Hydrochlorides
Medchemexpress LLC Gr 55562 dihydrochloride | 159533-25-2 | 99.0% | 448.39 | C23H27Cl2N3O2 | 5 MG
GR 55562 dihydrochloride is a selective serotonin 5-HT1B and 5-HT1D receptor antagonist supplied as the dihydrochloride salt for research use. It is commonly used in receptor pharmacology and behavioral studies to probe serotonergic mechanisms in vitro and in vivo.
- Selective 5-HT1B/5-HT1D receptor antagonist.
- Suitable for in vivo and in vitro studies.
- High purity (99.0%).
- Provided as the dihydrochloride salt for improved solubility.
- Available in small quantities for research use (5 MG, 10 MG).
- Includes documentation: datasheet, COA, and SDS.
Medchemexpress LLC CP 93129 dihydrochloride | 879089-64-2 | MFCD16875420 | 99.0% | 288.17 g/mol | C12H15Cl2N3O | 5 MG
CP 93129 dihydrochloride is the dihydrochloride salt of a potent and selective 5-HT1B receptor agonist used as a research reagent in neuroscience, including Parkinson's disease models. Supplied as an off-white to light yellow solid, it is intended for research and analytical applications.
- Potent, selective 5-HT1B receptor agonist for pharmacological studies.
- High purity (≈99.0%) suitable for analytical and in vitro work.
- CAS number 879089-64-2 for unambiguous identification.
- Molecular formula C12H15Cl2N3O; molecular weight ~288.17 g/mol.
- Recommended storage: 4°C; in solvent keep at -80°C (6 months) or -20°C (1 month).
eMolecules Medchem Express / PRE-084 (hydrochloride) / 10mg / 446268896 / HY-18100A / / 75136-54-8 / MFCD00673883 / 353.890 / C19H28ClNO3
Medchem Express / PRE-084 (hydrochloride) / 10mg / 446268896 / HY-18100A / / 75136-54-8 / MFCD00673883 / 353.890 / C19H28ClNO3
Medchemexpress LLC RS-102221 hydrochloride | 187397-18-8 | 98.0% | 649.08 g/mol | C27H32ClF3N4O7S | 5 MG
RS-102221 hydrochloride is the hydrochloride salt of a selective 5-HT2C receptor antagonist supplied as a solid for research use in pharmacology and neuroscience studies. It is intended for receptor binding and functional assays and includes manufacturer guidance for storage and solubility to support reliable preparation.
- Selective 5-HT2C receptor antagonist for pharmacology research.
- White to off-white solid suitable for in vitro and in vivo studies.
- High purity: 98.0%.
- Molecular weight: 649.08 g/mol.
- Soluble in DMSO at 125 mg/mL (ultrasonic recommended).
- Store powder at -20°C for long term; stock solutions at -80°C.
Apexbio Technology LLC Tirofiban hydrochloride monohydrate 150915-40-5 25mg
Tirofiban hydrochloride monohydrate (CAS 150915-40-5) is a small-molecule inhibitor targeting platelet glycoprotein IIb/IIIa receptors It is designed to reversibly antagonize the binding of fibrinogen to these receptors thereby inhibiting platelet aggregation and thrombus formation Tirofiban hydrochloride monohydrate exerts its biological activity primarily through selective reversible inhibition of glycoprotein IIb/IIIa-mediated platelet aggregation Based on these pharmacological properties tirofiban hydrochloride monohydrate holds research potential in antithrombotic therapy and the investigation of unstable angina and thrombus-associated cardiovascular conditions
Apexbio Technology LLC Tirofiban hydrochloride monohydrate 150915-40-5 5mg
Tirofiban hydrochloride monohydrate (CAS 150915-40-5) is a small-molecule inhibitor targeting platelet glycoprotein IIb/IIIa receptors It is designed to reversibly antagonize the binding of fibrinogen to these receptors thereby inhibiting platelet aggregation and thrombus formation Tirofiban hydrochloride monohydrate exerts its biological activity primarily through selective reversible inhibition of glycoprotein IIb/IIIa-mediated platelet aggregation Based on these pharmacological properties tirofiban hydrochloride monohydrate holds research potential in antithrombotic therapy and the investigation of unstable angina and thrombus-associated cardiovascular conditions
Medchemexpress LLC Iso-H7 dihydrochloride | 140663-38-3 | 99.1% | 364.29 | 25 MG
Iso-H7 dihydrochloride is an inhibitor of protein kinase with IC50 values of 22 and 34 μM for PKC and PKA, respectively. It has a negative control effect on PKA in satellite cell myogenesis.
- Protein kinase inhibitor.
- Inhibits PKC (IC50 = 22 μM).
- Inhibits PKA (IC50 = 34 μM).
- Negative control of PKA on satellite cell myogenesis.
Medchemexpress LLC Harmalol hydrochloride | 6028-07-5 | 25 MG
Harmalol hydrochloride is a beta carboline alkaloid found in medicinal plants like *Peganum harmala*. It is the 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 and is intended for research use only.
- Beta carboline alkaloid
- Found in medicinal plants such as *Peganum harmala*
- Main metabolite of Harmaline
- Inhibits CYP1A1 induction
- Exhibits antioxidant properties
- Possesses hydroxyl radical-scavenging properties
- For research use only
Apexbio Technology LLC Nitrocaramiphen hydrochloride 98636-73-8 50mg
Nitrocaramiphen hydrochloride (CAS 98636-73-8) is a small molecule that acts as a selective antagonist of muscarinic acetylcholine M1 receptors exhibiting a Ki of 5 5 nM Studies indicate that it effectively inhibits the hyperpolarizing effects induced by muscarinic agonists in muscle fibers Due to its receptor specificity nitrocaramiphen hydrochloride is widely utilized in neurobiological research to investigate cholinergic signaling pathways and the physiological roles of M1 receptor modulation
Medchemexpress LLC 3α-bis-(4-fluorophenyl) methoxytropane hydrochloride | 202646-03-5 | 100.0% | 379.87 g/mol | C21H24ClF2NO | 1 ML
AHN 1-055 hydrochloride is a dopamine uptake inhibitor that binds with high affinity to the dopamine transporter (DAT). It is provided as a 10 mM solution in DMSO for use in pharmacology and neuroscience research probing DAT function and dopamine reuptake. Key chemical identifiers include CAS 202646-03-5 and molecular weight 379.87 g/mol.
- Supplied as a ready-to-use 10 mM solution in DMSO.
- High potency DAT inhibitor (IC50 = 71 nM).
- High purity suitable for research use (~99.96%).
- Compact 1 mL format for small-volume assays.
Medchemexpress LLC L-733060 hydrochloride | 148687-76-7 | 99.9% | 439.82 | 1 MG
L-733060 hydrochloride is a selective neurokinin-1 (NK-1) receptor antagonist. It primarily regulates pain transmission and neural plasticity by blocking the binding of Substance P to the NK-1 receptor. It blocks the promoting effect of Substance P on long-term potentiation (LTP) in the hippocampus and reverses orofacial hyperalgesia induced by experimental occlusal interference (EOI) in rats. Additionally, it inhibits neurogenic plasma extravasation and acts as an anti-tumor agent, making it suitable for studying chronic orofacial pain.
- Selective neurokinin-1 (NK-1) receptor antagonist
- Regulates pain transmission and neural plasticity
- Blocks Substance P binding to NK-1 receptor
- Reverses orofacial hyperalgesia
- Inhibits neurogenic plasma extravasation
- Acts as an anti-tumor agent
- Suitable for studying chronic orofacial pain
Medchemexpress LLC (R)-VU 6008667 | 2097818-14-7 | 99.8% | 438.85 | C24H17ClF2N2O2 | 1 ML
(R)-VU 6008667 is the (R)-enantiomer of VU 6008667 supplied for research use. It is described as the less active enantiomer and lacks M5 negative allosteric modulator activity (IC50 > 10 μM). Available as a solid or as a 10 mM solution in DMSO, the product includes purity, molecular, and storage information for laboratory applications.
- High purity (99.8%).
- Available as solid or 10 mM solution in DMSO.
- White to off-white solid appearance.
- Molecular weight 438.85 and formula C24H17ClF2N2O2.
- Storage: solid at 4°C under nitrogen; in solvent at -80°C (6 months) or -20°C (1 month).
- Intended for research use only; not for human or clinical use.