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2 aminoanthracene 2 aa

Manufactured by Fujifilm
Sourced in Japan

2-aminoanthracene (2-AA) is a chemical compound used in laboratory applications. It serves as a substrate or intermediate in various organic synthesis reactions. The core function of 2-AA is to provide a specific molecular structure that can be utilized for further chemical transformations or analyses. Detailed information about its intended use or applications is not available.

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5 protocols using 2 aminoanthracene 2 aa

1

Chemical Standards for Analysis

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Aflatoxin B1 (AFB1) and sodium azide (NaN3) were obtained from Sigma-Aldrich (St. Louis, USA). 2-Amino-3,4 dimethylimidazo[4,5-f]quinolone (MeIQ), 2-aminoanthracene (2-AA) and 2-(2-furyl)-3-(5-nitro-2-furyl)-acrylamide (AF-2) were purchased from Wako Pure Chemicals (Osaka, Japan). Collagenase type IV and 4′-6-diamidino-2-phenylindole (DAPI) were obtained from Gibco/ Invitrogen Corp. (Carlsbad, USA). The phenolic acid, flavonoid and anthocyanin standards for chemical analysis were high performance liquid chromatography grade. All other chemicals were at least analytical grade.
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2

Cytotoxicity and Oxidative Stress Analysis

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Aflatoxin B1 (AFB1), sodium azide (NaN3), phenylmethylsulfonyl fluoride (PMSF), resorufin, ethoxyresorufin, methoxyresorufin, erythromycin, phorbol 12-myristate 13-acetate (PMA), dihydrorhodamine 123 (DHR), and lipopolysaccharides (LPS) were obtained from Sigma Aldrich Corp (St. Louis, MO, USA). 2-Amino-3,4 dimethylimidazo [4,5-f] quinolone (MeIQ), 2-aminoanthracene (2-AA), and 2-(2-furyl)-3-(5-nitro-2-furyl)-acrylamide (AF-2) were provided by Wako Pure Chemicals (Osaka, Japan). Furthermore, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox) were acquired from Merck (Darmstadt, Germany). Collagenase type IV and 4′-6-diamidino-2-phenylindole (DAPI) were bought from the Gibco/Invitrogen Corp (Waltham, MA, USA). Fetal bovine serum (FBS), Dulbecco’s Modified Eagle Medium (DMEM) and Roswell Park Memorial Institute (RPMI) medium were purchased from Thermo Fisher Scientific Inc. (Waltham, MA, USA). All standard phytochemicals were of high-performance liquid chromatography (HPLC) grade, and all other chemicals were of analytical grade.
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3

Micronucleus Assay: Evaluating Genotoxicity

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The chemicals used as positive controls included: 2-(2-furyl)-3-(5-nitro-2furyl)acrylamide (AF-2), 2-aminoanthracene (2AA), and sodium azide (NaN3), purchased from Wako Pure Chemical Industries, Ltd., (Osaka, Japan); and 9-aminoacridine hydrochloride hydrate (9AA), purchased from Sigma-Aldrich Chemical Corp, Inc., (St. Louis, MO, USA). Mitomycin C (MMC), cyclophosphamide monohydrate (CP), and colchicine (CLC) were purchased from Kyowa Hakko Kirin Co., Ltd., (Tokyo, Japan), Sigma-Aldrich Chemical Corp, Inc., (St. Louis, MO, USA), and Wako Pure Chemical Industries, Ltd., (Osaka, Japan), respectively. The olive oil used as a negative control in the bone marrow micronucleus assay in mice was purchased from Wako Pure Chemical Industries, Ltd. (Osaka, Japan). The bacterial strains Salmonella typhimurium and Escherichia coli were obtained from the National Institute of Technology and Evaluation (Chiba, Japan).
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4

Ames Test with Bacterial Strains

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Tester microorganisms used in the Ames test included Salmonella typhimurium strains TA100, TA1535, TA98, and TA1537 (provided by Dr Bruce N. Ames, University of California, Berkeley, CA, USA) and Escherichia coli WP2uvrA (provided by the National Institute of Technology and Evaluation, Chiba, Japan).
Water for injection was used as a negative control for all test microorganisms. The following compounds were employed as positive controls in studies conducted according to the preincubation method without metabolic activation: 2-(2-furyl)-3-(5-nitro-2-furyl) acrylamide (AF-2) (FUJIFILM Wako Pure Chemical, Lot No. CAH4001) at 0.01 µg/plate for TA100 and WP2uvrA and at 0.1 µg/plate for TA98, 0.5 µg/plate of sodium azide (NaN3) (FUJIFILM Wako Pure Chemical, Lot No. RSJ7863) for TA1535, and 80 µg/plate of 9-aminoacridine hydrochloride (9-AA) (Sigma-Aldrich, St. Louis, MO, USA, Lot No. BCBW4667) for TA1537. In assays conducted using the same method in the presence of metabolic activation, 2-aminoanthracene (2-AA) (FUJIFILM Wako Pure Chemical, Lot No. PTL0822) was used as the positive control at the following concentrations: 0.5 µg/plate for TA98, 1.0 µg/plate for TA100, 2.0 µg/plate for TA1535 and TA1537, and 10 µg/plate for WP2uvrA.
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5

Characterization of Xenobiotic Metabolism Enzymes

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2-Aminoanthracene (2-AA) and 2-(2-furyl)-3-(5-nitro-2-furyl)-acrylamide (AF-2) were obtained from Wako pure chemicals (Osaka, Japan). Aflatoxin B1 (AFB1), β-carotene, lycopene, resorufin, ethoxyresorufin and methoxyresorufin, erythromycin, cytochrome C, reduced glutathione, and 2, 6-dichlorophenolindolephenol (DCPIP) were provided by Sigma-Aldrich (St. Louis, MO, USA). Uridine-5′-diphosphoglucuronic acid was purchased from US Biological (Salem, MA, USA). Collagenase type IV and 4′-6-diamidino-2-phenylindole (DAPI) were acquired from Gibco/Invitrogen Corp. (Waltham, MA, USA), and anti-GSTA1 antibody and anti-UGT1A1 were purchased from Abcam (Cambridge, UK), respectively. All other chemicals were at least analytical grade.
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