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Filtered Search Results
eMolecules Oakwood Chemicals Triethylsilane 25g 480104453 005243 617-86-7 MFCD00009018 116.279 C6H16Si
Oakwood Chemicals Triethylsilane 25g 480104453 005243 617-86-7 MFCD00009018 116.279 C6H16Si
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000746738 DDGTP TRISODIUM 1 50UL
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5000723801 PTEROSTILBENE GLUCOS 25G
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Medchemexpress LLC E-Selectin/CD62E Hu 10ug
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E-selectin/CD62E Protein a cell-surface glycoprotein crucially mediates immunoadhesion by interacting with SELPLG/PSGL1 for the adhesion of neutrophils to cytokine-activated endothelium It also potentially influences capillary morphogenesis and interacts with SELPLG/PSGL1 and PODXL2 through the sialyl Lewis X epitope independently of SELPLG sulfation E-Selectin/CD62E Protein Human (HEK293 His-Fc) is the recombinant human-derived E-Selectin/CD62E protein expressed by HEK293 with C-hFc C-His labeled tag
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Medchemexpress LLC Prednisolone | 50-24-8 | MFCD00003649 | 99.9% | 25 G
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Prednisolone is a potent, orally active corticosteroid and a glucocorticoid. It exhibits approximately four times the anti-inflammatory activity of hydrocortisone while causing less salt and water retention. Prednisolone is suitable for ocular and anti-inflammatory research purposes.
- Potent, orally active corticosteroid and glucocorticoid.
- Exhibits anti-inflammatory activity, approximately four times that of hydrocortisone.
- Causes less salt and water retention.
- Suitable for ocular and anti-inflammatory research.
- Inhibits human leukocyte mitosis and prevents renal disease.
- Demonstrates agonist activity at human mineralocorticoid receptor.
- Involved in clinical trials for conditions such as metastatic cancer and and lupus nephritis.
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Medchemexpress LLC Tranylcypromine hydrochloride | 1986-47-6 | 99.9% | 169.66 | 100 MG
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Tranylcypromine hydrochloride is an irreversible inhibitor of lysine-specific demethylase 1 (LSD1/BHC110) and monoamine oxidase (MAO). It inhibits LSD1, MAO A, and MAO B with IC50s of 20.7, 2.3, and 0.95 μM, respectively, and can be used for the research of depression.
- Irreversible inhibitor of lysine-specific demethylase 1 and monoamine oxidase.
- Inhibits LSD1, MAO A, and MAO B with IC50s of 20.7, 2.3, and 0.95 μM, respectively.
- Used for research on depression.
- Inhibits histone and nucleosomal demethylation.
- Shows specific derepression of OCT4 transcription.
- Decreases LPS-mediated microglial activation and proinflammatory cytokine COX-2 and IL-6 levels in wild-type mice.
- Down-regulates Aβ-mediated microglial activation in 5xFAD mice.
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Medchemexpress LLC Diamthazole hydrochloride | 17140-69-1 | 99.9% | 329.89 | 25 MG
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Diamthazole (Dimazole) hydrochloride is an antifungal agent. It can be used for the research of infection and is intended for research use only.
- Antifungal agent
- Used for research of infection
- High purity
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Medchemexpress LLC N-Benzylhydroxylamin | 25G
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N-Benzylhydroxylamin | 25G
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Medchemexpress LLC Dithiooxamide | 79-40-3 | 99.9% | 120.20 | 100 G
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Dithiooxamide (Rubeanic Acid) is a selective chelating agent and sulfur-containing analog of Oxamide.
It forms stable chelates with various metal ions, which can be separated, enriched, and detected by adsorption on solid adsorbents or electrode surfaces.
- Selective chelating agent
- Sulfur-containing analog of Oxamide
- Forms stable chelates with metal ions (lead, iron, cadmium, manganese, aluminum)
- Chelates can be separated, enriched, and detected by adsorption on solid adsorbents or electrode surfaces
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eMolecules 111409-79-1 | (Bromoethynyl)triisopropylsilane | Ambeed | MFCD11036302 | 261.278 | C11H21BrSi | 98.000 | CC(C)[Si](C#CBr)(C(C)C)C(C)C | 25g | 595928668
(Bromoethynyl)triisopropylsilane | Ambeed | 111409-79-1 | MFCD11036302 | 261.278 | C11H21BrSi | 98.000 | CC(C)[Si](C#CBr)(C(C)C)C(C)C | 25g | 595928668
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Medchemexpress LLC 4-(1H-indol-4-yl)-N-phenylpiperazine-1-carboxamide | 882256-55-5 | MFCD00830676 | 99.8% | 320.39 g/mol | C19H20N4O | 10MM 1ML
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iGOT1-01 is a small-molecule inhibitor of aspartate aminotransferase 1 (GOT1) intended for research use. It is supplied as a ready-to-use 10 mM solution in DMSO (1 mL) and is also available as a solid in various sizes. Key identifiers include CAS 882256-55-5, molecular formula C19H20N4O, and molecular weight ~320.4 g/mol. Reported purity is approximately 99.77%.
- Potent GOT1 inhibitor suitable for biochemical and cell-based assays.
- Provided as a 10 mM solution in DMSO for immediate use.
- Also available as a solid for custom formulation and storage.
- High reported purity suitable for research applications.
- Stable under recommended storage conditions for powder and solvent forms.
- Contains CAS 882256-55-5 for unambiguous identification.
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Medchemexpress LLC KRAS G12C inhibitor 14 | 2349393-95-7 | 99.0% | 484.88 | C24H19ClF2N4O3 | 10MM 1ML
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KRAS G12C inhibitor 14 (Compound 17) is a potent small-molecule inhibitor selective for the KRAS G12C mutant (reported IC50 = 18 nM). It is supplied as a solid and as a 10 mM solution in DMSO for research use and is suitable for in vitro and in vivo studies of KRAS-driven signaling.
- Potency: IC50 = 18 nM against KRAS G12C.
- Molecular formula: C24H19ClF2N4O3; molecular weight: 484.88 g/mol.
- Purity: 99.0%.
- Available formats: solid (1 mg-500 mg) and 10 mM, 1 mL solution in DMSO.
- Solubility: DMSO 100 mg/mL; in vivo formulation yields ≥9 mg/mL in 10% DMSO/40% PEG300/5% Tween-80/45% saline.
- Storage: solid at -20°C; stock solution -80°C (6 months) or -20°C (1 month); protect from light and avoid repeated freeze-thaw.
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5000734882 LEVOGLUCOSAN 25G
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eMolecules 609-21-2 | 4-Amino-2,6-dibromophenol | MFCD00007874 | 1g
Combi-Blocks | 4-Amino-2,6-dibromophenol | 1g | 537621083 | OS-2353 | 95.000 | 609-21-2 | MFCD00007874 | 266.920 | C6H5Br2NO
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Medchemexpress LLC Resminostat (hydrochloride) | 1187075-34-8 | 99.67% | 385.87 | 25 MG
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Resminostat hydrochloride is a potent inhibitor of HDAC1, HDAC3, and HDAC6, with IC50 values in the nanomolar range. It is used for research applications and appears as a white to off-white solid. This compound shows less potent activity against HDAC8.
- Potent inhibitor of HDAC1, HDAC3, and HDAC6
- Exhibits less potent activity against HDAC8
- Induces histone acetylation in myeloma cells
- Inhibits cell growth and induces apoptosis in myeloma cells
- Synergistic activity with anti-myeloma agents
- Reduces viability of HCC cells when co-treated with AZD-2014
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