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Filtered Search Results
Medchemexpress LLC ONO-2952 | 895169-20-7 | 99.5% | 398.86 | 50 MG
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ONO-2952 is a potent, selective, and orally active antagonist of translocator protein 18 kDa (TSPO), exhibiting a Ki range of 0.33-9.30 nM for both rat and human TSPO. It demonstrates greater selectivity for TSPO compared to other receptors, transporters, ion channels, and enzymes. This compound achieves anti-stress effects by inhibiting the excessive activation of the noradrenergic system in the brain, without inducing amnesic effects. ONO-2952 shows potential for the treatment of irritable bowel syndrome.
- Potent, selective and orally active.
- More selective for TSPO than other receptors, transporters, ion channels and enzymes.
- Exerts anti-stress effects through inhibition of excessive activation of noradrenergic system in the brain.
- Does not cause amnesic effects.
- Has potential for irritable bowel syndrome treatment.
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Medchemexpress LLC HY-109002 5mg Medchemexpress, Apararenone CAS:945966-46-1 Purity:>98%
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Medchemexpress, HY-109002 5mg Apararenone CAS:945966-46-1 Apararenone (MT-3995) is a novel non-steroidal mineralocorticoid receptor antagonists under development for the treatment of diabetic nephropathies and non-alcoholic steatohepatitis. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-118284 10mg Medchemexpress, Vicagrel CAS:1314081-53-2 Purity:>98%
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Medchemexpress, HY-118284 10mg Vicagrel CAS:1314081-53-2 Vicagrel, an acetate derivative of Clopidogrel, is a P2Y12 platelet inhibitor potentially for the treatment of thrombosis, the substrate of carboxylesterase 2 (CES2). Vicagrel demonstrates a favorable safety profile and excellent anti-platelet activity, which could be an anti-platelet drug and for the unmet medical needs of cardiovascular diseases. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-112945 10mg Medchemexpress, MLS0315771 CAS:727664-91-7 Purity:>98%
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Medchemexpress, HY-112945 10mg MLS0315771 CAS:727664-91-7 MLS0315771 is a potent and biologically active competitive phosphomannose isomerase (MPI) inhibitor, with an IC50 ~1 μM and a Ki of 1.4 μM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-101437 10mg Medchemexpress, Ralfinamide CAS:133865-88-0 Purity:>98%
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Medchemexpress, HY-101437 10mg Ralfinamide CAS:133865-88-0 Ralfinamide (FCE-26742A) is an orally available Na + blocker derived from α-aminoamide, with function of suppressing pain [1] [2] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC A1874 | 100MG
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A1874 is a nutlin-based (MDM2 ligand) and BRD4-degrading PROTAC with a DC50 of 32 nM (induce BRD4 degradation in cells) Effective in inhibiting many cancer cell lines proliferation[1]
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eMolecules 1270391-53-1 | 1-(5-Chloro-2-fluorophenyl)ethan-1-amine | ChemScene | MFCD18705334 | 173.620 | C8H9ClFN | 95.000 | CC(N)c1cc(Cl)ccc1F | 100mg | 714293709
1-(5-Chloro-2-fluorophenyl)ethan-1-amine | ChemScene | 1270391-53-1 | MFCD18705334 | 173.620 | C8H9ClFN | 95.000 | CC(N)c1cc(Cl)ccc1F | 100mg | 714293709
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Medchemexpress LLC CCR2 antagonist 4 (hydrochloride) | 1313730-14-1 | MFCD16618399 | 99.9% | 476.32 | C21H22Cl2F3N3O2 | 5 MG
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CCR2 antagonist 4 hydrochloride is a small-molecule research compound that selectively antagonizes the chemokine receptor CCR2b. It is used to study CCR2-mediated chemotaxis and inflammatory signaling and is supplied as a white to off-white solid with high reported purity and defined physicochemical data.
- Potent CCR2b antagonist with reported IC50 180 nM.
- Inhibits MCP-1-induced chemotaxis (IC50 24 nM).
- High purity (99.91%).
- White to off-white solid appearance.
- Molecular weight 476.32.
- Available in small research pack sizes including 5 mg.
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Chemscene ChemScene | 2,4-Dimethoxy-3-fluoroaniline | 250MG | CS-0195063 | 0.98 | 195136-66-4| MFCD09258660 | 171.17
ChemScene | 2,4-Dimethoxy-3-fluoroaniline | 250MG | CS-0195063 | 0.98 | 195136-66-4| MFCD09258660 | 171.17
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Accela Chembio Inc 2 | 3-difluorophenylboronic Acid | 100g | 121219-16-7 | MFCD01863170 | 97+% | Shelf Life: 2160 Days | Moisture Sensitive/+4/n2
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2 | 3-difluorophenylboronic Acid | 100g | 121219-16-7 | MFCD01863170 | 97+% | Shelf Life: 2160 Days | Moisture Sensitive/+4/n2
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eMolecules 113299-40-4 | Medchem Express | (R)-Bicalutamide | 5mg | 572596461 | HY-108250 | MFCD00870866 | 430.37 | C18H14F4N2O4S
Ambeed | 4-Ethoxy-3-methoxyphenylacetic acid | 1g | 521439743 | A381850 | 120-13-8 | MFCD00016831 | 210.229 | C11H14O4
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Enzo Life Sciences Rucaparib (free base) (50mg). CAS: 283173-50-2
Rucaparib is a poly (ADP ribose) polymerase (PARP) inhibitor. PARP is a DNA damage-activated nuclear enzyme that has a key signaling role in the base excision repair pathway. Purity: ≥99% (HPLC). Solubility: Soluble in DMSO. Long Term Storage: -20°C.
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eMolecules 1218791-15-1 | 3-Cyano-2-fluorophenylboronic acid, pinacol ester | Combi-Blocks | MFCD11506358 | 247.080 | C13H15BFNO2 | 98.000 | CC1(C)OB(OC1(C)C)c1cccc(C#N)c1F | 1g | 117545216
3-Cyano-2-fluorophenylboronic acid, pinacol ester | Combi-Blocks | 1218791-15-1 | MFCD11506358 | 247.080 | C13H15BFNO2 | 98.000 | CC1(C)OB(OC1(C)C)c1cccc(C#N)c1F | 1g | 117545216
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eMolecules 903580-39-2 | Medchem Express | PRX-07034 (hydrochloride) | 5mg | 599150833 | HY-14559 | 490.44 | C21H29Cl2N3O4S
Medchem Express | PRX-07034 (hydrochloride) | 5mg | 599150833 | HY-14559 | 903580-39-2 | 490.440 | C21H29Cl2N3O4S
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Medchemexpress LLC Golgicide A-2 | 1394285-50-7 | 99.5% | 284.30 g/mol | C17H14F2N2 | 10 MG
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Golgicide A-2 is a synthetic derivative of Golgicide A that selectively inhibits GBF1, an Arf guanine nucleotide exchange factor. Supplied as a research reagent, it is used to study Golgi function, vesicular trafficking, and antiviral mechanisms against enteroviruses.
- Selective GBF1 (ArfGEF) inhibitor used to probe Golgi function.
- Useful in vesicular trafficking and membrane dynamics studies.
- Applied in antiviral research against enteroviruses and coxsackievirus.
- High purity supports reproducible experimental results.
- Available in small quantities suitable for laboratory assays.
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