authentic standards for metabolites Search Results


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Onyx Pharmaceuticals authentic metabolite standards
In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and <t>metabolite</t> formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.
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Nemoto Science Co Ltd authentic standards of sesamin metabolites sc-1 and sc-2
In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and <t>metabolite</t> formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.
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Celgene authentic standards for metabolites
In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and <t>metabolite</t> formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.
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INDOFINE Inc ilg metabolites butein and sulfarein
In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and <t>metabolite</t> formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.
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Daiichi Sankyo authentic standard of the metabolites
In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and <t>metabolite</t> formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.
Authentic Standard Of The Metabolites, supplied by Daiichi Sankyo, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Taisho Pharmaceutical Co Ltd authentic metabolite standards
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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Eisai Inc authentic metabolite standards
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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Yoshitomi Pharmaceutical Industries authentic standards of the metabolites m1 to m4
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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Taisho Pharmaceutical Co Ltd authentic metabolite standards for m1, m2, m3 and m17
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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Eli Lilly authentic standard metabolites m5, m7, m8, m11, m17, and m18
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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Human Metabolome Technologies America authentic metabolite standard database
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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Shima Laboratories authentic standards of methylone metabolites
Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).
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In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and metabolite formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.

Journal: Drug Metabolism and Disposition

Article Title: In Vitro Metabolism of Oprozomib, an Oral Proteasome Inhibitor: Role of Epoxide Hydrolases and Cytochrome P450s

doi: 10.1124/dmd.117.075226

Figure Lengend Snippet: In vitro metabolism of oprozomib in human hepatocytes. (A) Representative ion chromatograms of oprozomib metabolites formed in human hepatocytes. Dash line: control sample, cell suspensions spiked with oprozomib; solid line: cell suspensions after 1-hour incubation with oprozomib. (B) Quantitative oprozomib (OPZ) disappearance and metabolite formation in human hepatocytes. At each time point, the levels of oprozomib, PR-176, and PR-025 diol in cell suspensions were quantified and then normalized as the percentage of initial oprozomib concentration at zero minutes. Data represent mean ± S.D. from three replicate incubations. PR-176 was the predominant metabolite formed via epoxide hydrolysis within 1-hour incubation.

Article Snippet: Oprozomib and authentic metabolite standards were synthesized and characterized at Onyx Pharmaceuticals, an Amgen subsidiary (South San Francisco, CA).

Techniques: In Vitro, Control, Incubation, Concentration Assay

Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).

Journal: Pharmacology Research & Perspectives

Article Title: Preclinical metabolism and the disposition of vornorexant/TS‐142, a novel dual orexin 1/2 receptor antagonist for the treatment of insomnia

doi: 10.1002/prp2.1183

Figure Lengend Snippet: Composition of the metabolites of the drug in the urine and feces of rats and dogs after a single oral administration of [ 14 C]vornorexant (3 mg/kg).

Article Snippet: Vornorexant and authentic metabolite standards were synthesized at Taisho Pharmaceutical (Saitama, Japan).

Techniques: