Hydrochlorides
eMolecules 28356-58-3 | 4-Pyridineacetic acid | Combi-Blocks | MFCD03701446 | 137.138 | C7H7NO2 | 98.000 | OC(=O)Cc1ccncc1 | 1g | 357561050
4-Pyridineacetic acid | Combi-Blocks | 28356-58-3 | MFCD03701446 | 137.138 | C7H7NO2 | 98.000 | OC(=O)Cc1ccncc1 | 1g | 357561050
Medchemexpress LLC N,N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid dihydrochloride | 35369-53-0 | MFCD04113603 | >95.0% | 461.34 | C20H26Cl2N2O6 | 1 ML
HBED dihydrochloride is an orally active, hexadentate phenolic aminocarboxylate iron chelator (N,N'-bis(2-hydroxybenzyl)ethylenediamine-N,N'-diacetic acid dihydrochloride) supplied for research use in solution and solid formats for studies of iron binding and chelation biology.
- Orally active hexadentate iron chelator.
- Suitable for iron chelation research and biochemical assays.
- Supplied as ready-to-use 10 mM in DMSO solution and as solid material.
- Solid sizes available: 100 mg, 250 mg, 500 mg, 1 g.
- Molecular weight 461.34; formula C20H26Cl2N2O6.
- Typical purity specification ≥95.0% (batch dependent).
Medchemexpress LLC T-3775440 hydrochloride | 1422535-52-1 | 99.1% | 346.85 g/mol | C18H23ClN4O | 5 MG
T-3775440 hydrochloride is a small-molecule, irreversible inhibitor of lysine-specific histone demethylase 1 (KDM1/LSD1) used in biochemical and cellular research. It is supplied as a light yellow to yellow solid with high purity and characterized solubility and storage recommendations.
- Irreversible KDM1/LSD1 inhibitor; IC50 = 2.1 nM.
- Molecular formula C18H23ClN4O; molecular weight 346.85 g/mol.
- Purity approximately 99.1% by HPLC.
- Physical state: light yellow to yellow solid.
- Solubility: DMSO ≥ 30.18 mg/mL; water 8.33 mg/mL with ultrasonic warming to 60°C.
- Storage: powder at 4°C under inert atmosphere; solutions: -80°C (6 months), -20°C (1 month).
- Supplied as a 5 mg quantity.
Medchemexpress LLC Zinterol hydrochloride | 38241-28-0 | 99.7% | C19H27ClN2O4S | 1 ML
Zinterol hydrochloride is a potent and selective β2-adrenoceptor agonist. It increases ICa in a concentration-dependent manner with an EC50 of 2.2 nM. This compound has been shown to induce ventricular arrhythmias in conscious heart failure rabbits at specific dosages. It is intended strictly for research purposes.
- Potent and selective β2-adrenoceptor agonist.
- Increases ICa with an EC50 of 2.2 nM.
- Induces ventricular arrhythmias in heart failure animal models.
- For research use only.
- High purity of 99.7%.
- Solid form can be stored at 4°C, sealed, away from moisture.
- Solution form can be stored at -80°C for 6 months or -20°C for 1 month, sealed, away from moisture.
Medchemexpress LLC Y13g dihydrochloride | 99.9% | 381.29 g/mol | C16H26Cl2N2O4 | 5 MG
Y13g dihydrochloride is a research-grade small molecule inhibitor of acetylcholinesterase (AChE) and interleukin-6 (IL-6), used in in vitro and in vivo pharmacology studies. It has been shown to reverse STZ-induced memory deficits in animal models. For research use only; not for human or diagnostic use.
- High purity (99.9%)
- Molecular formula C16H26Cl2N2O4; molecular weight 381.29 g/mol
- Solid, off-white to light yellow
- Soluble in DMSO (≈125 mg/mL)
- Storage: sealed at -20°C; in solution: -80°C (6 months), -20°C (1 month)
- Targets acetylcholinesterase and interleukin-6
- Suitable for in vitro and in vivo studies
- Not for human or diagnostic use
Medchemexpress LLC Lycorine Hydrochloride Monohydrate | 6150-58-9 | 99.2% | 341.79 | 100 MG
Lycorine Hydrochloride Monohydrate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- Biochemical reagent.
- Can be used as a biological material.
- Can be used as an organic compound for life science related research.
Medchemexpress LLC GSK-LSD1 dihydrochloride | 2102933-95-7 | 99.5% | 289.24 g/mol | C14H22Cl2N2 | 1 ML
GSK-LSD1 dihydrochloride is a potent, selective, and irreversible inhibitor of lysine-specific demethylase 1 (LSD1) with an IC50 of 16 nM. It is intended for research use to probe LSD1 function, study gene expression changes, and evaluate effects on cancer cell proliferation. Supplied as a high-purity solid or as a solution in DMSO.
Medchemexpress LLC 4-amino-3-phenylbutanoic acid hydrochloride | 3060-41-1 | 98.0% | 215.68 | C10H14ClNO2 | 5 G
Phenibut hydrochloride is the hydrochloride salt of β-phenyl-GABA, an orally active GABAB receptor agonist used as a research reagent with anxiolytic and cognition-enhancing effects. Supplied as a high-purity powder for laboratory research and pharmacology studies.
- Orally active GABAB receptor agonist used in pharmacology research.
- Anxiolytic and nootropic effects relevant to central nervous system studies.
- High purity suitable for analytical and experimental use.
- Molecular weight 215.68 g/mol and chemical formula C10H14ClNO2.
- Available in multiple pack sizes including 5 g.
Medchemexpress LLC N-(1,3-diphenylpyrazol-5-yl)-4-nitrobenzamide | 890764-36-0 | MFCD12546140 | 99.6% | 384.39 g/mol | C22H16N4O3 | 10 MG
VU-29 is a research-stage positive allosteric modulator of the metabotropic glutamate receptor 5 (mGlu5), used in preclinical pharmacology to selectively potentiate mGlu5 signaling. It is supplied as a powder with high chemical purity and is intended for in vitro and in vivo formulation following recommended solvent systems and storage conditions.
- Positive allosteric modulator of mGlu5 receptor, suitable for receptor pharmacology studies.
- High purity (99.6%) for reliable experimental results.
- Powder form for flexible dosing and formulation.
- Soluble in DMSO at 50 mg/mL; recommended vehicle progression for in vivo administration.
- Stable under recommended storage conditions for extended shelf life in powder form.
Medchemexpress LLC T-3775440 hydrochloride | 1422535-52-1 | 99.1% | 346.85 g/mol | C18H23ClN4O | 1 ML
T-3775440 hydrochloride is an irreversible lysine-specific histone demethylase 1 (LSD1) inhibitor used in biochemical and cellular research to probe epigenetic regulation. The hydrochloride salt is provided as a concentrated solution for in vitro applications.
- Irreversible LSD1 inhibitor with IC50 2.1 nM.
- High purity (99.1%) suitable for research use.
- Molecular weight 346.85 g/mol; formula C18H23ClN4O.
- Supplied as 10 mM solution in DMSO, 1 mL vial.
- Soluble in DMSO (≥ 30.18 mg/mL) and soluble in water with ultrasonic/warming.
- Storage recommendations: in solvent, -80°C for up to 6 months or -20°C for 1 month.
Medchemexpress LLC H3B-6545 hydrochloride | 2052132-51-9 | 99.2% | 604.04 | 1 ML
H3B-6545 hydrochloride | 2052132-51-9 | 99.2% | 604.04 | 1 ML
Medchemexpress LLC Verubulin hydrochloride | 917369-31-4 | 98.7% | 50 MG
Verubulin hydrochloride is the hydrochloride salt of verubulin (MPC-6827), a quinazoline-derived microtubule polymerization inhibitor with reported antitumor activity. It is supplied as a solid research reagent for preclinical studies investigating microtubule dynamics and anticancer mechanisms.
- Hydrochloride salt suitable for enhanced solubility in polar solvents.
- Potent microtubule polymerization inhibitor used in anticancer research.
- Reported to be brain-penetrant, enabling neurobiology applications.
- High purity typical for analytical and preclinical work (98.7%).
- Stable as a solid at 4°C; follow recommended storage conditions for solutions.
Medchemexpress LLC Terbinafine hydrochloride | 78628-80-5 | 99.9% | 327.89 | 500 MG
Terbinafine hydrochloride (TDT 067 hydrochloride) is an orally active and potent antifungal agent. It is a potent non-competitive inhibitor of squalene epoxidase from Candida, with a Ki of 30 nM. It also demonstrates antibacterial activity against certain Gram-positive and Gram-negative bacteria. Terbinafine hydrochloride functions as a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Potent antifungal agent
- Orally active
- Inhibits squalene epoxidase from Candida
- Demonstrates antibacterial activity against certain Gram-positive and Gram-negative bacteria
- Functions as a click chemistry reagent with an Alkyne group
- Exhibits primary fungicidal action against most fungal pathogens
- Effective topically and orally in experimental dermatophytoses
Apexbio Technology LLC RS 127445 199864-87-4 10mM (in 1mL DMSO)
RS 127445 (CAS 199864-87-4) is a highly selective antagonist of the serotonin 5-HT2B receptor displaying nanomolar affinity (pKi 9 5 pIC50 10 4) and approximately 1000-fold selectivity over other receptor subtypes By inhibiting 5-HT2B-mediated signaling RS 127445 suppresses serotonin-induced increases in inositol phosphate and intracellular calcium in cellular models In vivo administration in rat models reduces stress- and TNBS-induced visceral hypersensitivity and attenuates colonic motility responses RS 127445 is widely used to elucidate 5-HT2B receptor functions in neurogastroenterology and mechanisms of gastrointestinal hypersensitivity
Medchemexpress LLC Benzamil hydrochloride | 161804-20-2 | 99.7% | 5 MG
Benzamil hydrochloride, an Amiloride analogue, is a Na+/Ca2+ exchanger (NCX) inhibitor with an IC50 of approximately 100 nM. It also functions as a non-selective blocker of Deg/epithelial sodium channels (ENaC) and can enhance myogenic vasoconstriction. It inhibits TRPP3-mediated Ca2+-activated currents with an IC50 of 1.1 μM.
- Inhibits neuronal and heterologously expressed small conductance Ca2+-activated K-channels.
- Treatment with the compound (0.7 mg/kg/day; s.c.) resulted in an average survival until 16.1 weeks of age in stroke-prone spontaneously hypertensive rats (SHRSP).