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Filtered Search Results
Medchemexpress LLC Yeast peptone dextrose | 25 G
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Yeast peptone dextrose is a common and nutrient-rich culture medium composed of yeast extract, peptone, and dextrose, primarily used for cultivating yeast in research settings.
- Composed of yeast extract, peptone, and dextrose.
- Nutrient-rich medium.
- Primarily for cultivating yeast.
- For research use only.
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Cayman Chemical 8piperazin1ylIsoquinoline hy
A synthetic intermediate useful for pharmaceutical synthesis.
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Medchemexpress LLC 5-(1,3-benzodioxol-5-ylmethylene)-2,4-thiazolidinedione | 6318-41-8 | MFCD18382117 | 99.0% | 249.24 g/mol | C11H7NO4S | 1 ML
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AS-041164 is a potent, selective, orally active PI3Kγ inhibitor supplied either as a ready-to-use solution (10 mM in DMSO, 1 mL) or as a solid in multiple mg sizes for research applications investigating PI3Kγ signaling and inflammatory responses.
- Potent, selective PI3Kγ inhibition with IC50 ≈ 70 nM.
- Available as 10 mM solution (1 mL) or solids in multiple milligram sizes.
- High purity (≈99.0%) suitable for research use.
- Soluble in DMSO, convenient for in vitro assays.
- Store protected from light; in solvent conditions extend stability at low temperatures.
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Medchemexpress LLC 4-[(3aS,4R,9bR)-6-ethoxy-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinolin-4-yl]benzoic acid | 1357248-83-9 | 98.7% | 335.40 g/mol | C21H21NO3 | 10MM 1ML
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LIN28 inhibitor LI71 is a research small-molecule inhibitor that disrupts LIN28:let-7 binding and LIN28-mediated oligouridylation. It is used in LIN28-driven cancer research and related biochemical studies, and has demonstrated activity against Plasmodium falciparum cold shock protein interactions. Available as a 10 mM solution in DMSO and as multiple solid pack sizes.
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Apexbio Technology LLC MGCD-265 875337-44-3 10mM (in 1mL DMSO)
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MGCD-265 (CAS 875337-44-3) is a multi-targeted ATP-competitive small molecule inhibitor primarily targeting c-Met and the vascular endothelial growth factor receptors VEGFR1 VEGFR2 and VEGFR3 with IC50 values of 1 nM 3 nM 3 nM and 4 nM respectively In preclinical non-small cell lung cancer (NSCLC) xenograft models including models with TKI-resistant EGFR T790M mutations MGCD-265 in combination with agents such as paclitaxel docetaxel or erlotinib demonstrated enhanced antitumor activity and antiangiogenic effects compared to monotherapy MGCD-265 has been investigated in phase I clinical trials as a single agent and in combination with docetaxel or erlotinib in patients with advanced solid tumors
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TARGETMOL CHEMICALS INC I-191 2MG
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Also available in 1 mL, 1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. I-191 is a potent antagonist of protease-activated receptor 2 (PAR2), inhibits multiple signaling functions in human cancer cells. Purity 99.8%
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Medchemexpress LLC Norverapamil hydrochloride | 67812-42-4 | MFCD00078605 | 99.8% | 477.04 g/mol | C26H37ClN2O4 | 100 MG
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Norverapamil hydrochloride is the N-demethylated metabolite of verapamil. It functions as an L-type calcium channel blocker and a P-glycoprotein (P-gp) function inhibitor and is supplied for research use in solid form or as a DMSO solution.
- High purity: 99.8% for reliable experimental results.
- White to off-white solid for easy handling.
- Soluble in water (≥50 mg/mL) and DMSO (≥31 mg/mL) for formulation flexibility.
- Stable when stored sealed at 4°C; in solvent store -80°C (6 months) or -20°C (1 month).
- Suitable as a research reagent for studies of calcium channel modulation and P-gp function.
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Medchemexpress LLC Asimadoline hydrochloride | 185951-07-9 | 99.6% | 451.00 | 5 MG
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Asimadoline hydrochloride is an orally active, selective, and peripherally active κ-opioid agonist. It demonstrates low permeability across the blood-brain barrier and exhibits peripheral anti-inflammatory actions. Research indicates its potential for treating irritable bowel syndrome (IBS) and ameliorating allodynia in diabetic rats.
- Orally active and selective κ-opioid agonist
- Low permeability across the blood-brain barrier
- Exhibits peripheral anti-inflammatory actions
- Potential for irritable bowel syndrome treatment
- Ameliorates allodynia in diabetic rats
- Rapid metabolism across species
- Highly selective for κ-opioid receptors
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Medchemexpress LLC N-(3-tert-butyl-4-hydroxyphenyl)-2,6-dichloro-4-(cyclopentylamino)benzamide HCl | 100.0% | 457.82 | 25 MG
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FXR antagonist 2 hydrochloride is a chemical compound that functions as an FXR antagonist.
- Functions as an FXR antagonist
- Tested to comply with given specifications
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Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC
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5000587295 CD62E/E-SELECTIN F3A3Z RABBIT
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Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC
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5000587303 F4/80 D2S9R RABBIT MONOCLONAL
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Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC
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5000587680 BETA3-TUBULIN D71G9 RABBIT MON
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Cell Signaling Technology CELL SIGNALING TECHNOLOGY INC
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5000587223 TOTAL CDK5 MATCHED ANTIBODY PA
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371492 - -U-50488 HYDROCH 25MG
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Apexbio Technology LLC eukaryotic translation elongation factor 1 alpha 1 (EEF1A1) (387-394) [Multiple species] 5mg
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eukaryotic translation elongation factor 1 alpha 1 EEF1A1 387-394 is a peptide fragment derived from EEF1A1 a protein centrally involved in protein synthesis by delivering aminoacyl-tRNAs to the ribosome This conserved peptide segment (LEU-GLU-ASP-GLY-PRO-LYS-PHE-LEU residues 387 394) is widely expressed across multiple species and serves as a reference antigen in biomedical research for studying autoimmune responses in certain diseases Based on these properties eukaryotic translation elongation factor 1 alpha 1 EEF1A1 387-394 is employed as a molecular tool to investigate translational regulation-associated cell death mechanisms and the immunological aspects of EEF1A1-related pathologies
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