Acyl bromides
Medchemexpress LLC N6-benzoyl-2'-deoxyadenosine monohydrate | 305808-19-9 | 98.0% | 373.36 | C17H19N5O5 | 25 G
N6-benzoyl-2'-deoxyadenosine monohydrate is a nucleoside analog used in biochemical research and oligonucleotide synthesis. Supplied as a solid monohydrate, it is used in diagnostic and analytical workflows that require modified nucleosides.
- Nucleoside analog used in oligonucleotide synthesis and nucleoside research.
- Monohydrate solid form for easier handling and storage.
- High purity (98.0%) suitable for research applications.
- Chemical formula C17H19N5O5; molecular weight 373.36.
- Available in common laboratory pack sizes, including 25 G.
- Applicable in diagnostic and analytical workflows requiring DNA binding or modification.
Medchemexpress LLC Aclidinium Bromide | 320345-99-1 | 98.96% | C26H30BrNO4S2 | 1 ML
Aclidinium Bromide is a long-acting, inhaled muscarinic antagonist with potential for research into chronic obstructive pulmonary disease (COPD). It has shown potent antagonism of human muscarinic receptors preclinically, with a long residence time at M3 receptors, suggesting potential for sustained bronchodilation. Early clinical studies have indicated low systemic bioavailability and a favorable safety profile.
- Long-acting muscarinic antagonist
- Potential for chronic obstructive pulmonary disease (COPD) research
- Exhibits potent antagonism of human muscarinic receptors
- Long residence time at M3 receptors for sustained bronchodilation
- Low systemic bioavailability
- Favorable safety profile
- Rapidly hydrolyzed in human plasma
Medchemexpress LLC N-Benzoyl-(2R,3S)-3-phenylisoserine | 132201-33-3 | 25 MG
N-Benzoyl-(2R,3S)-3-phenylisoserine is a Taxol C-13 Side Chain, crucial for the strong antitumor activity of Taxol. It has a molecular weight of 285.29 and a chemical formula of C16H15NO4. This compound appears as a white to off-white solid with a purity of 99.48%.
- Crucial for the strong antitumor activity of Taxol
- Taxol C-13 side chain
- Purity of 99.48%
- Molecular weight: 285.29
- Chemical formula: C16H15NO4
- Appears as a white to off-white solid
- Structure classification: Alkaloids, other alkaloids
- Initial source: Plants, Taxaceae, *Taxus wallichiana Zucc.*
Medchemexpress LLC Ipratropium bromide hydrate | 66985-17-9 | 99.9% | 1 ML
Ipratropium bromide (Sch 1000) hydrate is a muscarinic receptor antagonist, with IC50s of 2.9 nM, 2 nM, and 1.7 nM for M1, M2, and M3 receptors, respectively. It relaxes smooth muscle and can be used in the research for COPD (chronic obstructive pulmonary disease) and asthma.
- Muscarinic receptor antagonist
- Relaxes smooth muscle
- Potential for research in COPD and asthma
- IC50s: 2.9 nM for M1, 2 nM for M2, and 1.7 nM for M3 receptors
Selleck Chemical LLC Domiphen Bromide S4186-1g
Domiphen bromide (NSC-39415) is a quaternary ammonium antiseptic with actions as a cationic surfactant
Medchemexpress LLC Aclidinium (Bromide) | 320345-99-1 | C26H30BrNO4S2 | 100 MG
Aclidinium (Bromide) | 320345-99-1 | C26H30BrNO4S2 | 100 MG
Medchemexpress LLC N4-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine | 67219-55-0 | 98.9% | 633.69 | 5 G
N4-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxycytidine, also known as 5'-O-DMT-N4-Bz-dC, is a compound that can be used for the synthesis of oligodeoxynucleotides containing a 3'-S-phosphorothiolate (3'-PS) linkage. It serves as a useful tool for probing enzyme-catalyzed cleavage processes in DNA.
- Used for synthesis of oligodeoxynucleotides.
- Useful tool for probing enzyme-catalyzed cleavage processes in DNA.
Medchemexpress LLC N4-Benzoyl-2 -O-meth 500mg
N4-Benzoyl-2 -O-methylcytidine is a natural cytidine nucleoside analog Cytidine analogs have the mechanism of inhibiting DNA methyltransferase (such as Zebularine (HY-13420)) and have potential antimetabolite and antitumor activities[1][2]
Medchemexpress LLC (2e)-1-(3,4-dimethoxyphenyl)-5-fluoro-3-(4-fluorophenyl)-2-(2-fluorophenyl)pent-1-en-4-one bromide | 1390654-28-0 | >98.8% | 524.38 | 100 MG
KRN2 bromide is a selective inhibitor of nuclear factor of activated T cells (NFAT5), with an IC50 of 0.1 μM. It selectively suppresses the expression of pro-inflammatory genes, including Nos2 and Il6, without hindering high-salt-induced NFAT5 and its target gene expressions. KRN2 also dose-dependently inhibits NF-κB p65 binding to Nfat5 promoter 1 and directly blocks the interaction between NF-κB p65 and its DNA binding sequence in the upstream site of Nfat5 exon 1.
- Effectively suppresses AIA in which innate immune cells play a predominant role.
- Effectively suppresses CIA as well as AIA in mice.
- Decreases the production of pro-inflammatory cytokines and autoantibodies.
- Reduces macrophage infiltration.
Medchemexpress LLC Bromoacetyl-PEG3-DBCO | 00-00-0 | 98.6% | 600.50 | C29H34BrN3O6 | 5 MG
Bromoacetyl-PEG3-DBCO is a heterobifunctional PEG-based linker for bioconjugation and PROTAC synthesis. It combines a DBCO bioorthogonal handle with a bromoacetyl electrophile and a short PEG3 spacer to enable efficient, selective conjugation and good solubility in small-scale synthetic workflows.
- Contains a DBCO moiety for strain-promoted alkyne-azide cycloaddition (SPAAC).
- Provides a bromoacetyl reactive handle for selective conjugation to thiols.
- PEG3 spacer enhances solubility and flexibility in conjugates.
- High purity (~98.6%) suitable for synthetic applications.
- Oil appearance facilitates handling for small-scale synthesis.
- Recommended storage at -20°C in pure form for long-term stability.
- Available in milligram-scale quantities for research use.
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
AdipoGen 10-Dodecylacridine Orange Br
Chemical. CAS 41387-42-2. Formula C29H44BrN3. MW 514.58. Synthetic. Hydrophobic fluorescent probe. Selectively stains inner mitochondrial membranes, but in contrast to rhodamine-123 staining is not membrane potential-dependent. Dye binding to surfactant micellar surfaces and used for the determination of cationic surfactants.
TARGETMOL CHEMICALS INC Tarloxotinib bromide 1MG
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%
Selleck Chemical LLC Methylbenactyzine Bromide S4623-25mg
Methylbenactyzine Bromide (Gastrimade Noinarin Paragone Semulgin) is a kind of muscarinic cholinergic receptor antagonist with antispasmodic activity