Alcohols and polyols
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- (1)
- (1)
- (26)
- (1)
- (1)
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- (1)
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- (1)
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- (24)
- (1)
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- (22)
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- (24)
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- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
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- (2)
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- (11)
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- (1)
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- (14)
- (7)
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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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- (1)
- (1)
- (10)
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- (3)
- (7)
- (1)
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- (12)
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- (30)
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Filtered Search Results
Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 | C16H22Cl2N2O2S | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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W-7 isomer hydrochloride is the hydrochloride salt of a W-7 isomer used as a selective calmodulin antagonist in biochemical and cell biology research. It is provided as a purified solid or as a DMSO solution for small-scale laboratory experiments and mechanistic studies of Ca2+/calmodulin-dependent processes.
- Selective calmodulin antagonist suitable for biochemical assays and cell signaling studies.
- High purity, 99.7%, for reproducible experimental results.
- Available as powder and as a 10 mM solution in DMSO for ready-to-use applications.
- Small pack sizes support pilot experiments and dose-response testing.
- Long-term stability when stored at recommended low temperatures.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC M-PEG-NH2 hydrochloride | 99.1% | 2000 (Mn) | 50 MG
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m-PEG-NH2 hydrochloride (Mn 2000) is a methoxy-terminated polyethylene glycol bearing a terminal primary amine as its hydrochloride salt. Supplied as a solid reagent, it is used for PEGylation, surface functionalization, and preparation of gels for adsorption-size-exclusion (AdSEC) separations in biochemical workflows.
- Primary amine hydrochloride form for conjugation reactions.
- Average molecular weight Mn 2000 for consistent polymer properties.
- High purity: 99.13%.
- Soluble in DMSO at 100 mg/mL with sonication (use dry DMSO).
- Storage: store at -20°C, protect from light; in solution store at -80°C up to 6 months.
- For research use only.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC mAChR-IN-1 hydrochloride | 119391-73-0 | MFCD01725710 | 99.6% | 524.82 g/mol | C23H26ClIN2O2 | 10MG
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mAChR-IN-1 hydrochloride is a research-grade muscarinic acetylcholine receptor antagonist provided as the hydrochloride salt. It exhibits high potency (IC50 = 17 nM) and is characterized by a defined molecular formula and high reported purity, making it suitable for in vitro pharmacology and biochemical assays.
- Potent mAChR antagonist (IC50 = 17 nM).
- Hydrochloride salt form for consistent handling.
- High reported purity (99.6%).
- Molecular weight 524.82 g/mol; formula C23H26ClIN2O2.
- Intended for in vitro research applications.
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Medchemexpress LLC Etifoxine (hydrochloride) | 56776-32-0 | 99.8% | 337.24 | 100 MG
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Etifoxine hydrochloride is a non-benzodiazepine GABAergic compound that acts as a positive allosteric modulator of α1β2γ2 and α1β3γ2 subunit-containing GABAA receptors. It exhibits anxiolytic and anticonvulsant properties in rodents. This product is intended for research and analytical applications.
- Positive allosteric modulator of GABAA receptors.
- Exhibits anxiolytic properties.
- Exhibits anticonvulsant properties.
- Intended for research and analytical applications.
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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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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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Medchemexpress LLC AR-R17779 hydrochloride | 178419-42-6 | 99.0% | C9H15ClN2O2 | 10MG
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AR-R17779 hydrochloride is a research-grade, potent and selective full agonist of the α7 subtype of neuronal nicotinic acetylcholine receptors, provided as the hydrochloride salt for preclinical pharmacology studies. It is intended for in vitro and in vivo research to probe receptor signaling, cognitive effects, and neuroprotective mechanisms.
- Potent, selective α7 nicotinic acetylcholine receptor agonist.
- High purity (99.0%) suitable for research applications.
- Supplied as a white to off-white solid for ease of handling.
- Stable under recommended storage conditions to preserve activity.
- Suitable for in vitro assays and in vivo pharmacology studies.
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Medchemexpress LLC SB-269970 hydrochloride | 261901-57-9 | MFCD03788020 | C18H29ClN2O3S | 10 MM * 1 ML
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SB-269970 hydrochloride is a potent, selective, and brain-penetrant antagonist of the 5-HT7 receptor. It demonstrates over 50-fold selectivity against other 5-HT receptors with a pKi of 8.3.
- Potent and selective 5-HT7 receptor antagonist
- Brain-penetrant
- Exhibits over 50-fold selectivity against other 5-HT receptors
- Significantly blocks amphetamine and ketamine-induced hyperactivity in animal models
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Medchemexpress LLC SB-612111 hydrochloride | 99.6% | 454.86 | 100 MG
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SB-612111 hydrochloride is a novel and potent opiate receptor-like orphan receptor (ORL-1) antagonist with a high affinity for hORL-1 (Ki=0.33 nM). It exhibits selectivity for μ-, κ- and δ-receptors with Ki values of 57.6 nM, 160.5 nM, and 2109 nM, respectively. SB-612111 hydrochloride effectively antagonizes the pronociceptive action of Nociceptin in an acute pain model.
- Novel and potent ORL-1 antagonist
- High affinity for hORL-1 (Ki=0.33 nM)
- Selectivity for μ-, κ- and δ-receptors
- Effectively antagonizes pronociceptive action of Nociceptin in an acute pain model
- Purity: 99.64%
- Available in solid form (white to off-white)
- In-stock for 100 mg quantity
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Medchemexpress LLC Czc-54252 hydrochloride | 1784253-05-9 | 98.4% | 1 ML
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CZC-54252 hydrochloride is a potent and selective LRRK2 inhibitor with IC50 values of 1.28 nM for wild-type LRRK2 and 1.85 nM for G2019S LRRK2. It attenuates G2019S LRRK2-induced human neuronal injury with an EC50 of approximately 1 nM and demonstrates neuroprotective activity. This compound is intended for research use only.
- Potent and selective LRRK2 inhibitor
- Attenuates G2019S LRRK2-induced human neuronal injury
- Demonstrates neuroprotective activity
- For research use only
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Medchemexpress LLC Rufloxacin hydrochloride | 106017-08-7 | 99.25% | 100 MG
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Rufloxacin hydrochloride is a fluoroquinolone antibacterial that inhibits B-cell differentiation in human mononuclear cells and inhibits Topo. It is for research use only.
- Fluoroquinolone antibacterial
- Inhibits B-cell differentiation in human mononuclear cells
- Inhibits Topo
- Solid appearance
- Light yellow to yellow color
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Medchemexpress LLC W-7 isomer hydrochloride | 69762-85-2 | 99.7% | 377.33 g·mol⁻1 | C16H22Cl2N2O2S | 1 MG
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W-7 isomer hydrochloride is the positional isomer of W-7 hydrochloride, a selective calmodulin antagonist. Provided for research use, the compound is supplied as a solid in multiple sizes and as a DMSO solution, and is intended for studies probing calcium-dependent signaling where calmodulin inhibition is required.
- High purity (99.65%).
- Molecular weight 377.33 g·mol⁻1.
- Available as solid and 10 mM DMSO solution.
- Offered in multiple pack sizes from milligram quantities to larger amounts.
- Documents available: data sheet, certificate of analysis, and safety data sheet.
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Medchemexpress LLC Clorgyline hydrochloride | 17780-75-5 | MFCD00052012 | 99.9% | 308.63 g/mol | C13H16Cl3NO | 5 MG
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Clorgyline hydrochloride is an irreversible, selective monoamine oxidase A (MAO-A) inhibitor used in biochemical and pharmacological research. Supplied as the hydrochloride salt with high reported purity, it is used to probe MAO-A activity, neurotransmitter metabolism, and related signaling pathways. The molecule's alkyne functionality also enables copper-catalyzed azide-alkyne cycloaddition (CuAAC) applications.
- Selective irreversible MAO-A inhibitor.
- High purity suitable for research applications.
- Available in small, precise quantities for laboratory use.
- Contains an alkyne group compatible with CuAAC click chemistry.
- Useful for studies of neurotransmitter metabolism and MAO-A function.
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