Alcohols and polyols
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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)
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Filtered Search Results
Medchemexpress LLC W-7 (isomer hydrochloride) | 69762-85-2 | 99.7% | 377.33 | C16H22Cl2N2O2S | 50 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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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 a hydrochloride salt provided as a solid research reagent that acts as a calmodulin antagonist. It is used in biochemical and cellular studies to probe calmodulin-dependent signaling and enzyme activity; handle and store according to the supplier SDS for safety and stability.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Imeglimin (hydrochloride) | 775351-61-6 | 99.3% | 191.66 | 25 MG
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Imeglimin hydrochloride (EMD 387008) is an oral glucose-lowering agent that reduces reactive oxygen species (ROS) production, increases mitochondrial DNA, and improves mitochondrial function. This compound appears as a white to off-white solid.
- Oral glucose-lowering agent
- Reduces reactive oxygen species (ROS) production
- Increases mitochondrial DNA
- Improves mitochondrial function
- Soluble in H2O (≥ 50 mg/mL)
- Soluble in DMSO (25 mg/mL)
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Oxyfedrine hydrochloride | 16777-42-7 | MFCD01695148 | 99.9% | 349.85 g/mol | C19H24ClNO3 | 1 ML
Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Oxyfedrine hydrochloride is a β-adrenoreceptor agonist supplied as a ready-to-use 10 mM solution in DMSO (1 mL) for research applications. The accurately prepared solution simplifies assay setup and reduces measurement variability. Storage and handling recommendations are provided to maintain product stability.
- Prepared 10 mM solution in DMSO, 1 mL.
- High purity (99.9% by HPLC).
- Suitable for in vitro assays and compound screening.
- Includes storage and stability guidance for solvent and solid forms.
- Molecular formula C19H24ClNO3; molecular weight 349.85 g/mol.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Ravidasvir (hydrochloride) | 1303533-81-4 | MFCD32705191 | 99.9% | 835.82 | C42H52Cl2N8O6 | 5MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Ravidasvir hydrochloride is the hydrochloride salt of ravidasvir, a pan-genotypic hepatitis C virus (HCV) NS5A inhibitor supplied for research use. It is provided as solid vials in multiple sizes and as DMSO solutions for immediate assay use. Intended for in vitro research and assay development; not for human or clinical use.
- High purity suitable for analytical and biological research.
- Multiple solid vial sizes available, including small research quantities.
- Available as a ready-to-use 10 mM solution in DMSO for rapid testing.
- Molecular weight 835.82 and formula C42H52Cl2N8O6 for precise calculations.
- CAS number 1303533-81-4 for unambiguous identification.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC EPZ004777 hydrochloride | 1380316-03-9 | 99.5% | 576.13 g·mol⁻¹ | C28H42ClN7O4 | 10 MG
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EPZ004777 hydrochloride is a potent, selective inhibitor of the histone methyltransferase DOT1L used in epigenetic and leukemia research. It inhibits DOT1L with an IC50 of 0.4 nM, reduces H3K79 methylation in cells, and has been used to selectively kill MLL-rearranged leukemia cells. This material is supplied for research use only.
- Potent DOT1L inhibition (IC50 0.4 nM).
- Selective activity in biochemical and cellular assays.
- Reduces H3K79 methylation and downregulates leukemogenic gene expression.
- High chemical purity (99.5%).
- Available as solid and as DMSO solution for flexible use in experiments.
- CAS number 1380316-03-9; molecular weight 576.13 g·mol⁻¹.
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Medchemexpress LLC Ceftiofur hydrochloride | 103980-44-5 | 98.4% | C19H18ClN5O7S3 | 1 ML
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Ceftiofur hydrochloride is a potent cell wall synthesis inhibitor that targets bacterial penicillin-binding proteins (PBPs). It exerts bactericidal effects by inhibiting bacterial cell wall peptidoglycan synthesis, leading to cell lysis. Additionally, it possesses anti-inflammatory properties, inhibiting NF-κB and MAPKs, which reduces the secretion of pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6. This compound has been shown to improve survival rates in endotoxemia models.
- Targets bacterial penicillin-binding proteins (PBPs)
- Inhibits bacterial cell wall peptidoglycan synthesis
- Induces bacterial cell lysis
- Reduces secretion of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6)
- Inhibits phosphorylation of ERK, JNK, and p38
- Blocks nuclear translocation of NF-κB p65
- Improves survival in endotoxemia models
- Cited in 4 scientific publications
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Medchemexpress LLC Nevanimibe hydrochloride | 133825-81-7 | 99.5% | 458.08 g/mol | C27H40ClN3O | 50 MG
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Nevanimibe hydrochloride is the hydrochloride salt of nevanimibe, an orally active and selective ACAT1 inhibitor supplied as a research-grade solid for in vitro and preclinical studies. The material is characterized by molecular identity and high purity suitable for biochemical and pharmacological assays.
- High purity suitable for analytical and biological assays.
- Hydrochloride salt form for improved stability and solubility in polar solvents.
- Well-characterized molecular identity and molecular weight for reproducible results.
- Available in small pack sizes appropriate for laboratory research.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC Berubicin hydrochloride | 293736-67-1 | 95.1% | 670.10 | 1 MG
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Berubicin hydrochloride is an analog of Doxorubicin that can cross the blood-brain barrier. It inhibits P-gp and MRP1-mediated efflux and suppresses glioblastoma multiforme (GBM). This product exerts toxic effects on leukemia cells by activating nuclear factor κB (NF-κB) and induces apoptosis in neuroblastoma cells. It can be used in the study of tumors related to the nervous system.
- Crosses the blood-brain barrier
- Inhibits P-gp and MRP1-mediated efflux
- Suppresses glioblastoma multiforme (GBM)
- Activates nuclear factor κB (NF-κB)
- Induces apoptosis in neuroblastoma cells
- More potent activity than Doxorubicin in activating NF-κB and inhibiting DNA synthesis
- Prolongs survival time in intracranial orthotopic glioma models in mice
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Medchemexpress LLC Aptiganel hydrochloride | 137160-11-3 | 99.8% | 339.86 g·mol⁻1 | C20H22ClN3 | 5 MG
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Aptiganel hydrochloride is the hydrochloride salt of aptiganel, a non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist with reported neuroprotective activity. It is provided as a purified research chemical for studies of excitotoxicity and NMDA receptor-mediated signaling.
- Non-competitive NMDA receptor antagonist
- Reported neuroprotective activity
- Hydrochloride salt form
- High purity (99.8%)
- Suitable for in vitro and in vivo research
- Molecular weight 339.86 g·mol⁻1
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Medchemexpress LLC SSR180711 hydrochloride | 446031-79-4 | 99.9% | 361.66 | 25 MG
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SSR180711 hydrochloride | 446031-79-4 | 99.9% | 361.66 | 25 MG
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Medchemexpress LLC OTS186935 hydrochloride | 2093400-18-9 | 99.6% | 522.31 | 1 ML
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OTS186935 hydrochloride | 2093400-18-9 | 99.6% | 522.31 | 1 ML
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Medchemexpress LLC Tocainide hydrochloride | 71395-14-7 | 99.5% | 1 ML
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Tocainide hydrochloride is a sodium channel blocker that blocks sodium channels in pain-producing foci in nerve membranes. It is a primary amine analog of lidocaine and can be used for the treatment of tinnitus.
- Suppresses ventricular ectopic activity.
- Suitable for laboratory centrifugation and storage.
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Medchemexpress LLC Verapamil hydrochloride | 152-11-4 | 99.8% | C27H39ClN2O4 | 100 MG
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Verapamil hydrochloride | 152-11-4 | 99.8% | C27H39ClN2O4 | 100 MG
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Medchemexpress LLC Azasetron hydrochloride | 123040-16-4 | 99.8% | C17H21Cl2N3O3 | 1 ML
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Azasetron hydrochloride (Y-25130 hydrochloride) is a benzamide derivative that functions as a potent and selective 5-HT3 receptor antagonist. It is currently under study for its application in treating chemotherapy-induced nausea and vomiting (CINV).
- Potent and selective 5-HT3 receptor antagonist.
- Used to study chemotherapy-induced nausea and vomiting (CINV).
- Can effectively penetrate the skin and enter systemic circulation.
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Medchemexpress LLC mAChR-IN-1 (hydrochloride) | 119391-73-0 | 99.6% | 524.82 g/mol | C23H26ClIN2O2 | 10MM 1ML
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mAChR-IN-1 hydrochloride is a potent muscarinic cholinergic receptor antagonist (IC50 17 nM) provided for research use. It is offered as a solid and as a pre-made solution in DMSO, intended for in vitro pharmacology and receptor binding studies.
- Potent mAChR antagonist (IC50 17 nM).
- High purity: 99.6% (LCMS).
- Chemical formula: C23H26ClIN2O2.
- Molecular weight: 524.82 g/mol.
- Physical appearance: white to off-white solid.
- Available as solids (5-100 mg) and 10 mM solution in DMSO, 1 mL.
- Supplied for research use only.
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