Hydrobromides
Selleck Chemical LLC Homatropine Bromide S4025-50mg
Homatropine Bromide is an muscarinic AChR antagonist inhibits endothelial and smooth muscle muscarinic receptors of WKY-E and SHR-E with IC50 of 162 5 nM and 170 3 nM respectively
![eMolecules Oakwood Chemicals 1 8-Diazabicyclo[5 4 0]undec-7-ene 1kg 480122918 033415 0 000 6674-22-2 MFCD00006930 152 241 C9H16N2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
eMolecules Oakwood Chemicals 1 8-Diazabicyclo[5 4 0]undec-7-ene 1kg 480122918 033415 0 000 6674-22-2 MFCD00006930 152 241 C9H16N2
Oakwood Chemicals 1 8-Diazabicyclo[5 4 0]undec-7-ene 1kg 480122918 033415 0 000 6674-22-2 MFCD00006930 152 241 C9H16N2
Apexbio Technology LLC TC-E 5003 17328-16-4 50mg
TC-E 5003 (CAS 17328-16-4) is a selective inhibitor of protein arginine methyltransferase 1 (PRMT1) exhibiting an IC50 of 1 5 M1 PRMT1 a member of the PRMT family mediates post-translational arginine methylation and is implicated in regulating diverse cellular processes Aberrant PRMT1 activity has been associated with a range of malignancies making it of interest for oncology research In cellular studies TC-E 5003 has been shown to inhibit proliferation and induce apoptosis in MCF7a breast cancer and LNCaP prostate cancer cell lines as well as attenuate androgen-induced gene expression in LNCaP cells This compound serves as a useful tool for investigating PRMT1 function and its role in cancer biology
Medchemexpress LLC Rociletinib hydrobromide | 1446700-26-0 | MFCD28386290 | 98.0% | 636.46 g/mol | C27H29BrF3N7O3 | 10 MG
Rociletinib hydrobromide is the hydrobromide salt of rociletinib, an orally active kinase inhibitor selective for mutant forms of the epidermal growth factor receptor (EGFR) including T790M. It is supplied as a solid research reagent for biochemical, cellular, and analytical studies.
- Hydrobromide salt of rociletinib.
- Selective inhibitor of mutant EGFR, including T790M.
- Intended for research and analytical applications.
- Purity 98.04% (HPLC).
- Molecular weight 636.46 g/mol.
- CAS number 1446700-26-0.
- Store sealed, away from moisture; in solvent: -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC BC-11 hydrobromide | 443776-49-6 | 99.0% | 290.97 g/mol | C8H12BBrN2O2S | 5 MG
BC-11 hydrobromide is a research-grade small-molecule inhibitor that targets TMPRSS2 and urokinase (uPA). It is used in biochemical and cellular studies of viral entry and cancer biology, and is supplied as a hydrobromide salt to aid stability and handling.
- Selective TMPRSS2 and urokinase (uPA) inhibition for mechanistic studies.
- Suitable for biochemical and cellular assays, including viral entry research.
- Hydrobromide salt form for improved stability and solubility.
- High purity (99.0%) and available in small research sizes (5-100 mg).
Cayman Chemical Clobenpropit hydrobromide
A selective histamine H3 receptor antagonist (Ki = 0.17 nM in rat cortical membranes); reduces inhibition of electrically induced contractions in isolated guinea pig ileum longitudinal muscle by (R)-α-methylhistamine at 0.3, 0.1, and 3 nM; decreases the duration of the tonic, clonic, and convulsive coma phases of electrically induced convulsions in mice at 1 and 3 mg/kg, an effect that can be blocked by (R)-α-methylhistamine or imetit; increases GABA release and inhibits NMDA-induced neurotoxicity in primary rat cortical neurons at 0.1 μM
Selleck Chemical LLC Homatropine Methylbromide S4024-50mg
Homatropine Methylbromide is muscarinic AChR antagonist inhibits endothelial and smooth muscle muscarinic receptors of WKY-E and SHR-E with IC50 of 162 5 nM and 170 3 nM respectively
Accela Chembio Inc 3-(bromomethyl)pyridine Hydrobromide | 25g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
3-(bromomethyl)pyridine Hydrobromide | 25g | 4916-55-6 | MFCD01321314 | 95+% | Shelf Life: 1260 Days | Light Sensitive/nitrogen Or Argon/+4
Medchemexpress LLC Sulfone, bis((4-chloroacetylamino)phenyl). | 17328-16-4 | MFCD00028183 | 98.0% | 401.26 g/mol | C16H14Cl2N2O4S | 1 ML
TC-E 5003 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor supplied as a ready-to-use 10 mM solution in DMSO for research use in biochemical and cell-based assays. Handle and store according to laboratory safety and storage guidelines.
- Selective PRMT1 inhibitor with reported IC50 ≈ 1.5 μM.
- Supplied as a 10 mM solution in DMSO, 1 mL vial.
- Purity 98.0% by HPLC.
- Molecular weight 401.26 g/mol.
- Store solution at -80°C for long-term stability; short-term storage at -20°C.
Medchemexpress LLC Halofuginone hydrobromide | 64924-67-0 | MFCD00946455 | 100.0% | 495.59 g·mol⁻¹ | C16H18Br2ClN3O3 | 10 MG
Halofuginone hydrobromide is a febrifugine derivative and a competitive prolyl-tRNA synthetase inhibitor used as a research standard for studies of collagen synthesis, TGF-β signaling, fibrosis, cancer biology, and anti-parasitic activity.
- Competitive prolyl-tRNA synthetase inhibitor with reported Ki ≈ 18.3 nM.
- Inhibits type-I collagen synthesis, useful for fibrosis and TGF-β studies.
- High reported purity (99.99%), suitable as a reference standard.
- Characterized molecular weight (495.59 g·mol⁻¹) and CAS number (64924-67-0).
- Available in small mg quantities for in vitro and pharmacological assays.
eMolecules Ambeed 3-Bromopiperidine-2 6-dione 250mg 506392068 A875928 0 000 62595-74-8 MFCD11053059 192 012 C5H6BrNO2
Ambeed 3-Bromopiperidine-2 6-dione 250mg 506392068 A875928 0 000 62595-74-8 MFCD11053059 192 012 C5H6BrNO2
Medchemexpress LLC Arecoline hydrobromide | 300-08-3 | 99.95% | 500 MG
Arecoline hydrobromide is a naturally occurring, brain-penetrant, and orally active psychoactive alkaloid. It functions as a partial agonist for both nicotinic and muscarinic acetylcholine receptors, influencing various neurological processes. This compound has been noted for its ability to induce stimulation, alertness, anxiolysis, and anti-parasitic effects, though it can also cause oxidative stress.
- Naturally occurring psychoactive alkaloid
- Brain-penetrant and orally active
- Acts as a partial agonist of nicotinic and muscarinic acetylcholine receptors
- Can induce stimulation, alertness, anxiolysis, and anti-parasitic effects
- Induces reactive oxygen species and cell cycle arrest in HaCaT cells
- Alleviates anxiety and depression in CFA-induced mice
Medchemexpress LLC MTSEA hydrobromide | 16599-33-0 | 97.9% | 50 MG
MTSEA hydrobromide is a sulfhydryl-reactive reagent used to modify free cysteine residues in proteins, introducing a positively charged side chain approximately the size of lysine. The hydrobromide salt is supplied as a solid and is used in biochemical assays and site-directed cysteine modification to probe protein structure and function.
- Sulfhydryl-reactive reagent for cysteine modification.
- Introduces a positively charged side chain similar in size to lysine.
- Suitable for biochemical assays and site-directed mutagenesis studies.
- Soluble in water and common organic solvents such as DMSO.
- High purity suitable for research applications.
Medchemexpress LLC SCH-202676 (hydrobromide) | 265980-25-4 | 96.8% | 348.26 | 1 ML
SCH-202676 hydrobromide is an allosteric modulator of G protein-coupled receptors (GPCRs) and adenosine receptor (AR). It demonstrates antiviral activity and inhibits 3CLpro in a time-dependent manner with an IC50 value of 0.655 μM.
- Purity: 96.81%
- Appearance: Solid
- Color: White to off-white
- Solubility: DMSO: 10 mg/mL
Cayman Chemical FenoterolhydrobromIde 10mg
An analytical reference standard categorized as a β2-adrenergic receptor agonist; has been used as a performance-enhancing drug in sports doping and is banned by WADA; intended for research and forensic applications