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Filtered Search Results
Medchemexpress LLC FC131 TFA | 842166-42-1 | 99.9% | 843.85 | 10 MG
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FC131 TFA is a CXCR4 antagonist that inhibits [125I]-SDF-1 binding to CXCR4 with an IC50 of 4.5 nM. It also exhibits anti-HIV activity. It is for research use only and not sold to patients.
- Inhibits [125I]-SDF-1 binding to CXCR4 with an IC50 of 4.5 nM
- Exhibits anti-HIV activity
- Appearance: solid
- Color: white to off-white
- Soluble in DMSO (100 mg/mL)
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eMolecules 1314988-10-7 | 1-Benzyl-5-bromo-6-fluorobenzimidazole | Combi-Blocks | MFCD19684120 | 305.150 | C14H10BrFN2 | 98.000 | Fc1cc2n(Cc3ccccc3)cnc2cc1Br | 1g | 117535474
1-Benzyl-5-bromo-6-fluorobenzimidazole | Combi-Blocks | 1314988-10-7 | MFCD19684120 | 305.150 | C14H10BrFN2 | 98.000 | Fc1cc2n(Cc3ccccc3)cnc2cc1Br | 1g | 117535474
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eMolecules 20651-66-5 | AstaTech | 1-BUTYL-3-FLUOROBENZENE | 1g | 721956234 | 36944 | 97 | MFCD22482823 | 152.212 | C10H13F
Ambeed | 5-Chloro-124-thiadiazole | 1g | 525052791 | A142955 | 38362-15-1 | MFCD09743974 | 120.550 | C2HClN2S
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eMolecules 947-04-6 | 2-Azacyclotridecanone | Oakwood Chemicals | MFCD00005104 | 197.322 | C12H23NO | 99.000 | O=C1CCCCCCCCCCCN1 | 25g | 480149481
2-Azacyclotridecanone | Oakwood Chemicals | 947-04-6 | MFCD00005104 | 197.322 | C12H23NO | 99.000 | O=C1CCCCCCCCCCCN1 | 25g | 480149481
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Medchemexpress LLC HY-19712 5mg Medchemexpress, LJH685 CAS:1627710-50-2 Purity:>98%
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Medchemexpress, HY-19712 5mg LJH685 CAS:1627710-50-2 LJH685 is a potent, specific and selective RSK inhibitor, inhibits RSK1, 2, and 3 biochemical activities with IC50s of 6, 5, 4 nM, respectively. 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 Cdk9-in-7 | 2369981-71-3 | 98.1% | 547.71 | C29H37N7O2S | 5MG
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CDK9-IN-7 is a selective, potent, orally active small-molecule inhibitor of CDK9/cyclin T for research use. It exhibits strong biochemical potency (IC50 = 11 nM), preferential selectivity versus other CDKs, and has demonstrated antitumor activity in preclinical non-small-cell lung cancer models by inducing apoptosis, causing G2 cell-cycle arrest, and reducing cancer stemness.
- Selective CDK9/cyclin T inhibition with reduced activity against CDK4 and CDK6
- Potent biochemical activity (IC50 = 11 nM) for target engagement studies
- Demonstrated antitumor effects in NSCLC models, including apoptosis and G2 arrest
- Suitable for in vitro and in vivo research, including oral administration studies
- Available as powder and as a 10 mM solution in DMSO for screening
- High purity (~98.1%) for reliable experimental results
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Medchemexpress LLC Op-5244 sodium | 00-00-0 | 99.9% | C19H28ClN5NaO9P | 10MG
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OP-5244 sodium is the sodium salt of a potent, orally active small-molecule CD73 inhibitor that reverses immunosuppression by blocking adenosine production. Supplied for research use as a characterized solid with accompanying purity and analytical data.
- Potent CD73 inhibitor (IC50 0.25 nM).
- Reverses adenosine-mediated immunosuppression.
- High purity (99.9%).
- Chemical formula C19H28ClN5NaO9P; molecular weight 559.87 g·mol⁻¹.
- Available in small research quantities such as 10 mg.
- Solid form; store sealed at 4 °C.
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eMolecules 749269-83-8 | Medchem Express | Itanapraced | 5mg | 446264139 | HY-14399 | MFCD18633206 | 325.16 | C16H11Cl2FO2
Medchem Express | Itanapraced | 5mg | 446264139 | HY-14399 | 749269-83-8 | MFCD18633206 | 325.160 | C16H11Cl2FO2
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eMolecules 1040526-12-2 | Medchem Express | LP-533401 hydrochloride | 5mg | 434310676 | HY-15849A | MFCD18803629 | 562.95 | C27H23ClF4N4O3
Ambeed | Methyl 4-bromo-3-(trifluoromethyl)benzoate | 1g | 525050786 | A141504 | 107317-58-8 | MFCD10566409 | 283.044 | C9H6BrF3O2
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eMolecules 1218918-62-7 | Medchem Express | MK-7246 | 5mg | 446266791 | HY-15853 | MFCD22741619 | 416.47 | C21H21FN2O4S
Ambeed | 1-Ethylpiperidin-3-ol | 5g | 599118762 | A231304 | 13444-24-1 | MFCD00006508 | 129.203 | C7H15NO
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Medchemexpress LLC (Rac)-lunresertib | 2719749-28-5 | 99.7% | C18H20N4O2 | 100 MG
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(Rac)-lunresertib, also known as (Rac)-RP-6306, is a potent membrane-associated tyrosine and threonine-specific cdc2-inhibitory kinase (Myt1) inhibitor with an IC50 of less than 10 nM. This compound exhibits significant anticancer effects.
- Potent Myt1 inhibitor
- Inhibits PKMYT1 with an IC50 of <10 nM
- Exhibits anticancer effects
- Solid, off-white to yellow appearance
- Molecular weight of 324.38
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Medchemexpress LLC Sodium 2-(3-(2,6-difluoro-4-(1H-pyrazol-4-yl)phenyl)-3-oxoprop-1-en-1-yl)-4-(1-methyl-1H-pyrazol-4-yl | 2519537-70-1 | 98.9% | 50 MG
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HOIPIN-8 is a research small-molecule inhibitor of the linear ubiquitin chain assembly complex (LUBAC) used to probe ubiquitination and NF-κB signaling in biochemical and cell-based studies. It is supplied as a sodium salt with a molecular weight of 456.38 g/mol.
- Molecular weight 456.38 g/mol
- Molecular formula C23H15F2N4NaO3
- Potent LUBAC inhibitor with IC50 of 11 nM
- Soluble in DMSO at 50 mg/mL and formulatable for in vivo dosing
- Store sealed at -20°C; in solution store at -80°C for long-term stability
- Suitable for biochemical assays and cell-based research
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Enzo Life Sciences Gefitinib-based PROTAC 3 (10mg). CAS: 2230821-27-7
Gefitinib-based PROTAC 3 is targeting on EGFR, consisting of Gefitinib as the warhead linked to VHL-recruiting ligand. Purity: ≥99%. Solubility: Soluble in DMSO (75 mg/mL). Insoluble in water. Long Term Storage: -20°C.
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eMolecules 851881-60-2 | Medchem Express | ADX-47273 | 5mg | 446262353 | HY-13058 | MFCD17167026 | 369.372 | C20H17F2N3O2
Medchem Express | ADX-47273 | 5mg | 446262353 | HY-13058 | 851881-60-2 | MFCD17167026 | 369.372 | C20H17F2N3O2
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eMolecules 1491150-77-6 | Medchem Express | Syk-IN-1 | 5mg | 559839583 | HY-12657 | 366.429 | C18H22N8O
Ambeed | 3-Bromo-N-methoxy-N-methylbenzamide | 5g | 600835375 | A252486 | 207681-67-2 | MFCD02684302 | 244.088 | C9H10BrNO2
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