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Filtered Search Results
Apexbio Technology LLC PND-1186 10MM IN 1ML DMSO
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PND-1186 10MM IN 1ML DMSO APEXBIO TECHNOLOGIES
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eMolecules 4-(3-methoxypropoxy)phenylboronic acid | 279262-35-0 | MFCD12807145 | 1g
Combi-Blocks | 4-(3-methoxypropoxy)phenylboronic acid | 1g | 117529635 | FA-4162 | 98.000 | 279262-35-0 | MFCD12807145 | 210.040 | C10H15BO4
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eMolecules Medchem Express / TMPA / 2mg / 446269084 / HY-18555 / / 1258275-73-8 / MFCD28160842 / 380.481 / C21H32O6
Medchem Express / TMPA / 2mg / 446269084 / HY-18555 / / 1258275-73-8 / MFCD28160842 / 380.481 / C21H32O6
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eMolecules Medchem Express / iMDK / 5mg / 721434566 / HY-110171 / / 881970-80-5 / MFCD07528492 / 376.410 / C21H13FN2O2S
Medchem Express / iMDK / 5mg / 721434566 / HY-110171 / / 881970-80-5 / MFCD07528492 / 376.410 / C21H13FN2O2S
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Medchemexpress LLC N-[(3R,4S)-3-hydroxy-2,2-dimethyl-6-(4,4,4-trifluorobutoxy)chroman-4-yl]-N-methylmethanesulfonamide | 223749-46-0 | MFCD12756323 | 100.0% | 411.44 | C17H24F3NO5S | 10 MG
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HMR 1556 is a chromanol-derived small molecule that selectively inhibits the I_Ks (slow delayed rectifier potassium) current. It exhibits potent activity in cardiac myocytes with reported IC50 values in the low nanomolar range and is supplied as a high-purity research reagent in solid and solution formats.
- Potent and selective Iks channel blocker.
- Reported IC50s of 10.5 nM (canine) and 34 nM (guinea pig).
- High reported purity (99.95%).
- Available as solid and as DMSO solution formats.
- Multiple package sizes to suit experimental scale.
- For research use only; not for human or clinical use.
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eMolecules Medchem Express / Sirt2-IN-1 / 5mg / 451965719 / HY-112427 / / 1862238-00-3 / [null] / 557.690 / C28H27N7O2S2
Medchem Express / Sirt2-IN-1 / 5mg / 451965719 / HY-112427 / / 1862238-00-3 / [null] / 557.690 / C28H27N7O2S2
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Medchemexpress LLC Betrixaban-d6 | 2098655-51-5 | 99.0% | 457.94 g/mol | C23H16D6ClN5O3 | 1 MG
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Betrixaban-d6 is a deuterium-labeled analog of betrixaban, provided for use as an internal standard and tracer in quantitative analytical workflows. The compound is intended for LC-MS, GC-MS, NMR, and other assays where isotopic labeling improves quantitation and peak identification.
- Deuterium-labeled analog suitable for use as internal standard
- High purity for reliable analytical results
- Compatible with LC-MS, GC-MS, and NMR assays
- Supplied in small quantities for analytical method development
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Medchemexpress LLC Hg-9-91-01-5Mg | HY-15776-5MG
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Hg-9-91-01-5Mg
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Selleck Chemical LLC Briciclib
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Briciclib (ON-014185) is a water soluble derivative of ON-013100 a small molecule that binds to and inhibits eukaryotic translation initiation factor 4E (eIF4E)
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Medchemexpress LLC Roflumilast N-oxide | 292135-78-5 | MFCD04112984 | 99.5% | 419.21 g/mol | C17H14Cl2F2N2O4 | 100 MG
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Roflumilast N-oxide is the N-oxide metabolite of roflumilast and acts as a phosphodiesterase type 4 (PDE4) inhibitor. It is provided as a high-purity analytical standard for research and analytical applications, supplied as a solid powder with defined storage conditions and a range of pack sizes including 100 mg.
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Medchemexpress LLC Ly2365109 hydrochloride | 1779796-27-8 | 98.7% | 421.91 | C22H28ClNO5 | 25 MG
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LY2365109 hydrochloride is a potent, selective glycine transporter 1 (GlyT1) inhibitor that increases glycine levels in cerebrospinal fluid and raises seizure thresholds in preclinical models. It is provided as a solid research reagent with characterized purity and stability profiles.
- Potent and selective GlyT1 inhibitor, IC50 15.8 nM for glycine uptake.
- Elevates CSF glycine levels in preclinical studies.
- Shown to increase seizure thresholds in animal models.
- High purity suitable for research use (98.69%).
- White to off-white solid, molecular weight 421.91, formula C22H28ClNO5.
- Soluble in DMSO (≥31 mg/mL) and insoluble in water (<0.1 mg/mL).
- Recommended storage sealed at 4°C; in solvent store at -80°C for long term.
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Medchemexpress LLC V-9302 | 1855871-76-9 | 99.5% | 538.68 | 100 MG
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V-9302 is a competitive antagonist of transmembrane glutamine flux. It selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) but not ASCT1, inhibiting ASCT2-mediated glutamine uptake in HEK-293 cells.
- Selectively targets the amino acid transporter ASCT2 (SLC1A5) over ASCT1.
- Inhibits glutamine uptake (IC50=9.6 μM) in HEK-293 cells.
- Pharmacological blockade of ASCT2 leads to attenuated cancer cell growth and proliferation, increases cell death, and increases oxidative stress.
- Prevents tumor growth in HCT-116 and HT29 xenograft models (75 mg/kg; i.p.; daily for 21 days).
- When combined with CB-839, it elicits strong growth inhibition in SNU398 and MHCC97H xenograft models.
- High purity: 99.46%.
- Intended for research use only, not for sale to patients.
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eMolecules 2-Phenyl-1,3-thiazolane-4-carboxylic acid | 42607-21-6 | MFCD00170683 | 1g
Matrix Scientific | 2-Phenyl-1,3-thiazolane-4-carboxylic acid | 1g | 389716519 | 7990 | | 42607-21-6 | MFCD00170683 | 209.260 | C10H11NO2S
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eMolecules Medchem Express / Irinotecan / 50mg / 446267501 / HY-16562 / / 97682-44-5 / MFCD00866307 / 586.689 / C33H38N4O6
Medchem Express / Irinotecan / 50mg / 446267501 / HY-16562 / / 97682-44-5 / MFCD00866307 / 586.689 / C33H38N4O6
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Medchemexpress LLC 2- Hydroxy 4-phenoxy 1g | 1G
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2- Hydroxy 4-phenoxy 1g | 1G
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