Home Transmembrane Transporters Proton Pump inhibitor - ATPase inhibitor Dexlansoprazole For research use only.

Dexlansoprazole

Synonyms: T 168390, TAK 390,(R)-Lansoprazole

Dexlansoprazole (T 168390, TAK 390,(R)-Lansoprazole), the dextrorotatory enantiomer of lansoprazole, is a proton pump inhibitor (PPI) formulated to have dual delayed-release properties. Dexlansoprazole selectively suppresses gastric acid secretion by direct inhibition of the H(+),K(+)-ATPase proton pump in the gastric parietal cell.

Dexlansoprazole Chemical Structure

Dexlansoprazole Chemical Structure

CAS: 138530-94-6

Selleck's Dexlansoprazole has been cited by 2 publications

Purity & Quality Control

Batch: S409901 DMSO] 74 mg/mL] false] Water] Insoluble] false] Ethanol] Insoluble] false Purity: 99.92%
99.92

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Biological Activity

Description Dexlansoprazole (T 168390, TAK 390,(R)-Lansoprazole), the dextrorotatory enantiomer of lansoprazole, is a proton pump inhibitor (PPI) formulated to have dual delayed-release properties. Dexlansoprazole selectively suppresses gastric acid secretion by direct inhibition of the H(+),K(+)-ATPase proton pump in the gastric parietal cell.
Features A modified release formulation of an enantiomer of lansoprazole.
Targets
Proton pump [1] H(+),K(+)-ATPase [1]
In vitro
In vitro

Dexlansoprazole, constitutes >80% of circulating drug after oral administration of lansoprazole, provides lower clearance and 5-fold greater systemic exposure than the S-enantiomer following oral administration of lansoprazole. Dexlansoprazole MR is a modified release formulation of dexlansoprazole, which employs a novel Dual Delayed Release (DDR) technology that delivers the drug in two discrete phases of release, thereby inhibiting newly activated proton pumps that turn over following initial PPI inactivation of H+,K+-ATPase. Dexlansoprazole MR maintains plasma drug concentrations above the threshold level longer than lansoprazole at all doses, resulting in an optimized drug exposure-intragastric pH relationship. [1] Dexlansoprazole selectively suppresses gastric acid secretion by direct inhibition of the H+K+-ATPase proton pump in the gastric parietal cell, inhibition of this cell membrane enzyme ultimately blocks the final step in acid production. [2]
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT02442752 Withdrawn Pediatric Gastroesophageal Reflux Disease Takeda June 15 2025 Phase 1
NCT03316976 Completed Healthy Volunteers Takeda November 22 2017 Phase 1
NCT03079050 Completed GERD|Proton Pump Inhibitor American University of Beirut Medical Center|Takeda February 27 2017 Phase 4

Chemical lnformation & Solubility

Molecular Weight 369.36 Formula

C16H14F3N3O2S
CAS No. 138530-94-6 SDF Download Dexlansoprazole SDF
Smiles CC1=C(C=CN=C1CS(=O)C2=NC3=CC=CC=C3N2)OCC(F)(F)F
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 74 mg/mL ( (200.34 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble


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In vivo
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Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

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