Hydrochlorides
Medchemexpress LLC 4-(2-aminoethyl)-7-(methylamino)chromen-2-one dihydrochloride | 1883548-88-6 | MFCD30182251 | 99.5% | 291.17 g/mol | C12H16Cl2N2O2 | 5 MG
FFN 206 dihydrochloride is a fluorescent vesicular monoamine transporter 2 (VMAT2) substrate used as a research probe to visualize and study monoamine uptake into synaptic vesicles. The compound is supplied as a stable dihydrochloride salt in small pack sizes for laboratory use.
- Fluorescent VMAT2 substrate for visualization of vesicular uptake.
- High purity suitable for analytical and preparative experiments.
- Stable dihydrochloride salt with defined molecular weight and formula.
- Recommended storage at -20°C; in solvent stability varies with temperature.
- Available in small pack sizes for research use.
![Medchemexpress LLC N-[3-oxo-3-[4-(4-pyridinyl)-1-piperazinyl]propyl]-2,1,3-benzothiadiazole-4-sulfonamide | 1135243-19-4 | MFCD18086889 | 99.8% | 432.52 g/mol | C18H20N6O3S2 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000244005.png-250.jpg)
Medchemexpress LLC N-[3-oxo-3-[4-(4-pyridinyl)-1-piperazinyl]propyl]-2,1,3-benzothiadiazole-4-sulfonamide | 1135243-19-4 | MFCD18086889 | 99.8% | 432.52 g/mol | C18H20N6O3S2 | 25 MG
VU 0255035 is a selective, competitive antagonist of the M1 muscarinic acetylcholine receptor used as a research compound for central nervous system studies, including seizure models and investigations of neuronal excitability. It is supplied with high purity and is available in solid and solution formats for in vitro and in vivo experiments.
- Selective M1 antagonist with reported nanomolar activity.
- Brain-penetrant compound suitable for in vivo CNS studies.
- High supplied purity (≈99.8%).
- Molecular weight 432.52 g/mol (C18H20N6O3S2).
- Available in multiple pack sizes and DMSO solution formats for easy dosing.
Medchemexpress LLC 2-iminothiolane hydrochloride | 4781-83-3 | MFCD00039013 | 99.9% | 137.63 g/mol | C4H8ClNS | 50 MG
2-Iminothiolane hydrochloride is a thiolating reagent that introduces sulfhydryl (-SH) groups into primary amines of proteins, peptides, and oligosaccharides for bioconjugation and cross-linking. Supplied as a white to off-white solid, it is intended for research use and should be stored sealed and away from moisture.
- High purity suitable for biochemical applications
- Efficient thiolation of primary amines under mild conditions
- Useful for protein and peptide modification and cross-linking
- Solid form easy to weigh and dissolve for reactions
- Stable when stored sealed and protected from moisture
Medchemexpress LLC Co 101244 hydrochloride | 193356-17-1 | 99.9% | 377.90 | C21H28ClNO3 | 5 MG
Co 101244 hydrochloride | 193356-17-1 | 99.9% | 377.90 | C21H28ClNO3 | 5 MG
Medchemexpress LLC JDTic dihydrochloride | 785835-79-2 | MFCD22419279 | 98.0% | 538.55 | C28H41Cl2N3O3 | 25 MG
JDTic dihydrochloride is the dihydrochloride salt of JDTic, a potent and selective kappa-opioid receptor (KOR) antagonist used as a research reagent to inhibit κ-agonist (e.g., U50,488)-induced antinociception and to study KOR signaling. It is supplied as a characterized solid for laboratory assays and is not for human use.
- Potent kappa-opioid receptor (KOR) antagonist used in pharmacological research.
- Blocks κ-agonist U50,488-induced antinociception in model systems.
- High purity (98.03%) suitable for research applications.
- White to off-white solid appearance.
- Dissolves in DMSO (100 mg/mL) and H2O (50 mg/mL); ultrasonic assistance recommended.
- Store sealed, away from moisture; in solvent store at -80°C (6 months) or -20°C (1 month).
- For research use only; not for human or patient use.
Medchemexpress LLC Dasatinib hydrochloride | 854001-07-3 | 99.3% | 524.47 g/mol | C22H27Cl2N7O2S | 500 MG
Dasatinib hydrochloride is the hydrochloride salt of dasatinib, a potent ATP-competitive dual Src/Bcr-Abl kinase inhibitor used in cancer research and cell signaling studies. It is supplied as a high-purity research reagent intended for in vitro and in vivo kinase inhibition assays and related biochemical applications.
- Potent ATP-competitive inhibitor of Src and Bcr-Abl kinases.
- Suitable for in vitro and in vivo research applications.
- Hydrochloride salt for improved solubility and handling.
- High purity (99.31% by HPLC) for reliable experimental results.
- Molecular formula C22H27Cl2N7O2S; molecular weight 524.47 g/mol.
- Available in a 500 mg research package.
Medchemexpress LLC Nilotinib hydrochloride dihydrate | 00-00-0 | MFCD09833716 | 99.9% | 602.01 g/mol | C28H27ClF3N7O3 | 100 MG
Nilotinib hydrochloride dihydrate is the hydrochloride salt, dihydrate form of nilotinib, supplied as a white to off-white solid for research use. It functions as a Bcr-Abl tyrosine kinase inhibitor and is intended for biochemical and cell-based studies of Bcr-Abl signaling and leukemia models, provided in laboratory-scale quantities for in vitro and preclinical experiments.
- High purity suitable for research-grade assays.
- Hydrochloride dihydrate salt form for improved handling and reproducibility.
- Soluble in DMSO at high concentrations (≈100 mg/mL) with ultrasonic assistance.
- Stable when stored sealed at 4°C; long-term storage in solvent at -80°C.
- White to off-white powder form for easy weighing and dissolution.
Medchemexpress LLC Doxapram hydrochloride hydrate | 7081-53-0 | 99.3% | 25 MG
Doxapram hydrochloride hydrate | 7081-53-0 | 99.3% | 25 MG
Medchemexpress LLC Kevetrin hydrochloride | 66592-89-0 | 98.0% | 179.67 | 1 ML
Kevetrin hydrochloride is a potent activator of p53, inducing apoptosis in TP53 wild-type and mutant acute myeloid leukemia cells. It exhibits preferential cytotoxic activity against blast cells.
- Potent activator of p53.
- Induces apoptosis in TP53 wild-type and mutant acute myeloid leukemia cells.
- Exhibits preferential cytotoxic activity against blast cells.
eMolecules 19524-06-2 | 4-Bromopyridine hydrochloride | Combi-Blocks | MFCD00012828 | 194.460 | C5H5BrClN | 98.000 | Cl.Brc1ccncc1 | 5g | 117556755
4-Bromopyridine hydrochloride | Combi-Blocks | 19524-06-2 | MFCD00012828 | 194.460 | C5H5BrClN | 98.000 | Cl.Brc1ccncc1 | 5g | 117556755
Medchemexpress LLC VU-1545 | 890764-63-3 | 99.0% | 402.38 | 25 MG
VU-1545 is a potent metabotropic glutamate receptor 5 (mGluR5) positive allosteric modulator (PAM) with a Ki of 156 nM and an EC50 of 9.6 nM. It promotes AKT activation, efficiently doing so at concentrations as low as 0.1 and 1.0 μM. Studies have shown that VU-1545 at 10 and 100 μM promotes Akt phosphorylation. This compound is used for research purposes and is not intended for patient use.
- Potent mGluR5 positive allosteric modulator
- Ki of 156 nM for mGluR5
- EC50 of 9.6 nM for mGluR5
- Promotes AKT activation in neuronal cells
- Efficiently promotes Akt phosphorylation at 10.0 μM and 100.0 μM
Medchemexpress LLC Doxapram (hydrochloride hydrate) | 7081-53-0 | 99.3% | 1 ML
Doxapram hydrochloride hydrate is a respiratory stimulant that increases breathing rate and depth by acting on the brain's respiratory centers and peripheral chemoreceptors. It can be used for the study of respiratory depression such as post-anesthesia respiratory depression, chronic obstructive pulmonary disease, and apnea of prematurity.
- Inhibits TASK-1, TASK-3, and TASK-1/TASK-3 heterodimeric channel function
- Inhibits Ca²⁺-activated and Ca²⁺-independent potassium current in type I cells of the carotid body
- Significantly prolongs the effective refractory period of the atrium
- Has an anti-arrhythmic effect
Medchemexpress LLC Aldoxorubicin hydrochloride | 480998-12-7 | 98.0% | 787.21 g/mol | C37H43ClN4O13 | 5 MG
Aldoxorubicin hydrochloride is an albumin-binding proagent of doxorubicin that functions as a DNA topoisomerase II inhibitor and exhibits acid-sensitive release properties. It is supplied as a high-purity research reagent for preclinical laboratory use.
- Albumin-binding proagent of doxorubicin
- Acid-sensitive release of active doxorubicin
- Acts as a DNA topoisomerase II inhibitor
- Available as small-mass research packs (e.g., 5 mg)
- High reported purity (around 98%)
Medchemexpress LLC Urapidil (hydrochloride) | 64887-14-5 | MFCD00078601 | 99.98% | 100 MG
Urapidil hydrochloride (Standard) is an analytical standard intended for research and analytical applications. It is an orally active α1-adrenoceptor antagonist and 5-HT1A receptor agonist, showing an antihypertensive effect.
- Analytical standard grade
- Used in qualitative research experiments
- Used in quantitative research experiments
- Used in methodological research experiments
- Applicable in HPLC
- Applicable in GC
- Applicable in MS