Acyl bromides
Medchemexpress LLC MitoB bromide | 1247025-84-8 | MFCD28976194 | 99.8% | 477.14 g·mol⁻¹ | C25H23BBrO2P | 5 MG
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.
Medchemexpress LLC Pinaverium bromide | 53251-94-8 | MFCD08063574 | 98.0% | 591.42 g/mol | C26H41Br2NO4 | 5 MG
Pinaverium bromide is an analytical research standard of an L-type calcium channel blocker with selectivity for the gastrointestinal tract. Supplied in small laboratory pack sizes, it is intended for analytical and pharmacological research, method development, and use as a reference material. The compound has formula C26H41Br2NO4, molecular weight 591.42 g/mol, and CAS 53251-94-8.
- Research-grade analytical standard for L-type calcium channel studies.
- Supplied in small, lab-friendly pack sizes for routine use.
- High purity suitable for analytical and pharmacological assays.
- Datasheet, safety data sheet, and certificate of analysis available on request.
- Stable bromide salt form appropriate for gastrointestinal pharmacology research.
Cayman Chemical N4-benzoyl-2-DeoxycytIdIn 10g
A building block; has been used in the synthesis of nucleosides and nucleotides with anticancer activity, as well as oligonucleotides
eMolecules AOBChem USA / 5-Chloro-2-(methythio)phenylboronic acid / 250mg / 532120225 / 24620 / / 1451392-55-4 / MFCD22543736 / 202.460 / C7H8BClO2S
AOBChem USA / 5-Chloro-2-(methythio)phenylboronic acid / 250mg / 532120225 / 24620 / / 1451392-55-4 / MFCD22543736 / 202.460 / C7H8BClO2S
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
Cayman Chemical N4-benzoyl-2-DeoxycytIdIn 5g
A building block; has been used in the synthesis of nucleosides and nucleotides with anticancer activity, as well as oligonucleotides
Rieke Metals LLC 3-BUTENYLMAGNESIUM BROMIDE | 7103-09-5 | 159.31 g/mol |
3-BUTENYLMAGNESIUM BROMIDE | 7103-09-5 | 159.31 g/mol |
Medchemexpress LLC Benzoyl coenzyme A trilithium | 102185-37-5 | MFCD00078942 | 94.0% | 889.44 g·mol⁻¹ | C28H37Li3N7O17P3S | 5 MG
Benzoyl coenzyme A trilithium is the trilithium salt of benzoyl coenzyme A supplied for research use as an intermediate in CoA-dependent metabolic pathways (CAS 102185-37-5). It is provided as a white to off-white solid with specified storage and solvent stability for biochemical studies.
- White to off-white solid for biochemical research.
- Molecular weight 889.44 g·mol⁻¹.
- Purity 94.0%.
- Store sealed at -20°C; in solution -80°C (up to 6 months) or -20°C (up to 1 month).
- Used to study benzoate metabolism and CoA-dependent pathways in vitro.
Apexbio Technology LLC Tiotropium Bromide hydrate 139404-48-1 10mg
Tiotropium Bromide hydrate is a small-molecule antagonist targeting muscarinic acetylcholine receptors (mAChRs) It is designed to competitively inhibit mAChRs thereby modulating airway smooth muscle contraction and mediating bronchodilation Tiotropium Bromide hydrate exerts its biological activity primarily through competitive antagonism at mAChRs resulting in relaxation of airway smooth muscle Based on these pharmacological properties Tiotropium Bromide hydrate holds research potential in respiratory pharmacology particularly for investigating mechanistic pathways in chronic obstructive pulmonary disease (COPD) receptor-ligand interactions and pulmonary pharmacodynamics associated with airway obstruction