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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Q SepharoseR Xl Cytiva 17
Q Sepharose(R) XL is a strong anion exchanger designed for use in the capture steps of biomolecules from clarified feed-stocks.Q Sepharose(R) XL is based on a highly cross-linked bead formed 6% agarose matrix similar to the well established Q Sepharose(R) Fast Flow media. Dextran chains are covalently coupled to the agarose matrix and modified with quaternary ammonium (Q) strong anion exchange groups through chemically stable ether bonds. The stable agarose matrix and long flexible chains of dextran with bound charged groups work together to increase loading capacity whilst allowing high flow rates.With its high loading capacities and excellent physical and chemical stability Q Sepharose(R) XL is suitable for the capture stage of a downstream process which is characterised by large loads of crude samples.As member of the BioProcess media range Q Sepharose(R) XL meets industrial demands with security of supply and comprehensive technical and regulatory support.
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eMolecules 58794-09-5 | 7-bromoisoquinoline | AA Blocks LLC | MFCD07368661 | 208.058 | C9H6BrN | 0.000 | Brc1ccc2ccncc2c1 | 2g | 795063184
7-bromoisoquinoline | AA Blocks LLC | 58794-09-5 | MFCD07368661 | 208.058 | C9H6BrN | 0.000 | Brc1ccc2ccncc2c1 | 2g | 795063184
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Sigma Aldrich Fine Chemicals Biosciences Ciprofloxacin hydrochloride European Pharmacopoeia (EP) Reference Standard | 86393-32-0 | MFCD00242856 |
Ciprofloxacin hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 385.82 | 86393-32-0 | MFCD00242856 |
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Apexbio Technology LLC Resiquimod (R-848) 144875-48-9 100mg
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Resiquimod (R-848) is an immunomodulatory small molecule structurally related to imiquimod It functions primarily by activating immune responses via inducing cytokine release In vitro studies with human peripheral blood mononuclear cells (PBMC) indicate that Resiquimod promotes dose-dependent production of cytokines including interferon-alpha (IFN- ) tumor necrosis factor (TNF) interleukin-1 (IL-1 ) and interleukin-6 (IL-6) Mechanistically Resiquimod increases intracellular IL-1 levels and both monocytes and B-cells respond by secreting IFN upon stimulation In addition it elevates mRNA expression of IFN- TNF and IL-8 in treated PBMC relative to untreated controls Resiquimod demonstrates antiviral and antitumor activities in preclinical animal models frequently utilized as an immune response potentiator and Toll-like receptor (TLR) agonist in biomedical investigations (IC50 values typically range in low micromolar)
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Medchemexpress LLC Quinine hydrochloride dihydrate | 6119-47-7 | 99.7% | 10 G
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Quinine hydrochloride dihydrate is an orally active compound primarily used in anti-malarial studies. It functions as a potassium channel inhibitor, specifically targeting WT mouse Slo3 (KCa5.1) channel currents. This compound has also demonstrated effects against Dengue virus proliferation in HepG2 cell lines and exhibited some tumor-suppressing activity in skin cancer models.
- Acts as a potassium channel inhibitor
- Inhibits WT mouse Slo3 (KCa5.1) channel currents
- Inhibits DENV proliferation and cytostatic effects in HepG2 cell lines
- Reduces viral DENV RNA and protein levels
- Shows tumor-suppressing effects on skin cancer in mice
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Medchemexpress LLC Quin-C7 | 871100-12-8
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Quin-C7 | 871100-12-8
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Apexbio Technology LLC APEXBIO TECHNOLOGY LLC
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5000569993 DANSYL-CHLORIDE-200MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000760361 2 5 -DIMETHOXY-1 1 100MG
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Ambeed AMBEED
5000847698 7-NITROQUINOLINE 250MG
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Medchemexpress LLC Hydroquinidine | 1435-55-8 | 99.9% | 1 ML
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Hydroquinidine (Dihydroquinidine) is a potent ion channel blocker that demonstrates strong anti-cancer activity against colon, pancreatic, and hepatocellular cancer cells. It also prolongs the QT interval and possesses antiarrhythmic efficacy.
- Potent ion channel blocker
- Exhibits strong anti-cancer activity on colon, pancreatic, and hepatocellular cancer cells
- Prolongs the QT interval
- Possesses antiarrhythmic efficacy
- For research use only
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eMolecules 957486-82-7 | Azido-PEG6-amine | ChemScene | MFCD03453240 | 350.416 | C14H30N4O6 | 97.000 | NCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] | 500mg | 632318427
Azido-PEG6-amine | ChemScene | 957486-82-7 | MFCD03453240 | 350.416 | C14H30N4O6 | 97.000 | NCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] | 500mg | 632318427
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eMolecules 1805137-37-4 | 3-Bromo-2-chloro-4-(difluoromethoxy)pyridine | MFCD28733844 | 250mg
Ambeed | (4S4S)-22-(23-Dihydro-1H-indene-22-diyl)bis(4-(tert-butyl)-45-dihydrooxazole) | 100mg | 633659832 | A1220210 | 2757082-06-5 | 368.521 | C23H32N2O2
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Ambeed 3Chloro5nitrobenzoic acid
3-Chloro-5-nitrobenzoic acid, 34662-36-7, 98%
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Medchemexpress LLC Bromocriptine mesylate | 22260-51-1 | 99.90% | 1 ML
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Bromocriptine mesylate is a potent dopamine D2/D3 receptor agonist that readily crosses the blood-brain barrier. It stimulates [35S]-GTPγS binding at the D2 dopamine receptor expressed in CHO cells with a pEC50 of 8.15±0.05. It also acts as a strong inhibitor of brain nitric oxide synthase and a potent inhibitor of CYP3A4.
- It is a potent dopamine D2/D3 receptor agonist.
- It is permeable to the blood-brain barrier.
- It shows significant anti-immobility action in experimental models of depression.
- It induces a significant, dose-dependent decrease in pain scores in specific models.
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Aobchem AOBCHEM
5000906168 N- 2-FLUORO-4- 4 4 5 5-TETRAME
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