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Filtered Search Results
Medchemexpress LLC Terazosin hydrochloride dihydrate | 70024-40-7 | 99.5% | 1 ML
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Terazosin hydrochloride dihydrate is a quinazoline derivative and a competitive, orally active α1-adrenoceptor antagonist. It functions by relaxing blood vessels and aiding in the opening of the bladder. This compound has potential applications in the treatment of benign prostatic hyperplasia (BPH) and high blood pressure. This product is for research use only.
- Competitive α1-adrenoceptor antagonist
- Relaxes blood vessels
- Aids in opening the bladder
- Potential for treating benign prostatic hyperplasia (BPH)
- Potential for treating high blood pressure
- Does not differentiate cloned α1-adrenoceptor subtypes
- Can promote stone discharge in the treatment of ureteral stones
- Reportedly safe and effective for distal ureteral stones, especially those >5 mm
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Melitracen hydrochloride | 10563-70-9 | MFCD00242905 | 99.8% | 327.89 g·mol⁻¹ | C21H26ClN | 500 MG
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Melitracen hydrochloride is an orally active tricyclic antidepressant research compound that inhibits norepinephrine and serotonin reuptake. Supplied as the hydrochloride salt, it is intended for in vitro and preclinical investigation of monoaminergic activity.
- Inhibits norepinephrine and serotonin reuptake, increasing monoamine availability.
- Provided as the hydrochloride salt for improved stability and solubility.
- High reported purity (≈99.8%) suitable for research applications.
- Molecular formula C21H26ClN, molecular weight 327.89 g·mol⁻¹.
- Soluble in DMSO and water at high concentrations with sonication.
- Recommended sealed storage away from moisture; short-term storage in solution at low temperatures.
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 | C42H52Cl2N8O6 | 10MG
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Ravidasvir hydrochloride is a research-grade small-molecule inhibitor of the hepatitis C virus NS5A protein, supplied as the hydrochloride salt for laboratory studies. It exhibits potent, pan-genotypic antiviral activity and is provided with high purity and supporting documentation for use in biochemical and cellular assays.
- Pan-genotypic NS5A inhibitor with potent antiviral activity.
- High purity (99.9%) suitable for research applications.
- Supplied as a hydrochloride salt for improved solubility handling.
- Recommended storage conditions provided to preserve stability.
- Includes product datasheet and safety data sheet for lab use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Repinotan hydrochloride | 144980-77-8 | 97.1% | 25 MG
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Repinotan hydrochloride (BAY x 3702) is a potent, selective, brain-penetrant, and orally active 5-HT1A receptor agonist with Ki values of 0.19 nM (calf hippocampus), 0.25 nM (rat and human cortex), and 0.59 nM (rat hippocampus). It has a weak affinity for other related receptors and exhibits pronounced neuroprotective effects. It is intended for research use only.
- Potent, selective, brain-penetrant, and orally active 5-HT1A receptor agonist.
- Exhibits pronounced neuroprotective effects.
- Weak affinity for other related receptors.
- For research use only.
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Medchemexpress LLC Aptiganel hydrochloride (CNS 1102) | 137160-11-3 | 99.9% | 339.86 | 1 ML
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Aptiganel hydrochloride is a non-competitive NMDA receptor antagonist that demonstrates a neuroprotective effect.
- Acts as a non-competitive NMDA receptor antagonist.
- Shows neuroprotective effect.
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Medchemexpress LLC Terazosin hydrochloride dihydrate | 70024-40-7 | 99.9% | 50 MG
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Terazosin hydrochloride dihydrate is a quinazoline derivative, and it acts as a competitive and orally active α1-adrenoceptor antagonist. It functions by relaxing blood vessels and facilitating the opening of the bladder. This compound shows potential for treating benign prostatic hyperplasia (BPH) and high blood pressure. It is intended for research use only and is not sold to patients.
- Competitively blocks α1-adrenoceptors.
- Can be administered orally.
- Helps in relaxing blood vessels.
- Aids in the opening of the bladder.
- Has potential for the treatment of benign prostatic hyperplasia (BPH) and high blood pressure.
- Suitable for research applications.
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Medchemexpress LLC Tetraphenylethene maleimide | 1245606-71-6 | 98.9% | C31H23NO2 | 100 MG
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Tetraphenylethene maleimide | 1245606-71-6 | 98.9% | C31H23NO2 | 100 MG
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Medchemexpress LLC Morin | 480-16-0 | 302.24 | 5 MG
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Morin | 480-16-0 | 302.24 | 5 MG
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Medchemexpress LLC 1-Undecanol (Undecyl alcohol) | 112-42-5 | 172.31 | 100 G
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1-Undecanol (Undecyl alcohol) is primarily produced from bacteria through the oxidation of 2-tridecanone. It is also the main product resulting from the degradation of 2-tridecanone by Pseudomonas bacteria found in soil. This compound has been observed to enhance the attraction of Grapholita molesta to sex pheromone traps.
- Main product generated from the degradation of 2-tridecanone by Pseudomonas bacteria.
- Enhances attraction of Grapholita molesta to sex pheromone traps.
- Acts as a synergist for Grapholita molesta sex pheromone at 50-200 μg doses, with 50 μg showing the most significant effect.
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eMolecules [(CYCLOHEX-3-EN-1-YLOXY)METHYL]BENZENE | 100611-66-3 | | 0.25g
AstaTech | [(CYCLOHEX-3-EN-1-YLOXY)METHYL]BENZENE | 0.25g | 559764104 | D84459 | 95.000 | 100611-66-3 | | 188.270 | C13H16O
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Medchemexpress LLC Isoforskolin | 64657-21-2 | 1 MG
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Isoforskolin is the principal active component of C. forskohlii, native to China. It functions as an anti-inflammatory agent by reducing the secretion of lipopolysaccharide (LPS)-induced cytokines, specifically TNF-α, IL-1β, IL-6, and IL-8, in human mononuclear leukocytes. It is used for the treatment of Lyme arthritis.
- Principal active component of C. forskohlii.
- Reduces LPS-induced cytokine secretion (TNF-α, IL-1β, IL-6, and IL-8).
- Acts as an anti-inflammatory agent.
- Potentially treats Lyme arthritis.
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Medchemexpress LLC Iretol (2,4,6-trihydroxyanisole) | 487-71-8 | 99.4% | 156.14 | 50 MG
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Iretol (2,4,6-trihydroxyanisole) is a degradation product of a glucoside obtained from Iris Jorentina. It serves as an intermediate in the synthesis of natural isoflavones.
- Used to synthesize Tectorigenin, Irigenin, and Caviunin.
- For research use only.
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eMolecules Ambeed / Potassium tetrakis(perfluorophenyl)borate / 100mg / 591798290 / A702695 / / 89171-23-3 / MFCD06797410 / 718.140 / C24BF20K
Ambeed / Potassium tetrakis(perfluorophenyl)borate / 100mg / 591798290 / A702695 / / 89171-23-3 / MFCD06797410 / 718.140 / C24BF20K
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eMolecules AstaTech / BENZAMIDOXIME HCL / 1g / 449771892 / L10027 / 95.000 / 99277-23-3 / MFCD06656049 / 172.610 / C7H9ClN2O
AstaTech / BENZAMIDOXIME HCL / 1g / 449771892 / L10027 / 95.000 / 99277-23-3 / MFCD06656049 / 172.610 / C7H9ClN2O
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eMolecules AstaTech / 34-DIMETHOXYBICYCLO[4.2.0]OCTA-135-TRIENE-7-CARBOXYLIC ACID / 0.1g / 696739738 / 88612 / 95.000 / 41234-23-5 / MFCD01846125 / 208.213 / C11H12O4
AstaTech / 34-DIMETHOXYBICYCLO[4.2.0]OCTA-135-TRIENE-7-CARBOXYLIC ACID / 0.1g / 696739738 / 88612 / 95.000 / 41234-23-5 / MFCD01846125 / 208.213 / C11H12O4
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