Alcohols and polyols
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- (50)
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- (1)
- (25)
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- (1)
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- (1)
- (463)
- (9)
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- (10)
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- (1)
- (6)
- (13)
- (148)
- (114)
- (9)
- (5)
- (1)
- (1)
- (1)
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- (1)
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- (1)
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- (30)
- (1)
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- (1)
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- (1)
- (20)
- (10)
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- (15)
- (1)
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- (6)
- (2)
- (1)
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- (2)
- (2)
- (1)
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- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
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- (17)
- (14)
- (4)
- (5)
- (1)
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- (1)
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- (37)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (9)
- (7)
- (7)
- (2)
- (1)
- (1)
- (26)
- (1)
- (1)
- (1)
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- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (1)
- (14)
- (24)
- (1)
- (8)
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- (1)
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- (1)
- (22)
- (2)
- (6)
- (5)
- (2)
- (1)
- (5)
- (3)
- (4)
- (24)
- (5)
- (3)
- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (6)
- (4)
- (1)
- (3)
- (6)
- (11)
- (5)
- (4)
- (1)
- (2)
- (11)
- (14)
- (7)
- (2)
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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)
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- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
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- (2)
- (3)
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- (1)
- (1)
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- (1)
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- (60)
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- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (81)
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- (1)
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- (1)
- (81)
- (3)
- (378)
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- (1)
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- (1)
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- (281)
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- (28)
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- (731)
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Filtered Search Results
Medchemexpress LLC SGK1-IN-3 hydrochloride | 00-00-0 | 96.7% | 567.88 g/mol | C23H21Cl3N6O3S | 5 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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SGK1-IN-3 hydrochloride is the hydrochloride salt of a small-molecule inhibitor of serum- and glucocorticoid-regulated kinase 1 (SGK1). It has reported potent activity (IC50 <1 μM) and is supplied as a solid research reagent for biochemical and cellular studies, including exploratory research in osteoarthritis.
- Potent SGK1 inhibition (IC50 <1 μM).
- Supplied as a solid suitable for biochemical and cellular assays.
- High reported purity for reliable experimental results.
- Available in small research pack sizes for screening and optimization.
- Useful for exploratory studies of SGK1-related pathways and disease models.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Carmoterol hydrochloride | 137888-11-0 | 98.7% | 404.89 | C21H25ClN2O4 | 50MG
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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Carmoterol hydrochloride is a long-acting, selective β2-adrenoceptor agonist supplied for laboratory research. It is provided as a solid for studies of bronchodilation in asthma and chronic obstructive pulmonary disease (COPD) models, with supplier-provided purity and storage data to support experimental planning.
- High purity suitable for research (98.7%).
- Solid, white to light yellow appearance.
- Available in multiple package sizes, including 50 MG.
- Store sealed at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
- Useful for in vitro and in vivo respiratory pharmacology studies.
- 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 mAChR-IN-1 (hydrochloride) | 119391-73-0 | 99.6% | 524.82 g/mol | C23H26ClIN2O2 | 10MM 1ML
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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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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Medchemexpress LLC Aptiganel hydrochloride | 137160-11-3 | 99.9% | 339.86 | 10 MG
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Aptiganel hydrochloride (Cerestat) is a non-competitive NMDA receptor antagonist that demonstrates a neuroprotective effect.
- Non-competitive NMDA receptor antagonist
- Neuroprotective effect
- Purity: 99.89%
- Appearance: Solid
- Color: Off-white to light yellow
- Molecular weight: 339.86
- Formula: C20H22ClN3
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Medchemexpress LLC Indotecan hydrochloride | 1228035-68-4 | 99.8% | 514.95 | 5 MG
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Indotecan hydrochloride, an indenoisoquinoline derivative, is a potent Topoisomerase I inhibitor. It prevents the relaxation of supercoiled DNA and can be used for the research of visceral leishmaniasis.
- Potent Topoisomerase I inhibitor.
- Can be used for the research of visceral leishmaniasis.
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Medchemexpress LLC Bambuterol hydrochloride | 81732-46-9 | MFCD03427293 | 99.9% | 403.90 | 100 MG
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Bambuterol hydrochloride, also known as (±)-Bambuterol hydrochloride, is a long-acting beta-adrenoceptor agonist (LABA). It is primarily utilized in the treatment of asthma and functions as a proagent of terbutaline. Intended for research use only, this product is contraindicated in pregnancy and for individuals with severely impaired liver function, requiring dose adjustments for renal impairment.
- Used in the treatment of asthma.
- Functions as a proagent of terbutaline.
- Intended for research use only.
- Purity of 99.9%.
- Available in solid form.
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Medchemexpress LLC Bambuterol hydrochloride | 81732-46-9 | 403.90 | 5 MG
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Bambuterol hydrochloride is a long-acting beta-adrenoceptor agonist (LABA) and a prodrug of terbutaline, utilized in the treatment of asthma. It targets the Adrenergic Receptor and is involved in GPCR/G Protein and Neuronal Signaling pathways.
- Acts as a long-acting beta-adrenoceptor agonist (LABA)
- Targets the adrenergic receptor
- Functions as a prodrug of terbutaline
- Used in the treatment of asthma
- Storage conditions include 4°C sealed, away from moisture; in solvent, -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC Bevantolol hydrochloride | 42864-78-8 | 99.0% | 5 MG
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Bevantolol hydrochloride is a selective β1 and α1-adrenergic receptor antagonist and calcium channel antagonist provided as a research-grade analytical standard for pharmacology and signaling studies.
- Selective β1 and α1-adrenergic receptor antagonist.
- Also acts as a calcium channel antagonist.
- Available in small milligram pack sizes suitable for research.
- Soluble in DMSO and water; formulation guidance provided.
- Store sealed at 4°C; solvent storage recommendations provided.
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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 Melitracen hydrochloride | 10563-70-9 | MFCD00242905 | 99.8% | 327.89 g/mol | C21H26ClN | 1 ML
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Melitracen hydrochloride is a research-grade small molecule antidepressant and anxiolytic agent supplied for in vitro pharmacology, mechanism-of-action studies, and analytical reference. The material is provided with solubility and stock-solution guidance, and recommended storage conditions for both solid and solution forms.
- High purity of 99.8%.
- CAS number 10563-70-9, formula C21H26ClN, molecular weight 327.89 g/mol.
- Available as solid samples and as a pre-made 10 mM solution (1 mL) in DMSO.
- Soluble in DMSO and water at up to 100 mg/mL; ultrasonic assistance may be required.
- Storage: solid at 4°C; in solution store at -80°C up to 6 months or -20°C up to 1 month.
- Includes stock solution preparation guidance for common concentrations.
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Medchemexpress LLC Clorgyline hydrochloride | 17780-75-5 | 99.9% | C13H16Cl3NO | 50 MG
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Clorgyline hydrochloride is an irreversible and selective inhibitor of monoamine oxidase A (MAO-A) used in scientific research. It has minimal effect on conjugated dopamine (DA) amounts in superfusates of rat striatum slices. This compound contains an Alkyne group, enabling it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Irreversible and selective inhibitor of monoamine oxidase A (MAO-A)
- Structurally related to Pargyline
- Contains an Alkyne group for copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Azide groups
- Increases nicotine infusions and motivation to obtain nicotine in rats at 2 mg/kg daily for 28 days
- Pretreatment with 1 mg/kg intravenously for 1 hour has little effect on the efflux of conjugated dopamine (DA) and p-tyramine-evoked release of conjugated DA from slices of rat striatum
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Medchemexpress LLC Ansofaxine hydrochloride | 916918-84-8 | 417.97 | 100 MG
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Ansofaxine hydrochloride is a triple reuptake inhibitor that targets serotonin, dopamine, and norepinephrine. It is a solid, white to off-white compound intended for research use only.
- Inhibits serotonin, dopamine, and norepinephrine reuptake
- Solid appearance
- White to off-white color
- For research use only
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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 SB-277011 hydrochloride | 215804-67-4 | 99.59% | 475.02 | 50 MG
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SB-277011 hydrochloride is a potent and selective dopamine D3 receptor (D3R) antagonist, demonstrating high oral bioavailability and brain penetrance. It exhibits significant selectivity over other dopamine receptors and possesses an excellent pharmacokinetic profile in rats. This compound has been shown to effectively reverse the effects of quinelorane and reduce cocaine self-administration in preclinical studies.
- Potent and selective D3 receptor antagonist
- High oral bioavailability and brain penetrance
- 80- to 100-fold selectivity over other dopamine receptors
- Excellent pharmacokinetic profile
- Reverses quinelorane effects in nucleus accumbens
- Reduces intravenous cocaine self-administration
- Inhibits basal and cocaine-enhanced locomotion
- Appearance: solid, off-white to light yellow
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Medchemexpress LLC Clorgyline hydrochloride | 17780-75-5 | 99.9% | C13H16Cl3NO | 100 MG
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Clorgyline hydrochloride is an irreversible and selective inhibitor of monoamine oxidase A (MAO-A) used in scientific research. It is structurally related to Pargyline. It has little effect on the amounts of conjugated dopamine (DA) in superfusate of slices from rat striatum. It contains an Alkyne group, allowing it to undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. This product is for research use only, not sold to patients.
- Irreversible and selective inhibitor of monoamine oxidase A (MAO-A)
- Used in scientific research
- Structurally related to Pargyline
- Has little effect on conjugated dopamine (DA) in superfusate of slices from rat striatum
- Contains an Alkyne group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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