Alcohols and polyols
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- (395)
- (6)
- (102)
- (21)
- (50)
- (31)
- (61)
- (13)
- (14)
- (1)
- (2)
- (1)
- (26)
- (6)
- (4)
- (1)
- (6)
- (1)
- (462)
- (9)
- (46)
- (11)
- (45)
- (6)
- (1)
- (7)
- (10)
- (145)
- (114)
- (6)
- (5)
- (1)
- (1)
- (1)
- (1)
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- (1)
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- (2)
- (2)
- (2)
- (16)
- (2)
- (30)
- (2)
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- (1)
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- (20)
- (10)
- (4)
- (15)
- (1)
- (4)
- (6)
- (2)
- (2)
- (2)
- (2)
- (4)
- (3)
- (1)
- (28)
- (29)
- (7)
- (3)
- (5)
- (1)
- (36)
- (5)
- (4)
- (2)
- (5)
- (4)
- (17)
- (15)
- (4)
- (5)
- (2)
- (5)
- (4)
- (33)
- (4)
- (2)
- (6)
- (8)
- (2)
- (2)
- (8)
- (7)
- (7)
- (2)
- (1)
- (26)
- (1)
- (1)
- (1)
- (2)
- (1)
- (3)
- (4)
- (3)
- (1)
- (15)
- (12)
- (1)
- (2)
- (2)
- (7)
- (12)
- (1)
- (14)
- (24)
- (1)
- (8)
- (4)
- (1)
- (2)
- (1)
- (17)
- (2)
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- (5)
- (2)
- (1)
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- (3)
- (4)
- (24)
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- (5)
- (14)
- (1)
- (1)
- (1)
- (11)
- (3)
- (2)
- (4)
- (11)
- (2)
- (7)
- (4)
- (1)
- (1)
- (3)
- (6)
- (11)
- (5)
- (3)
- (1)
- (2)
- (11)
- (14)
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- (2)
- (2)
- (1)
- (3)
- (2)
- (10)
- (1)
- (2)
- (4)
- (4)
- (3)
- (1)
- (3)
- (5)
- (1)
- (1)
- (2)
- (10)
- (2)
- (2)
- (3)
- (7)
- (1)
- (5)
- (4)
- (1)
- (2)
- (9)
- (4)
- (2)
- (12)
- (4)
- (1)
- (1)
- (5)
- (3)
- (10)
- (2)
- (5)
- (1)
- (1)
- (1)
- (10)
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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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- (11)
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Filtered Search Results
Medchemexpress LLC Nebivolol hydrochloride | 152520-56-4 | 99.9% | 1 ML
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Nebivolol hydrochloride (R 065824) is an orally active beta receptor blocker with high beta(1)-receptor affinity. It possesses direct vasodilator properties and adrenergic blocking characteristics.
- Used for research into various diseases
- High beta(1)-receptor affinity
- Direct vasodilator properties
- Adrenergic blocking characteristics
- Orally active beta receptor blocker
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Amiloride hydrochloride | 2016-88-8 | MFCD03703482 | 99.8% | 500 MG
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Amiloride hydrochloride is a research chemical that acts as an inhibitor of both epithelial sodium channel (ENaC) and urokinase-type plasminogen activator receptor (uTPA). It also functions as a blocker of the polycystin-2 (PC2; TRPP2) channel. This compound is intended for research use only.
- Inhibits epithelial sodium channel (ENaC).
- Inhibits urokinase-type plasminogen activator receptor (uTPA).
- Blocks polycystin-2 (PC2; TRPP2) channel.
- Selective inhibitor of ENaC with an IC50 ranging from 0.1 to 0.5 μM.
- Reverses and prevents increases in collagen deposition in DOCA-salt hypertensive rats.
- Delays proteinuria and improves brain and kidney scores in SHRSP rats.
- Antagonizes aldosterone actions in cardiovascular and renal tissues.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Tiagabine (hydrochloride) | 145821-59-6 | MFCD00892911 | ≥98% | 1 ML
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Tiagabine (hydrochloride) is an anticonvulsant agent and a selective inhibitor of the GAT-1 GABA transporter. It potently and selectively inhibits GABA reuptake and demonstrates neuroprotective properties.
- Selective inhibitor of GAT-1 GABA transporter
- Potently and selectively inhibits GABA reuptake
- Exhibits neuroprotective properties
- Protects neurons against mutant huntingtin-induced toxicity
- Increases viability of SH-SY5Y cells
- Inhibits GABA uptake in mouse GAT1 expressed in HEK293 cells
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Betaxolol hydrochloride | 63659-19-8 | 98.12% | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Betaxolol Hydrochloride is a selective beta1 adrenergic receptor blocker that can be used for the research of hypertension and glaucoma. It is a cardioselective beta-adrenergic receptor blocking agent. It has been shown to diminish anxiety-like behavior during early withdrawal from chronic cocaine administration in rats, and it produces less systemic beta 2- and possibly beta 1-adrenergic receptor blockade than either timolol or levobunolol, potentially making it safer for patients with reactive airway disease.
- Selective beta1 adrenergic receptor blocker
- Used in research for hypertension and glaucoma
- Cardioselective beta-adrenergic receptor blocking agent
- Diminishes anxiety-like behavior during withdrawal from chronic cocaine administration in rats
- Produces less systemic beta 2- and possibly beta 1-adrenergic receptor blockade
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Amprolium hydrochloride | 137-88-2 | 98.79% | 250 MG
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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. It is for research use only and not sold to patients.
- Acts as an antagonist to thiamine in intestinal absorption
- Targets Coccidia
- Suitable for in vivo and in vitro applications
- For research use only
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Medchemexpress LLC Alfuzosin hydrochloride | 81403-68-1 | 99.7% | 50 MG
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Alfuzosin hydrochloride is an orally active, selective and competitive α1-adrenoceptor antagonist. It relaxes the muscles of the prostate and bladder neck, aiding in urination. This compound can be used in the study of benign prostatic hyperplasia (BPH).
- Orally active
- Selective and competitive α1-adrenoceptor antagonist
- Relaxes the muscles of the prostate and bladder neck
- Aids in urination
- Can be used in the study of benign prostatic hyperplasia (BPH)
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Medchemexpress LLC Nebivolol hydrochloride | 152520-56-4 | MFCD07357273 | 99.9% | 50 MG
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Nebivolol hydrochloride is an orally active beta receptor blocker with high beta(1)-receptor affinity. It possesses direct vasodilator properties and adrenergic blocking characteristics. This compound is used for the research of various diseases such as hypertension, coronary artery disease, congestive heart failure, and ischemic heart disease.
- Orally active beta receptor blocker
- High beta(1)-receptor affinity
- Direct vasodilator properties
- Adrenergic blocking characteristics
- Improves endothelial dysfunction
- Stimulates endothelial nitric oxide synthase activity
- Antioxidative properties
- Inhibits haCSMC and haEC proliferation
- Induces moderate apoptosis
- Increases NO formation and decreases endothelin-1 secretion
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Medchemexpress LLC Articaine hydrochloride | 23964-57-0 | 99.4% | 1 ML
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Articaine hydrochloride is a selective inhibitor of voltage-gated sodium channels, demonstrating local anesthetic activity by blocking nerve impulse conduction. It also exhibits anti-inflammatory functions by inhibiting NF-κB activation and NLRP3 inflammasome pathways. It is used in the study of dental local anesthesia and inflammatory-related diseases.
- Inhibits voltage-gated sodium channels
- Exhibits local anesthetic activity
- Inhibits NF-κB activation and NLRP3 inflammasome pathways
- Reduces inflammatory factors like TNF-α, IL-6, and IL-1β
- Ameliorates LPS-induced acute kidney injury in animal models
- Can enhance anesthetic effect in zebrafish model
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Medchemexpress LLC Amprolium (hydrochloride) | 137-88-2 | 98.8% | 1 ML
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Amprolium hydrochloride is provided as a 10 mM solution in 1 mL, with a purity of 98.8%. This product is intended for research use only and should be handled by qualified personnel in appropriately equipped facilities.
- 10 mM solution in 1 mL
- Purity: 98.8% (HPLC)
- Recommended storage: 4°C for sealed solutions, away from moisture
- For longer-term storage in solvent: -80°C for 6 months or -20°C for 1 month
- Can be shipped at room temperature if shipment duration is less than 2 weeks
- Intended for research applications
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Medchemexpress LLC Fendiline (hydrochloride) | 13636-18-5 | 99.8% | 1 ML
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Fendiline hydrochloride is a diphenylalkylamine type of antianginal agent that acts as an L-type calcium channel blocker with an IC50 of 17 μM. It is also identified as a selective K-Ras inhibitor, showing no effect on H-Ras and N-Ras. It inhibits K-Ras plasma membrane localization (IC50 of 9.64 μM) and K-Ras signal output. Additionally, Fendiline hydrochloride is a STING agonist and has demonstrated the ability to inhibit the growth of multiple refractory cold tumors. This product is provided as a 10 mM solution in 1 mL of DMSO with a purity of 99.78%.
- Acts as an L-type calcium channel blocker
- Functions as a selective K-Ras inhibitor
- Inhibits K-Ras plasma membrane localization
- Suppresses K-Ras signal output
- Prevents proliferation of various cancer cell lines
- Serves as a STING agonist
- Inhibits growth of refractory cold tumors
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Medchemexpress LLC Trazodone hydrochloride | 25332-39-2 | 99.6% | 5 G
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Trazodone hydrochloride is a triazolopyridine derivative that acts as a serotonin receptor antagonist and reuptake inhibitor (SARI). It demonstrates anti-depressant and anti-insomnious activity by antagonizing α1- and α2-adrenergic receptors and histamine H1 receptors, with minimal anticholinergic effects. It is suitable for various laboratory applications and research.
- Exhibits anti-depressant and anti-insomnious activity
- Acts as an antagonist against α1- and α2-adrenergic receptors
- Antagonizes histamine H1 receptors
- Demonstrates minimal anticholinergic effects
- Binds to 5-HT1A receptor
- Reduces expression of neuroinflammatory markers
- Increases mRNA expression of BDNF and CREB
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Medchemexpress LLC 9h-Carbazole-3-methanamine, 9-ethyl-N-methyl-, hydrochloride (1:1) | 1050480-30-2 | 99.3% | 274.79 | 1 ML
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PhiKan 083 hydrochloride is a carbazole derivative that binds to the surface cavity and stabilizes Y220C (a p53 mutant), with a Kd of 167 μM, and a relative binding affinity (Kd) of 150 μM in Ln229 cells.
- Slows down its thermal denaturation rate.
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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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Medchemexpress LLC SAR407899 hydrochloride | 923262-96-8 | MFCD20485429 | 99.1% | 280.75 g/mol | C14H17ClN2O2 | 10 MG
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SAR407899 hydrochloride is a selective, potent, ATP-competitive inhibitor of Rho-associated kinases (ROCK), supplied as a high-purity solid for preclinical biochemical and cellular research. It is used to probe ROCK-mediated signaling, vascular tone, and smooth muscle responses in vitro and in vivo.
- Selective ATP-competitive ROCK inhibitor with ROCK-2 IC50 ≈135 nM.
- Demonstrates Ki values of 36 nM (human) and 41 nM (rat).
- High purity (99.1%) suitable for research applications.
- Solid, light yellow to khaki appearance; stable when stored sealed at 4°C.
- Applicable to studies of vascular tone, smooth muscle relaxation, and ROCK signaling pathways.
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Medchemexpress LLC Sematilide hydrochloride | 101526-62-9 | MFCD01667315 | 99.3% | 349.88 g·mol⁻1 | C14H24ClN3O3S | 100 MG
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Sematilide hydrochloride is a class III antiarrhythmic research compound that selectively blocks the cardiac IKr (hERG) potassium channel. It inhibits the delayed rectifier K+ current in a concentration-dependent manner (reported IC50 ≈ 25 μM) and is supplied as the hydrochloride salt for in vitro electrophysiology and pharmacology studies. Typical purity is 99.33%.
- Selective IKr (hERG) channel blocker
- Inhibits delayed rectifier K+ current (IC50 ≈ 25 μM)
- Intended for in vitro electrophysiology and pharmacology studies
- High purity suitable for analytical applications
- Available in milligram pack sizes for research use
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