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6 n propyl 2 thiouracil

Manufactured by Merck Group
Sourced in Italy

6-n-propyl-2-thiouracil is a laboratory reagent used for various research and analytical applications. It is a chemical compound with the formula C7H10N2OS. The primary function of this product is to serve as a precursor or intermediate in the synthesis of other chemical compounds. No further details on its intended use or applications are provided.

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4 protocols using 6 n propyl 2 thiouracil

1

Determining PROP Taster Status

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PROP taster status was assessed using a 3.2 mm PROP solution, prepared by dissolving 0.545 g/L of 6-n-propyl-2-thiouracil (Sigma-Aldrich, Burlington, MA, USA) into deionized water. Subjects rated the intensity of bitterness of two identical samples by using the generalized labelled magnitude scale (gLMS) [51 (link)]. Sample presentation and evaluation procedure were reported in Bartoshuk et al. [55 (link)]. PROP taster status of each subject was defined based on the average rating of the two replicates. Subjects were classified for responsiveness to PROP bitterness into three classes, applying previously used cut-off values [45 (link)], as follows: no-taster = NT (ratings on gLMS ≤ moderate, 17), medium-taster = MT (17 < ratings on gLMS < 53), and super-taster = ST (ratings on gLMS ≥ very strong, 53).
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2

Antioxidant Assay Protocol for Liver Cells

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Flutamide (2-methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]-propanamide), glucose oxidase from Aspergillus niger (type II, 15,000–50,000 units/g solid), peroxidase from horseradish (type II, 150–250 units/mg solid), 6-N-propyl-2-thiouracil (PTU), N-acetyl-L-cysteine (NAC), (±)-6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox), 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL), N,N′-diphenyl-p-phenylenediamine (DPPD), resveratrol (3,5,4′-trihydroxy-trans-stilbene), and all other chemicals were purchased from Sigma-Aldrich Corp. (Oakville, ON, Canada). Type II collagenase (from Clostridium histolyticum) was purchased from Worthington Biochemical Corp. (Lakewood, NJ, USA). 4-(2-Hydroxyethyl) piperazine-1-ethanesulfonic acid (HEPES) was purchased from Boehringer-Mannheim Ltd. (Montreal, QC, Canada).
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3

Assessing Chemosensory Responsiveness and PROP Taster Status

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To assess individual responsiveness to chemosensory stimulation, seven aqueous solutions containing only one stimulus at a time were included in the study. The stimuli corresponded to the basic tastes (i.e., bitterness, sourness, sweetness, saltiness, and umami), the chemesthetic sensation of pungency, and the tactile sensation of astringency. The aqueous solutions were prepared to elicit an expected moderate/strong sensation on a general Labeled Magnitude Scale (gLMS) presented in vertical position [51 (link)]. The concentrations of the chemical reagents (European Pharmacopoeia Reference Standard Sigma-Aldrich, Milano, Italy) were as follows: citric acid, 4 g/kg (sourness); caffeine, 3 g/kg (bitterness); sucrose, 200 g/kg (sweetness); sodium chloride, 15 g/kg (saltiness); monosodium glutamate, 10 g/kg (umami); capsaicin, 1.5 mg/kg (pungent); and aluminium sulphate, 0.8 g/kg (astringency).
To assess participants’ PROP taster status, supra-threshold 3.2 mM PROP solution was prepared by dissolving 0.5447 g/L of 6-n-propyl-2-thiouracil (European Pharmacopoeia Reference Standard, Sigma-Aldrich, Milano, Italy) in deionized water in accordance with the PROP status assessment procedure described in [52 (link)].
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4

Bitter Taste Perception Evaluation

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A 3.2 mM solution of 6-n-propyl-2-thiouracil (European Pharmacopoeia Reference Standard, Sigma Aldrich, Milano, Italy) was prepared by dissolving 0.5447 g/L in deionized water [11 (link)]. Respondents evaluated the bitter intensity of two identical samples (10 mL) using the gLMS, presented monadically in white plastic cups and coded with two different three-digit codes [7 (link)]. Participants were instructed to hold each sample in their mouth for 10 s, expectorate, and then wait 20 s before evaluating the bitterness intensity. In order to control for carry-over effects after the first evaluation, a break of 90 s was taken between the two evaluations. During this break, participants rinsed their mouth with water (30 s), had a cracker (30 s) then rinsed their mouth again. Participants were grouped according to their PROP status on the basis of arbitrary cut-offs reported in previous studies [63 (link),69 (link),70 (link)] corresponding to Non Taster (NT; gLMS ≤moderate, 17), Medium Taster (MT) and Super Taster (ST; gLMS ≥very strong, 53).
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