Alcohols and polyols
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- (1)
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- (1)
- (462)
- (9)
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- (11)
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- (1)
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- (145)
- (114)
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- (1)
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- (1)
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- (1)
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- (6)
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- (2)
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- (2)
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- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
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- (2)
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- (2)
- (5)
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- (33)
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- (1)
- (26)
- (1)
- (1)
- (1)
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- (1)
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- (3)
- (1)
- (15)
- (12)
- (1)
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- (1)
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- (24)
- (1)
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- (1)
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- (1)
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- (24)
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- (1)
- (1)
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- (1)
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- (1)
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Filtered Search Results
Medchemexpress LLC Naluzotan hydrochloride | 740873-82-9 | 99.6% | 487.10 g/mol | C23H39ClN4O3S | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Naluzotan hydrochloride is the hydrochloride salt of a potent, selective amidosulfonamide 5-HT1A receptor agonist used in preclinical research. It is supplied as a solid research chemical with characterized purity and analytical data, intended for laboratory use only.
- High purity (99.6%) suitable for research applications.
- Potent, selective 5-HT1A receptor agonist (IC50 ≈ 20 nM; Ki ≈ 5.1 nM).
- Weak hERG K+ channel blocker (IC50 ≈ 3,800 nM), relevant for cardiac safety studies.
- Solid form; molecular weight 487.10 g/mol; formula C23H39ClN4O3S.
- Supplied in a 10 mg research pack and 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 | 99.6% | 524.82 g/mol | C23H26ClIN2O2 | 25MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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mAChR-IN-1 hydrochloride is a research-grade small-molecule antagonist of muscarinic cholinergic receptors (mAChR). It exhibits potent inhibition of mAChR (reported IC50 17 nM) and is supplied as the hydrochloride salt for use in biochemical and pharmacological studies.
- Potent mAChR antagonist with an IC50 of 17 nM.
- High chemical purity (99.6%).
- Molecular weight 524.82 g/mol and formula C23H26ClIN2O2.
- Available in multiple pack sizes, including a 25 MG option.
- Supplied as the hydrochloride salt for improved solubility.
- Suitable for in vitro pharmacology and receptor profiling.
- Provided with supporting product documentation and datasheet.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Ravidasvir hydrochloride | 1303533-81-4 | 99.9% | 835.82 g·mol⁻1 | C42H52Cl2N8O6 | 100MG
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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 a research-grade, pan-genotypic inhibitor of hepatitis C virus (HCV) nonstructural protein 5A (NS5A), supplied as a white to off-white solid and used in antiviral in vitro and preclinical studies.
- Pan-genotypic NS5A inhibitor with low-nanomolar EC50 against multiple HCV genotypes.
- High purity: 99.9% (reported by supplier).
- Molecular weight: 835.82 g·mol⁻1; formula C42H52Cl2N8O6.
- Appearance: white to off-white solid, suitable for analytical and biological assays.
- Storage: store sealed at 4°C; in solvent, -80°C for up to 6 months or -20°C for 1 month.
- Intended for research use only; not for human or clinical use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Snap 94847 hydrochloride | 1781934-47-1 | >98.0% | 515.03 g/mol | C29H32F2N2O2·HCl | 1 ML
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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SNAP 94847 hydrochloride is a potent, selective melanin-concentrating hormone receptor 1 (MCH1) antagonist supplied as a concentrated research solution. It is used to probe MCH1 signaling in neuroscience studies and has demonstrated effects on appetite-related behavior, anxiety, and hippocampal neurogenesis in preclinical models.
- Potent MCH1 antagonist with Ki = 2.2 nM and Kd = 530 pM.
- High selectivity over α1A and D2 receptors (>80-fold and >500-fold).
- Provided as a 10 mM solution in DMSO for laboratory use.
- Purity ≥98.0% by HPLC.
- Molecular weight 515.03 g/mol; formula C29H32F2N2O2·HCl.
- Store desiccated at room temperature; handle solvents per safety guidance.
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Medchemexpress LLC Nordoxepin hydrochloride | 2887-91-4 | 99.9% | 301.81 | C18H20ClNO | 5 MG
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Nordoxepin hydrochloride is the major metabolite of the tricyclic antidepressant doxepin, provided as a research-grade chemical standard for analytical and laboratory applications. This compound is intended for non-clinical research use only.
- Major metabolite of doxepin, useful as an analytical standard.
- Purity 99.9%.
- Molecular formula C18H20ClNO and molecular weight 301.81.
- White to off-white solid appearance.
- Available in small solid quantities suitable for analytical work.
- Store sealed at 4°C; solutions are stable at -80°C for long-term storage.
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Medchemexpress LLC Ru-ski 43 hydrochloride | 1782573-67-4 | 99.6% | 423.01 g/mol | C22H31ClN2O2S | 10 MG
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RU-SKI 43 hydrochloride is the hydrochloride salt of a small-molecule inhibitor of hedgehog acyltransferase (Hhat) used in research to probe hedgehog signaling and evaluate anticancer effects in cellular models.
- Potent and selective Hhat inhibitor (IC50 850 nM).
- Useful for hedgehog pathway and oncology research.
- Reduces hedgehog signaling and Shh palmitoylation in cellular assays.
- High purity suitable for biochemical and cell-based studies (~99.6%).
- Characterized by formula C22H31ClN2O2S and molecular weight 423.01 g/mol.
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Medchemexpress LLC D-Glucose, 3-amino-3-deoxy-, hydrochloride | 57649-10-2 | 99.0% | 215.63 | 1 MG
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D-Glucose, 3-amino-3-deoxy-, hydrochloride | 57649-10-2 | 99.0% | 215.63 | 1 MG
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Medchemexpress LLC Dyclonine hydrochloride | 536-43-6 | 99.3% | 5 G
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Dyclonine hydrochloride is an orally effective ALDH covalent inhibitor that crosses the blood-brain barrier. It has an IC50 of 35 μM for ALDH2 and 76 μM for ALDH3A1. This compound exhibits sensitizing activities for targeted cancer cells and possesses antibacterial properties. Additionally, it functions as a local agent, capable of suppressing or relieving pain by blocking nerve impulse transmission and inhibiting the sensation of touch and pain.
- Orally effective ALDH covalent inhibitor
- Crosses the blood-brain barrier
- Sensitizes targeted cancer cells
- Exhibits antibacterial properties
- Suppresses or relieves pain as a local agent
- Blocks transmission of nerve impulses
- Inhibits sensation of touch and pain
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Medchemexpress LLC Amprolium (hydrochloride) | 137-88-2 | 98.8% | 500 MG
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Amprolium hydrochloride is an anti-parasitic drug administered orally, functioning as a thiamine antagonist in intestinal absorption. It has been used as a preventive measure, particularly when combined with other anti-coccidial drugs. Its antagonistic effect on thiamine absorption primarily occurs at the intestinal epithelial cells. This product is for research use only and has not been fully validated for medical applications.
- Anti-parasitic drug
- Administered orally
- Acts as a thiamine antagonist in intestinal absorption
- Used for preventive measures against coccidiosis
- Targets coccidia
- Antagonistic effect primarily at intestinal epithelial cells
- For research use only
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Medchemexpress LLC mAChR-IN-1 hydrochloride | 119391-73-0 | MFCD01725710 | 99.6% | 524.82 | C23H26ClIN2O2 | 50MG
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mAChR-IN-1 hydrochloride is a research-grade muscarinic cholinergic receptor antagonist supplied as the hydrochloride salt. It exhibits high potency (IC50 = 17 nM) and is provided as a high-purity solid for in vitro pharmacology and receptor profiling.
- High potency mAChR antagonist (IC50 = 17 nM).
- High purity: 99.6%.
- Hydrochloride salt form for improved stability and handling.
- White to off-white solid suitable for in vitro assays.
- Available in multiple pack sizes and a solution format for convenience.
- Store sealed at 4°C; in solvent, store at -80°C for long-term stability.
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Medchemexpress LLC Flavoxate hydrochloride | 3717-88-2 | 99.7% | 427.92 | C24H26ClNO4 | 10 MG
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Flavoxate hydrochloride (standard) is an analytical reference standard supplied for research and analytical applications. It is used as a reference in studies of phosphodiesterase activity and lower urinary tract disorders, and displays antispasmodic, muscarinic antagonist, calcium antagonistic, and local anesthetic properties.
- Analytical standard for research and method development.
- High purity suitable for reference and analytical use.
- Available in small, defined package sizes for assay calibration.
- Defined chemical identity with molecular weight and formula for traceability.
- Applicable to studies of overactive bladder and lower urinary tract conditions.
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Medchemexpress LLC Olprinone hydrochloride | 119615-63-3 | 99.9% | C14H11ClN4O | 25 MG
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Olprinone Hydrochloride, also known as Loprinone Hydrochloride, is a potent phosphodiesterase (PDE) 3 inhibitor with an IC50 of 0.35 μM. It is utilized in research for heart failure due to its positive inotropic and vasodilative effects, and it also demonstrates anti-inflammatory activity.
- Potent PDE3 inhibitor (IC50 of 0.35 μM)
- Used in research for heart failure
- Exhibits positive inotropic and vasodilative effects
- Demonstrates anti-inflammatory activity
- Modulates inflammation associated with myocardial ischemia-reperfusion injury in rats
- Reduces histological evidence of myocardial injury
- Decreases pro-inflammatory cytokines (TNF-α and IL-1β)
- Reduces adhesion molecules (ICAM-1 and P-Selectin)
- Decreases nitrotyrosine formation and NF-κB expression
- Reduces PAR formation and apoptosis
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Medchemexpress LLC Nevanimibe hydrochloride | 133825-81-7 | 99.5% | 458.08 g·mol⁻¹ | C27H40ClN3O | 100 MG
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Nevanimibe hydrochloride is an orally active, selective inhibitor of acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) used in preclinical research. It has low-nanomolar activity against ACAT1 and has been investigated in cell models for effects on cholesterol metabolism and adrenocortical cancer.
- Selective ACAT1 inhibitor with EC50 ≈ 9 nM.
- Orally active small molecule suitable for in vitro and in vivo research.
- High chemical purity (~99.5%) for reliable experimental results.
- Available as solid and as 10 mM solution in DMSO for flexible dosing.
- Characterized by CAS 133825-81-7 and molecular weight 458.08 g·mol⁻¹.
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Medchemexpress LLC SRI-011381 hydrochloride | 2070014-88-7 | 99.6% | 365.94 g/mol | C20H32ClN3O | 25 MG
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SRI-011381 hydrochloride is an orally active TGF-β signaling agonist used as a research reagent to modulate TGF-β/Smad pathways and to investigate neuroprotective effects. It is supplied as a white to off-white solid and is intended for laboratory research applications.
- Orally active TGF-β signaling agonist with reported neuroprotective effects.
- High purity (99.6%).
- Molecular weight 365.94 g/mol; formula C20H32ClN3O.
- White to off-white solid physical form suitable for handling in lab settings.
- Available in milligram to gram quantities for in vitro and preclinical research.
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Medchemexpress LLC Olcegepant hydrochloride | 586368-06-1 | MFCD30738010 | 99.1% | 906.11 | C38H47Br2N9O5·HCl | 10 MG
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Olcegepant hydrochloride is a selective non-peptide antagonist of the calcitonin gene-related peptide (CGRP) receptor supplied as the hydrochloride salt for laboratory research. It is provided as a high-purity solid for use in neuroscience and GPCR pharmacology studies.
- Hydrochloride salt form, suitable for aqueous formulations.
- CAS number 586368-06-1.
- Molecular formula C38H47Br2N9O5·HCl and molecular weight 906.11.
- High purity (~99.1%) suitable for analytical and preparative studies.
- Available in small-scale quantities, e.g., 10 MG, for laboratory use.
- Used to probe calcitonin gene-related peptide (CGRP) receptor signaling in preclinical research.
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