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11 cooh thc

Manufactured by Merck Group
Sourced in United States

11-COOH-THC is a chemical compound that can be used for laboratory research purposes. It is a metabolite of tetrahydrocannabinol (THC), the main psychoactive compound found in cannabis. This compound can be utilized in various analytical and research applications, but its specific functions and intended uses should not be extrapolated upon.

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2 protocols using 11 cooh thc

1

Quantitative Analysis of Cannabinoids

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Acetonitrile and methanol (LC/MS grade), anhydrous magnesium sulfate (99.5% powder; MgSO4) and sodium chloride were purchased from Merck (Darmstadt, Germany); the Sepra C18-E sorbent (50 µm, 65 Å) used in the QuEChERS process was obtained from Phenomenex (Torrance, CA, USA).
The standards (certified reference materials) of THC (1.0 mg/mL in methanol T-005 Cerilliant), THC-d3 (1.0 mg/mL in methanol T-011 Cerilliant), 11-OH-THC (1.0 mg/mL in methanol H-027 Cerilliant), 11-OH-THC-d3 (100 µg/mL in methanol H-041 Cerilliant), 11-COOH-THC (1.0 mg/mL in methanol T-010 Cerilliant) and 11-COOH-THC-d3 (100 µg/mL in methanol T-004 Cerilliant) were acquired from Sigma-Aldrich (St. Louis, MO, USA). Deionized water was purified on a Milli-Q system (MilliporeSigma, Bedford, MA, USA). Working solutions were prepared in methanol. They were all kept under stable conditions at − 20 °C.
A standard mixture was prepared from individual stock standard solutions to obtain a concentration of 1 μg/mL in acetonitrile. All other working solutions for determining calibration curves, recovery percentages, and limits of detection were prepared by diluting the standard mixture in acetonitrile or in a blank blood sample.
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2

Mitigating ER Stress in Trophoblast Cells

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To prevent Δ9-THC-induced ER stress, we used tauroursodeoxycholic acid (TUDCA); TUDCA has been shown to relieve ER stress in several cell and tissue types, including the placenta [35, (link)37] (link). After seeding cells in 12-well plate, cells were pretreated for 1 h with 100 μM of TUDCA (Sigma-Aldrich), and then treated with 15 μM Δ9-THC for 24 h. This dose of TUDCA has been effective to ameliorate nicotine-induced ER stress and UPR activation in rat Rcho-1 trophoblast giants cells after 24 h [35] (link). Additionally, BeWo cells were also treated with 15 μM 11-COOH-THC (Sigma-Aldrich), the inactive THC metabolic, to assess its potential effects on ER stress.
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