelés

20 mL Clear Glass Screw Cap Vial (791056P-1g)

Jogi információk

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Tárolási osztály kódja

11 - Combustible Solids


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Analitikai tanúsítványok (COA)

Lot/Batch Number

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Dokumentumtár megtekintése

2-Hydroxyoleic acid: a new hypotensive molecule
Alemany R, et al.
Hypertension, 43(2), 249-254 (2004)
Structure-effect relation of C18 long-chain fatty acids in the reduction of body weight in rats
Vogler O, et al.
International Journal of Obesity, 32(3), 464-464 (2008)
Victoria Lladó et al.
Biochimica et biophysica acta, 1838(6), 1619-1627 (2014-02-15)
This review summarizes the cellular bases of the effects of NaCHOleate (2-hydroxyoleic acid; 2OHOA; Minerval) against glioma and other types of tumors. NaCHOleate, activates sphingomyelin synthase (SGMS) increasing the levels of cell membrane sphingomyelin (SM) and diacylglycerol (DAG) together with
Silvia Terés et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(22), 8489-8494 (2012-05-16)
Despite recent advances in the development of new cancer therapies, the treatment options for glioma remain limited, and the survival rate of patients has changed little over the past three decades. Here, we show that 2-hydroxyoleic acid (2OHOA) induces differentiation
Alena Khmelinskaia et al.
Langmuir : the ACS journal of surfaces and colloids, 30(8), 2117-2128 (2014-02-05)
Recent research regarding 2-hydroxylated fatty acids (2OHFAs) showed clear evidence of their benefits in the treatment of cancer, inflammation, and neurodegenerative disorders such as Alzheimer's disease. Monolayer compressibility isotherms and isothermal titration calorimetry of 2OHFA (C18-C22) in phosphatidylcholine/phosphatidylethanolamine/sphingomyelin/cholesterol (1:1:1:1 mole

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