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Filtered Search Results
Medchemexpress LLC HPMC (Viscosity: 11250-21000 mPa.s) | 9004-65-3 | 500 MG
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HPMC (Viscosity:11250-21000mPa.s) is a hydrophilic, non-ionic cellulose ether used to form swellable-soluble matrices. It provides controlled release of a drug, effectively increasing the duration of release to prolong its therapeutic effect. When used in matrix tablets, it hydrates on contact with water to produce a viscous gel barrier.
- Hydrophilic, non-ionic cellulose ether
- Forms swellable-soluble matrices
- Provides controlled release of drugs
- Increases duration of drug release
- Forms a viscous gel barrier
- Effective in improving blood glucose metabolism
- Suppresses oxidative stress
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Medchemexpress LLC Cefazolin | 25953-19-9 | 99.7% | 100 MG
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Cefazolin (Cephazolin) is a first-generation cephalosporin antibiotic that can be used in research for various bacterial infections. It also exhibits anti-inflammatory effects and can mitigate post-operative cognitive dysfunction (POCD).
- Antibiotic properties: First-generation cephalosporin antibiotic effective against various bacterial infections.
- Anti-inflammatory effect: Can attenuate post-operative cognitive dysfunction (POCD).
- High purity of 99.73%.
- Research use only.
- Versatile forms: Available as a solid and in solution.
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Medchemexpress LLC Spectinomycin (dihydrochloride pentahydrate) | 22189-32-8 | 98.0% | 1 G
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Spectinomycin (dihydrochloride pentahydrate) | 22189-32-8 | 98.0% | 1 G
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Sigma Aldrich Fine Chemicals Biosciences Teicoplanin | 61036-62-2 | 100MG
Teicoplanin | Purity: >=80% (teicoplanins A2, HPLC) | 61036-62-2 | 100MG
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Sigma Aldrich Fine Chemicals Biosciences Bafilomycin A1 Ready Made Solution | 88899-55-2 | MFCD06795130 | 0.1mL
Bafilomycin A1 Ready Made Solution | 0.16 mM in DMSO, from Streptomyces griseus | MW:622.83 | 88899-55-2 | MFCD06795130 | 0.1mL
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Carbosynth LLC. Hydroxy-itraconazole (powder), 50 mg
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Hydroxy-itraconazole chemical reference substance
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AG Scientific Inc Ampicillin, Sodium Salt, 25 G
Ampicillin Sodium Salt is a Beta-Lactam antibiotic within the penicillin family. It inhibits synthesis of bacterial cell wall by inactivation of transpeptidases. It is used as a selective agent of ampicillin resistance in mutated and transformed cells having plasmid encoding for Beta-Lactamase production such as pBR322 or pUC.It is sensitive to Beta-lactamase, which hydrolyzes Beta-lactam ring. This antibiotic is effective against gram positive and highly effective against gram negative bacteria.CAS Number: 69-52-3Molecular Weight: 371.4 DaChemical Formula: C16H18N3O4S NaSolubility: Soluble in waterStorage Temperature: +4CResearch or further manufacturing use only, not for food or drug use.
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Medchemexpress LLC Bemnifosbuvir hemisulfate | 2241337-84-6 | 99.4% | C24H33FN7O7P.1/2H2O4S | 10MG
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Bemnifosbuvir hemisulfate is the hemisulfate salt of a guanosine nucleotide prodrug developed as an orally active antiviral. It demonstrates potent activity against hepatitis C virus and in vitro activity against SARS-CoV-2 (reported EC90 ≈ 0.47 μM). Supplied for research use, the compound is provided at high purity and in laboratory-scale quantities suitable for pharmacology and mechanism-of-action studies.
- Hemisulfate salt form for improved handling and solubility
- High purity (≈99.4%) suitable for in vitro research
- Orally bioactive nucleotide prodrug mechanism for antiviral studies
- Demonstrated activity against HCV and in vitro SARS-CoV-2 models
- Suitable for pharmacology and mechanism-of-action experiments
- Supplied in laboratory-scale sizes for research flexibility
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Bioworld AMPICILLIN HP
HP-Ampicillin eliminates the problem of satellite or background colonies, even after a prolonged incubation (2-4 days) or the plating of competent cells at 20 fold higher density. -Lactamase secreted into the medium from ampicillin-resi...
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Medchemexpress LLC 2',5'-dideoxyadenosine | 6698-26-6 | MFCD00210904 | 99.9% | C10H13N5O2 | 10MG
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2',5'-Dideoxyadenosine is a nucleoside analog and a potent, non-competitive inhibitor of adenylyl cyclase that binds the P-site. It is used as a research reagent to probe cAMP signaling, adenylyl cyclase activity, and downstream phosphorylation events in vitro and in vivo. Supplied as a solid with high purity and recommended storage for stability.
- Potent, non-competitive adenylyl cyclase inhibitor (IC50 = 3 μM).
- Reduces cAMP production and modulates phosphorylation of signaling proteins such as GluA1 and Akt.
- Effective in vitro and in vivo for studying antiadrenergic and diuretic/natriuretic responses.
- High purity suitable for biochemical and cell-based assays.
- Stable when stored as powder at recommended temperatures for extended periods.
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Medchemexpress LLC Geldanamycin-FITC | 2969156-01-0 | MFCD32068377 | 98.4% | 1,034.18 g·mol⁻¹ | C55H63N5O13S | 5 MG
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Geldanamycin-FITC is a fluorescently labeled geldanamycin derivative used as a probe for Hsp90-binding studies, fluorescence polarization assays, and cellular imaging. It is supplied as a light brown solid of high purity intended for research applications requiring a fluorescent Hsp90 ligand.
- High purity (98.43%) for reliable assay results.
- Emission at ~515 nm suitable for fluorescence detection.
- Soluble in DMSO at 25 mg/mL; may require ultrasonication.
- Light brown solid; store protected from light and at low temperature.
- Suitable for Hsp90 binding assays, fluorescence polarization, and cellular imaging.
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Bioworld Amphotericin B (FUNGIZONE) (100X), 100 mL
Amphotericin B is one of the earliest compounds designed to kill fungi. It acts by forming channels in fungal membranes, causing the cells to become leaky. It is toxic to eukaryotic cells in culture. Thus, very low doses are recommended. Typical concentrations in media range from 0.5 to 2.5 µg/mL. High concentrations of amphotericin B solution (FUNGIZONE) are not recommended for routine prophylactic use.SpecificationsSterile-filteredConcentration: 250µg/mlRecommended use: 10ml/LStability: It is stable at 2-8°C for 3 - 4 weeks and at 37°C for 3-5 days. Avoid freeze thaw cycles. Don't expose to light.RTECS Number: BU2625000
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Selleck Chemical LLC Tanespimycin (17-AAG) S1141-5mg
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Tanespimycin (17-AAG CP127374 NSC-330507 KOS 953) is a potent HSP90 inhibitor with IC50 of 5 nM in a cell-free assay having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells Tanespimycin (17-AAG) induces apoptosis necrosis autophagy and mitophagy Phase 3
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Research Products International Corp Anisomycin, 100 MG
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Anisomycin is an antibiotic derived from Streptomyces griseolus. It inhibits protein synthesis in eukaryotic cells by blocking the peptidyl transferase activity of the 60S ribosomal subunit. This interference disrupts the elongation phase of protein synthesis, leading to the inhibition of new protein formation.
Anisomycin is widely used as a tool in cell biology and biochemistry to study cellular responses to stress, apoptosis, and various signaling pathways. Its ability to selectively inhibit protein synthesis allows researchers to investigate the role of specific proteins in cellular processes. Anisomycin induces cellular stress and activates various stress response pathways, making it valuable in studies focused on understanding how cells respond to environmental challenges.
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Research Products International Corp Phleomycin 20mg/ml Solution, 1 ML
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Phleomycin is an antibiotic and antitumor agent commonly used in molecular biology and life science research. It is known for its ability to cleave DNA, making it useful for studies involving DNA damage and repair mechanisms.
Phleomycin 20mg/ml Solution is a formulation often employed in molecular biology experiments to induce controlled DNA damage in cells. Phleomycin accomplishes this by causing single- and double-strand breaks in DNA, making it a valuable tool for investigating cellular responses to DNA damage and the mechanisms involved in DNA repair.
Researchers may use Phleomycin 20mg/ml Solution to study the impact of DNA damage on cellular processes, gene expression, and other aspects of molecular biology.
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