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17 octadecynoic acid 17 odya

Manufactured by Bio-Techne
Sourced in Germany

17-octadecynoic acid (17-ODYA) is a long-chain fatty acid analogue used in various research applications. It serves as a tool compound for studying lipid metabolism and signaling pathways. The core function of 17-ODYA is to act as a substrate or inhibitor in in vitro and in vivo experiments, enabling researchers to investigate specific enzymes and biological processes.

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2 protocols using 17 octadecynoic acid 17 odya

1

Vascular Reactivity Pharmacological Study

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The following drugs were used in this experiment: Nω-nitro L-arginine methyl ester (L-NAME), indomethacin, acetylcholine hydrochloride (ACh), phenylephrine, 1H-(1, 2, 4) oxadiazole (4, 3-alpha) quinoxaline-1-one (ODQ), catalase, baicalein 18 alpha-glycyrrhetinic acid (18α-GA), ouabain, glibenclamide, barium chloride (BaCl2), and psora-4 [5-(4-Phenylbutoxy)psoralen] (all purchased from Sigma-Aldrich Chemie GmbH, Steinheim, Germany), 17-octadecynoic acid (17-ODYA) and 1-[(2-chlorophenyl) Fdiphenylmethyl]-1H-pyrazole (TRAM-34) (Tocris Bioscience, Bristol, UK), iberiotoxin (IbTX), charybdotoxin (ChTX) and apamin (AnaSpec Inc., Fremont, CA, USA), margatoxin (MgTX), maurotoxin (MTX), α- and β-dendrotoxin (α- and β- DTX) (Alomone Labs, Jerusalem, Israel). indomethacin, ODQ, 17-ODYA, baicalein, glibenclamide and TRAM-34 were dissolved in dimethyl sulfoxide (DMSO). DMSO at ≤ 0.2% (v/v) did not influence vascular reactivity to agonists and antagonists tested, as described elsewhere73 (link). 18α-GA was dissolved in chloroform: ethanol (2:3) according to the manufacturer’s instructions and this solvent mixture did not affect the vasoreactivity (personal observation). Apamin, charybdotoxin, iberiotoxin and L-NAME were dissolved in phosphate buffer saline (PBS), whereas all other drugs were dissolved in distilled water.
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2

Vascular Function Drug Interactions

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The following drugs were used in this experiment: Nω-nitro L-arginine methyl ester (L-NAME), indomethacin, acetylcholine hydrochloride (ACh), phenylephrine, catalase, baicalein, 18 alpha-glycyrrhetinic acid (18α-GA), ouabain, glibenclamide, barium chloride (BaCl2), (all purchased from Sigma-Aldrich Chemie GmbH, Steinheim, Germany), 17-octadecynoic acid (17-ODYA) and 1-[(2-chlorophenyl) diphenylmethyl]-1H-pyrazole (TRAM-34) (Tocris Bioscience, Bristol, UK), iberiotoxin (IbTX), charybdotoxin (ChTX) and apamin (AnaSpec Inc., Fremont, CA, USA), margatoxin (MgTX), α- and β-dendrotoxin (α- and β- DTX) (Alomone Labs, Jerusalem, Israel). indomethacin, 17-ODYA, baicalein, glibenclamide and TRAM-34 were dissolved in dimethyl sulfoxide (DMSO). 18α-GA was dissolved in chloroform: ethanol (2:3) according to the manufacturer’s instructions. Apamin, ChTX, IbTX and L-NAME were dissolved in phosphate-buffered saline (PBS), whereas all other drugs were dissolved in distilled water.
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