Acyl bromides
AdipoGen Stain 3-I
Chemical. CAS 155862-91-2. Formula C18H16BrN3O2S. MW 418.31. Synthetic. Class of highly photostable, water soluble fluorescent labels with large Stokes shift, high QY in aqueous media and pH tolerance. Relatively low extinction coefficient Epsilon∼ >20,000 in EtOH.
AdipoGen Stain 7-II
Chemical. CAS 155863-03-9. Formula C29H24BrN3O6. MW 590.42. Synthetic. New class of highly photostable, water soluble fluorescent labels with large Stokes shift, high QY in aqueous media and pH tolerance.
Selleck Chemical LLC Domiphen Bromide S4186-50mg
Domiphen bromide (NSC-39415) is a quaternary ammonium antiseptic with actions as a cationic surfactant
Cayman Chemical N4-benzoyl-2'-Deoxycytidine, Purity: ≥98%, CAS: 4836-13-9, 50 g
A building block; has been used in the synthesis of nucleosides and nucleotides with anticancer activity, as well as oligonucleotides
Medchemexpress LLC Bromoacetyl-PEG3-DBCO | 00-00-0 | 98.6% | C29H34BrN3O6 | 10MG
Bromoacetyl-PEG3-DBCO is a heterobifunctional PEG linker containing a dibenzocyclooctyne (DBCO) moiety and a bromoacetyl reactive handle. It is designed for conjugation and linker installation in PROTAC and bioconjugation workflows, enabling click chemistry and selective nucleophile coupling.
- Facilitates SPAAC via a strained alkyne DBCO group.
- Provides a bromoacetyl handle for selective conjugation to thiols or amines.
- PEG3 spacer improves solubility and reduces steric hindrance.
- High purity suitable for research and synthesis workflows.
- Available in small-scale pack sizes for discovery chemistry.
eMolecules 89520-11-6 | N-Bromoacetyl-beta-alanine | Combi-Blocks | MFCD07369176 | 210.027 | C5H8BrNO3 | 97.000 | OC(=O)CCNC(=O)CBr | 1g | 267178577
N-Bromoacetyl-beta-alanine | Combi-Blocks | 89520-11-6 | MFCD07369176 | 210.027 | C5H8BrNO3 | 97.000 | OC(=O)CCNC(=O)CBr | 1g | 267178577
Medchemexpress LLC N6-benzoyl-2'-deoxyadenosine monohydrate | 305808-19-9 | MFCD00009628 | ≥98.0% | 373.37 g/mol | C17H19N5O5 | 1 G
N6-Benzoyl-2'-deoxyadenosine monohydrate is a purine nucleoside analog provided as a monohydrate solid for research and diagnostic applications. It is used to study DNA duplex interactions and related biochemical assays, and is supplied at research-grade purity for laboratory use.
- High purity (≥98.0%).
- Monohydrate solid form suitable for laboratory assays.
- Used as a nucleoside analog to probe DNA duplex structure in assays.
- CAS number 305808-19-9.
- Molecular weight 373.37 g/mol.
- Available in a 1 g pack and larger sizes.
TARGETMOL CHEMICALS INC DEMECARIUM BROMIDE 50MG
Also available in 2 mg 5 mg 10 mg 25 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Demecarium bromide (BC-48) is a potent cholinesterase inhibitorand is treatment glaucoma agent. purity: 98%
Medchemexpress LLC Rocuronium Bromide (ORG 9426 Bromide) | 119302-91-9 | 98.0% | 609.68 | 5 MG
Rocuronium Bromide is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation. It is intended for research use only.
- Aminosteroid non-depolarizing neuromuscular blocker
- Muscle relaxant
- Used in modern anaesthesia
- Facilitates endotracheal intubation
- Provides skeletal muscle relaxation during surgery or mechanical ventilation
- For research use only
Medchemexpress LLC Domiphen bromide | 538-71-6 | 98.7% | 1 ML
Domiphen bromide is a cationic active quaternary ammonium salt that inhibits HERG channels, aminopeptidase-like enzymes, Escherichia coli alkaline phosphatase, and α-chymotrypsin. It exhibits antibacterial, antimalarial, and disinfectant properties, and acts as a synergist for Colistin. This compound can be utilized as a chemical preservative and cationic surfactant, and is also relevant for research into bacterial infectious diseases such as pharyngitis, thrush, and oral ulcers.
- Cationic active quaternary ammonium salt
- Inhibitor of HERG channels (IC50: 9 nM), aminopeptidase-like enzymes, Escherichia coli alkaline phosphatase, and α-chymotrypsin
- Antibacterial, antimalarial, and disinfectant properties
- Synergist of colistin
- Can be used as a chemical preservative and cationic surfactant
- Applicable in research of bacterial infectious diseases like pharyngitis, thrush, and oral ulcers
Medchemexpress LLC N6-Benzoyl-5'-O-DMT-3'-O-methyladenosine 3'CE-phosphoramidite | 179479-02-8 | 98.04% | C48H54N7O8P | 100 MG
N6-Benzoyl-5'-O-DMT-3'-O-methyladenosine 3'CE-phosphoramidite is an adenosine analog that primarily acts as a smooth muscle vasodilator. It has also been shown to inhibit cancer progression. This product is for research use only.
- Appears as a solid with a color ranging from white to off-white
- Molecular weight: 887.96
- Primarily functions as a smooth muscle vasodilator
- Demonstrated ability to inhibit cancer progression
Medchemexpress LLC Demecarium Bromide | 56-94-0 | 50 MG
Demecarium Bromide is a potent cholinesterase inhibitor with an apparent affinity (Kiapp) of 0.15 μM. It is primarily used as a glaucoma agent. This product serves as an analytical standard, suitable for research and analytical applications.
- Potent cholinesterase inhibitor
- Used as a glaucoma agent
- Suitable for research and analytical applications
Medchemexpress LLC Umeclidinium bromide | 869113-09-7 | 508.49 | 100 MG
Umeclidinium bromide is a novel mAChR antagonist with an affinity (Ki) for cloned human M1-M5 mAChRs ranging from 0.05 to 0.16 nM. It inhibits the human ether-a-go-go-related gene channel tail current in a concentration-dependent manner.
- Novel mAChR antagonist
- Inhibits human ether-a-go-go-related gene channel tail current
- Shows slow functional reversibility at cloned human M3 mAChRs
- Shows slow functional reversibility at endogenous mAChR in isolated human bronchus
- For research use only
Medchemexpress LLC Roslin 2 bromide | 29574-21-8 | 99.0% | C13H19BrN4 | 1 MG
Roslin 2 bromide (Benzylhexamethylenetetramine bromide) is a p53 reactivator that exhibits anticancer effects. It functions by binding to FAK, thereby disrupting the interaction between FAK and p53.
- Decreases cancer cell viability and clonogenicity in a p53-dependent manner.
- Increases p53 transcriptional activity, which is inhibited by FAK, using p21, Mdm-2, and Bax-promoter targets.
- Leads to increased expression of p53 targets: p21, Mdm-2, and Bax proteins.
- Significantly reduces tumor growth, disrupts the FAK and p53 complex, and up-regulates p21 in HCT116 p53+/+ xenografts (not in HCT116 p53-/- xenografts).