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Filtered Search Results
eMolecules 95-85-2 | 2-AMINO-4-CHLOROPHENOL | AstaTech | MFCD00007694 | 143.570 | C6H6ClNO | 95.000 | Nc1cc(Cl)ccc1O | 25g | 718059141
2-AMINO-4-CHLOROPHENOL | AstaTech | 95-85-2 | MFCD00007694 | 143.570 | C6H6ClNO | 95.000 | Nc1cc(Cl)ccc1O | 25g | 718059141
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eMolecules 1433286-70-4 | Medchem Express | 666-15 | 5mg | 446256484 | HY-101120 | MFCD30182343 | 620.53 | C33H31Cl2N3O5
Medchem Express | GNE-781 | 5mg | 455325966 | HY-108696 | 1936422-33-1 | 525.605 | C27H33F2N7O2
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Medchemexpress LLC Methoxamine hydrochloride | 61-16-5 | MFCD00058607 | 99.3% | 247.72 g/mol | C11H18ClNO3 | 10 MG
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Methoxamine hydrochloride is a selective α1-adrenergic receptor agonist used in vascular and receptor pharmacology research. Supplied as the hydrochloride salt in solid form, it is used to induce vasoconstriction and study α1-adrenergic signaling in tissue and cellular assays.
- Selective α1-adrenergic agonist for receptor and vascular studies.
- High purity suitable for research applications.
- Available as a solid powder for formulation or assay use.
- Soluble in polar solvents, compatible with common assay preparations.
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Medchemexpress LLC Ticlopidine hydrochloride | 53885-35-1 | 99.99% | 1 G
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Ticlopidine hydrochloride is an antithrombotic proagent that acts as an allosteric, noncompetitive inhibitor of CD39 with an IC50 of 81.7 μM. It blocks several NTPDase isoenzymes, showing IC50s of 170 μM for NTPDase2 and 149 μM for NTPDase3. This compound is also an inhibitor of human liver cytochrome CYP2C19, and it inhibits CYP2C9 and CYP3A4 with IC50s of 26.0 μM and 32.3 μM, respectively.
- Functions as an allosteric, noncompetitive inhibitor of CD39
- Blocks multiple NTPDase isoenzymes
- Inhibits human liver cytochrome CYP2C19, CYP2C9, and CYP3A4
- Demonstrates antiplatelet aggregation activity
- Soluble in water and DMSO
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Medchemexpress LLC -Coniine hydroch 10mg
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( )-Coniine hydrochloride (2-Propylpiperidine hydrochloride) is a potent nAChR agonist with an EC50 value of 0 3 mM ( )-Coniine hydrochloride shows acute toxicity with an LD50 value of 7 7 mg/kg[1]
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Medchemexpress LLC Pardoprunox hydrochloride | 269718-83-4 | MFCD09833663 | 99.5% | 269.73 g/mol | C12H16ClN3O2 | 10 MG
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Pardoprunox hydrochloride is the hydrochloride salt of SLV-308, a research compound used in pharmacology studies of dopaminergic and serotonergic signaling. It is provided as a high-purity solid and formulated for both in vitro and in vivo experiments.
- Acts as a partial agonist at dopamine D2 and D3 receptors and an agonist at 5-HT1A receptors.
- Reported pEC50 values: D2 = 8, D3 = 9.2, 5-HT1A = 6.3.
- Supplied as an off-white to pink solid suitable for laboratory use.
- High purity appropriate for research applications.
- Soluble in DMSO and water; in vivo formulations and concentrations provided for dosing.
- Storage recommendations: solid at 4°C; dissolved samples at -80°C for long-term storage.
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Medchemexpress LLC Quinagolide hydrochloride | 94424-50-7 | MFCD00893553 | 99.7% | C20H34ClN3O3S | 10MG
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Quinagolide hydrochloride is the hydrochloride salt of quinagolide, a non-ergot-derived selective dopamine D2 receptor agonist used in research on prolactin regulation and dopaminergic signaling. Supplied as a research-grade solid with high purity for reliable in vitro and in vivo pharmacology studies.
- Selective dopamine D2 receptor agonist for prolactin research.
- Hydrochloride salt improves aqueous solubility.
- High purity (≈99.7%) for reproducible results.
- Suitable for in vitro and in vivo pharmacology studies.
- Available in research-scale pack sizes for dose-ranging experiments.
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eMolecules 56962-01-7 | 3-Amino-2-chlorophenol | MFCD11044694 | 250mg
Ambeed | 3-Amino-2-chlorophenol | 250mg | 602850772 | A796202 | 56962-01-7 | MFCD11044694 | 143.570 | C6H6ClNO
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Medchemexpress LLC (1R,2R)-2-pcca (hydrochloride) | 1609563-71-4 | 98.1% | 528.56 | C30H39Cl2N3O | 1 ML
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(1R,2R)-2-PCCA hydrochloride is the (1R,2R) diastereomer of 2-PCCA and is used as a pharmacological agonist to study GPR88 signaling in biochemical and cell-based assays. It is available as a solid and as a pre-prepared 10 mM solution in DMSO for convenient use in experiments.
- Potent GPR88 receptor agonist with low-nanomolar activity in cell-free assays.
- Documented cell-based activity and functional inhibition of GPR88-mediated cAMP.
- Molecular weight 528.56 and formula C30H39Cl2N3O for precise dosing calculations.
- High purity (98.08%) with enantiomeric excess ~99% for stereochemical consistency.
- Available as solid quantities and as 10 mM solution in DMSO for immediate use.
- Storage recommendations provided for solids and solutions to preserve stability.
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Sigma Aldrich Fine Chemicals Biosciences 3-NN-Dimethylpalmitylammon5G
3-(N N-Dimethylpalmitylammonio)propanesulfonate is a zwitterionic detergent.
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Sigma Aldrich Fine Chemicals Biosciences Riboflavin 100G
Riboflavin belongs to the vitamin-B family and contains a pentose side chain ribitol.
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Medchemexpress LLC AMPK activator 2 hydrochloride | 00-00-0 | 99.7% | 337.77 | C13H19ClF3N5 | 5 MG
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AMPK activator 2 hydrochloride is a fluorine-containing proguanil derivative that activates AMP-activated protein kinase (AMPK), modulating downstream mTOR/4EBP1/p70S6K signaling. It is reported to inhibit proliferation and migration of human cancer cell lines and is provided as a research reagent for in vitro studies.
- Up-regulates AMPK signaling pathway.
- Downregulates mTOR/4EBP1/p70S6K signaling.
- Inhibits proliferation and migration in UMUC3, T24, and A549 cell lines.
- Available in small quantities suitable for assay development.
- High reported purity for biochemical experiments.
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Medchemexpress LLC Bay 61-3606 hydrochloride | 1615197-10-8 | MFCD29073361 | 98.1% | 426.86 | C20H19ClN6O3 | 10 MG
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BAY 61-3606 hydrochloride is the hydrochloride salt of BAY 61-3606, a selective ATP-competitive Syk inhibitor used for in vitro research on Syk-mediated signaling and apoptosis. The product is supplied as a solid with a reported CAS number 1615197-10-8, molecular formula C20H19ClN6O3, molecular weight 426.86, and high purity for research applications.
- Selective Syk inhibitor suitable for cell signaling studies.
- ATP-competitive and reversible mechanism of action.
- Hydrochloride salt form improves solubility for aqueous assays.
- High reported purity supports reproducible experimental results.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC CARM1-IN-3 dihydrochloride | 912970-67-3 | 98.8% | 481.46 | C24H34Cl2N4O2 | 10 MG
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CARM1-IN-3 dihydrochloride is a small-molecule inhibitor selective for co-activator associated arginine methyltransferase 1 (CARM1). Supplied as a white to off-white solid, it shows potent inhibition of CARM1 (IC50 = 0.07 μM) with minimal activity versus CARM3, and is intended for research use in biochemical and cellular assays. Store sealed and away from moisture; follow recommended cold storage for long-term stability.
- Potent and selective CARM1 inhibition (IC50 = 0.07 μM).
- High purity for reproducible experimental results (98.77%).
- White to off-white solid suitable for analytical and biological applications.
- Dihydrochloride salt form compatible with aqueous preparations.
- Recommended storage: sealed, away from moisture; in solvent -80°C (6 months), -20°C (1 month).
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eMolecules 621-38-5 | 3-Bromoacetanilide | Combi-Blocks, Inc. | MFCD00461391 | 214.062 | C8H8BrNO | 98.000 | CC(=O)Nc1cccc(Br)c1 | 500g | 837473975
3-Bromoacetanilide | Combi-Blocks, Inc. | 621-38-5 | MFCD00461391 | 214.062 | C8H8BrNO | 98.000 | CC(=O)Nc1cccc(Br)c1 | 500g | 837473975
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