Alcohols and polyols
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- (462)
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- (1)
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- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
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- (17)
- (15)
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- (2)
- (5)
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- (33)
- (4)
- (2)
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- (8)
- (2)
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- (8)
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- (7)
- (2)
- (1)
- (26)
- (1)
- (1)
- (1)
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- (1)
- (3)
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- (3)
- (1)
- (15)
- (12)
- (1)
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- (7)
- (12)
- (1)
- (14)
- (24)
- (1)
- (8)
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- (1)
- (2)
- (1)
- (17)
- (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)
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- (11)
- (14)
- (7)
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- (10)
- (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)
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- (10)
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- (1)
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- (30)
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- (11)
- (82)
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- (378)
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Filtered Search Results
Medchemexpress LLC Molindone hydrochloride | 15622-65-8 | 99.8% | 5 MG
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Molindone hydrochloride (EN-1733A) is an orally active, brain-penetrant dopamine D2/D5 receptor antagonist. It demonstrates antipsychotic and antidepressant-like activities, suppresses spontaneous locomotion, and antagonizes apomorphine-induced emesis. This compound is suitable for research related to neurological diseases.
- Orally active and brain-penetrant D2/D5 receptor antagonist
- Exhibits antipsychotic and antidepressant-like activities
- Suppresses spontaneous locomotion
- Antagonizes apomorphine-induced emesis
- Targeted to D2 and D5 receptors
- Soluble in water (100 mg/mL; ultrasonic needed)
- Soluble in DMSO (17.5 mg/mL; ultrasonic and warming needed)
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Medchemexpress LLC Ladostigil hydrochlo 5mg | 209394-18-3 | 5MG
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Ladostigil (TV-3326) hydrochloride is an orally active dual inhibitor of cholinesterase and brain-selective monoamine oxidase (MAO) with IC50s of 37 1 and 31 8 M for MAO-B and AChE respectively Ladostigil hydrochloride exhibits neuroprotective antioxidant and anti-inflammatory activities Ladostigil can be used for the research of depression and Alzheimer s disease[1 [2 Ladostigil (hydrochloride) is a click chemistry reagent it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups
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Medchemexpress LLC Amprolium (hydrochloride) | 137-88-2 | 98.8% | 1 G
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Amprolium hydrochloride is an anti-parasitic drug that is taken orally and acts as an antagonist to thiamine in intestinal absorption. With a molecular formula of C14H20Cl2N4 and a molecular weight of 315.24, this compound is supplied as a white to off-white solid with a high purity of 98.79%.
- Anti-parasitic drug targeting coccidia
- Acts as a thiamine antagonist
- High purity of 98.79%
- White to off-white solid appearance
- Soluble in water (≥ 200 mg/mL)
- Recommended storage at 4°C, sealed, away from moisture
- In solvent, store at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC Trazodone hydrochloride | 25332-39-2 | 99.9% | 5 MG
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Trazodone hydrochloride is an antidepressant classified as a serotonin receptor antagonist and reuptake inhibitor. It is primarily intended for research and analytical applications, particularly in the study of anxiety disorders, and serves as a reference standard.
- Analytical standard for research
- Used in analytical applications
- Functions as a serotonin receptor antagonist and reuptake inhibitor
- Employed for treatment of anxiety disorders
- Suitable for qualitative, quantitative, and methodological research experiments
- Compatible with HPLC, GC, and MS techniques
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Medchemexpress LLC Pitofenone hydrochloride | 1248-42-6 | 99.9% | 403.90 | 10 MG
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Pitofenone hydrochloride is a spasmolytic compound that inhibits acetylcholinesterase (AChE) activity. It exhibits anticonvulsant activity when combined with diclofenac and fenpivirine.
- Inhibits acetylcholinesterase (AChE) activity.
- Exhibits anticonvulsant activity.
- Suitable for neurological disease research.
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Medchemexpress LLC VU0357017 hydrochloride | 1135242-13-5 | MFCD17215959 | 99.9% | 369.89 | C18H28ClN3O3 | 10 MG
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VU0357017 hydrochloride is a brain-penetrant, selective allosteric agonist of the M1 muscarinic acetylcholine receptor used as a research tool to probe M1 receptor pharmacology and signaling. Supplied as the hydrochloride salt, the compound is characterized by a defined molecular weight and high reported purity.
- Potent M1 allosteric agonist with reported EC50 ≈ 477 nM.
- Brain-penetrant small molecule suitable for in vitro and in vivo studies.
- High chemical purity as provided by manufacturer.
- Provided as a hydrochloride salt for improved solubility.
- Available in small research pack sizes for laboratory use.
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Medchemexpress LLC Alectinib (Hydrochloride) | 1256589-74-8 | 99.9% | 100 MG
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Alectinib Hydrochloride is a potent, selective, and orally available ALK inhibitor with an IC50 of 1.9 nM and a Kd value of 2.4 nM (in an ATP-competitive manner). It effectively inhibits ALK F1174L and ALK R1275Q with IC50s of 1 nM and 3.5 nM, respectively, and demonstrates effective central nervous system (CNS) penetration.
- Potent, selective, and orally available ALK inhibitor
- Effective central nervous system (CNS) penetration
- Molecular formula: C30H35ClN4O2
- Molecular weight: 519.08
- Appearance: White to off-white solid
- Recommended storage at 4°C, sealed and away from moisture
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Medchemexpress LLC Midodrine hydrochloride | 43218-56-0 | 99.9% | 10 MG
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Midodrine hydrochloride is a selective and orally active adrenergic α1-receptor agonist. It strengthens vascular contraction and is utilized in research concerning cardiovascular diseases, such as orthostatic hypotension.
- Selective and orally active adrenergic α1-receptor agonist
- Strengthens vascular contraction
- Utilized in research for cardiovascular diseases like orthostatic hypotension
- Increases p-AMPK and PPARδ expression
- Increases Ca2+ in C2C12, HL1 and HepG2 cells
- Increases maximal mitochondrial oxidative phosphorylation and ATP content in C2C12 cells
- Reduces cellular lipid content in 3T3-L1 cells
- Reduces platelet-activating factor-induced death in mice
- Shows anti-hypotensive effects in orthostatic hypotension rat models
- Relieves hypertension in spontaneously hypertensive rat models
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Medchemexpress LLC CHK1-IN-4 hydrochlo | 1MG
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CHK1-IN-4 hydrochlo | 1MG
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Medchemexpress LLC Pumosetrag hydrochloride | 194093-42-0 | MFCD00939557 | 99.8% | 339.84 g/mol | C15H18ClN3O2S | 10 MG
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Pumosetrag hydrochloride is an orally active, small-molecule partial agonist of the 5-HT3 receptor investigated for treatment of irritable bowel syndrome and gastroesophageal reflux disease. Supplied as a high-purity white to off-white solid for laboratory research (for research use only).
- Acts as a partial agonist at 5-HT3 receptors.
- Investigated for irritable bowel syndrome and gastroesophageal reflux disease.
- Supplied as a white to off-white solid with high purity.
- Molecular weight 339.84 g/mol; formula C15H18ClN3O2S.
- Available in small laboratory pack sizes, including 10 mg.
- Store sealed at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
- For research use only; not for human or clinical use.
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Medchemexpress LLC Carmoterol hydrochloride | 137888-11-0 | 98.7% | 404.89 | C21H25ClN2O4 | 10MG
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Carmoterol hydrochloride is a potent, selective, long-acting β2-adrenoceptor agonist supplied as a solid research chemical. It is used in pharmacological and respiratory research to study bronchoconstriction and treatments for asthma and chronic obstructive pulmonary disease (COPD), exhibiting strong bronchodilatory activity and high β2 vs β1 selectivity.
- Potent, selective β2-adrenoceptor agonist.
- Long-acting bronchodilator activity suitable for respiratory research.
- High β2 vs β1 selectivity, reducing off-target cardiac β1 activation.
- Supplied as a solid research-grade chemical for laboratory use.
- High purity (98.7% by HPLC reported on certificate of analysis).
- Molecular formula C21H25ClN2O4, molecular weight 404.89 g·mol-1.
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Medchemexpress LLC Deterenol hydrochloride | 23239-36-3 | MFCD28898982 | 99.7% | 231.72 g/mol | C11H18ClNO2 | 25 MG
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Deterenol hydrochloride is the hydrochloride salt of deterenol, a selective beta-adrenergic agonist used as a research reagent. Provided as a solid with high purity, it is intended for in vitro and in vivo pharmacology studies involving beta-adrenergic receptors and cardiovascular response assessment.
- Selective beta-adrenergic agonist activity.
- High purity suitable for research applications.
- Hydrochloride salt form for improved stability and handling.
- Common use in receptor pharmacology and cardiovascular studies.
- Molecular formula C11H18ClNO2; molecular weight 231.72 g/mol.
- CAS number 23239-36-3 for unambiguous identification.
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Medchemexpress LLC Ravidasvir hydrochloride | 1303533-81-4 | 99.9% | 835.82 g·mol⁻1 | C42H52Cl2N8O6 | 100MG
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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.
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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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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 2,4-Pyrimidinediamine, N2-(2-methylpropyl)-N4-[[5-[4-(phenylmethoxy)phenyl]-2-thienyl]methyl]- | 1802650-31-2 | 99.5% | C26H28N4OS | 25 MG
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2,4-Pyrimidinediamine, N2-(2-methylpropyl)-N4-[[5-[4-(phenylmethoxy)phenyl]-2-thienyl]methyl]- | 1802650-31-2 | 99.5% | C26H28N4OS | 25 MG
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