Phenylhydrazines
Medchemexpress LLC S-remoxipride hydrochloride | 73220-03-8 | 99.9% | 371.27 g/mol | C16H23BrN2O3 | 10 MG
(S)-Remoxipride hydrochloride is the S-enantiomer of remoxipride supplied as the hydrochloride salt for laboratory research. It is a selective dopamine D2 receptor antagonist used in neuroscience and pharmacology studies, supplied as a solid powder with reported high purity and characterized by CAS 73220-03-8.
- Selective dopamine D2 receptor antagonist for receptor pharmacology studies.
- S-enantiomeric form for stereospecific research.
- Hydrochloride salt form, solid powder suitable for in vitro use.
- High purity, typically reported as 99.9%.
- Molecular weight 371.27 g/mol and formula C16H23BrN2O3.
- Intended for research use only; not for human or clinical applications.
Medchemexpress LLC Fabomotizole hydrochloride | 173352-39-1 | 99.9% | 343.87 | 50 MG
Fabomotizole hydrochloride (CM346 hydrochloride) is a compound recognized for its anxiolytic and neuroprotective properties. It also demonstrates activity against *Giardia lamblia*, showing potential to inhibit giardiasis. While its precise mechanism of action is still being elucidated, research suggests possible involvement in GABAergic pathways, promotion of NGF and BDNF release, antagonism of MT1 and MT3 receptors, sigma agonism, reversible inhibition of MAO-A, and potential interaction with serotonin receptors.
- Anxiolytic activity
- Neuroprotective activity
- Activity against Giardia lamblia with potential to inhibit giardiasis
Medchemexpress LLC Bendamustine hydrochloride | 3543-75-7 | 99.9% | C16H22Cl3N3O2 | 50 MG
Bendamustine hydrochloride is a purine analogue and a DNA cross-linking agent. It activates DNA-damage stress response and apoptosis, possessing potent alkylating, anticancer, and antimetabolite properties. This product is for research use only.
- Purine analogue
- DNA cross-linking agent
- Activates DNA-damage stress response and apoptosis
- Possesses potent alkylating, anticancer, and antimetabolite properties
- Induces caspase-dependent MM cell death
- Inhibits the spindle-assembly checkpoint
Medchemexpress LLC Bendamustine (hydrochloride) | 3543-75-7 | 99.89% | C16H22Cl3N3O2 | 100 MG
Bendamustine hydrochloride is a purine analogue and a DNA cross-linking agent that activates DNA-damage stress response and apoptosis. It possesses potent alkylating, anticancer, and antimetabolite properties.
- A purine analogue.
- Acts as a DNA cross-linking agent.
- Activates DNA-damage stress response.
- Induces apoptosis.
- Exhibits potent alkylating properties.
- Demonstrates anticancer effects.
- Possesses antimetabolite characteristics.
- Induces p21 (Cip1/Waf1) and NOXA genes.
- Increases the expression of p53 in SU-DHL-1 cells.
- Blocks mitotic checkpoints and causes mitotic catastrophe.
- Reduces the viability of multiple myeloma cell lines.
- Induces specific caspase-dependent multiple myeloma cell death.
- Inhibits the spindle-assembly checkpoint.
eMolecules 1977535-33-3 | Medchem Express | 3-Nitrophenylhydrazine-13C6 (hydrochloride) | 1mg | 705860714 | HY-133689AS | 195.55 | C6H8ClN3O2
Ambeed | N-(3-fluoro-4-nitrophenyl)acetamide | 250mg | 600850122 | A943212 | 345-30-2 | MFCD01463345 | 198.153 | C8H7FN2O3
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Chem-Impex International, Inc. 1,5-Diphenylcarbazone compound with 1,5-Diphenylcarbazide | MFCD00013218 | 5G
1,5-Diphenylcarbazone compound with 1,5-Diphenylcarbazide, MFCD00013218, 5G
Medchemexpress LLC Diclofensine (hydrochloride) | 34041-84-4 | 99.79% | 358.69 | 50 MG
Diclofensine (hydrochloride) | 34041-84-4 | 99.79% | 358.69 | 50 MG
Medchemexpress LLC Ampreloxetine hydrochloride | 1227056-87-2 | 99.5% | 357.80 g/mol | C18H19ClF3NO | 100 MG
Ampreloxetine hydrochloride is an orally active, CNS-penetrant inhibitor of norepinephrine and serotonin transporters used as a research compound to investigate monoamine reuptake and central nervous system pharmacology. Supplied as the hydrochloride salt, it is intended for preclinical and biochemical assays and is characterized by high reported purity.
- Orally active, CNS-penetrant norepinephrine and serotonin transporter inhibitor.
- Useful for studies of monoamine reuptake and central nervous system pharmacology.
- Provided as a hydrochloride salt to aid solubility in formulations.
- High reported purity suitable for biochemical and preclinical assays.
- Available in laboratory-scale quantity for research use.
- Molecular weight 357.80 g/mol and formula C18H19ClF3NO.
![Medchemexpress LLC Piperidine, 4-[2-[(2,4,6-trifluorophenoxy)methyl]phenyl]-, hydrochloride | 1227056-87-2 | 99.5% | 357.80 g·mol⁻¹ | C18H19ClF3NO | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000240486.png-250.jpg)
Medchemexpress LLC Piperidine, 4-[2-[(2,4,6-trifluorophenoxy)methyl]phenyl]-, hydrochloride | 1227056-87-2 | 99.5% | 357.80 g·mol⁻¹ | C18H19ClF3NO | 1 ML
Ampreloxetine hydrochloride (TD-9855) is a research-grade small molecule inhibitor of the norepinephrine transporter (NET) and serotonin transporter (SERT). It is CNS-penetrant and supplied for in-vitro research in solid form and as a ready-to-use 10 mM solution in DMSO; intended for research use only.
- Inhibits NET and SERT for neurotransmitter uptake studies.
- Supplied as a 10 mM solution in DMSO for immediate use.
- Also available as solid quantities for formulation or storage.
- High reported purity (99.5%).
- Molecular weight 357.80 g·mol⁻¹ for dose calculations.
- Intended for research use only.
Medchemexpress LLC Sucunamostat (hydrochloride) | 00-00-0 | 98.1% | 506.89 g/mol | C22H23ClN4O8 | 5 MG
Sucunamostat hydrochloride is the hydrochloride salt of sucunamostat, a reversible enteropeptidase inhibitor supplied for research use. It is formulated as a high-purity, small-scale reagent intended for in vitro and preclinical studies.
- Molecular formula C22H23ClN4O8.
- Molecular weight 506.89 g/mol.
- Purity 98.1%.
- Target enteropeptidase with low-nanomolar potency (IC50 ~4.6-5.4 nM).
- Chemical form hydrochloride salt for improved solubility.
- Available in small pack sizes suitable for lab-scale use.