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Organic compounds that contain a carbon atom bonded to a halogen atom, and an oxygen atom via a double bond; commonly derived from an oxoacid by replacing a hydroxyl group with a halogen atom.
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Also available in 1 mL, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Tarloxotinib bromide (TH-4000) is an irreversible inhibitor of EGFR/HER2. Purity 97.15%
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N3-Cho bromide (azido-choline bromide) is an azide-bearing choline analogue supplied as a ready-to-use 10 mM solution in DMSO for bioorthogonal labeling and click chemistry applications. It is intended for incorporation into membrane mimetics and for use in azide-alkyne cycloaddition workflows.
Contains an azide functional group compatible with click chemistry reactions.
Supplied as a 10 mM solution in DMSO, ready for dilution or reaction.
High purity (listed at 99.63%), suitable for research use.
Soluble in DMSO and water.
Stable in solution when sealed at -80°C (up to 6 months) or -20°C (up to 1 month).
Useful for membrane labeling and synthesis of phospholipid head-group analogues.
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Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Umeclidinium bromide (GSK573719A) is a novel mAChR antagonist. purity: 99%
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2-Bromoisobutyryl bromide (Bromodimethylacetyl bromide -Bromoisobutyryl bromide 2-Bromoisobutylyl bromide) is a biochemical reagent that can be used as a biological material or organic compound for life science related research[1]
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A photoreactive derivative of L-phenylalanine; can be incorporated into synthetic peptides and used as a photolabel to identify the residues involved in peptide-protein interactions; has been incorporated into GPCRs to identify potential ligand binding sites
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Rocuronium Bromide (CAS 119302-91-9) is an aminosteroid compound that functions as a non-depolarizing neuromuscular blocking agent It acts by competitively antagonizing nicotinic acetylcholine receptors at the neuromuscular junction thereby inhibiting acetylcholine-induced depolarization and subsequent muscle contraction In research settings Rocuronium Bromide is utilized to investigate neuromuscular transmission and to model pharmacological blockade of skeletal muscle activity supporting studies in anesthesia muscle physiology and synaptic transmission mechanisms
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A nonpeptide substrate of proteases and deiminases; has been used as a substrate for the quantification of papain, carboxypeptidase B, PAD2, and PAD4 activities
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A membrane-impermeant lidocaine derivative that when combined with capsaicin selectively blocks sodium channels on nociceptive neurons via the TRPV1 channel; decreases the pain response without imparting numbness or paralysis associated with other local anesthetics
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MitoB bromide is a mitochondria-targeted ratiometric probe used as an exomarker to detect mitochondrial hydrogen peroxide (H2O2) in living animals. It accumulates in mitochondria and is converted by H2O2 to a reaction product that allows quantification of mitochondrial oxidative stress by analytical methods such as mass spectrometry.
Targeted detection of mitochondrial hydrogen peroxide in vivo.
Enables ratiometric quantification via conversion to a measurable product.
Compatible with mass spectrometry and analytical assays for in vivo studies.
Provided in research-scale quantities with high purity for reproducible results.
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1,3,5-Tri-O-benzoyl-α-D-ribofuranose is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms involve the inhibition of DNA synthesis and the induction of apoptosis. This product is intended for research use only and is not sold to patients.
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Ipratropium Bromide is an antagonist of M3 type muscarinic acetylcholine receptors used for the treatment of chronic obstructive pulmonary disease (COPD)
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Benzoyl coenzyme A (Benzoyl CoA) is an intermediate in the CoA-dependent epoxide pathway synthesized from benzoate in the presence of the enzyme benzoate-CoA ligase. It is further converted to 2 3-epoxybenzoyl-CoA and this step is catalyzed by benzoyl-CoA reductase (BoxA) and benzoyl-CoA oxygenase(BoxB).
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