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Filtered Search Results
Apexbio Technology LLC Synephrine HCl 5985-28-4 100mg
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Synephrine HCl (CAS 5985-28-4) also known as Oxedrine or p-Synephrine is a small molecule that functions as a sympathomimetic agent by activating -adrenergic receptors Through its agonist activity at these receptors Synephrine HCl modulates adrenergic signaling pathways involved in vasoconstriction and other physiological processes It is commonly utilized in biomedical research to investigate adrenergic receptor pharmacology signal transduction mechanisms and cardiovascular responses associated with adrenergic stimulation
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Medchemexpress LLC Tylvalosin (tartrate) | 63428-13-7 | 96.0% | 50 MG
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Tylvalosin tartrate is an orally active, broad-spectrum macrolide antibiotic and antiviral agent. It is useful in studying PRRSV infection, induces apoptosis, and possesses anti-inflammatory activity by relieving oxidative stress and alleviating acute lung injury through inhibiting NF-κB activation.
- Increases caspase-3 cleavage and promotes endocytosis in porcine neutrophils.
- Reduces stress and improves health in pigs during PRRSV vaccine immunization.
- Attenuates increase in white blood cells and reduction in CD8+ T cells after immunization.
- Relieves oxidative stress and alleviates acute lung injury by inhibiting NF-κB activation.
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Medchemexpress LLC Morantel tartrate | 26155-31-7 | 99.0% | 1 ML
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Morantel tartrate is an anthelmintic agent primarily used to control subclinical gastrointestinal parasitism in cattle. This compound can be detected in various biological fluids and feces for extended periods after administration, making it suitable for research applications. It is intended for research use only.
- Anthelmintic agent
- Controls subclinical gastrointestinal parasitism
- Can be detected in biological fluids and feces for over 98 days
- For research use only
- Purity of 99.01%
- Molecular weight of 370.42
- Off-white to light yellow solid appearance
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Medchemexpress LLC Morantel tartrate | 26155-31-7 | 99.0% | 100 MG
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Morantel tartrate is an anthelmintic agent primarily used for the control of subclinical gastrointestinal parasitism in cattle on pasture. This broad-spectrum anthelmintic is effective and demonstrates low toxicity, with detectable presence in ruminal, abomasal, ileal fluids, and feces for over 98 days post-administration.
- Anthelmintic agent.
- Controls subclinical gastrointestinal parasitism.
- Broad spectrum effectiveness.
- Low toxicity.
- Extended detection in biological fluids and feces.
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Medchemexpress LLC 2-Hydroxybutyric acid | 600-15-7 | 98.0% | 104.10 | 1 ML
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2-Hydroxybutyric acid (α-Hydroxybutyric acid) is an endogenous metabolite converted from 2-Aminobutyric acid, with 2-oxobutyric acid as an intermediate. It is recognized as a potential biomarker for type 2 diabetes and preeclampsia. It has also been shown to prevent acetaminophen (AP)-induced liver injury.
- Derived from 2-Aminobutyric acid.
- Potential biomarker for type 2 diabetes and preeclampsia.
- Prevents acetaminophen-induced liver injury.
- Synthesized as a co-product of insulin resistance.
- Enhances cell viabilities and reduces AP-induced cytotoxicities in studies.
- Administration in C57 mice prevented AP-induced liver injury and normalized gene expression.
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Medchemexpress LLC Varenicline tartrate | 375815-87-5 | 100.0% | C17H19N3O6 | 1 ML
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Varenicline tartrate is the tartrate salt of varenicline, a nicotinic acetylcholine receptor ligand used in research as a partial agonist of α4β2 nAChR. Supplied as a 10 mM solution in DMSO, this product is intended for laboratory research and analytical applications and is not for human use.
- Ready-to-use 10 mM solution in DMSO.
- High purity (99.96%) suitable for analytical applications.
- Small 1 mL vial minimizes freeze-thaw and waste.
- Validated for receptor pharmacology and in vitro assays.
- Stable when stored under recommended conditions.
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Medchemexpress LLC L-Glyceric acid sodium | 146298-95-5 | 99.0% | 128.06 | 10 MG
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L-Glyceric acid sodium is a urinary metabolite that accumulates in the rare inherited metabolic disease L-glyceric aciduria. It is used to diagnose primary hyperoxaluria type 2 (PH2) and to distinguish PH1 from PH2 based on its excretion.
- Urinary metabolite
- Used to diagnose primary hyperoxaluria type 2 (PH2)
- Helps distinguish PH1 from PH2
- For research use only
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Apexbio Technology LLC Ifenprodil Tartrate 23210-58-4 10mM (in 1mL DMSO)
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Ifenprodil Tartrate (CAS 23210-58-4) is a small molecule recognized as an atypical noncompetitive antagonist of the NMDA (N-methyl-D-aspartate) receptor It demonstrates high-affinity binding to a uniform population of NMDA receptors in neonatal rat forebrain tissue exhibiting an IC50 value of 0 3 M By selectively modulating NMDA receptor activity Ifenprodil Tartrate serves as a valuable tool in neuropharmacological research particularly for investigating glutamatergic neurotransmission excitotoxicity and the roles of NMDA receptor subtypes in neuronal development and pathology
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eMolecules 6168-83-8 | (S)-3-Hydroxybutanoic acid | AA Blocks LLC | MFCD00137685 | 104.105 | C4H8O3 | 0.000 | C[C@H](O)CC(O)=O | 100mg | 524649694
(S)-3-Hydroxybutanoic acid | AA Blocks LLC | 6168-83-8 | MFCD00137685 | 104.105 | C4H8O3 | 0.000 | C[C@H](O)CC(O)=O | 100mg | 524649694
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Medchemexpress LLC 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, tartrate (2:1) | 56392-17-7 | 100.0% | 342.41 | 500 MG
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Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist, demonstrating anti-inflammation, antitumor, and anti-angiogenic properties. It is intended for research use only and not sold to patients.
- Purity: 99.98%
- Appearance: White to light yellow solid
- Storage: 4°C, sealed storage, away from moisture and light
- In solvent storage: -80°C for 6 months; -20°C for 1 month
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Medchemexpress LLC 3-HYDROXYBUTYRIC ACI 100UG | 100UG
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3-HYDROXYBUTYRIC ACI 100UG | 100UG
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Medchemexpress LLC 3-Hydroxybutyric acid sodium | 150-83-4 | 98.0% | 126.09 | 10MM/1ML
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3-Hydroxybutyric acid sodium is a metabolite that is elevated in type I diabetes. It can modulate the properties of membrane lipids. It is also capable of interacting with lipids (modeled using a DPPC monolayer) and altering phase behavior at clinical concentrations, and diminishes the interfacial viscosity of DPPC Monolayers.
- Target: Endogenous Metabolite
- Research Areas: Metabolic Disease
- Classification of Application Fields: Ketones, Aldehydes, Acids
- Modulates membrane lipid properties
- Interacts with lipids and alters phase behavior
- Diminishes interfacial viscosity of DPPC Monolayers
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Medchemexpress LLC Metoprolol tartrate | 56392-17-7 | 100.0% | 342.41 | 200 MG
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Metoprolol tartrate is an orally active, selective β1-adrenoceptor antagonist. It exhibits anti-inflammation, antitumor, and anti-angiogenic properties. This product is intended for research use only and is not sold to patients.
- Acts as a selective β1-adrenoceptor antagonist.
- Exhibits anti-inflammatory effects.
- Demonstrates antitumor properties.
- Shows anti-angiogenic effects.
- Cytotoxic to U937 and MOLT-4 cells.
- Reduces proinflammatory cytokines.
- Decreases myocardial virus titers.
- Inhibits myocardial apoptosis.
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Apexbio Technology LLC Tolterodine tartrate 124937-52-6 100mg
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Tolterodine tartrate (CAS 124937-52-6) is the tartrate salt form of tolterodine a small molecule that acts as a competitive antagonist at muscarinic acetylcholine receptors By selectively inhibiting these receptors particularly subtypes involved in urinary bladder contraction tolterodine tartrate reduces detrusor muscle activity This mechanism underlies its utility in studies related to bladder function muscarinic receptor pharmacology and disorders characterized by overactive bladder The compound is commonly employed in preclinical and clinical research investigating the modulation of cholinergic signaling in urological and neurological contexts
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Medchemexpress LLC 2-Propanol, 1-[4-(2-methoxyethyl)phenoxy]-3-[(1-methylethyl)amino]-, (2R,3R)-2,3-dihydroxybutanedioate (2:1) | 56392-17-7 | 99.98% | 342.41 | 25MG
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Metoprolol tartrate is characterized as an orally active, selective β1-adrenoceptor antagonist. It has demonstrated various biological activities, including anti-inflammatory, antitumor, and anti-angiogenic properties. Studies have shown its ability to reduce proinflammatory cytokines and atherosclerosis, protect myocardial tissue from viral damage, decrease myocardial virus titers, and inhibit myocardial apoptosis.
- Orally active compound.
- Selective antagonist of a specific adrenoceptor.
- Exhibits anti-inflammatory effects.
- Demonstrates antitumor properties.
- Possesses anti-angiogenic activity.
- Reduces proinflammatory cytokines.
- Decreases atherosclerosis.
- Protects heart muscle from viral damage.
- Lowers myocardial virus titers.
- Inhibits programmed cell death in heart tissue.
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