Hydrobromides
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 S-(2-aminoethyl) methanethiosulfonate hydrobromide | 16599-33-0 | 97.9% | 25 MG
MTSEA hydrobromide is a sulfhydryl-reactive reagent that selectively modifies free cysteine residues to introduce a positively charged side chain roughly the size of lysine. It is used in biochemical and electrophysiological studies to probe cysteine accessibility and to introduce charge at engineered cysteine sites.
- Sulfhydryl-reactive reagent for targeted cysteine modification.
- High supplied purity of 97.9%.
- Molecular weight 236.15 g/mol; formula C3H10BrNO2S2.
- Available in small solid packs suitable for research use.
- Store sealed at -20°C; in solution store at -80°C for long-term stability.
- CAS number 16599-33-0 for unambiguous identification.
Medchemexpress LLC Guvacoline hydrobrom 5mg | 17210-51-4 | 222.08 g/mol | C7H12BrNO2 | 5 MG
Guvacoline hydrobromide is the hydrobromide salt of guvacoline, a pyridine alkaloid that acts as a weak full agonist of atrial and ileal muscarinic acetylcholine receptors (mAChR). It is supplied as a solid reagent intended for biochemical and pharmacological research applications.
- Hydrobromide salt form suitable for laboratory handling
- CAS number 17210-51-4
- Molecular formula C7H12BrNO2; molecular weight 222.08 g/mol
- Purity 96.09% as verified by certificate of analysis
- Used as a pharmacological tool for muscarinic receptor studies
Sigma Aldrich Fine Chemicals Biosciences 4-Bromopiperidine hydrobromide 98% | 54288-70-9 | MFCD00191858 | 1G
4-Bromopiperidine hydrobromide 98% | Purity: 98% | Mol Wt: 244.96 | 54288-70-9 | MFCD00191858 | 1G
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.
TARGETMOL CHEMICALS INC Halofuginone hydrobromide 10MG
Also available in 1 mL, 1 mg, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Halofuginone specifically inhibits collagen type I gene expression and matrix metalloproteinase 2 (MMP-2) gene expression, which may result in the suppression of angiogenesis, tumor stromal cell development, and tumor cell growth. Halofuginone Hydrobromide is the hydrobromide salt of halofuginone, a semisynthetic quinazolinone alkaloid anticoccidial derived from the plant Dichroa febrifuga, with antifibrotic and potential antineoplastic activities. These effects appear to be due to halofuginone-mediated inhibition of the collagen type I and MMP-2 promoters. Collagen type I and MMP-2 play important roles in fibroproliferative diseases. Purity 98.5%
Medchemexpress LLC Dihydro-β-erythroidine hydrobromide | 29734-68-7 | MFCD00153793 | >98.0% | 356.25 g/mol | C16H22BrNO3 | 10 MG
Dihydro-β-erythroidine hydrobromide is a competitive antagonist of neuronal nicotinic acetylcholine receptors (nAChRs), with selectivity for α4β2 and α4β4 subtypes. It is used as a pharmacological tool in receptor characterization, electrophysiology, and behavioral studies to probe cholinergic signaling.
- Competitive nAChR antagonist selective for α4β2 and α4β4.
- CAS number 29734-68-7.
- Chemical formula C16H22BrNO3; molecular weight 356.25 g/mol.
- Purity >98.0% (HPLC) as reported by catalog vendors.
- Typical research pack sizes: 1 mg, 5 mg, 10 mg.
- Common applications: electrophysiology, receptor pharmacology, and behavioral assays.