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Filtered Search Results
Ethos Biosciences Quick I Red, 16oz, Ethos
ready-to-use, two-step, staining solution replicating Wright Stain designed for hematology and cytology. Commonly used for rapid staining of peripheral blood smears and bone marrow specimens, it provides clear differentiation of cellular components for reliable microscopic evaluation. The formulation delivers consistent color intensity and rapid results, making it ideal for routine diagnostic workflows and high-throughput laboratories. Suitable for clinical, research, and educational settings, Quick I Red supports accurate cell morphology assessment and dependable staining performance.
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Chemscene CHEMSCENE
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5000577686 2-BROMO-1 3-DIMETHOXYBENZEN 5G
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Medchemexpress LLC Bromo-PEG1-CH2COOH | 1135131-50-8 | ≥97.0% | 1 G
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Bromo-PEG1-CH2COOH is a PROTAC linker that can be used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PROTAC linker for synthesis of PROTACs
- Exploits intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
- For research use only
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Medchemexpress LLC Milnacipran hydrochloride | 101152-94-7 | 99.7% | 10 MM x 1 ML
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Milnacipran hydrochloride is an orally active Serotonin and Norepinephrine reuptake inhibitor. It inhibits monoamine transporters, specifically the norepinephrine transporter and the serotonin transporter (Ki values of 31 and 8.5 nM, respectively). It also inhibits pERK1/2 activation.
- Antidepressant, anxiolytic, and analgesic properties.
- Inhibits biting behavior in mice.
- Can be used in the study of major depressive disorder, anxiety disorders, and neuropathic pain (e.g., fibromyalgia).
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Medchemexpress LLC LX-1031 | 945976-76-1 | 99.14% | 1 ML
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LX-1031 is a potent, orally available tryptophan 5-hydroxylase (TPH) inhibitor that reduces serotonin (5-HT) synthesis peripherally.
- Potent and orally available: effective when administered orally.
- Peripheral serotonin reduction: specifically reduces serotonin (5-HT) synthesis in the periphery, without affecting brain 5-HT levels.
- Reversible effects: in mice, the effects on jejunal mucosa 5-HT levels were reversible within 2 days of discontinuation.
- Research use only: this product is intended for research use only and is not for sale to patients.
- Clinical trial information: has been investigated in a Phase 2 clinical trial (NCT00813098) for Irritable Bowel Syndrome.
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Medchemexpress LLC Rimantadine hydrochloride | 1501-84-4 | 98.0% | 5 G
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Rimantadine hydrochloride is an orally active inhibitor for M2 protein, designed for research applications. It functions by blocking hydrogen ion channel activity, thereby preventing viral entry and replication, and demonstrating broad-spectrum antiviral effects. This compound is intended for research use only.
- Orally active M2 protein inhibitor
- Blocks hydrogen ion channel activity
- Prevents virus entry and replication
- Exhibits broad-spectrum antiviral activity
- Inhibits RNA levels of hepatitis A virus (HAV) in Huh7 and IHH cells
- Induces autophagy in HAV-infected Huh7 cells
- Exhibits anti-infectious activity in H3N2-infected mouse models
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Medchemexpress LLC Allylthiourea (Thiosinamine) | 109-57-9 | 99.95% | 100 G
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Allylthiourea can selectively inhibit the oxidation of ammonia. It is commonly used to inhibit nitrification by targeting ammonia monooxygenase and chelating copper in the active site to suppress its activity. Allylthiourea also exhibits anticancer activity, showing cytotoxicity against the MCF-7 cell line with an IC50 of 5.22 mM. It can be utilized in research related to micropollutant biodegradability and cancer studies.
- Selectively inhibits ammonia oxidizers.
- Decreases intracellular copper in *Methylosinus trichosporium* OB3b.
- Used to inhibit nitrification by targeting ammonia monooxygenase.
- Exhibits cytotoxicity against MCF-7 cell line.
- Useful for micropollutant biodegradability and cancer studies.
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Medchemexpress LLC Copper(II) oxalate | 814-91-5 | MFCD00064789 | 98.0% | 151.56 g/mol | C2CuO4 | 25 G
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Copperoxalate (Copper(II) oxalate, C2CuO4) is an inorganic copper salt supplied as a blue to blue-green solid and used as a reagent in research and synthesis. It provides a stable source of Cu(II) for catalysis, materials preparation, and laboratory studies, and is offered in small laboratory packaging for analytical and preparative work.
- Blue to blue-green solid and stable source of Cu(II).
- Suitable for catalysis and materials synthesis applications.
- Appropriate for laboratory reagent and analytical use.
- Molecular formula C2CuO4; molecular weight 151.56 g/mol.
- Supplied in 25 G packaging; typical purity 98%.
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eMolecules 617-86-7 | Triethylsilane | Oakwood Chemicals | MFCD00009018 | 116.279 | C6H16Si | 99.000 | CC[SiH](CC)CC | 500g | 480104455
Triethylsilane | Oakwood Chemicals | 617-86-7 | MFCD00009018 | 116.279 | C6H16Si | 99.000 | CC[SiH](CC)CC | 500g | 480104455
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Medchemexpress LLC Ethambutol dihydrochloride | 1070-11-7 | 99.9% | 100 MG
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Ethambutol dihydrochloride is an antimycobacterial compound that prevents cell wall formation by inhibiting arabinosyltransferase activity. It can be used to establish animal models of hyperuricemia and optic neuropathy.
- Prevents cell wall formation by inhibiting arabinosyltransferase activity.
- Can be used to establish animal models of hyperuricemia.
- Can be used to establish animal models of optic neuropathy.
- Increases uric acid levels by reducing renal uric acid clearance in hyperuricemia models.
- Induction of hyperuricemia is often combined with adenine for better model construction.
- Induction of optic neuropathy involves oral administration at specific doses and durations.
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eMolecules 56-81-5 | Glycerin | Oakwood Chemicals | MFCD00004722 | 92.094 | C3H8O3 | 99.000 | OCC(O)CO | 1kg | 480144972
Glycerin | Oakwood Chemicals | 56-81-5 | MFCD00004722 | 92.094 | C3H8O3 | 99.000 | OCC(O)CO | 1kg | 480144972
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Medchemexpress LLC Succinimide (pyrrolidine-2,5-dione) | 123-56-8 | 99.9% | 99.09 | 25 G
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Succinimide rapidly hydrolyzes into aspartic acid during the reduction/alkylation process. It is utilized in the development of antiepileptic agents.
- High purity: available at 99.92% purity.
- Research use: intended for research purposes.
- Solubility: soluble in DMSO (100 mg/mL), with specific protocols for in vivo dissolution using co-solvents like PEG300, Tween-80, and Saline, or SBE-β-CD in Saline, or Corn Oil.
- Stability: powder form is stable for 3 years at -20°C and 2 years at 4°C. In solvent, it's stable for 6 months at -80°C and 1 month at -20°C.
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Ambeed AMBEED
5000846752 Z -1 2-BIS PHENYLSULFON 25G
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Ambeed AMBEED
5000846758 3-BROMO-5-METHOXYBENZAL 100G
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Medchemexpress LLC SAG-524 | 2246696-89-7 | 98.5% | 594.12 g·mol⁻1 | C30H32ClN5O4S | 10 MG
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SAG-524 is a novel, orally bioavailable small-molecule inhibitor of hepatitis B virus (HBV) replication that destabilizes HBV RNA. In cell-based assays it reduced extracellular HBV-DNA and HBsAg levels with IC50 values of 0.92 nM and 1.4 nM, respectively. It is supplied as a high-purity research solid for in vitro studies.
- Potent HBV RNA destabilizer reducing HBV-DNA and HBsAg (IC50 0.92 nM and 1.4 nM).
- Orally bioavailable small molecule suitable for preclinical research.
- High purity (98.5%).
- Provided as a 10 mg solid for research use.
- Key identifiers: CAS 2246696-89-7; molecular formula C30H32ClN5O4S; molecular weight 594.12 g·mol⁻1.
- Not intended for human or veterinary use; for laboratory research only.
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