Alcohols and polyols
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- (462)
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- (1)
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- (1)
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- (1)
- (36)
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- (1)
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- (1)
- (1)
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- (1)
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- (1)
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- (12)
- (1)
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- (1)
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Filtered Search Results
Medchemexpress LLC Adrogolide hydrochloride | 166591-11-3 | 99.6% | 435.96 g/mol | C22H26ClNO4S | 5 MG
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Adrogolide hydrochloride is the hydrochloride salt of adrogolide, a prodrug that is converted in plasma to the dopamine D1 receptor agonist A-86929. It is provided as a research-grade compound for pharmacology and neuroscience studies where selective D1 activation is required.
- High purity suitable for research applications.
- Soluble in DMSO; documented in vivo formulation options for administration.
- Available in small and larger pack sizes to support screening and in vivo studies.
- Stable when stored dry at room temperature; stock solutions stable at -20°C to -80°C.
- Used to study dopamine D1 receptor-mediated pharmacology in vitro and in vivo.
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Medchemexpress LLC VU6036720 hydrochloride | 99.7% | 473.39 | 100 MG
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VU6036720 hydrochloride is a potent and specific in vitro inhibitor of Kir4.1/5.1 channels. It can inhibit these channels with an IC50 value of 0.24 μM and is suitable for research related to brain and kidney.
- Potent and specific in vitro inhibitor of Kir4.1/5.1 channels
- Inhibits Kir4.1/5.1 channels with an IC50 value of 0.24 μM
- Can be used for the research of brain and kidney
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Medchemexpress LLC AR-C102222 hydrochloride | 1781934-50-6 | 99.8% | 10MM 1ML
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AR-C102222 hydrochloride | 1781934-50-6 | 99.8% | 10MM 1ML
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Medchemexpress LLC Befiradol hydrochloride | 2436760-81-3 | 99.93% | 430.32 | 25 MG
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Befiradol hydrochloride is a selective 5-HT1A receptor agonist, suitable for research use only.
- Reduces activity of dorsal raphe serotonergic neurons
- Increases discharge rate of mPFC pyramidal neurons
- Decreases extracellular 5-HT in the hippocampus and mPFC
- Increases extracellular DA in mPFC
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Medchemexpress LLC Imeglimin (hydrochloride) | 775351-61-6 | 99.98% | 191.66 | 5 MG
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Imeglimin hydrochloride is an oral glucose-lowering agent. It functions by reducing reactive oxygen species (ROS) production, increasing mitochondrial DNA, and improving mitochondrial function.
- Oral glucose-lowering agent.
- Reduces reactive oxygen species (ROS) production.
- Increases mitochondrial DNA.
- Improves mitochondrial function.
- Prevents human endothelial cell death by inhibiting mitochondrial permeability transition without inhibiting mitochondrial respiration.
- Significantly decreases hyperglycemia and restores normal glucose tolerance in models.
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Medchemexpress LLC VU6036720 hydrochloride | 99.65% | 473.39 | 50 MG
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VU6036720 hydrochloride is a potent and specific inhibitor of Kir4.1/5.1 channels. It is suitable for various research applications.
- Inhibits Kir4.1/5.1 channels with an IC50 value of 0.24 μM.
- Can be used for the research of brain and kidney.
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Medchemexpress LLC Flavoxate hydrochloride (Standard) | 3717-88-2 | 99.7% | 100 MG
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Flavoxate hydrochloride (Standard) | 3717-88-2 | 99.7% | 100 MG
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Medchemexpress LLC Arg1-in-1 (hydrochloride) | 00-00-0 | 90.0% | 292.57 g·mol⁻1 | C11H22BClN2O4 | 5 MG
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ARG1-IN-1 hydrochloride is a small-molecule inhibitor of human arginase 1 with a reported IC50 of 29 nM. It is intended for research use in biochemical and cellular studies to probe arginase-related pathways. The hydrochloride form improves handling and aqueous compatibility for assay preparation.
- Potent arginase 1 inhibition (IC50 29 nM).
- Suitable for biochemical and cellular assays.
- Provided as a 5 mg quantity for small-scale research use.
- Molecular weight 292.57 g·mol⁻1; formula C11H22BClN2O4.
- Purity typically 90.0% as reported on the certificate of analysis.
- Store at -20°C under nitrogen and protect from moisture; in solvent store at -80°C for long-term.
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Medchemexpress LLC Pirlimycin hydrochloride | 78822-40-9 | MFCD27952783 | 99.1% | 447.42 g·mol⁻¹ | C17H32Cl2N2O5S | 1 MG
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Pirlimycin hydrochloride is a lincosamide-class antibiotic supplied as the hydrochloride salt for research use. It inhibits bacterial protein synthesis by binding the 50S ribosomal subunit and is primarily active against Gram-positive organisms. The material is provided as a solid at high purity for analytical and laboratory applications.
- Lincosamide antibiotic.
- Inhibits bacterial protein synthesis via 50S ribosomal binding.
- Primarily active against Gram-positive bacteria.
- High purity (99.1%).
- Supplied as a solid suitable for analytical use.
- Available in small-scale quantities for research.
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Medchemexpress LLC Pargyline hydrochloride | 306-07-0 | MFCD00012492 | 99.91% | C11H14ClN | 100 MG
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Pargyline hydrochloride is an irreversible monoamine oxidase (MAO) inhibitor with antihypertensive and anticancer activities. It functions as a click chemistry reagent, containing an Alkyne group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Irreversible monoamine oxidase (MAO) inhibitor
- Exhibits antihypertensive activities
- Demonstrates anticancer activities
- Functions as a click chemistry reagent
- Contains an alkyne group for CuAAc reactions
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Medchemexpress LLC Azasetron hydrochloride | 123040-16-4 | MFCD00209913 | 99.8% | C17H21Cl2N3O3 | 5 MG
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Azasetron hydrochloride is a benzamide derivative functioning as a potent and selective 5-HT3 receptor antagonist. It is utilized in studies concerning chemotherapy-induced nausea and vomiting (CINV).
- Potent and selective 5-HT3 receptor antagonist
- Used in studies for chemotherapy-induced nausea and vomiting (CINV)
- Purity of 99.76%
- Solid, white to off-white appearance
- Effectively penetrates skin in in vivo studies
- IC50 for 5-HT3 Receptor is 0.33 nM
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Medchemexpress LLC SAR407899 (hydrochloride) | 923262-96-8 | 99.1% | 280.75 | 5 MG
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SAR407899 hydrochloride is a selective, potent, and ATP-competitive ROCK inhibitor. It has an IC50 of 135 nM for ROCK-2, and Kis of 36 nM and 41 nM for human and rat ROCK-2, respectively. It inhibits ROCK-2 more effectively than ROCK-1. This product exhibits potent vasorelaxant activity in various isolated arteries and dose-dependently lowers blood pressure in hypertensive SHRs. It also increases penile length in healthy and diabetic rabbits.
- Selective and potent ROCK inhibitor
- ATP-competitive mechanism of action
- Inhibits MYPTT696 phosphorylation
- Blocks thrombin-induced effects
- Inhibits cell proliferation and migration
- Potent vasorelaxant activity
- Reduces blood pressure
- Increases penile length
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Medchemexpress LLC Ravidasvir hydrochloride | 1303533-81-4 | MFCD32705191 | 99.9% | 835.82 | C42H52Cl2N8O6 | 50MG
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Ravidasvir hydrochloride is the hydrochloride salt of ravidasvir, a pan-genotypic hepatitis C virus (HCV) NS5A inhibitor supplied as a high-purity research compound in solid form. It inhibits HCV replication at low nanomolar concentrations and is provided for laboratory research applications.
- High purity (99.9%).
- White to off-white solid physical form.
- Molecular weight 835.82 g/mol.
- Packaged as 50 MG for research use.
- Storage: sealed at 4°C; in solvent: -80°C (up to 6 months) or -20°C (up to 1 month).
- Provides potent pan-genotypic NS5A inhibition with low nanomolar activity.
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eMolecules (+)-2,3-O-Isopropylidene-l-threitol | 50622-09-8 | 5G | Purity: 95%
Combi-Blocks | (+)-2,3-O-Isopropylidene-l-threitol | 5G | 50622-09-8 | MFCD00063761
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eMolecules 1,4,7,17,20,23-HEXAAZA-CYCLODOTRIACONTANE 6HCL | 106961-22-2 | MFCD05863898 | 1g
AstaTech | 1,4,7,17,20,23-HEXAAZA-CYCLODOTRIACONTANE 6HCL | 1g | 112530030 | 68632 | 97.000 | 106961-22-2 | MFCD05863898 | 673.540 | C26H64Cl6N6
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