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Organic bicyclic compounds that consist of a seven-membered ring fused with a thiophene ring; thiophenes are a five-membered ring with four carbon atoms and one sulfur atom.
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Ocifisertib fumarate is the fumarate salt of CFI-400945, a potent, selective, and orally bioavailable inhibitor of polo-like kinase 4 (PLK4) supplied for research use in biochemical and cellular studies of PLK4-related pathways and antineoplastic activity.
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Bedaquiline fumarate is an analytical standard and a diarylquinoline antibiotic that targets ATP synthase. It is effective for the treatment of Mycobacterium tuberculosis infections and is intended for research and analytical applications.
Analytical standard grade
Reference standard supplied assay
Effective against Mycobacterium tuberculosis infections
Commonly used in qualitative, quantitative, and methodological research experiments
Suitable for HPLC, GC, and MS applications
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Bedaquiline fumarate is a diarylquinoline antibiotic that targets ATP synthase and is effective for the treatment of Mycobacterium tuberculosis infections.
Inhibits the growth of TDR Mycobacterium tuberculosis strains.
Highest activity against Mycobacterium avium among slowly growing mycobacteria.
Shows moderate in vitro activity against NTM species.
Excellent in vitro activity against multidrug-resistant Mycobacterium tuberculosis.
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Diethyl fumarate is a decomposition product of Malathion 9 and a reactant in the Diels-Alder reaction. It is a reputed skin irritant and can cause non-immunologic contact urticaria on the skin. Diethyl fumarate and Curcumin hybridize to exert neuroprotective effects.
Decomposition product of Malathion 9.
Reactant in Diels-Alder reaction.
Causes dose-dependent swelling of ears in guinea pigs.
Curcumin hybrids show neuroprotective effects in C. elegans model of PD.
For research use only.
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Cevipabulin fumarate (TTI-237 fumarate) is an oral, microtubule-active, antitumor compound. It inhibits the binding of [3H]NSC 49842 to tubulin, with an IC50 of 18-40 nM for cytotoxicity in human tumor cell lines.
Microtubule-active, antitumor compound
Shows good activity (18-40 nM IC50 values) on ovarian, breast, prostate, and cervical tumor cell lines
Produces sub-G1 nuclei at low concentrations (20-40 nM)
Causes a strong G2-M block at concentrations above 50 nM
Active via intravenous (i.v.) and oral (p.o.) administration against human tumor xenografts in mice, with good antitumor activity at 20 and 15 mg/kg
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Iron (II) fumarate is an orally effective active dietary supplement. It can alleviate metabolic damage and damage to silkworms caused by cypermethrin and can be used for research on iron deficiency anemia.
In vitro: Can restore metabolic pathway disruption and enhance cell viability in BmN cells treated with cypermethrin.
In vivo: Alleviates damage caused by cypermethrin in silkworms.
In vivo: Induces oxidative stress in the liver and colon of rats.
In vivo: Alters intestinal morphology and microbiota in Yellow River carp, increasing diversity and richness.
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Formoterol fumarate is a selective β2-adrenoceptor agonist, at least as selective as Salbutamol and Terbutaline. It relaxes acetylcholine-pre-contracted human isolated segmental bronchi and can be used for research related to chronic obstructive pulmonary disease and bronchial asthma.
Selective β2-adrenoceptor agonist
Relaxes acetylcholine-pre-contracted human isolated segmental bronchi
Suitable for research on chronic obstructive pulmonary disease
Suitable for research on bronchial asthma
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Diroximel fumarate is supplied as a research-grade small-molecule reagent intended for laboratory studies. This listing represents a 50 MG pack of the prodrug of monomethyl fumarate and is provided for experimental and analytical use in research settings; it is not for clinical or human use.
For research use only, not for human or clinical use.
Supplied as a small 50 MG pack suitable for laboratory testing.
High purity, typically ≥98.0%.
Molecular weight 255.23 g/mol and formula C11H13NO6.
Useful for studies of fumarate metabolism and related biochemical pathways.
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Ibutilide Fumarate (CAS 122647-32-9) is a small molecule classified as a Class III antiarrhythmic agent It acts primarily by enhancing slow inward sodium currents and delaying repolarization through inhibition of the rapid component of the cardiac delayed rectifier potassium current (IKr) resulting in prolongation of the cardiac action potential Ibutilide is utilized in research to investigate pharmacological cardioversion of atrial arrhythmias specifically studying the acute conversion of atrial fibrillation and atrial flutter to normal sinus rhythm Its properties make it valuable for exploring the mechanisms of antiarrhythmic therapy and cardiac electrophysiology
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