Alcohols and polyols
- (1)
- (55)
- (343)
- (39)
- (4)
- (8)
- (7)
- (55)
- (3)
- (7)
- (18)
- (1)
- (4)
- (156)
- (1)
- (64)
- (27)
- (14)
- (3)
- (1)
- (1)
- (10)
- (3)
- (2)
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- (1)
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- (6)
- (3)
- (30)
- (4)
- (20)
- (10)
- (2)
- (10)
- (4)
- (5)
- (395)
- (6)
- (102)
- (21)
- (50)
- (31)
- (62)
- (13)
- (14)
- (1)
- (2)
- (1)
- (25)
- (6)
- (4)
- (1)
- (6)
- (1)
- (464)
- (9)
- (46)
- (11)
- (46)
- (6)
- (1)
- (7)
- (12)
- (145)
- (116)
- (7)
- (5)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (4)
- (7)
- (14)
- (2)
- (1)
- (6)
- (5)
- (1)
- (12)
- (21)
- (5)
- (2)
- (2)
- (2)
- (16)
- (2)
- (30)
- (1)
- (4)
- (1)
- (2)
- (1)
- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (1)
- (2)
- (2)
- (2)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (1)
- (2)
- (5)
- (1)
- (4)
- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (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)
- (7)
- (4)
- (1)
- (1)
- (3)
- (6)
- (11)
- (5)
- (3)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
- (2)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
- (2)
- (4)
- (4)
- (1)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (1)
- (5)
- (4)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
- (5)
- (1)
- (2)
- (2)
- (6)
- (14)
- (2)
- (4)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (1)
- (4)
- (2)
- (3)
- (2)
- (4)
- (3)
- (1)
- (4)
- (5)
- (1)
- (4)
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- (9)
- (1)
- (5)
- (5)
- (2)
- (1)
- (1)
- (2)
- (5)
- (3)
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- (1)
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- (1)
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- (2)
- (11)
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- (1)
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- (1)
- (1)
- (10)
- (1)
- (1)
- (1)
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- (4)
- (11)
- (1)
- (2)
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- (20)
- (21)
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- (3)
- (1)
- (8)
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- (2)
- (1)
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- (1)
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- (1)
- (1)
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- (12)
- (9)
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- (4)
- (3)
- (1)
- (1)
- (4)
- (6)
- (1)
- (1)
- (1)
- (5)
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- (1)
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- (1)
- (1)
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- (1)
- (1)
- (1)
- (1)
- (1)
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- (2)
- (1)
- (1)
- (1)
- (1)
- (3)
- (14)
- (1)
- (1)
- (2)
- (1)
- (2)
- (2)
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- (1)
- (1)
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- (5)
- (2)
- (2)
- (1)
- (10)
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- (1)
- (9)
- (1)
- (8)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
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- (1)
- (1)
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- (1)
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- (5)
- (3)
- (4)
- (1)
- (1)
- (3)
- (2)
- (4)
- (1)
- (1)
- (1)
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- (1)
- (7)
- (1)
- (2)
- (1)
- (7)
- (1)
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- (1)
- (1)
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- (15)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
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- (1)
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- (1)
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- (1)
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- (1)
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- (1)
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- (2)
- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (82)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
- (4)
- (40)
- (21)
- (1)
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- (1)
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- (16)
- (1)
- (2)
- (21)
- (2)
- (2)
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- (1)
- (67)
- (1)
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- (1)
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- (279)
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- (1)
- (6)
- (278)
- (28)
- (2)
- (25)
- (2)
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- (2)
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- (2)
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- (2)
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- (48)
- (3)
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- (3)
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- (1)
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- (1)
- (8)
- (2)
- (733)
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- (1)
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Filtered Search Results
Medchemexpress LLC Betaxolol hydrochloride | 63659-19-8 | 98.1% | 10 MM * 1 ML
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Betaxolol hydrochloride is a selective beta1 adrenergic receptor blocker that can be used for the research of hypertension and glaucoma. It is a cardioselective beta-adrenergic receptor blocking agent.
- Functions as a selective beta1 adrenergic receptor blocker
- Cardioselective beta-adrenergic receptor blocking agent
- Applicable for research in hypertension
- Applicable for research in glaucoma
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Dyclonine hydrochloride | 536-43-6 | 99.3% | 10 G
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Dyclonine hydrochloride is an orally effective ALDH covalent inhibitor that crosses the blood-brain barrier. It functions as a local anesthetic, capable of suppressing or relieving pain by blocking nerve impulse transmission. It also exhibits sensitizing activities for targeted cancer cells and possesses antibacterial and fungicidal properties, demonstrating significant activity against various bacteria and fungi.
- Orally effective ALDH covalent inhibitor
- Crosses the blood-brain barrier
- Functions as a local anesthetic
- Sensitizes cancer cells to cysteine and GSH deficiency
- Demonstrates bactericidal and fungicidal activity
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC 2-pyridinecarbonitrile, 5-[(4'-amino-5',8'-difluoro-spiroquinazoline)carbonyl] hydrochloride | 1781934-50-6 | 99.8% | 100 MG
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This hydrochloride salt is a potent, selective inducible nitric oxide synthase (iNOS) inhibitor with reported IC50 = 37 nM. Supplied as a high-purity research reagent suitable for in vitro and in vivo studies of iNOS-mediated pathways and inflammatory responses.
- High purity 99.8% as reported by manufacturer.
- Molecular weight 418.83.
- Chemical formula C19H17ClF2N6O.
- Hydrochloride salt form for improved solubility.
- Potent, selective iNOS inhibition (IC50 = 37 nM).
- Suitable for pharmacology and inflammation research applications.
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Medchemexpress LLC N4-(4-(2-bromo-4,5-difluorophenoxy)phenyl)-L-asparagine hydrochloride | 2450268-84-3 | MFCD28405312 | 99.8% | 451.65 g/mol | C16H14BrClF2N2O4 | 1 ML
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WAY-213613 hydrochloride is a potent, selective inhibitor of the human excitatory amino acid transporter 2 (EAAT2) used in central nervous system research. It inhibits EAAT2 with an IC50 of approximately 85 nM and is provided as a ready-to-use solution for pharmacological studies.
- Potent EAAT2 inhibition (IC50 = 85 nM).
- Selectivity over EAAT1 and EAAT3.
- Supplied as a 10 mM solution in DMSO (1 mL).
- High purity (≈99.8%).
- Suitable for central nervous system research and transporter pharmacology.
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Medchemexpress LLC Skf-34288 (hydrochloride) | 320386-54-7 | 98.6% | 50 MG
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SKF-34288 hydrochloride is an orally active phosphoenolpyruvate carboxykinase (PEPCK) inhibitor with a Ki of 2-9 μM. It functions as a potent hypoglycemic agent by inhibiting glucose synthesis. Additionally, it inhibits Asn metabolism, leading to an increase in amino acids and amides.
- Inhibits C2C12 cell proliferation
- Induces myogenic differentiation of C2C12 cells
- Reduces mRNA expression of Pck2 and genes associated with serine biosynthesis
- Reduces blood glucose in starved rats
- Neutralizes Salbutamol-mediated hyperglycaemia in rabbits
- Reduces Pyruvate-induced blood glucose level in rats
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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
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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 SKF-34288 hydrochloride | 320386-54-7 | 98.6% | 10 MM * 1 ML
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SKF-34288 (3-Mercaptopicolinic acid) hydrochloride is an orally active phosphoenolpyruvate carboxykinase (PEPCK) inhibitor with a Ki of 2-9 μM. It acts as a potent hypoglycemic agent by inhibiting glucose synthesis. Additionally, it inhibits Asn metabolism and leads to an increase in amino acids and amides. It is intended for research use only.
- Potent phosphoenolpyruvate carboxykinase (PEPCK) inhibitor
- Inhibits glucose synthesis
- Increases amino acids and amides by inhibiting Asn metabolism
- Inhibits C2C12 cell proliferation
- Induces myogenic differentiation of C2C12 cells
- Reduces mRNA expression of Pck2 and genes associated with serine biosynthesis
- Reduces blood glucose in starved rats
- Neutralizes Salbutamol-mediated hyperglycaemia in rabbits
- Reduces pyruvate-induced blood glucose level in rats
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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 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 VU0357017 hydrochloride | 1135242-13-5 | 98.6% | 369.89 | 50 MG
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VU0357017 hydrochloride is a potent, selective, and brain-penetrant allosteric agonist of the M1 muscarinic acetylcholine receptor, exhibiting an EC50 of 477 nM. This compound demonstrates high selectivity for M1, showing no activity at M2-M5 receptors at concentrations up to 30 μM. It is being investigated for its potential use in the research of Alzheimer's disease and schizophrenia.
- Potent and selective allosteric agonist of M1 muscarinic acetylcholine receptor.
- Brain-penetrant.
- Highly selective for M1, with no activity at M2-M5 receptors at tested concentrations.
- Induces calcium release and ERK phosphorylation in CHO cells.
- Reverses scopolamine-induced cognitive deficits in animal models.
- Potential for research in Alzheimer's disease and schizophrenia.
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Medchemexpress LLC Taltobulin hydrochloride | 228266-40-8 | 99.3% | 510.11 g/mol | C27H44ClN3O4 | 50 MG
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Taltobulin hydrochloride is a synthetic analogue of the tripeptide hemiasterlin and a potent antimicrotubule agent used in research. It inhibits tubulin polymerization, disrupts microtubule organization, and induces mitotic arrest and apoptosis.
- Potent tubulin inhibitor for research applications
- High purity (typically 99.34%)
- Supplied as a white to off-white solid
- Available in multiple pack sizes, including 50 mg
- Used in vitro and in vivo to assess antimitotic activity
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eMolecules 485-47-2 | Ninhydrin | Oakwood Chemical | MFCD00003791 | 178.143 | C9H6O4 | 98.000 | OC1(O)C(=O)c2ccccc2C1=O | 100g | 537717969
Ninhydrin | Oakwood Chemical | 485-47-2 | MFCD00003791 | 178.143 | C9H6O4 | 98.000 | OC1(O)C(=O)c2ccccc2C1=O | 100g | 537717969
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