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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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Metaraminol tartrate is an α-adrenergic agonist and a sympathomimetic amine that directly and indirectly affects adrenergic receptors, with alpha effects being predominant. It acts as a vasopressor agent and is for research use only.
α-Adrenergic agonist
Sympathomimetic amine
Acts as a vasopressor agent
High purity: 99.9%
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Metaraminol tartrate is an α-adrenergic agonist and sympathomimetic amine that directly and indirectly affects adrenergic receptors. It acts as a vasopressor agent, primarily through its alpha effects, making it suitable for various research applications.
Acts as an α-adrenergic agonist
Functions as a sympathomimetic amine
Directly and indirectly affects adrenergic receptors
Exhibits predominant alpha effects
Serves as a vasopressor agent
High purity of 99.9%
Solid appearance, white to off-white color
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Fludrocortisone acetate is an orally active synthetic mineralocorticoid. It effectively controls sodium retention and is used in studies of cardiac injury, adrenal insufficiency, and orthostatic hypotension. Research indicates its role in managing conditions related to sodium balance and cardiovascular health.
Effectively controls sodium retention
Supports research into cardiac injury
Supports research into adrenal insufficiency
Supports research into orthostatic hypotension
Demonstrates efficacy in reducing specific enzyme activities related to cardiac injury
Shown to decrease UACR in healthy cats
Contributes to restoring quiescent morphology in choroidal endothelial cells
Assists in reducing membrane permeability in stimulated choroidal endothelial cells
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m-PEG3-Tos is a methoxy-terminated PEG3 tosylate used as a short, flexible PEG linker and intermediate in small-molecule synthesis. It provides three ethylene glycol units with a tosylate leaving group, making it suitable for nucleophilic substitution to install PEG chains and build PROTAC linkers or other conjugates.
Provides three ethylene glycol units for short, flexible spacing.
Contains a tosylate leaving group suitable for nucleophilic substitution.
High purity (98.75%) appropriate for synthetic applications.
Available in small-scale quantities for research use, such as 250 mg.
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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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Zinc gluconate is the zinc salt of gluconic acid provided as a white powder for research and analytical use. It serves as a source of bioavailable zinc ions for biochemical, pharmacological, and nutritional studies, and is supplied with supporting documentation for laboratory handling.
High purity (98.0%) for research-grade applications.
Anhydrous molecular weight 455.67 and formula C12H22O14Zn.
Soluble in DMSO and water at 50 mg/mL with sonication.
Supplied as a dry powder; store sealed at 4°C to protect from moisture.
Datasheet and certificate of analysis available for lot-specific data.
Suitable for biochemical, pharmacological, and nutritional research.
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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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Mal-PEG3-NH2 TFA is a linear, heterobifunctional polyethylene glycol (PEG) crosslinker supplied as the trifluoroacetic acid (TFA) salt. It contains a maleimide at one end and a primary amine at the other, enabling thiol-to-amine conjugation and use as a non-cleavable linker in PROTAC and bioconjugation workflows. For research use only.
Provides maleimide and primary amine reactive groups for orthogonal conjugation.
PEG3 spacer improves aqueous solubility and reduces steric hindrance.
TFA salt form enhances stability and handling compared with the free base.
Non-cleavable linker suitable for stable conjugates and PROTAC constructs.
High purity (>99%) for consistent conjugation performance.
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