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Filtered Search Results
Ambeed AMBEED
5000867733 3-BROMO-2-METHOXYQUINOLI 100MG
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Medchemexpress LLC PF-00356231 hydrochloride | 820223-77-6 | 99.0% | 464.96 | 100 MG
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PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12 (IC50=1.4 μM). It binds to MMP-12, forming a PF-00356231/MMP-12 complex. This compound also demonstrates potency against MMP-13, MMP-8, MMP-9, and MMP-3 with IC50 values of 0.00065, 1.7, 0.98, and 0.39 μM, respectively. It is intended for research use only.
- Specific inhibitor of matrix metalloproteinase MMP-12.
- Non-peptidic and non-zinc chelating ligand.
- Potency against MMP-13, MMP-8, MMP-9, and MMP-3.
- Available in solid and solution forms.
- Can be stored at 4°C (sealed, away from moisture) or -80°C/-20°C in solvent.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000371729 NUTRIENT BROTH 250G
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Medchemexpress LLC 5-Bromo-3-methylpyridin-2-ol | 89488-30-2 | 99.7% | C6H6BrNO | 10 G
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5-Bromo-3-methylpyridin-2(1H)-one is a biochemical reagent intended for life science research. This compound appears as a white to off-white solid with a molecular weight of 188.02 and a chemical formula of C6H6BrNO.
- High purity for research applications
- Biochemical reagent for life science research
- White to off-white solid appearance
- Stable as powder at -20°C for 3 years or 4°C for 2 years
- Stable in solvent at -80°C for 6 months or -20°C for 1 month
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Medchemexpress LLC 2-phenylmelatonin | 151889-03-1 | MFCD00673896 | 99.2% | 308.37 g/mol | C19H20N2O2 | 10 MG
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UCM 608 (2-Phenylmelatonin) is a high-affinity melatonin (MT) receptor agonist supplied as a purified solid for laboratory research. It binds MT1 and MT2 receptors with reported pKi values of 10.7 and 10.4, respectively, and is used in pharmacology and receptor-binding studies. Handle and store according to safety data and laboratory protocols.
- High affinity for MT1 and MT2 receptors.
- Reported pKi values: MT1 10.7, MT2 10.4.
- Molecular formula C19H20N2O2.
- Molecular weight 308.37 g/mol.
- Purity approximately 99.18% (reported).
- Solid, off-white to yellow appearance.
- Store powder at -20°C or 4°C per stability guidance.
- Intended for research use only.
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Medchemexpress LLC NOTA-P2-RM26 | 1446005-10-2 | 97.2% | 1543.76 | 1 MG
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NOTA-P2-RM26 is an antagonist of bombesin analogs. It targets the gastrin-releasing peptide receptor (GRPR/BB2), which is a molecular target for prostate cancer visualization. This product is utilized in imaging studies for prostate cancer using PET and SPECT/CT, where it is labeled with 111In and 68Ga.
- Antagonist of bombesin analogs
- Targets gastrin-releasing peptide receptor (GRPR/BB2)
- Used in prostate cancer imaging studies
- Can be labeled with 111In and 68Ga for PET and SPECT/CT applications
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Medchemexpress LLC Methoxyamiodarone im 5g | 5G
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Methoxyamiodarone im 5g | 5G
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Ambeed AMBEED
5000868808 6-BROMO-3-CHLOROISOQUINOLI 1GR
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Apexbio Technology LLC Imidapril HCl 89396-94-1 10mM (in 1mL DMSO)
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Imidapril hydrochloride (CAS 89396-94-1) is a synthetic angiotensin-converting enzyme (ACE) inhibitor that interrupts the renin-angiotensin-aldosterone system by preventing the conversion of angiotensin I to angiotensin II This inhibition leads to vasodilation and a reduction in blood pressure and has been associated with improvements in cardiac function Imidapril HCl is extensively utilized in biomedical research to investigate the molecular mechanisms underlying hypertension and chronic heart failure as well as to evaluate ACE inhibition in various experimental models
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431832 S -N-GLYCIDYLPHTHAL 100G
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Aobchem AOBCHEM
5000862546 4-HYDROXY-2-PHENYL-2-HYDROPHTH
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Apexbio Technology LLC Olsalazine Sodium 6054-98-4 10mM (in 1mL H2O)
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Olsalazine Sodium (CAS 6054-98-4) is a small-molecule anti-inflammatory agent It is designed to modulate inflammatory pathways thereby reducing the production of local inflammatory mediators Olsalazine Sodium exerts its biological activity primarily through inhibition of prostaglandin and leukotriene synthesis pathways after biotransformation by gut microbiota into 5-aminosalicylic acid (5-ASA) In experimental settings researchers employ olsalazine sodium to investigate disease mechanisms underlying colonic inflammation and to evaluate therapeutic responses in models of intestinal inflammation Currently precise IC50 values for olsalazine sodium have not been reported in the literature Based on these pharmacological properties olsalazine sodium holds research potential in inflammatory bowel disease (IBD) especially ulcerative colitis
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Medchemexpress LLC ODN 21158 (sodium) | DNA, d(P-thio)(C-C-T-G-G-C-G-G-G-G), sodium salt | 1 MG
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ODN 21158 sodium is a potent G-modified TLR3 and TLR9 inhibitor that effectively inhibits IFN-α secretion in a dose-dependent manner. It is supplied as a solid, white to off-white colored compound.
- Potent G-modified TLR3 and TLR9 inhibitor
- Inhibits IFN-α secretion
- Supplied as a solid, white to off-white powder
- Recommended storage for solid at -20°C, sealed and away from moisture. In solvent, store at -80°C for up to 6 months or -20°C for 1 month.
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Aobchem AOBCHEM
5000863566 5-BROMO-3-METHYL-2- 2 2 2-TRIF
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Aobchem AOBCHEM
5000862930 1-BROMO-3- 2-METHYLPROPOXY BEN
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