Halophenols
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Filtered Search Results
Medchemexpress LLC 2',4',6'-Trimethoxyacetophenone | 832-58-6 | 210.23 | 10 G
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2',4',6'-Trimethoxyacetophenone (2,4,6-Trimethoxyphenyl methyl ketone) is a Diterpenoids product that can be isolated from the herbs of Chloranthus elatior.
- Exhibits cytotoxicity against human A549 cells (IC50 9.8 μM)
- Exhibits cytotoxicity against HeLa cells (IC50 3.8 μM)
- Exhibits cytotoxicity against MIA PaCa-2 cells (IC50 14.3 μM)
- Exhibits cytotoxicity against U-937 cells (IC50 7.2 μM)
- Shows cytotoxicity against human HCT-116 and REH cells with an IC50 > 20 μM
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Cambridge Isotope Laboratories Fluoranthene (D10 98%) 0 1 g
Fluoranthene (D10 98%) 0 1 g
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Medchemexpress LLC Ferrous bisglycinate | 20150-34-9 | 98.0% | 100 G
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Ferrous bisglycinate is an orally active iron fortificant and therapeutic iron supplement. It can be used for the research of iron deficiency anemia.
- Does not affect Caco-2 cells viability (at 25-200 μM).
- Increases ferritin content in Caco-2 cells.
- Exerts a protective effect on colitis in mice.
- Demonstrated best survival rates (100%) in a colitis animal model.
- Caused the least body loss (9%) in a colitis animal model.
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Medchemexpress LLC 8-Azabicyclo[3.2.1]octan-3-ol, 8-methyl-, (3-endo)- | 120-29-6 | 100 G
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Tropine is a tropane alkaloid that serves as a crucial intermediate for synthesizing anticholinergics and bronchodilators such as Atropine and Scopolamine. It is naturally found in Solanaceae Plants and *Przewalskia tangutica Maximo*.
- Important intermediate for synthesis of anticholinergics and bronchodilators
- Suitable for research and analytical applications
- Appearance: white to light yellow solid
- Purity (GC): 99.26%
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Medchemexpress LLC Dimedone (5,5-dimethylcyclohexane-1,3-dione) | 126-81-8 | MFCD00001588 | 99.7% | 140.18 g/mol | C8H12O2 | 100 G
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Dimedone (5,5-dimethylcyclohexane-1,3-dione) is an organic biochemical reagent used in laboratory research. It is commonly employed as a nucleophilic trapping agent for sulfenic acids and as a building block in organic synthesis. Supplied as a high-purity solid, it is intended for research use and analytical characterization.
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Apexbio Technology LLC Conivaptan HCl 168626-94-6 10mM (in 1mL DMSO)
Conivaptan Hydrochloride (CAS 168626-94-6) is a non-peptide antagonist of the antidiuretic hormone vasopressin It selectively inhibits vasopressin V1A and V2 receptors thereby blocking vasopressin-mediated water reabsorption in renal collecting ducts This action promotes aquaresis without affecting sodium or potassium excretion Conivaptan Hydrochloride is utilized in biomedical research to investigate pathways involved in fluid balance sodium homeostasis and cardiovascular dysfunction including models of congestive heart failure and disorders of hyponatremia
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Medchemexpress LLC N-[2-hydroxy-3-(1-piperidinyl)propoxy]-3-pyridinecarboximidamide dihydrochloride | 66611-37-8 | 98.0% | 351.27 g/mol | C14H24Cl2N4O2 | 1 ML
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BGP-15 is a small-molecule poly(ADP-ribose) polymerase (PARP) inhibitor for research use, characterized in the literature for cytoprotective and insulin-sensitizing effects. It is available as a ready-to-use solution or as solid material and is commonly used to probe PARP-related pathways in biochemical and cellular studies.
- Available as 10 mM solution in DMSO (1 mL) and as solid quantities.
- Demonstrates PARP inhibition with IC50 = 120 μM and Ki = 57 μM.
- High purity, 98.0% by HPLC.
- Molecular weight approximately 351.27 g/mol.
- CAS number 66611-37-8 for unambiguous identification.
- Suitable for biochemical and cell-based research applications.
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Ambeed AMBEED
5000883664 ENBUCRILATE 25G
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Cayman Chemical 6-Bromo-2-oxIndole 5g
A secondary metabolite used in the synthesis of bioactive compounds; cytotoxic to MDA-MB-231 breast cancer cells (IC50 = 74.41 µM); has been used in the synthesis of anti-inflammatory p38α inhibitors
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Apexbio Technology LLC Butenafine HCl 101827-46-7 5g
Butenafine HCl (CAS 101827-46-7) is a small-molecule inhibitor targeting squalene epoxidase It is designed to inhibit this enzyme thereby disrupting fungal sterol biosynthesis Butenafine HCl exerts its biological activity primarily through inhibition of squalene epoxidase leading to impaired ergosterol synthesis and accumulation of squalene which disrupts fungal cell membrane integrity and results in cell death In biochemical studies Butenafine HCl demonstrates inhibitory activity with reported IC50 values ranging from approximately 0 03 M to 0 1 M depending on fungal species and experimental conditions Based on these pharmacological properties Butenafine HCl holds research potential in biomedical antifungal studies including investigations into fungal physiology antifungal efficacy and drug resistance mechanisms
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eMolecules 4009-98-7 | (Methoxymethyl)triphenylphosphonium chloride | Combi-Blocks | MFCD00011800 | 342.800 | C20H20ClOP | 98.000 | [Cl-].COC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 | 1kg | 335343585
(Methoxymethyl)triphenylphosphonium chloride | Combi-Blocks | 4009-98-7 | MFCD00011800 | 342.800 | C20H20ClOP | 98.000 | [Cl-].COC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 | 1kg | 335343585
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Ambeed AMBEED
5000867602 2-CHLORO-6-IODOPHENOL 1GR
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Medchemexpress LLC 500 BP DNA MARKER 1ML | 1 ML
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The 500 bp DNA Marker is provided in a solution of 1x DNA Loading Buffer and can be directly used for nucleic acid electrophoresis analysis. It contains 14 double-stranded DNA fragments ranging from 500 bp to 5000 bp.
- Contains 14 double-stranded DNA fragments.
- Suitable for nucleic acid electrophoresis analysis.
- Each 5 μL contains approximately 100 ng for the 2500 bp band and 40 ng for other bands.
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Medchemexpress LLC Benzoxonium chloride | 19379-90-9 | 99.7% | 500 MG
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Benzoxonium chloride is an anti-leishmanial agent that inhibits bacteria, certain protozoa, yeasts, and non-spore-forming organisms. It is an analytical standard intended for research and analytical applications.
- Anti-leishmanial agent
- Inhibits bacteria
- Inhibits certain protozoa
- Inhibits yeasts
- Inhibits non-spore-forming organisms
- Analytical standard
- Intended for research and analytical applications
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Medchemexpress LLC Sitaxsentan sodium | 210421-74-2 | 98.8% | 476.89 | 500 MG
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Sitaxsentan sodium is a potent, selective, and orally active endothelin A receptor (ETA) antagonist. It is suitable for pulmonary arterial hypertension (PAH) studies and can significantly alleviate PAH symptoms by inhibiting ET-1-induced phosphoinositide turnover.
- Potent and selective ETA receptor antagonist
- Inhibits ET-1-induced phosphoinositide turnover
- Alleviates pulmonary arterial hypertension symptoms
- Suitable for PAH research studies
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