Hydrochlorides
eMolecules 5987-82-6 | Oxybuprocaine hydrochloride | Combi-Blocks | MFCD00012512 | 344.880 | C17H29ClN2O3 | 98.000 | Cl.CCCCOc1cc(ccc1N)C(=O)OCCN(CC)CC | 25g | 537622054
Oxybuprocaine hydrochloride | Combi-Blocks | 5987-82-6 | MFCD00012512 | 344.880 | C17H29ClN2O3 | 98.000 | Cl.CCCCOc1cc(ccc1N)C(=O)OCCN(CC)CC | 25g | 537622054
Cayman Chemical Terbinafine hydrochloride
A broad-spectrum antifungal agent; has activity against T. rubrum, T. metagrophytes, T. verrucosum, E. floccosum, M. canis, A. fumigatus, and S. schenckii (MIC50s = 0.003-0.8 μg/ml); selectively inhibits C. albicans squalene epoxidase over rat liver epoxidase (IC50s = 0.03 and 77 μM, respectively); induces cell cycle arrest at the G0/G1 phase in COLO 205 tumor cells and HUVECs from 90-120 μM
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 VU 0240551 | 893990-34-6 | 99.7% | 342.44 | 100 MG
VU 0240551 is a potent neuronal K-Cl cotransporter KCC2 inhibitor (IC50=560 nM) that is selective versus NKCC1. It also inhibits hERG and L-type Ca2+ channels, making it a valuable tool in neuroscience research. This compound attenuates GABA-induced hyperpolarization of P cells, produces a positive shift in the P cell GABA reversal potential, and enhances P cell synaptic transmission.
- Potent neuronal K-Cl cotransporter KCC2 inhibitor
- Selective inhibition over NKCC1
- Inhibits hERG and L-type Ca2+ channels
- Attenuates GABA-induced hyperpolarization of P cells
- Enhances P cell synaptic transmission
Medchemexpress LLC VU0360172 hydrochloride | 1309976-62-2 | 98.9% | 330.78 g/mol | C18H16ClFN2O | 25 MG
VU0360172 hydrochloride is a potent and selective positive allosteric modulator of the metabotropic glutamate receptor 5 (mGlu5) used as a research tool in pharmacology and neuroscience. Supplied as the hydrochloride salt, the compound is intended for in vitro assays and preclinical in vivo studies and is provided with high purity and defined storage recommendations.
- Potent mGlu5 positive allosteric modulator (EC50 = 16 nM).
- Selective pharmacological tool for mGlu5 receptor studies.
- High purity suitable for biochemical and preclinical assays.
- Multiple milligram pack sizes available for laboratory experiments.
- Recommended storage conditions provided to maintain stability.
Medchemexpress LLC Asciminib hydrochlor 10mM 1mL | 2119669-71-3 | 10MM 1ML
Asciminib (ABL001) hydrochloride is a potent and selective allosteric BCR-ABL1 inhibitor which inhibits Ba/F3 cells grown with an IC50 of 0 25 nM[1
Sigma Aldrich Fine Chemicals Biosciences Olopatadine hydrochloride >=98% (HPLC) | 140462-76-6 | MFCD00875716 | 10MG
Olopatadine hydrochloride >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 373.87 | 140462-76-6 | MFCD00875716 | 10MG
Medchemexpress LLC OPC-14523 hydrochlor 10mM 1mL | 145969-31-9 | 450.40 g/mol | C23H29Cl2N3O2 | 1 ML
OPC-14523 hydrochloride is a sigma and 5-HT1A receptor agonist supplied as a hydrochloride salt for research use. It is available as a lyophilized solid and as a ready-to-use 10 mM solution in DMSO, with documented solubility and storage recommendations for in vitro and in vivo studies.
- Hydrochloride salt form for improved stability and handling.
- High purity (99.95%) suitable for pharmacology studies.
- Chemical formula C23H29Cl2N3O2; molecular weight 450.40 g/mol.
- Available as solid in multiple mg sizes and as a 10 mM, 1 mL solution in DMSO.
- Soluble in DMSO (~83.3 mg/mL) and moderately soluble in water with warming.
- Recommended storage: sealed, away from moisture; in solvent: -20°C short term, -80°C long term.
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 Arc 239 dihydrochloride | 55974-42-0 | MFCD02262215; MFCD16875414 | 99.2% | 480.43 | C24H31Cl2N3O3 | 5 MG
ARC 239 dihydrochloride is a small-molecule research compound that acts as a selective α2B/α2C adrenoceptor antagonist. It is supplied as a white to off-white solid intended for in vitro pharmacology and receptor-binding studies; reported binding data indicate greater affinity at α2B compared with α2A and α2C subtypes.
- Selective antagonist of α2B and α2C adrenoceptors.
- Reported pKd/pKi values indicate higher affinity for α2B subtype.
- High purity suitable for research applications.
- White to off-white solid form for convenient handling.
- Stable under recommended refrigerated storage.
- Useful for subtype-selective adrenergic receptor studies.
Medchemexpress LLC PXS-4787 hydrochloride | 2409964-40-3 | 99.7% | 265.73 g/mol | C10H13ClFNO2S | 10 MG
PXS-4787 hydrochloride is a research-use small-molecule pan-lysyl oxidase (LOX) inhibitor supplied as a solid. It inhibits LOX family enzymes with low micromolar potency, reduces collagen I deposition and crosslinking in fibroblasts, and is provided with analytical documentation for laboratory studies. Not for human or veterinary use.
- High purity (99.71%) suitable for research applications.
- Solid form for convenient handling and storage.
- Potent pan-LOX inhibitory activity with reported low micromolar IC50s.
- Reduces collagen I deposition and crosslinking in cell-based assays.
- Available in small research pack sizes for pilot and preclinical studies.
- Provided with COA, SDS, and handling documentation.
Sigma Aldrich Fine Chemicals Biosciences Cysteamine hydrochloride >=97.0% (RT) | 156-57-0 | MFCD00012904 | 100G
Cysteamine hydrochloride >=97.0% (RT) | Purity: >=97.0% (RT) | Mol Wt: 113.61 | 156-57-0 | MFCD00012904 | 100G