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Filtered Search Results
Accela Chembio Inc 2 | 6-dichlorophenethylamine | 5g | 14573-23-0 | MFCD00060612 | 97+% | D: 1.307 | Shelf Life: 1080 Days | Moisture Sensitive/n2
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2 | 6-dichlorophenethylamine | 5g | 14573-23-0 | MFCD00060612 | 97+% | D: 1.307 | Shelf Life: 1080 Days | Moisture Sensitive/n2
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Indofine Chemical Β-Nicotinamide Aden, 96%, 1 Gm
-NICOTINAMIDE ADENINE DINUCLEOTIDE, (REDUCED FORM) DISODIUM SALT, Products for Life Science, 606-68-8, >97%, 1 gm
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Accela Chembio Inc MF: C8H9Cl2N | MW: 190.07 | >97% | BP: 280¿C | Density: 1.268g/mLat25¿C.
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MF: C8H9Cl2N | MW: 190.07 | >97% | BP: 280¿C | Density: 1.268g/mLat25¿C.
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eMolecules 27854-93-9 | (1S)-1-(3-PYRIDYL)ETHYLAMINE | MFCD09256803 | 1g
Medchem Express | N-(p-Coumaroyl) Serotonin | 5mg | 536984750 | HY-129440 | 68573-24-0 | MFCD09840280 | 322.364 | C19H18N2O3
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Medchemexpress LLC PSB-0739 | 1052087-90-7 | 98.0% | 609.54 | 10 MG
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PSB-0739 is a high-affinity potent, competitive, nonselective platelet P2Y12 receptor antagonist with a Ki value of 24.9 nM. The P2Y12 receptor plays a crucial role in platelet aggregation, and PSB-0739 exhibits an antithrombotic effect.
- Is a potent competitive non-nucleotide antagonist at the human P2Y12 receptor with a pA2 value of 9.8.
- Inhibits ADP-evoked Ca2+ responses with an EC50 of 5.4±1.8 μM and causes a rightward parallel shift in the ADP concentration-response curve in THP-1 cells.
- In vivo, has dose-dependent and significant antihyperalgesic effect in low doses, with a minimal effective dose (mED) of 0.1 mg/kg.
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Medchemexpress LLC 3(2H)-Pyridazinone, 6-[3-fluoro-4-(4-morpholinyl)phenyl]-4,5-dihydro-5-methyl-, (5R)- | 1630760-75-6 | 98.4% | 291.32 | 50 MG
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BRD9500 is an orally active phosphodiesterases 3 (PDE3) inhibitor, demonstrating IC50s of 10 nM for PDE3A and 27 nM for PDE3B. This compound exhibits significant antitumor activity, primarily by inhibiting PDE3A and PDE3B, leading to cancer cell killing through the induction of PDE3A/B interactions with SFLN12.
- Orally active PDE3 inhibitor
- Potently inhibits PDE3A (IC50: 10 nM) and PDE3B (IC50: 27 nM)
- Exhibits antitumor activity
- Induces PDE3A/B interactions with SFLN12 to kill cancer cells
- Shows an EC50 of 1 nM for SK-MEL-3 melanoma cell line viability
- Demonstrates an EC50 of 1.6 nM for HeLa cell viability
- Stabilizes the PDE3A-SLFN12 interaction in HeLa cells
- Inhibits SK-MEL-3 melanoma growth in mice
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eMolecules 62-53-3 | Aniline, 99.5%, ACS grade | Oakwood Chemical | MFCD00007629 | 93.129 | C6H7N | 0.000 | Nc1ccccc1 | 5g | 854221463
Aniline, 99.5%, ACS grade | Oakwood Chemical | 62-53-3 | MFCD00007629 | 93.129 | C6H7N | 0.000 | Nc1ccccc1 | 5g | 854221463
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eMolecules 62-53-3 | Aniline | Oakwood Chemical | MFCD00007629 | 93.129 | C6H7N | 99.000 | Nc1ccccc1 | 2.5kg | 786489788
Aniline | Oakwood Chemical | 62-53-3 | MFCD00007629 | 93.129 | C6H7N | 99.000 | Nc1ccccc1 | 2.5kg | 786489788
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![Medchemexpress LLC N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly | 64967-39-1 | 99.8% | 399.40 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000453478-logo.png-250.jpg){kind=logo}
Medchemexpress LLC N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly | 64967-39-1 | 99.8% | 399.40 | 25 MG
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N-[3-(2-Furyl)acryloyl]-Phe-Gly-Gly | 64967-39-1 | 99.8% | 399.40 | 25 MG
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eMolecules AstaTech / 3-AMINOCYCLOBUTANE-1-CARBONITRILE HCL / 0.1g / 268491474 / 37826 / 95.000 / 1523572-04-4 / MFCD26959098 / 132.590 / C5H9ClN2
AstaTech / 3-AMINOCYCLOBUTANE-1-CARBONITRILE HCL / 0.1g / 268491474 / 37826 / 95.000 / 1523572-04-4 / MFCD26959098 / 132.590 / C5H9ClN2
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eMolecules 57260-73-8 | N-Boc-Ethylenediamine | AA Blocks LLC | MFCD00191871 | 160.217 | C7H16N2O2 | 0.000 | CC(C)(C)OC(=O)NCCN | 5g | 410167691
N-Boc-Ethylenediamine | AA Blocks LLC | 57260-73-8 | MFCD00191871 | 160.217 | C7H16N2O2 | 0.000 | CC(C)(C)OC(=O)NCCN | 5g | 410167691
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eMolecules 929-73-7 | Dodecylamine hydrochloride | Combi-Blocks | MFCD00042017 | 221.810 | C12H28ClN | 96.000 | Cl.CCCCCCCCCCCCN | 1g | 482932290
Dodecylamine hydrochloride | Combi-Blocks | 929-73-7 | MFCD00042017 | 221.810 | C12H28ClN | 96.000 | Cl.CCCCCCCCCCCCN | 1g | 482932290
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Apexbio Technology LLC ACTB-1003 939805-30-8 50mg
ACTB-1003 (CAS 939805-30-8) also known as EOC317 is an orally bioavailable small-molecule kinase inhibitor that selectively targets fibroblast growth factor receptor 1 (FGFR1) vascular endothelial growth factor receptor 2 (VEGFR2) and the endothelial-specific tyrosine kinase Tie-2 In vitro studies demonstrate that ACTB-1003 suppresses the activity of these kinases at nanomolar concentrations By modulating these angiogenesis-associated signaling pathways ACTB-1003 serves as a valuable tool for investigating tumor angiogenesis and related signal transduction mechanisms in biomedical research
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Medchemexpress LLC Tert-butylamine borane | 7337-45-3 | MFCD00075635 | ≥99.0% | 86.97 g/mol | C4H14BN | 10 G
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tert-Butylamine borane is a stable borane-amine complex used as a mild, selective reducing agent in organic synthesis. It provides controlled hydride transfer for the reduction of aldehydes and ketones to their corresponding alcohols, suitable for laboratory-scale reactions where selectivity and ease of handling are required.
- Mild, selective hydride source for aldehyde and ketone reductions.
- High purity (≥99.0%) for consistent reaction performance.
- Solid, easy-to-handle complex offering improved stability over gaseous borane reagents.
- Available in small pack sizes appropriate for bench-scale work.
- Compatible with common organic solvents under standard reaction conditions.
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eMolecules 4905-83-3 | Propylamine Hydrobromide | MFCD30749306 | 1g
Medchem Express | Iodo-PEG7-alcohol | 50mg | 761738499 | HY-143833 | | 436.283 | C14H29IO7
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