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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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Tolterodine tartrate is a mAChR inhibitor and a substrate for cytochrome P450 enzymes. It competitively binds acetylcholine, which reduces sympathetic excitation and inhibits involuntary bladder muscle contraction. It restores the Nrf2/NF-κB signaling pathway, providing protection against inflammatory response and ferroptosis, and ameliorates LPS-induced reactive oxygen species production and lipid oxidation. This product can be used for research related to urinary tract infections and overactive bladder.
Competitively binds acetylcholine
Reduces sympathetic excitation
Inhibits involuntary bladder muscle contraction
Restores Nrf2/NF-κB signaling pathway
Provides protection against inflammatory response and ferroptosis
Ameliorates LPS-induced reactive oxygen species production and lipid oxidation
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Budiodarone tartrate is a chemical analogue of Amiodarone with balanced, multiple cardiac ion channel (potassium, sodium and calcium channels) inhibiting activity. It acts as an antiarrhythmic agent.
Chemical analogue of Amiodarone.
Inhibits multiple cardiac ion channels (potassium, sodium, and calcium channels).
Antiarrhythmic agent.
Has a short plasma half-life (7 h) and a lower volume of distribution (13 L/kg) in vitro.
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Budiodarone tartrate is a chemical analogue of Amiodarone, exhibiting balanced inhibitory activity across multiple cardiac ion channels, including potassium, sodium, and calcium channels. It functions as an antiarrhythmic agent. The compound is characterized by a short plasma half-life of 7 hours and a lower volume of distribution at 13 L/kg.
Functions as a chemical analogue of Amiodarone.
Exhibits balanced, multiple cardiac ion channel inhibiting activity, targeting potassium, sodium, and calcium channels.
Acts as an antiarrhythmic agent.
Demonstrates a short plasma half-life of 7 hours.
Possesses a lower volume of distribution of 13 L/kg.
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Rivastigmine Tartrate (ENA 713) is a cholinesterase inhibitor with IC50 of 5 5 M and used as a parasympathomimetic or cholinergic agent for the treatment of mild to moderate Alzheimer disease
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Gemigliptin tartrate hydrate is a selective, reversible, competitive dipeptidyl peptidase-4 (DPP-4) inhibitor supplied as a white to off-white solid hydrate for research use. It is provided in research-scale packages with high chemical purity and characterized molecular weight, appropriate for biochemical and cellular studies, including investigations of advanced glycation end products and diabetic complications.
Selective inhibitor of DPP-4 with low nanomolar potency.
High purity suitable for analytical and biological research.
Solid white to off-white appearance for easy handling.
Hydrated salt form with defined molecular weight for reproducibility.
Recommended storage conditions help preserve stability.
Available in small, research-scale package sizes for laboratory use.
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Also available in 1 mL, 25 mg, 50 mg, 200 mg and bulk. Please contact Fisher for quotes. Ifenprodil is a selective NMDA receptor (glutamate) antagonist. Purity 99.7%
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Budiodarone tartrate, also known as ATI-2042 tartrate, is a chemical analogue of Amiodarone. This antiarrhythmic agent exhibits balanced and multiple cardiac ion channel inhibiting activity.
Inhibits potassium, sodium, and calcium cardiac ion channels
Possesses a short plasma half-life (7 h)
Has a lower volume of distribution (13 L/kg)
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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, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Tylosin tartrate, a macrolide antibiotic, is approved for the control of mycoplasmosis in poultry. Purity 99.16%
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