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Organoantimony compounds possess direct bonds between carbon and antimony atoms. Organoantimony compounds commonly have Sb(V) or Sb(III) oxidation states and are studied in organometallic chemistry.
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Gemigliptin tartrate, also known as LC15-0444 tartrate, is a highly selective, reversible, and competitive dipeptidyl peptidase-4 (DPP-4) inhibitor with an IC50 of 10.3 nM for human recombinant DPP-4. It demonstrates potent anti-glycation properties and can be used in research concerning advanced glycation end products (AGE)-related diabetic complications.
Highly selective DPP-4 inhibitor.
Exhibits potent anti-glycation properties.
Useful for research on AGE-related diabetic complications.
Dose-dependently inhibits AGE-BSA formation.
Suppresses cross-linking of preformed AGE-BSA.
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Tolterodine tartrate is a muscarinic acetylcholine receptor (mAChR) inhibitor and a substrate for cytochrome P450 enzymes. It works by competitively binding acetylcholine, reducing sympathetic excitation and inhibiting involuntary bladder muscle contraction. This compound restores the Nrf2/NF-κB signaling pathway, protecting against inflammatory responses and ferroptosis. It is used in research for urinary tract infections and overactive bladder.
Inhibits mAChR
Substrate for cytochrome P450 enzymes
Reduces sympathetic excitation
Inhibits involuntary bladder muscle contraction
Restores Nrf2/NF-κB signaling pathway
Protects against inflammatory responses
Protects against ferroptosis
Ameliorates reactive oxygen species production
Ameliorates lipid oxidation
Applied in urinary tract infection research
Applied in overactive bladder research
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Also available in 100 mg and bulk. Please contact Fisher for quotes. Brimonidine Tartrate (AGN190342 tartrate) is a quinoxaline derivative and adrenergic (alpha)-2 receptor agonist (EC50 0.45 nM) that is used to manage intraocular pressure associated with open-angle glaucoma or ocular hypertension. purity: 99%
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Norepinephrine (Levarterenol; L-Noradrenaline) tartrate is a potent adrenergic receptor (AR) agonist that activates α1, α2, and β1 receptors. It is intended for research use only. This compound is known to induce cardiomyopathy in animal models and plays a role in cellular processes such as increasing cAMP and inducing lipolysis in adipocytes.
Potent adrenergic receptor agonist
Activates α1, α2, and β1 receptors
Induces cardiomyopathy in animal models
Increases cAMP and induces lipolysis in adipocytes
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
Budiodarone tartrate is the tartrate salt form of budiodarone (ATI-2042), an antiarrhythmic research compound and analogue of amiodarone. It exhibits balanced inhibition of multiple cardiac ion channels and is supplied for laboratory research in solid and solution formats with supporting analytical documentation.
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Giredestrant tartrate (Estrogen receptor antagonist 1) is a novel orally active selective and effective non-steroidal estrogen receptor antagonist. Giredestrant tartrate strongly binds to ER resulting in the failure of ER to activate the transcription of targeted genes and promoting the degradation of ER protein. Giredestrant tartrate can be used to treat tumor diseases. purity: 98%
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Ifenprodil is an atypical noncompetitive antagonist at the NMDA receptor it interacts with high affinity at a homogeneous population of NMDA receptors in neonatal rat forebrain with IC50 of 0 3 M
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Also available in 1 mL, 1 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Levalbuterol tartrate is a short-acting beta2-adrenergic receptor agonist and the R enantiomer of salbutamol. Purity 98.97%
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