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Filtered Search Results
eMolecules 21926-00-1 | 4-Aminotetrahydro-2H-thiopyran | Apollo Scientific | MFCD07371524 | 117.210 | C5H11NS | 98.000 | NC1CCSCC1 | 1g | 600855493
4-Aminotetrahydro-2H-thiopyran | Apollo Scientific | 21926-00-1 | MFCD07371524 | 117.210 | C5H11NS | 98.000 | NC1CCSCC1 | 1g | 600855493
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Chemscene CHEMSCENE
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5000580052 2-NAPHTHOL 100G
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Aobchem AOBCHEM
5000865945 2-CHLORO-6-METHOXYNAPHTHALENE
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Medchemexpress LLC Prodigiosin hydrochloride | 56144-17-3 | 98.1% | 359.89 g/mol | C20H26ClN3O | 250 UG
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Prodigiosin hydrochloride is the hydrochloride salt of the natural product prodigiosin, provided as a research reagent with reported antibacterial, antifungal, antiprotozoal, antimalarial, immunosuppressive, and anticancer activities. It is supplied as a solid for use in biochemical and cell biology studies and analytical assays.
- Small-molecule hydrochloride salt with reported broad-spectrum bioactivity.
- High purity suitable for research use (≈98.1%).
- Solid, purple to purplish red appearance.
- Molecular weight 359.89 g/mol.
- Store sealed at -20°C; in solution store at -80°C for long-term stability.
- Available in microgram and milligram quantities for assay development.
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Apexbio Technology LLC GSK 5959 901245-65-6 10mg
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GSK 5959 (CAS 901245-65-6) is a selective small-molecule inhibitor targeting the bromodomain of BRPF1 (bromodomain and PHD finger-containing protein 1) By binding specifically to the BRPF1 bromodomain GSK 5959 disrupts its interaction with acetylated histones thereby modulating associated epigenetic regulatory pathways In vitro studies report an IC50 of 80 nM for inhibition of BRPF1 bromodomain activity Due to its favorable cell permeability GSK 5959 is widely utilized in research investigating BRPF1-dependent mechanisms of gene expression and in the exploration of epigenetic contributions to disease models
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eMolecules 94749-08-3 | Medchem Express | Salmeterol (xinafoate) | 10mg | 446268457 | HY-17453 | MFCD00897708 | 603.756 | C36H45NO7
Medchem Express | Salmeterol (xinafoate) | 10mg | 446268457 | HY-17453 | 94749-08-3 | MFCD00897708 | 603.756 | C36H45NO7
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Medchemexpress LLC Givinostat hydrochloride monohydrate | 732302-99-7 | 99.6% | 475.97 | 100 MG
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Givinostat hydrochloride monohydrate is a potent histone deacetylase (HDAC) inhibitor, demonstrating inhibitory activity against HDAC1 (IC50 of 198 nM) and HDAC3 (IC50 of 157 nM). It can penetrate the blood-brain barrier (BBB), making it suitable for neurological research.
- Potent HDAC inhibitor targeting HDAC1 and HDAC3.
- Can penetrate the blood-brain barrier (BBB).
- Suitable for in vitro and in vivo studies related to HDAC inhibition.
- Available as a stable hydrochloride monohydrate form.
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Medchemexpress LLC Fluoxetine hydrochloride | 56296-78-7 | 100.0% | C17H19ClF3NO | 500 MG
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Fluoxetine hydrochloride is an antidepressant and a selective serotonin reuptake inhibitor, intended for research use only.
- Acts as an antidepressant and selective serotonin reuptake inhibitor.
- Blocks downregulation of cell proliferation in hippocampal cells.
- Increases neurogenesis in the hippocampus and prelimbic cortex.
- Enhances neurogenesis-dependent long-term potentiation.
- Increases norepinephrine and dopamine extracellular levels.
- Reverses deficits in escape latency in animal models.
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![eMolecules 9001-62-1 | Sustine? 131 | Strem Chemicals238.201 | C11H9N3NaO2 | 0.000 | [Na+].OC1=CC(=O)C=C\C1=N\Nc1ccccn1 | 5g | 576207975](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215933.jpg-250.jpg)
eMolecules 9001-62-1 | Sustine? 131 | Strem Chemicals238.201 | C11H9N3NaO2 | 0.000 | [Na+].OC1=CC(=O)C=C\C1=N\Nc1ccccn1 | 5g | 576207975
Sustine? 131 | Strem Chemicals | 9001-62-1238.201 | C11H9N3NaO2 | 0.000 | [Na+].OC1=CC(=O)C=C\C1=N\Nc1ccccn1 | 5g | 576207975
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Medchemexpress LLC Rotigotine Hydrochloride | 125572-93-2 | 99.45% | C19H26ClNOS | 500 MG
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Rotigotine Hydrochloride is a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. It is suitable for research use only.
- Full agonist of dopamine receptor
- Partial agonist of the 5-HT1A receptor
- Antagonist of the α2B-adrenergic receptor
- Ki values of 0.71 nM for the dopamine D3 receptor
- Ki values of 4-15 nM for D2, D5, and D4 receptors
- Ki value of 83 nM for the dopamine D1 receptor
- White to off-white solid appearance
- Suitable for research use only
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Medchemexpress LLC Givinostat hydrochloride | 199657-29-9 | 98.06% | 457.95 | 25 MG
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Givinostat hydrochloride (ITF-2357) is a potent Histone Deacetylase (HDAC) inhibitor, with IC50 values of 198 nM for HDAC1 and 157 nM for HDAC3. This compound can also penetrate the blood-brain barrier (BBB) and is typically a white to off-white solid.
- Potent HDAC inhibitor
- Penetrates the blood-brain barrier
- White to off-white solid appearance
- Store solid at 4°C, sealed, away from moisture
- Store in solvent at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC 4-(4-((dimethylamino)methyl)-2,5-dimethoxyphenyl)-2-methyl-2,7-naphthyridin-1(2H)-one | 1883429-22-8 | 98.7% | 353.41 | C20H23N3O3 | 10 MG
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BI-9564 is a potent, selective, and cell-permeable inhibitor of BRD9 and BRD7 bromodomains used as a chemical probe in epigenetics research. It exhibits low-nanomolar affinity for BRD9, displays selectivity versus BET family bromodomains, and is supplied as a white to off-white solid for laboratory use.
- Potent inhibition of BRD9 with low-nanomolar affinity.
- Selectivity for BRD9/BRD7 over BET family bromodomains.
- Cell-permeable for use in cellular assays.
- High purity suitable for research applications.
- Supplied as a solid with defined storage recommendations.
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Medchemexpress LLC Anpirtoline hydrochloride | 99201-87-3 | 99.9% | 265.21 | C10H14Cl2N2S | 100 MG
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Anpirtoline hydrochloride is a research-grade serotonergic compound that functions primarily as a 5-HT1B receptor agonist, with activity at 5-HT1A and 5-HT2 subtypes. It is supplied for laboratory research use only and is not for human or veterinary use. CAS: 99201-87-3; molecular weight: 265.21 g/mol.
- Potent 5-HT1B receptor agonist with activity at related 5-HT subtypes.
- High reported purity, suitable for pharmacological experiments.
- Available in multiple pack sizes to support screening or preparative work.
- Provided with documentation useful for research-grade handling and QC.
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Selleck Chemical LLC BI-847325
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BI-847325 is an orally bioavailable and selective dual MEK/Aurora kinase inhibitor with IC50 of 3 nM 25 nM 15 nM 25 nM and 4 nM for Xenopus laevis Aurora B human Aurora A and Aurora C as well as human MEK1 and MEK2 respectively Phase 1
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Apexbio Technology LLC Adapalene sodium salt 911110-93-5 50mg
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Adapalene sodium salt (CAS 911110-93-5) is a small-molecule agonist targeting retinoic acid receptors (RARs) It is designed to selectively modulate RAR-mediated signaling thereby regulating cellular differentiation and proliferation Adapalene sodium salt exerts its biological activity primarily through specific binding and activation of nuclear RAR subtypes influencing gene transcription It demonstrates agonist activity toward RARs with EC50 values of 2 3 nM 9 3 nM and 22 nM for different RAR subtypes Additionally Adapalene sodium salt noncompetitively inhibits an unspecified enzyme s activity Based on these pharmacological properties Adapalene sodium salt holds research potential in studies of retinoid signaling cellular differentiation mechanisms dermatological disease models and antitumor investigations
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