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Verdinexor (KPT-335, ATG-527) is an orally bioavailable, selective XPO1/CRM1 inhibitor. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
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This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Pantoprazole is an orally active and potent proton pump inhibitor (PPI). It is a substituted benzimidazole and a potent H+/K+-ATPase inhibitor. It improves pH stability and has anti-secretory and anti-ulcer activities. This product is intended for research and analytical applications.
Improves pH stability
Has anti-secretory activities
Has anti-ulcer activities
Potent H+/K+-ATPase inhibitor
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Meclizine dihydrochloride (Meclizine 2HCl CAS 1104-22-9) is a small molecule antagonist of histamine H1 receptors commonly investigated for its antiemetic properties In addition to its antihistaminic activity meclizine exhibits antimuscarinic effects and inhibits oxidative phosphorylation It has also been identified as an agonist of the mouse constitutive androstane receptor (mCAR) and demonstrates inverse agonist activity at other signaling pathways These multifunctional pharmacological properties make meclizine 2HCl a useful tool in research exploring receptor-mediated signaling mitochondrial function and metabolism-related diseases
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Riluzole (RP-54274, PK 26124) is a glutamate release inhibitor with neuroprotective, anticonvulsant, anxiolytic and anesthetic qualities. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
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Rosuvastatin (CAS 287714-41-4) is a small molecule that acts as a competitive inhibitor of the enzyme hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase a critical enzyme catalyzing the rate-limiting step in cholesterol biosynthesis The compound exhibits potent inhibitory activity demonstrated by an IC50 value of approximately 11 nM By inhibiting HMG-CoA reductase rosuvastatin effectively reduces the biosynthesis of cholesterol facilitating its application in research focused on lipid metabolism cardiovascular diseases and related cellular pathways
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