Alcohols and polyols
- (1)
- (55)
- (350)
- (41)
- (4)
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- (55)
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- (18)
- (1)
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- (155)
- (1)
- (63)
- (29)
- (14)
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- (1)
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- (10)
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- (1)
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- (6)
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- (30)
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- (20)
- (10)
- (2)
- (10)
- (4)
- (5)
- (399)
- (6)
- (102)
- (22)
- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (463)
- (9)
- (46)
- (10)
- (46)
- (6)
- (1)
- (6)
- (13)
- (148)
- (114)
- (9)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
- (6)
- (5)
- (1)
- (1)
- (12)
- (21)
- (5)
- (2)
- (2)
- (1)
- (2)
- (16)
- (2)
- (30)
- (1)
- (4)
- (1)
- (2)
- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (14)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (9)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (5)
- (4)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (6)
- (1)
- (2)
- (2)
- (6)
- (14)
- (2)
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- (1)
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- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
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- (2)
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- (1)
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- (1)
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- (1)
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- (1)
- (1)
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- (1)
- (1)
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- (1)
- (1)
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- (1)
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- (1)
- (1)
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- (3)
- (1)
- (1)
- (4)
- (6)
- (1)
- (1)
- (1)
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- (1)
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- (1)
- (1)
- (1)
- (2)
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- (1)
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- (2)
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- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (14)
- (1)
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- (1)
- (1)
- (4)
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- (1)
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- (1)
- (9)
- (1)
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- (3)
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- (1)
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- (3)
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- (7)
- (1)
- (18)
- (16)
- (1)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (81)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
- (4)
- (40)
- (21)
- (1)
- (19)
- (1)
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- (16)
- (1)
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- (21)
- (2)
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- (1)
- (67)
- (1)
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- (2)
- (7)
- (4)
- (86)
- (1)
- (5)
- (72)
- (3)
- (5)
- (238)
- (4)
- (2)
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- (21)
- (281)
- (17)
- (1)
- (6)
- (279)
- (28)
- (2)
- (25)
- (2)
- (3)
- (2)
- (2)
- (2)
- (6)
- (3)
- (2)
- (3)
- (48)
- (3)
- (418)
- (6)
- (3)
- (6)
- (5)
- (47)
- (6)
- (3)
- (1)
- (4)
- (21)
- (16)
- (2)
- (4)
- (11)
- (1)
- (8)
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- (731)
- (11)
- (3)
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- (1)
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- (66)
- (2)
- (2)
- (18)
- (3)
- (4)
- (33)
- (2)
- (31)
- (39)
- (2)
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- (1)
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Medchemexpress LLC CP-640186 hydrochloride | 591778-70-0 | C30H36ClN3O3 | 50 MG
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CP-640186 hydrochloride is an orally active, cell-permeable Acetyl-CoA carboxylase (ACC) inhibitor. It has IC50s of 53 nM for rat liver ACC1 and 61 nM for rat skeletal muscle ACC2. This compound can stimulate muscle fatty acid oxidation and inhibit fatty acid synthesis.
- Orally active and cell-permeable ACC inhibitor
- Inhibits rat liver ACC1 and rat skeletal muscle ACC2
- Stimulates muscle fatty acid oxidation
- Inhibits H460 cell growth
- Increases fatty acid metabolism in C2C12 cells and muscle strips
- Inhibits fatty acid and TG synthesis in HepG2 cells
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Amelparib hydrochloride | 98.4% | 379.88 | 1 MG
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Amelparib hydrochloride is a potent, orally active, and water-soluble inhibitor of PARP-1. It inhibits PARP-1 activity (IC50 = 18.5 nM) and cellular PAR formation (IC50 = 10.7 nM). This compound is a potential neuroprotective agent and has potential for the research of acute ischaemic stroke.
- Potent, orally active, and water-soluble inhibitor of PARP-1
- Inhibits PARP-1 activity (IC50 = 18.5 nM)
- Inhibits cellular PAR formation (IC50 = 10.7 nM)
- Potential neuroprotective agent
- Potential for research of acute ischaemic stroke
- Appearance: Solid
- Color: Off-white to light yellow
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Medchemexpress LLC Agn 192403 hydrochloride | 175521-95-6 | >95.0% | 189.73 | C10H19N·HCl | 25 MG
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AGN 192403 hydrochloride is a small-molecule I1 (imidazoline-1) receptor ligand used in cardiovascular and neurological research. It has been reported to show neuroprotective effects, and in cellular studies to bind the TMED9 cargo receptor, affecting MUC1-fs trafficking. The compound is used as a research tool to probe imidazoline receptor pharmacology and related mitochondrial pathways.
- Selective I1 receptor activity suitable for receptor pharmacology studies.
- Reported neuroprotective effects for neurological research applications.
- Demonstrated interaction with TMED9, useful in cellular trafficking studies.
- Applicable to in vitro assays and exploratory in vivo models.
- Available from multiple research suppliers with supporting COA/technical data.
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Medchemexpress LLC VU6036720 hydrochloride | 99.7% | 473.39 | 5 MG
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VU6036720 hydrochloride is a potent and specific in vitro inhibitor of Kir4.1/5.1. It can inhibit Kir4.1/5.1 channels with an IC50 value of 0.24 μM and can be used for the research of brain and kidney.
- Potent and specific in vitro inhibitor of Kir4.1/5.1.
- Inhibits Kir4.1/5.1 channels with an IC50 value of 0.24 μM.
- Useful for research pertaining to the brain.
- Useful for research pertaining to the kidney.
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Medchemexpress LLC 4-hydroxy-N-(4-(4-methylthiazol-5-yl)benzyl)pyrrolidine-2-carboxamide hydrochloride | 2115897-23-7 | MFCD32062443 | 99.2% | 467.02 | C22H31ClN4O3S | 10MG
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(S,S,S)-AHPC hydrochloride is a research-grade VHL ligand provided as the hydrochloride salt. It is used as a building block or negative control in protein degrader (PROTAC) development and biochemical studies of von Hippel-Lindau (VHL) E3 ligase recruitment.
- Research-grade VHL ligand for protein degrader and binding studies.
- High purity suitable for biochemical and cell-based assays (99.2%).
- Hydrochloride salt form to enhance solubility in polar solvents.
- Molecular weight 467.02 and formula C22H31ClN4O3S.
- Supplied as a 10 mg vial for small-scale research use.
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Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 g/mol | C16H22Cl2N2O2S | 5 MG
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W-7 isomer hydrochloride is the hydrochloride salt of an isomer of W-7, a selective calmodulin antagonist used in biochemical and cellular research to inhibit calmodulin-dependent signaling. Supplied as a powdered research reagent with specified purity and handling instructions, it is intended for laboratory research use only.
- Selective calmodulin antagonist for biochemical and cellular assays.
- High purity suitable for analytical and experimental applications.
- Supplied as a stable powder for convenient storage and handling.
- Available in small research quantities for assay development.
- Refer to safety data and handling instructions for proper use.
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Medchemexpress LLC Zoniporide hydrochloride hydrate | 863406-85-3 | MFCD04113213 | 99.4% | 374.82 g·mol⁻¹ | C17H19ClN6O2 | 50 MG
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Zoniporide hydrochloride hydrate is the hydrated hydrochloride salt of zoniporide, a potent and selective inhibitor of the sodium-hydrogen exchanger type 1 (NHE-1). Supplied as a white to off-white solid for research use, the hydrated salt form improves aqueous solubility and is intended for in vitro and preclinical studies.
- Potent NHE-1 inhibitor (IC50 ≈ 14 nM).
- Greater than 150-fold selectivity over other NHE isoforms.
- High aqueous solubility (H2O ≥ 100 mg/mL).
- High purity (≈ 99.4%).
- White to off-white solid appearance.
- Stable when stored sealed and protected from moisture; in solution store at -80°C (6 months) or -20°C (1 month).
- Available as a 50 mg research pack.
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Medchemexpress LLC Pholedrine (hydrochloride) | 877-86-1 | 99.6% | 50 MG
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Pholedrine hydrochloride is the hydrochloride salt of pholedrine, a sympathomimetic amine that acts on adrenergic receptors and is used in cardiovascular and receptor signaling research. It is supplied for laboratory research use with accompanying safety documentation and a certificate of analysis.
- Hydrochloride salt form for improved stability and solubility.
- High purity: 99.6% (LCMS, per COA).
- Molecular formula C10H16ClNO; molecular weight 201.69 g/mol.
- Used in adrenergic receptor and cardiovascular pharmacology studies.
- Available as a 50 MG research pack.
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Medchemexpress LLC Defactinib hydrochloride | 1073160-26-5 | 99.4% | 1 ML
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Defactinib hydrochloride is a small-molecule focal adhesion kinase (FAK) inhibitor that suppresses FAK Tyr397 phosphorylation in a time- and dose-dependent manner. It is supplied as the hydrochloride salt and is available as a 10 mM solution in DMSO (1 mL) or as solid samples for biochemical and cellular research.
- Inhibits FAK phosphorylation at Tyr397
- Supplied as hydrochloride salt for improved solubility
- Available as 10 mM solution in DMSO (1 mL) and as solid samples
- High purity suitable for research assays
- Useful for studies of cell migration, invasion, and signaling
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Medchemexpress LLC GYKI 53655 hydrochloride | 143692-48-2 | MFCD01941362 | 98.4% | 388.85 g/mol | C19H21ClN4O3 | 50 MG
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GYKI 53655 hydrochloride is the hydrochloride salt of GYKI 53655, a selective antagonist of alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) receptors used as a research tool in neuropharmacology. The compound is supplied as a light yellow solid with high purity and documented solubility properties.
- Selective antagonist of AMPA receptors for neuropharmacology research.
- High purity suitable for in vitro pharmacology.
- Soluble in DMSO and partially soluble in water with warming or sonication.
- Supplied as a solid with recommended storage at 4°C, protected from moisture.
- Molecular weight 388.85 g/mol and formula C19H21ClN4O3.
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Medchemexpress LLC Trazodone hydrochloride | 25332-39-2 | MFCD00079603 | 99.6% | 1 G
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Trazodone hydrochloride is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors (SARIs). It is a triazolopyridine derivative with antidepressant and anti-insomnious activity. Trazodone hydrochloride is often used for the treatment of anxiety disorders and depression. It exerts antagonistic properties against α1- and α2-adrenergic receptors.
- Antidepressant and anti-insomnious activity.
- Serotonin receptor antagonist and reuptake inhibitor.
- Antagonizes α1- and α2-adrenergic receptors.
- Used in the treatment of anxiety disorders and depression.
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Medchemexpress LLC Butaxamine hydrochloride | 5696-15-1 | 99.9% | 303.82 g/mol | C15H26ClNO3 | 5 MG
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Butaxamine hydrochloride is the hydrochloride salt of butaxamine, a selective β2-adrenergic receptor antagonist used in pharmacological research to probe β2-adrenergic signaling and physiological responses. It is provided as a high-purity solid suitable for small-scale laboratory experiments.
- Selective β2-adrenergic receptor antagonist.
- Intended for in vitro and in vivo pharmacology studies.
- High purity (99.87%) for reproducible results.
- Supplied in small 5 mg quantities for bench-scale use.
- White to off-white solid, hydrochloride salt improves solubility.
- Store at 4°C, sealed, and protect from moisture.
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eMolecules 485-47-2 | Ninhydrin | Medchem Express (US) | MFCD00003791 | 178.143 | C9H6O4 | 98.000 | OC1(O)C(=O)c2ccccc2C1=O | 100g | 845732890
Ninhydrin | Medchem Express (US) | 485-47-2 | MFCD00003791 | 178.143 | C9H6O4 | 98.000 | OC1(O)C(=O)c2ccccc2C1=O | 100g | 845732890
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Medchemexpress LLC GW806742X hydrochloride | 98.3% | 610.01 | 5 MG
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GW806742X hydrochloride is an ATP mimetic and a potent MLKL (Mixed Lineage Kinase Domain-Like protein) inhibitor. It binds the MLKL pseudokinase domain with a Kd of 9.3 μM and exhibits activity against VEGFR2 with an IC50 of 2 nM. This compound retards MLKL membrane translocation and inhibits necroptosis. This product is for research use only.
- Potent MLKL inhibitor
- Activity against VEGFR2 (IC50=2 nM)
- Retards MLKL membrane translocation
- Inhibits necroptosis
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Medchemexpress LLC Viloxazine hydrochloride | 35604-67-2 | MFCD00661100 | 98.9% | 273.75 g/mol | C13H20ClNO3 | 25MG
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Viloxazine hydrochloride is the hydrochloride salt of viloxazine, a selective norepinephrine reuptake inhibitor supplied as a research-grade solid reference compound. It is intended for biochemical and pharmacological studies and includes analytical and storage guidance. For research use only; not for human or veterinary use.
- High purity: 98.9% (reported by supplier)
- Molecular formula: C13H20ClNO3
- Molecular weight: 273.75 g/mol
- Form: solid powder suitable for formulation or assay
- Storage: store sealed, away from moisture; recommended 4°C; in solvent, -80°C (6 months) or -20°C (1 month)
- Available in small quantities suitable for research (for example, 25 mg)
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