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rabeprazole sodium  (Sartorius AG)


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    Sartorius AG rabeprazole sodium
    Rabeprazole Sodium, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 93/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabeprazole+sodium/Entris+II+Essential+Line+Analytical+Balance+220+gr/pm38897632-23-12-20
    Average 93 stars, based on 14 article reviews
    rabeprazole sodium - by Bioz Stars, 2026-10
    93/100 stars

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    Formulation:

    Article Title: 13-Week Repeated Oral Toxicity and Toxicokinetic Studies of Rabeprazole Sodium and Sodium Bicarbonate Combination in Dogs.
    Article Snippet: The subchronic toxicity and toxicokinetics of a combination of rabeprazole sodium and sodium bicarbonate were investigated in dogs by daily oral administration for 13 consecutive weeks with a 4-week recovery period.. The dose groups consisted of control (vehicles), (5 + 200), (10 + 400), and (20 + 800) mg/kg of rabeprazole sodium + sodium bicarbonate, 20 mg/kg of rabeprazole sodium only, and 800 mg/kg of sodium bicarbonate only.. Esophageal ulceration accompanied by inflammation was observed in only one animal in the male (20 + 800) mg/kg rabeprazole sodium + sodium bicarbonate group.

    Capsules:

    Article Title: 13-Week Repeated Oral Toxicity and Toxicokinetic Studies of Rabeprazole Sodium and Sodium Bicarbonate Combination in Dogs.
    Article Snippet: The subchronic toxicity and toxicokinetics of a combination of rabeprazole sodium and sodium bicarbonate were investigated in dogs by daily oral administration for 13 consecutive weeks with a 4-week recovery period.. The dose groups consisted of control (vehicles), (5 + 200), (10 + 400), and (20 + 800) mg/kg of rabeprazole sodium + sodium bicarbonate, 20 mg/kg of rabeprazole sodium only, and 800 mg/kg of sodium bicarbonate only.. Esophageal ulceration accompanied by inflammation was observed in only one animal in the male (20 + 800) mg/kg rabeprazole sodium + sodium bicarbonate group.



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    <t>Rabeprazole</t> sodium inhibited CeENGASE in vitro and improved wild-type worms stress adaptivity in vivo. a CeENGASE expressed in E. coli BL21 (DE3) was purified and subjected to an in vitro assay to release N-glycans on RNaseB. The products of the assay were analyzed by MALDI-TOF MS, and N2H3F1X1 (1221) was used as an internal control. The ratio of the main product (N1H7, 1378) to the internal reference (N2H3F1X1, 1211) decreased by about 50 times, indicating that Rabeprazole sodium inhibited the enzymatic activity of CeENGASE. b The survival rate of wild-type worms (on plate supplied with 150 μL of Rabeprazole sodium [1 m m ]) after 7-h heat treatment. The survival rate of Rabeprazole sodium group was 26.48% more than the control group (control vs. Rabeprazole sodium: 10.12% vs. 36.60%).
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    LKT Laboratories rabeprazole
    Fig. 3. Inhibition of PNU-142586 uptake by PPIs in HEK-hOAT3 cells. HEK-hOAT3 cells were incubated at 37◦C for 5 min with 1 µM PNU-142586 (pH 7.4) in the absence or presence of various concentrations of lansoprazole (A), <t>rabeprazole</t> (B), omeprazole (C), and esomeprazole (D). Each point represents mean ± S.D. of three separate experiments using three monolayers. When the standard errors of the means are small, they are contained within the symbols. The apparent IC50 values were calculated by fitting the data to a sigmoidal dose-response regression curve.
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    Rabeprazole sodium inhibited CeENGASE in vitro and improved wild-type worms stress adaptivity in vivo. a CeENGASE expressed in E. coli BL21 (DE3) was purified and subjected to an in vitro assay to release N-glycans on RNaseB. The products of the assay were analyzed by MALDI-TOF MS, and N2H3F1X1 (1221) was used as an internal control. The ratio of the main product (N1H7, 1378) to the internal reference (N2H3F1X1, 1211) decreased by about 50 times, indicating that Rabeprazole sodium inhibited the enzymatic activity of CeENGASE. b The survival rate of wild-type worms (on plate supplied with 150 μL of Rabeprazole sodium [1 m m ]) after 7-h heat treatment. The survival rate of Rabeprazole sodium group was 26.48% more than the control group (control vs. Rabeprazole sodium: 10.12% vs. 36.60%).

    Journal: Cells, Tissues, Organs

    Article Title: Downregulation of Endo-Beta-N-Acetylglucosaminidase in Caenorhabditis elegans Improves Stress Adaptivity

    doi: 10.1159/000546244

    Figure Lengend Snippet: Rabeprazole sodium inhibited CeENGASE in vitro and improved wild-type worms stress adaptivity in vivo. a CeENGASE expressed in E. coli BL21 (DE3) was purified and subjected to an in vitro assay to release N-glycans on RNaseB. The products of the assay were analyzed by MALDI-TOF MS, and N2H3F1X1 (1221) was used as an internal control. The ratio of the main product (N1H7, 1378) to the internal reference (N2H3F1X1, 1211) decreased by about 50 times, indicating that Rabeprazole sodium inhibited the enzymatic activity of CeENGASE. b The survival rate of wild-type worms (on plate supplied with 150 μL of Rabeprazole sodium [1 m m ]) after 7-h heat treatment. The survival rate of Rabeprazole sodium group was 26.48% more than the control group (control vs. Rabeprazole sodium: 10.12% vs. 36.60%).

    Article Snippet: In brief, a 200-μL reaction system was incubated at 21°C for 24 h, which contained 50 m m sodium acetate reaction buffer (pH 5.5), 100 μg RNaseB (Sigma), 100 μg CeENGASE, and 50 μM Rabeprazole sodium (Topscience) [ ].

    Techniques: In Vitro, In Vivo, Purification, Matrix-assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry, Control, Activity Assay, Mass Spectrometry

    Rabeprazole sodium inhibited CeENGASE in vitro and improved wild-type worms stress adaptivity in vivo. a CeENGASE expressed in E. coli BL21 (DE3) was purified and subjected to an in vitro assay to release N-glycans on RNaseB. The products of the assay were analyzed by MALDI-TOF MS, and N2H3F1X1 (1221) was used as an internal control. The ratio of the main product (N1H7, 1378) to the internal reference (N2H3F1X1, 1211) decreased by about 50 times, indicating that Rabeprazole sodium inhibited the enzymatic activity of CeENGASE. b The survival rate of wild-type worms (on plate supplied with 150 μL of Rabeprazole sodium [1 m m ]) after 7-h heat treatment. The survival rate of Rabeprazole sodium group was 26.48% more than the control group (control vs. Rabeprazole sodium: 10.12% vs. 36.60%).

    Journal: Cells, Tissues, Organs

    Article Title: Downregulation of Endo-Beta-N-Acetylglucosaminidase in Caenorhabditis elegans Improves Stress Adaptivity

    doi: 10.1159/000546244

    Figure Lengend Snippet: Rabeprazole sodium inhibited CeENGASE in vitro and improved wild-type worms stress adaptivity in vivo. a CeENGASE expressed in E. coli BL21 (DE3) was purified and subjected to an in vitro assay to release N-glycans on RNaseB. The products of the assay were analyzed by MALDI-TOF MS, and N2H3F1X1 (1221) was used as an internal control. The ratio of the main product (N1H7, 1378) to the internal reference (N2H3F1X1, 1211) decreased by about 50 times, indicating that Rabeprazole sodium inhibited the enzymatic activity of CeENGASE. b The survival rate of wild-type worms (on plate supplied with 150 μL of Rabeprazole sodium [1 m m ]) after 7-h heat treatment. The survival rate of Rabeprazole sodium group was 26.48% more than the control group (control vs. Rabeprazole sodium: 10.12% vs. 36.60%).

    Article Snippet: In brief, a 200-μL reaction system was incubated at 21°C for 24 h, which contained 50 m m sodium acetate reaction buffer (pH 5.5), 100 μg RNaseB (Sigma), 100 μg CeENGASE, and 50 μM Rabeprazole sodium (Topscience) [ ].

    Techniques: In Vitro, In Vivo, Purification, Control, Activity Assay

    Journal: Bio-protocol

    Article Title: An Assay System for Plate-based Detection of Endogenous Peptide: N -glycanase/NGLY1 Activity Using A Fluorescence-based Probe

    doi: 10.21769/BioProtoc.5151

    Figure Lengend Snippet:

    Article Snippet: Rabeprazole sodium salt (Tokyo Chemical Industry Co. Ltd., catalog number: R0115) 10.

    Techniques: Concentration Assay, Protease Inhibitor

    Journal: Bio-protocol

    Article Title: An Assay System for Plate-based Detection of Endogenous Peptide: N -glycanase/NGLY1 Activity Using A Fluorescence-based Probe

    doi: 10.21769/BioProtoc.5151

    Figure Lengend Snippet:

    Article Snippet: Rabeprazole sodium salt (Tokyo Chemical Industry Co. Ltd., catalog number: R0115) 10.

    Techniques: Concentration Assay, Protease Inhibitor

    Fig. 3. Inhibition of PNU-142586 uptake by PPIs in HEK-hOAT3 cells. HEK-hOAT3 cells were incubated at 37◦C for 5 min with 1 µM PNU-142586 (pH 7.4) in the absence or presence of various concentrations of lansoprazole (A), rabeprazole (B), omeprazole (C), and esomeprazole (D). Each point represents mean ± S.D. of three separate experiments using three monolayers. When the standard errors of the means are small, they are contained within the symbols. The apparent IC50 values were calculated by fitting the data to a sigmoidal dose-response regression curve.

    Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    Article Title: Contribution of human organic anion transporter 3-mediated transport of a major linezolid metabolite, PNU-142586, in linezolid-induced thrombocytopenia.

    doi: 10.1016/j.biopha.2024.116801

    Figure Lengend Snippet: Fig. 3. Inhibition of PNU-142586 uptake by PPIs in HEK-hOAT3 cells. HEK-hOAT3 cells were incubated at 37◦C for 5 min with 1 µM PNU-142586 (pH 7.4) in the absence or presence of various concentrations of lansoprazole (A), rabeprazole (B), omeprazole (C), and esomeprazole (D). Each point represents mean ± S.D. of three separate experiments using three monolayers. When the standard errors of the means are small, they are contained within the symbols. The apparent IC50 values were calculated by fitting the data to a sigmoidal dose-response regression curve.

    Article Snippet: Linezolid and rabeprazole were sourced from LKT Laboratories, Inc. (St. Paul, MN).

    Techniques: Inhibition, Incubation