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Filtered Search Results
eMolecules 91940-87-3 | Medchem Express | Zatebradine (hydrochloride) | 5mg | 446262871 | HY-13422 | MFCD06798356 | 493.04 | C26H37ClN2O5
Medchem Express | Zatebradine (hydrochloride) | 5mg | 446262871 | HY-13422 | 91940-87-3 | MFCD06798356 | 493.040 | C26H37ClN2O5
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Medchemexpress LLC BRD4 Inhibitor-24 | 309951-18-6 | 99.3% | 262.26 | 100 MG
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BRD4 Inhibitor-24 (compound 3U) is a potent BRD4 inhibitor that exhibits antitumor activity against MCF7 and K652 cells. This compound is for research use only and is presented as a solid, white to off-white substance with the molecular formula C13H14N2O4.
- Potent BRD4 inhibitor
- Antitumor activity against MCF7 and K652 cells (IC50 values of 33.7 and 45.9 μM)
- Solid, white to off-white appearance
- Molecular formula C13H14N2O4
- Recommended storage at 4°C, protected from light
- In solvent, storage at -80°C for 6 months or -20°C for 1 month (protected from light)
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eMolecules 24088-59-3 | 3-(3-Phenyl-1,2,4-oxadiazol-5-yl)propanoic acid | MFCD05130956 | 25g
Ambeed | 3-(Pyrrolidin-2-yl)pyridine | 250mg | 552713526 | A348497 | 5746-86-1 | MFCD00016913 | 148.209 | C9H12N2
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Enzo Life Sciences Aristolochic acid. sodium salt (50mg). CAS: 10190-99-5
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Water soluble form of aristolochic acid. Purity: ≥97%. Solubility: Soluble in water. Long Term Storage: Ambient.
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eMolecules 1780259-94-0 | Medchem Express | ZK756326 (dihydrochloride) | 5mg | 446256361 | HY-101038A | MFCD09038571 | 429.38 | C21H30Cl2N2O3
Medchem Express | AICAR | 50mg | 446262850 | HY-13417 | 2627-69-2 | 258.234 | C9H14N4O5
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Medchemexpress LLC HY-119373 5mg Medchemexpress, Cav 2.2 blocker 1 CAS:1567335-29-8 Purity:>98%
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Medchemexpress, HY-119373 5mg Cav 2.2 blocker 1 CAS:1567335-29-8 Cav 2.2 blocker 1 (compound 9) is a N-type calcium channel (Cav 2.2) blocker for the treatment of pain, with an IC 50 of 1 nM [1] . 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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Strem, An Ascensus Company CAS# 1447963-71-4. 100MG. 2-Diphenylphosphino-2',6'-bis(dimethylamino)-1,1'-biphenyl, min. 98% PhCPhos
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CAS# 1447963-71-4. 100MG. 2-Diphenylphosphino-2',6'-bis(dimethylamino)-1,1'-biphenyl, min. 98%. PhCPhos Molecular Formula: C28H29N2P. Molecular Weight: 424.52. Color/Form: tan solid. Strem# 15-1125. www.strem.com/catalog/v3/15-1125/
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Selleck Chemical LLC Telaglenastat
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Telaglenastat (CB-839) is a potent selective and orally bioavailable glutaminase inhibitor with IC50 of 24 nM for recombinant human GAC CB-839(Telaglenastat) inudces autophagy and has antitumor activity Phase 1
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eMolecules 1488363-78-5 | Medchem Express | Adomeglivant | 5mg | 446270500 | HY-19904 | MFCD30343860 | 555.638 | C32H36F3NO4
Ambeed | Sodium 23-dimercaptopropane-1-sulfonate hydrate | 1g | 513350172 | A599319 | 207233-91-8 | MFCD00149543 | 228.270 | C3H9NaO4S3
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Medchemexpress LLC Dihydrodiol-ibrutinib | 1654820-87-7 | 99.9% | 474.51 g/mol | C25H26N6O4 | 5 MG
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Dihydrodiol-ibrutinib is a dihydrodiol active metabolite of ibrutinib that retains BTK inhibitory activity at a lower potency than the parent compound. Supplied as a white to off-white solid for laboratory research use, it is suitable for in vitro assays and formulation studies and can be prepared in common solvents for dosing formulations.
- Active metabolite with measurable BTK inhibition (~15x lower than parent)
- High reported purity, suitable for research applications
- White to off-white solid for convenient handling
- Soluble in DMSO and compatible with multiple in vivo formulation vehicles
- Stable under recommended cold storage conditions for extended periods
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eMolecules 1346242-31-6 | Medchem Express | Rivastigmine carbamate impurity | 25mg | 705860717 | HY-133776 | MFCD26390683 | 224.216 | C10H12N2O4
Ambeed | 7-Fluoro-1-hydroxy-13-dihydrobenzo[c][12]oxaborole-6-carboxylic acid | 100mg | 784394940 | A1670383 | 1628151-46-1 | 195.940 | C8H6BFO4
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Medchemexpress LLC GW6471 | 880635-03-0 | C35H36F3N3O4 | 100 MG
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GW6471 is a potent PPARα antagonist that inhibits GW409544-induced activation of PPARα with an IC50 of 0.24 μM. It significantly inhibits cell viability in Caki-1 and 786-O renal cell carcinoma cell lines in vitro. In vivo studies demonstrate its antitumor activity, showing decreased tumor growth and c-Myc levels in xenograft mouse models without observed toxicity.
- Potent PPARα antagonist
- Inhibits cell viability in renal cell carcinoma cell lines
- Demonstrates antitumor activity in vivo
- No toxicity observed at effective doses in animal studies
- Cited in numerous publications, including Nat Metab, Cell Metab, and Immunity
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Selleck Chemical LLC ZK756326 2HCl
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ZK756326 is a full agonist of CCR8 Chemokine receptor 8 with an IC50 of 1 8 M dose-responsively eliciting an increase in intracellular calcium and cross-desensitizing the response of the receptor to CCL1
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Medchemexpress LLC HY-111493 10mg Medchemexpress, LRRK2 inhibitor 1 CAS:1802525-61-6 Purity:>98%
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Medchemexpress, HY-111493 10mg LRRK2 inhibitor 1 CAS:1802525-61-6 LRRK2 inhibitor 1 is a potent, selective and oral LRRK2 inhibitor with an pIC50 of 6.8 nM. 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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Selleck Chemical LLC BTK inhibitor 1
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BTK inhibitor 1 (compound 27) is an inhibitor of BTK with an IC50 of 0 11 nM for Btk and inhibits B cell activation in hWB with an IC50 of 2 nM
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