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1 p hydroxyphenyl imidazole

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1-(p-hydroxyphenyl)imidazole is a chemical compound that functions as a laboratory reagent. It is used in various scientific and research applications, but a detailed description of its core function is not available while maintaining an unbiased and factual approach.

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Lab products found in correlation

Monobromobimane, by Merck Group (2 mentions) Cumene hydroperoxide, by Merck Group (2 mentions) Erastin, by Merck Group (2 mentions) Liproxstatin 1, by Merck Group (2 mentions) Disodium sulfide, by Merck Group (2 mentions) Diallyl tetrasulfide, by Thermo Fisher Scientific (2 mentions) 4 hydroxy 2 2 6 6 tetramethylpiperidin 1 oxyl tempol, by Merck Group (2 mentions) 7 diethylamino coumarin 3 carbohydrazide, by Merck Group (2 mentions) C11 bodipy, by Thermo Fisher Scientific (2 mentions) Depmpo, by Enzo Life Sciences (2 mentions) 3 6 di o thiosalicyl fluorescein ssp4, by Dojindo Laboratories (2 mentions) 3 mercaptopyruvate, by Merck Group (2 mentions) 5 aminolevulinic acid hydrochloride, by Merck Group (2 mentions) 2 2 azino bis 3 ethylbenzothiazoline 6 sulfonic acid, by Merck Group (2 mentions) Amplex red, by Thermo Fisher Scientific (2 mentions) S nitrosoglutathione, by Merck Group (2 mentions) 4 hydroxytamoxifen, by Merck Group (2 mentions) Cysteine, by Merck Group (2 mentions) Ferrocene, by Merck Group (2 mentions) Glutathione (gsh), by Merck Group (2 mentions)

2 protocols using 1 p hydroxyphenyl imidazole

1

Synthesis and Analysis of Sulfur Compounds

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3-aminophthalhydrazide (luminol), 1-(p-hydroxyphenyl)imidazole (HPI), disodium sulfide (Na2S), erastin, RSL3, cumene hydroperoxide (CHP), liproxstatin-1, 7-(diethylamino)coumarin-3-carbohydrazide (CHH), 4-hydroxytamoxifen (Tam), monobromobimane (MBB), cysteine (Cys), 3-mercaptopyruvate (3MP), cytochrome c (cyt c), glutathione reductase (GR), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), S-nitrosoglutathione (GSNO), ferrocene, 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL) and isopropyl β-d-1-thiogalactopyranoside (IPTG) were obtained from Sigma-Aldrich. BODIPY C11, diallyl tetrasulfide (DATS) and Amplex Red were obtained from Thermo Fisher Scientific. DEPMPO was obtained from Enzo. H2O2 was obtained from Roth. GSH and 5-aminolevulinic acid hydrochloride were obtained from Merck. Sodium disulfide (Na2S2), sodium tetrasulfide (Na2S4) and 3′,6′-di(O-thiosalicyl)fluorescein (SSP4) were obtained from Dojindo. The synthesis of GSSSG, GS34SSG and GSSSSG was performed as described previously43 . CSSSC was synthesized as described below.
Barayeu U., Schilling D., Eid M., Xavier da Silva T.N., Schlicker L., Mitreska N., Zapp C., Gräter F., Miller A.K., Kappl R., Schulze A., Friedmann Angeli J.P, & Dick T.P. (2022). Hydropersulfides inhibit lipid peroxidation and ferroptosis by scavenging radicals. Nature Chemical Biology, 19(1), 28-37.
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2

Redox Signaling Compound Synthesis and Detection

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3-Aminophthalhydrazide (luminol), 1-(p-hydroxyphenyl)imidazole (HPI), disodium sulfide (Na2S), erastin, RSL3, cumene hydroperoxide (CHP), liproxstatin-1, 7- (Diethylamino)coumarin-3-carbohydrazide (CHH), 4-hydroxytamoxifen (Tam), monobromobimane (MBB), cysteine (Cys), 3-mercaptopyruvate (3-MP), cytochrome c (cyt c), glutathione reductase (GR), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS), S- nitrosoglutathione (GSNO), ferrocene, 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPOL) and isopropyl β-D-1-thiogalactopyranoside (IPTG) were obtained from Sigma. BODIPY C11, diallyl tetrasulfide (DATS) and Amplex Red was obtained from ThermoFisher. DEPMPO was obtained from Enzo. H2O2 was obtained from Roth. Glutathione (GSH) and 5- aminolevulinic acid hydrochloride was obtained from Merck. Sodium disulfide (Na2S2), sodium tetrasulfide (Na2S4), and 3',6'-Di(O-thiosalicyl)fluorescein (SSP4) were obtained from Dojindo. The synthesis of GSSSG, GS34SSG and GSSSSG was performed as described previously 43 . CSSSC was synthesized as described below.
Barayeu U., Schilling D., Eid M., Xavier da Silva T.N., Schlicker L., Mitreska N., Zapp C., Gräter F., Miller A.K., Kappl R., Schulze A., Friedmann Angeli J.P, & Dick T.P. (2022). Hydropersulfides inhibit lipid peroxidation and ferroptosis by scavenging radicals. Nature Chemical Biology, 19(1), 28-37.
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