Acyl Halides
Cayman Chemical N4-benzoyl-2-DeoxycytIdIn 50g
A building block; has been used in the synthesis of nucleosides and nucleotides with anticancer activity, as well as oligonucleotides
Medchemexpress LLC N4-Benzoyl-2 -O-meth 10mM 1mL
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 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.
Medchemexpress LLC Domiphen bromide | 538-71-6 | 98.7% | 5 G
Domiphen bromide | 538-71-6 | 98.7% | 5 G
Medchemexpress LLC 1,3,5-Tri-O-benzoyl-a-D-ribofuranose | 22224-41-5 | 99.8% | 462.45 | 25 G
1,3,5-Tri-O-benzoyl-a-D-ribofuranose is a purine nucleoside analog. Purine nucleoside analogs exhibit broad antitumor activity, particularly against indolent lymphoid malignancies. Their anticancer mechanisms involve inhibiting DNA synthesis and inducing apoptosis.
- Broad antitumor activity
- Targets indolent lymphoid malignancies
- Inhibits DNA synthesis
- Induces apoptosis
Apexbio Technology LLC Umeclidinium bromide 869113-09-7 5mg
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
