Acyl bromides
Medchemexpress LLC Pinaverium bromide | 53251-94-8 | 99.7% | 591.42 | 25 MG
Pinaverium bromide | 53251-94-8 | 99.7% | 591.42 | 25 MG
TARGETMOL CHEMICALS INC Clidinium bromide 500MG
Also available in 1 mL, 50 mg, 100 mg, 200 mg and bulk. Please contact Fisher for quotes. Clidinium bromide (Ro 2-3773) , a synthetic anticholinergic agent, has been shown in experimental and clinical researchers to have a pronounced antisecretory and antispasmodic effect on the gastrointestinal tract. It can inhibit muscarinic actions of acetylcholine at postganglionic parasympathetic neuroeffector sites. It is used for the treatment of peptic ulcer disease and also to help relieve cramps or stomach spasms or abdominal due to colicky abdominal diverticulitis, pain, and irritable bowel syndrome. Purity 99.36%
Apexbio Technology LLC Umeclidinium bromide 869113-09-7 10mg
Umeclidinium bromide (CAS 869113-09-7) is a potent and long-acting antagonist of muscarinic acetylcholine receptors (mAChRs) displaying high affinity for subtypes M1 M5 with Ki values of 0 16 nM 0 15 nM 0 06 nM 0 05 nM and 0 13 nM respectively It selectively targets mAChRs without observable activity at unrelated receptors or channels such as / opioid receptors sodium channels or dopamine transporters In cell-based assays using CHO cells expressing recombinant human mAChRs umeclidinium inhibits acetylcholine-induced calcium flux with pA2 values between 9 6 and 10 6 for M1 M3 receptors In murine models it reverses acetylcholine-driven bronchoconstriction Umeclidinium bromide is broadly applied in research focused on pulmonary disease mechanisms and drug development
Apexbio Technology LLC Umeclidinium bromide 869113-09-7 2mg
Umeclidinium bromide (CAS 869113-09-7) is a potent and long-acting antagonist of muscarinic acetylcholine receptors (mAChRs) displaying high affinity for subtypes M1 M5 with Ki values of 0 16 nM 0 15 nM 0 06 nM 0 05 nM and 0 13 nM respectively It selectively targets mAChRs without observable activity at unrelated receptors or channels such as / opioid receptors sodium channels or dopamine transporters In cell-based assays using CHO cells expressing recombinant human mAChRs umeclidinium inhibits acetylcholine-induced calcium flux with pA2 values between 9 6 and 10 6 for M1 M3 receptors In murine models it reverses acetylcholine-driven bronchoconstriction Umeclidinium bromide is broadly applied in research focused on pulmonary disease mechanisms and drug development
Apexbio Technology LLC Mepenzolate Bromide 76-90-4 500mg
Mepenzolate bromide (CAS 76-90-4) is a synthetic quaternary ammonium compound that functions as a muscarinic acetylcholine receptor antagonist By inhibiting parasympathetic neural transmission it reduces gastric secretion and gastrointestinal motility Mepenzolate bromide is generally supplied as a white to light cream powder with high solubility in methanol limited solubility in water and chloroform and minimal solubility in ether This compound is widely employed in research investigating modulation of cholinergic signaling gastrointestinal physiology and autonomic pharmacology and serves as a tool compound for studying antimuscarinic mechanisms in vitro and in vivo
Medchemexpress LLC Iem-1925 bromide | 258282-23-4 | MFCD19690950 | 98.0% | 422.24 g/mol | C17H30Br2N2 | 10 MG
IEM-1925 bromide is the bromide salt of a small-molecule glutamate receptor antagonist provided for research use. It is supplied as a high-purity solid suitable for in vitro and in vivo studies, with a molecular weight of 422.24 g/mol and typical purity of 98.0%. Intended for laboratory research and not for human use.
- Glutamate receptor antagonist activity
- High purity solid powder for reliable results
- Suitable for in vitro and in vivo research applications
- Available in small milligram package sizes for early-stage studies
- Store sealed at 4°C; in solution store at -80°C for long-term
Medchemexpress LLC Fentonium bromide | 5868-06-4 | 98.8% | 25MG
Fentonium bromide | 5868-06-4 | 98.8% | 25MG
Selleck Chemical LLC Umeclidinium bromide S3735-5mg
Umeclidinium bromide(GSK573719A) is a long-acting muscarinic antagonist approved for the maintenance treatment of chronic obstructive pulmonary disease (COPD)
Medchemexpress LLC N6-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine | 64325-78-6 | 98.0% | 657.71 | 5 G
N6-Benzoyl-5′-O-(4,4′-dimethoxytrityl)-2′-deoxyadenosine can be used as an intermediate in various chemical processes. This compound is available in solid form and is suitable for laboratory research and manufacture of substances.
- Used as an intermediate
- Available in solid form
- Suitable for laboratory chemicals and manufacturing
- Relevant in oligonucleotides research, particularly nucleoside analogs and adenosine
- Associated with disease areas like cancer and blood diseases
- Related to cell cycle/DNA damage and nucleoside antimetabolite/analog classifications
Medchemexpress LLC Rapacuronium bromide | 156137-99-4 | 98.0% | 677.80 | 1 ML
Rapacuronium bromide (Org 9487) is a non-depolarizing neuromuscular blocker that also acts as an allosteric modulator of the muscarinic acetylcholine receptor (mAChR). It is intended for research use only.
- Acts as a non-depolarizing neuromuscular blocker.
- Functions as an allosteric modulator of the muscarinic acetylcholine receptor (mAChR).
- Binds to all muscarinic receptor subtypes.
- Shows micromolar affinity and slight selectivity towards the M2 receptor.
- Exhibits neuromuscular effects in vivo.
Medchemexpress LLC Rapacuronium bromide | 156137-99-4 | 98.0% | 677.80 | 50 MG
Rapacuronium bromide (Org 9487) is a non-depolarizing neuromuscular blocker and an allosteric modulator of muscarinic acetylcholine receptor (mAChR).
- Acts as a non-depolarizing neuromuscular blocker
- Functions as an allosteric modulator of muscarinic acetylcholine receptor (mAChR)
- Binds to all muscarinic receptor subtypes
- Exhibits micromolar affinity and slight selectivity towards M2 receptor
- Lowers [35S]GTPγS binding to membranes
Cayman Chemical QX314 bromide Other Receptor
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
Medchemexpress LLC N6-benzoyl-2',3'-isopropylidene adenosine | 39947-04-1 | MFCD15145205 | 98.8% | 411.41 g·mol⁻¹ | C20H21N5O5 | 100 MG
N6-Benzoyl-2',3'-isopropylidene adenosine is an adenosine analog used as a research reagent in pharmacological and biochemical studies. The compound is supplied as a small-mass solid with reported purity of 98.8%, molecular formula C20H21N5O5, and molecular weight 411.41 g·mol⁻¹.
- Research-grade adenosine analog for pharmacology studies.
- High reported purity (98.8%) suitable for analytical applications.
- Small 100 MG quantity appropriate for lab-scale experiments.
- Defined molecular formula and molecular weight for identification and QC.
- Suitable for biochemical assays and structure-activity investigations.
Medchemexpress LLC Azido-choline bromide | 2059973-54-3 | 99.6% | 239.11 g/mol | C6H15BrN4O | 25 MG
N3-Cho bromide (Azido-choline bromide) is an azide-functionalized choline analogue used as a click chemistry reagent to install or label choline head-groups in membrane lipids and related biomolecules. It is provided as a colorless to off-white solid-liquid mixture with high purity and good solubility in common solvents, intended for synthetic and labeling applications.
- Azide-functionalized choline analogue for click chemistry labeling.
- High purity suitable for synthetic and analytical use.
- Soluble in water (125 mg/mL) and DMSO (100 mg/mL); ultrasonic recommended.
- Storage recommendations for stability: solid at -20°C sealed; in solvent -80°C up to 6 months.
- Available in small research pack sizes for laboratory experiments.