Alcohols and polyols
- (1)
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- (350)
- (41)
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- (155)
- (1)
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- (50)
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- (13)
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- (1)
- (25)
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- (1)
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- (1)
- (463)
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- (46)
- (10)
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- (6)
- (1)
- (6)
- (13)
- (148)
- (114)
- (9)
- (5)
- (1)
- (1)
- (1)
- (1)
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- (1)
- (1)
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- (7)
- (14)
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- (1)
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- (1)
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- (21)
- (5)
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- (1)
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- (16)
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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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- (1)
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- (1)
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- (7)
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- (1)
- (36)
- (5)
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- (2)
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- (17)
- (14)
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- (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)
- (2)
- (1)
- (3)
- (4)
- (2)
- (1)
- (14)
- (12)
- (1)
- (3)
- (2)
- (7)
- (12)
- (1)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (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)
- (3)
- (1)
- (3)
- (1)
- (2)
- (1)
- (10)
- (1)
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- (4)
- (4)
- (1)
- (3)
- (1)
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- (5)
- (1)
- (1)
- (2)
- (1)
- (1)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (1)
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- (1)
- (2)
- (9)
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- (12)
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- (1)
- (5)
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- (10)
- (2)
- (5)
- (1)
- (1)
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- (6)
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- (1)
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- (1)
- (18)
- (16)
- (1)
- (4)
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- (4)
- (60)
- (5)
- (2)
- (1)
- (1)
- (30)
- (2)
- (2)
- (11)
- (81)
- (12)
- (4)
- (1)
- (3)
- (7)
- (5)
- (1)
- (81)
- (3)
- (378)
- (4)
- (40)
- (21)
- (1)
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- (16)
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- (1)
- (67)
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- (7)
- (4)
- (86)
- (1)
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- (72)
- (3)
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- (238)
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- (2)
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- (21)
- (281)
- (17)
- (1)
- (6)
- (279)
- (28)
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- (25)
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- (48)
- (3)
- (418)
- (6)
- (3)
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- (47)
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- (1)
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- (21)
- (16)
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- (731)
- (11)
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- (18)
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- (33)
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Medchemexpress LLC Amsacrine hydrochloride | 54301-15-4 | MFCD07799963 | 99.9% | 429.92 g/mol | C21H20ClN3O3S | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Amsacrine hydrochloride is a topoisomerase II inhibitor supplied as a research-grade analytical standard. It intercalates DNA and stabilizes topoisomerase II-DNA cleavage complexes, making it suitable for biochemical assays and cell biology studies of DNA damage, cell cycle, and autophagy. Available as a solid and as a DMSO solution, the material is characterized for consistent analytical performance.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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![Medchemexpress LLC Benzoic acid, 4-[4-[[(3R)-1-butyl-3-[(R)-cyclohexylhydroxymethyl]-2,5-dioxo-1,4,9-triazaspiro [5.5]undec-9-yl]methyl]phenoxy]-, hydrochloride (1:1) | 461023-63-2 | 99.9% | 614.17 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000384286-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Benzoic acid, 4-[4-[[(3R)-1-butyl-3-[(R)-cyclohexylhydroxymethyl]-2,5-dioxo-1,4,9-triazaspiro [5.5]undec-9-yl]methyl]phenoxy]-, hydrochloride (1:1) | 461023-63-2 | 99.9% | 614.17 | 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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Aplaviroc hydrochloride is a CCR5 antagonist derived from SDP, with IC50s ranging from 0.1-0.4 nM for HIV-1Ba-L, HIV-1JRFL, and HIV-1MOKW. It is intended for research use only.
- Target: CCR5 antagonist
- Potency: Potent activity against wild-type R5 HIV-1 strains with IC50 values of 0.1 to 0.4 nM
- Mechanism: Suppresses infectivity and replication of HIV-1MDR variants at low concentrations (IC50 values of 0.4 to 0.6 nM)
- Binding Affinity: Binds to CCR5 with high affinity (Kd value of 2.9±1.0 nM)
- Inhibition: Potently blocks rgp120/sCD4 binding to CCR5 with an IC50 value of 2.7 nM
- In Vivo Efficacy: Suppresses R5 HIV-1 viremia in hu-PBMC-NOG mice at a dosage of 60 mg/kg
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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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 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
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Medchemexpress LLC Yonkenafil hydrochloride | 804519-64-0 | 99.4% | 524.08 | C24H34ClN5O4S | 5MG
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Yonkenafil hydrochloride is the hydrochloride salt of a selective phosphodiesterase 5 (PDE5) inhibitor supplied for research use. It is provided as a high-purity solid suitable for in vitro and preclinical studies involving PDE5-related pathways, neuroscience, and pharmacology. Typical solvent compatibility includes DMSO; follow the SDS and laboratory safety procedures.
- High purity suitable for research.
- Solid form for accurate weighing and formulation.
- Soluble in DMSO for assay preparation.
- Appropriate for in vitro and preclinical pharmacology studies.
- Available in small-scale vials for dose-ranging experiments.
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Apexbio Technology LLC NINHYDRIN-1G
Ninhydrin (CAS No 485-47-2) is a chemical compound widely used in the biochemical and forensic sciences Originating as a synthetic reagent it primarily functions by reacting with free amino groups in proteins and peptides resulting in a deep blue or purple color known as Ruhemann s purple This makes it particularly useful for detecting amino acids and analyzing protein structure In vitro ninhydrin demonstrates high sensitivity for amino acid detection in the nanomolar to low micromolar range It is frequently used in applications including the visualization of fingerprints protein and amino acid quantification and various drug screening protocols In laboratory settings ninhydrin often serves in cell models and animal studies to detect and quantify biomolecules significantly aiding in the complex analysis of biochemical pathways Experimental concentrations typically depend on the specific research design
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Medchemexpress LLC Alectinib hydrochloride | 1256589-74-8 | MFCD27987893 | 99.9% | C30H35ClN4O2 | 10MG
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Alectinib hydrochloride is the hydrochloride salt of alectinib, a potent and selective anaplastic lymphoma kinase (ALK) inhibitor. It is supplied as a research-grade analytical standard for biochemical and cell-based assays and includes documentation to support analytical verification. Intended for research use only.
- High purity (99.9%) for analytical applications.
- Verified identity with CAS 1256589-74-8.
- Available in multiple small pack sizes for method development.
- Soluble in common organic solvents for assay preparation.
- Supplied with COA and datasheet for traceability.
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Medchemexpress LLC PAZOPANIB HYDROCHLO 25 mg
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PAZOPANIB HYDROCHLO 25MG
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Medchemexpress LLC Proadifen (hydrochloride) | 62-68-0 | 99.9% | 250 MG
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Proadifen (hydrochloride) | 62-68-0 | 99.9% | 250 MG
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Medchemexpress LLC SB 243213 HYDROCHLO 100 mg
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SB 243213 HYDROCHLO 100MG
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Medchemexpress LLC BMY-14802 hydrochloride | 105565-55-7 | 98.0% | 384.85 | 500 UG
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BMY-14802 hydrochloride (BMY-14802-1) is a selective and orally active sigma receptor antagonist with an IC50 of 112 nM. It is also a 5-HT1A and adrenergic α1 receptors agonist. BMY-14802 hydrochloride has antipsychotic effects.
- Selective and orally active sigma receptor antagonist.
- Acts as a 5-HT1A and adrenergic α1 receptor agonist.
- Exhibits antipsychotic effects.
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