Hydrochlorides
Medchemexpress LLC Harmalol hydrochloride | 6028-07-5 | 1 ML
Harmalol hydrochloride is a beta carboline alkaloid found in medicinal plants like *Peganum harmala*. It is a main metabolite of Harmaline and significantly inhibits the dioxin-mediated induction of CYP1A1 at both transcriptional and posttranslational levels. This compound also exhibits antioxidant and hydroxyl radical-scavenging properties.
- Purity: 99.91%
- Inhibits dioxin-mediated induction of CYP1A1
- Possesses antioxidant and hydroxyl radical-scavenging properties
- For research use only
Medchemexpress LLC Efaroxan hydrochloride | 89197-00-2 | 99.8% | 1 ML
Efaroxan hydrochloride is a potent, selective, and orally active α2-adrenoceptor antagonist with antidiabetic activity. It is also a selective I1-Imidazoline receptor antagonist. This product can be utilized for research related to cardiovascular disease.
- Potent, selective, and orally active α2-adrenoceptor antagonist
- Demonstrates antidiabetic activity
- Selective I1-Imidazoline receptor antagonist
- Suitable for research related to cardiovascular disease
Medchemexpress LLC Iso-H7 dihydrochloride | 140663-38-3 | MFCD00132899 | 99.1% | 364.29 g/mol | C14H19Cl2N3O2S | 5 MG
Iso-H7 dihydrochloride is a small-molecule protein kinase inhibitor supplied as the dihydrochloride salt for research use. It is intended for biochemical and cell-based studies to modulate kinase activity and is provided in small, high-purity quantities for assay screening and optimization.
- High purity for reliable experimental results.
- Dihydrochloride salt form to aid solubility in polar solvents.
- Available in small milligram pack sizes suitable for screening.
- Validated for use as a protein kinase inhibitor in biochemical and cellular assays.
- Accompanied by datasheet, certificate of analysis, and safety data sheet for quality and safety information.
Medchemexpress LLC L-745870 hydrochloride | 1173023-36-3 | 99.91% | C18H20Cl2N4 | 1 ML
L-745870 hydrochloride is a potent, selective, brain-penetrant, and orally active dopamine D4 receptor antagonist. It exhibits high affinity for D4 receptors, with weaker affinity for D2 and D3 receptors, and moderate affinity for 5-HT2 receptors, sigma sites, and α-adrenoceptors. This compound demonstrates good pharmacokinetic properties and excellent brain penetration in vivo.
- Potent, selective, brain-penetrant, and orally active dopamine D4 receptor antagonist
- High affinity for D4 receptors (Ki of 0.43 nM)
- Weaker affinity for D2 and D3 receptors
- Moderate affinity for 5-HT2 receptors, sigma sites, and α-adrenoceptors
- Good pharmacokinetic properties with 20-60% oral bioavailability
- Plasma t1/2 of 2.1-2.8 hours in rats and monkeys
- Excellent brain penetration in rats
eMolecules 21987-29-1 | 4,4-Difluoropiperidine | Ambeed | MFCD03094281 | 121.131 | C5H9F2N | 97.000 | FC1(F)CCNCC1 | 25g | 536284494
4,4-Difluoropiperidine | Ambeed | 21987-29-1 | MFCD03094281 | 121.131 | C5H9F2N | 97.000 | FC1(F)CCNCC1 | 25g | 536284494
eMolecules 89990-54-5 | Pyrazolidine dihydrochloride | ChemScene | MFCD16620353 | 145.030 | C3H10Cl2N2 | 95.000 | Cl.Cl.C1CNNC1 | 1g | 654759654
Pyrazolidine dihydrochloride | ChemScene | 89990-54-5 | MFCD16620353 | 145.030 | C3H10Cl2N2 | 95.000 | Cl.Cl.C1CNNC1 | 1g | 654759654
eMolecules 89990-54-5 | Pyrazolidine dihydrochloride | Combi-Blocks | MFCD16620353 | 145.030 | C3H10Cl2N2 | 96.000 | Cl.Cl.C1CNNC1 | 5g | 457917117
Pyrazolidine dihydrochloride | Combi-Blocks | 89990-54-5 | MFCD16620353 | 145.030 | C3H10Cl2N2 | 96.000 | Cl.Cl.C1CNNC1 | 5g | 457917117
Medchemexpress LLC Fipexide hydrochloride | 34161-23-4 | 25 MG
Fipexide hydrochloride is a parachloro-phenossiacetic acid derivative and an orally active nootropic agent. It reduces striatal adenylate cyclase activity and positively affects cognitive performance through dopaminergic neurotransmission. This product is intended for research and analytical applications, particularly in senile dementia research.
- Orally active nootropic agent
- Reduces striatal adenylate cyclase activity
- Positive effect on cognitive performance by dopaminergic neurotransmission
- Used for senile dementia research
- Acts as a chemical inducer in callus formation, shoot regeneration and Agrobacterium infection
- Intended for research and analytical applications
Sigma Aldrich Fine Chemicals Biosciences Benidipine hydrochloride >=98% (HPLC) | 91599-74-5 | 10MG
Benidipine hydrochloride >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 542.02 | 91599-74-5 | 10MG
Medchemexpress LLC Verubulin hydrochloride | 917369-31-4 | 98.7% | 10 MG
Verubulin hydrochloride is the hydrochloride salt of verubulin, a blood-brain barrier-permeable microtubule-disrupting agent used in research for studies of tubulin polymerization, microtubule dynamics, and anticancer pharmacology. It is supplied as a high-purity research reagent for in vitro and in vivo studies.
- Blood-brain barrier permeable microtubule disruptor.
- Potent, broad-spectrum cytotoxic and antitumor activity.
- Hydrochloride salt form.
- Available in multiple pack sizes, including 10 mg.
- High purity suitable for research applications.
Medchemexpress LLC Nitrocaramiphen hydrochloride | 98636-73-8 | 99.6% | 370.87 g/mol | C18H27ClN2O4 | 5 MG
Nitrocaramiphen hydrochloride is a selective muscarinic M1 receptor antagonist (Ki: 5.5 nM) that inhibits the hyperpolarizing effect induced by muscarine in muscle fibers. It is supplied as a high-purity solid for in vitro pharmacological and biochemical research.
- Selective M1 receptor antagonist (Ki: 5.5 nM).
- High reported purity (~99.6%).
- Solid form suitable for handling and formulation.
- Soluble in DMSO (10 mg/mL) and water with heating and sonication.
- Recommended storage: sealed, away from moisture; in solvent: -80°C (6 months), -20°C (1 month).
eMolecules 89990-54-5 | pyrazolidine dihydrochloride | Pharmablock | MFCD16620353 | 145.030 | C3H10Cl2N2 | 97.000 | Cl.Cl.C1CNNC1 | 1g | 717427045
pyrazolidine dihydrochloride | Pharmablock | 89990-54-5 | MFCD16620353 | 145.030 | C3H10Cl2N2 | 97.000 | Cl.Cl.C1CNNC1 | 1g | 717427045
Medchemexpress LLC VU-1545 | 890764-63-3 | 99.0% | 402.38 | 50 MG
VU-1545 is a metabotropic glutamate receptor 5 positive allosteric modulator (mGluR5 PAM). It exhibits a Ki of 156 nM and an EC50 of 9.6 nM. This compound promotes AKT activation at concentrations of 0.1 and 1.0 μM and is intended for research use only.
- Functions as a metabotropic glutamate receptor 5 positive allosteric modulator (mGluR5 PAM).
- Demonstrates a Ki of 156 nM and an EC50 of 9.6 nM.
- Promotes AKT activation.
- Promotes Akt phosphorylation in neuronal cells.
- Solid appearance, light yellow to yellow color.
- Powder storage: -20°C for 3 years, 4°C for 2 years.
- In solvent storage: -80°C for 6 months, -20°C for 1 month.
Medchemexpress LLC Gaboxadol hydrochloride | 85118-33-8 | MFCD00055180 | 99.9% | 176.60 g/mol | C6H9ClN2O2 | 5 MG
Gaboxadol hydrochloride is a small-molecule GABAA receptor agonist used in neuroscience and pharmacology research. Supplied as a solid with high reported purity, it is intended for in vitro and in vivo experimental studies.
- High purity for research applications.
- Solid form suitable for accurate weighing and formulation.
- Active at GABAA receptors; useful for GABAergic pharmacology studies.
- Stable under recommended storage conditions (sealed, away from moisture and light).
- Small quantity packaging suitable for experimental use.