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Filtered Search Results
Medchemexpress LLC MARK4 inhibitor 1 5mg | 2271081-58-2 | 5 MG
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MARK4 inhibitor 1 is a selective small-molecule inhibitor of microtubule affinity-regulating kinase 4 (MARK4) used for in vitro and preclinical research into MARK4-mediated signaling, apoptosis, and cancer cell biology. Supplied as a powder with reported high purity and standard storage recommendations.
- Selective MARK4 inhibitor with reported IC50 1.54 μM.
- Molecular formula C20H18N6O3; molecular weight 390.40.
- Reported purity 98.3% (manufacturer-reported).
- Soluble in DMSO (approx. 5 mg/mL with ultrasonication; pH adjustment may be required).
- Supplied as a powder with manufacturer-recommended storage conditions.
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Medchemexpress LLC MALAT1-IN-1 100mg | 827327-28-6 | 100 MG
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MALAT1-IN-1 is a research-grade small-molecule inhibitor of the long non-coding RNA MALAT1 that modulates downstream gene expression in a dose-dependent manner. It is supplied for laboratory use in solid and solution formats and is intended for in vitro and preclinical research. Purity is stated as 99.84%.
- Potent, selective modulation of MALAT1-related pathways
- High purity: 99.84% (manufacturer reported)
- Available in multiple pack sizes, including 100 MG
- Supplied as solid and as DMSO solution for flexible dosing
- Includes data sheet, COA, and SDS for experimental support
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Medchemexpress LLC DFP00173 | 672286-03-2 | MFCD00121277 | 99.5% | 332.16 g/mol | C11H7Cl2N3O3S | 50MG
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DFP00173 is a potent, selective small-molecule inhibitor of aquaporin-3 (AQP3) used for biochemical and pharmacological studies. It inhibits mouse and human AQP3 with an IC50 of approximately 0.1-0.4 μM, is supplied as a high-purity solid, and is soluble in DMSO with defined storage recommendations.
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eMolecules 635323-95-4 | Medchem Express | F-15599 | 5mg | 415688302 | HY-19863 | MFCD28502284 | 394.85 | C19H21ClF2N4O
Medchem Express | F-15599 | 5mg | 415688302 | HY-19863 | 635323-95-4 | MFCD28502284 | 394.850 | C19H21ClF2N4O
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eMolecules 1401090-53-6 | Medchem Express | Ibiglustat | 2mg | 446267809 | HY-16743 | MFCD28502073 | 389.49 | C20H24FN3O2S
Medchem Express | MSP-3 | 5mg | 781212789 | HY-118785 | 1820968-63-5 | 305.390 | C16H19NO3S
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Medchemexpress LLC Florbetapir (18F)-radiolabeled styrylpyridine tosylate precursor | 1205550-99-7 | 99.7% | 100 MG
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A styrylpyridine tosylate precursor used to synthesize 18F-radiolabeled florbetapir-type tracers for positron emission tomography (PET) research.
- High chemical purity suitable for radiolabeling workflows.
- Used to synthesize 18F-labeled PET imaging agents targeting amyloid plaques.
- White to yellow solid; easy handling and storage as a dry powder.
- Long-term stability when stored at -20°C; solvent solutions require colder storage.
- Available in small research-scale quantities for tracer development.
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eMolecules 451485-60-2 | 3-{3-[(2-Chloro-6-fluorobenzyl)oxy]phenyl}-1H-pyrazole | Apollo Scientific | MFCD03425750 | 302.730 | C16H12ClFN2O | 95.000 | Fc1cccc(Cl)c1COc1cccc(c1)-c1cc[nH]n1 | 1g | 562431119
3-{3-[(2-Chloro-6-fluorobenzyl)oxy]phenyl}-1H-pyrazole | Apollo Scientific | 451485-60-2 | MFCD03425750 | 302.730 | C16H12ClFN2O | 95.000 | Fc1cccc(Cl)c1COc1cccc(c1)-c1cc[nH]n1 | 1g | 562431119
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eMolecules 5527-94-6 | 4-Chloro-3-fluorotoluene | Ambeed | MFCD00143295 | 144.570 | C7H6ClF | 98.000 | Cc1ccc(Cl)c(F)c1 | 1g | 552760402
4-Chloro-3-fluorotoluene | Ambeed | 5527-94-6 | MFCD00143295 | 144.570 | C7H6ClF | 98.000 | Cc1ccc(Cl)c(F)c1 | 1g | 552760402
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eMolecules 851723-84-7 | Medchem Express | Timapiprant | 5mg | 446265491 | HY-15342 | MFCD18633254 | 348.377 | C21H17FN2O2
Medchem Express | Timapiprant | 5mg | 446265491 | HY-15342 | 851723-84-7 | MFCD18633254 | 348.377 | C21H17FN2O2
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Apexbio Technology LLC IMDK-10MG
iMDK (CAS No 881970-80-5) is a promising compound in the field of biomedical research particularly known for its potential in oncology studies Originating from extensive research efforts to identify effective anti-cancer agents iMDK functions primarily by targeting specific signaling pathways involved in cell proliferation and apoptosis such as the MAPK/ERK pathway It is known to exhibit potent in vitro activity in the nanomolar to low micromolar range making it an attractive candidate for laboratory investigations Frequently utilized in various cellular models and animal studies iMDK helps to elucidate mechanisms of tumor growth and explores potential therapeutic interventions Its role in high-throughput drug screening further highlights its importance in the discovery of novel cancer treatments Experimental concentrations typically depend on the specific research design offering flexibility in diverse experimental setups to assess its effectiveness and safety profiles
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eMolecules 2250323-50-1 | Medchem Express | JWG-071 | 5mg | 495799688 | HY-108886 | 612.779 | C34H44N8O3
Ambeed | Methyl 2-benzyl-56-dihydroxypyrimidine-4-carboxylate | 100mg | 596569375 | A851948 | 519032-07-6 | MFCD09031861 | 260.249 | C13H12N2O4
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eMolecules 2226789-82-6 | Medchem Express | UNC5293 | 5mg | 632433237 | HY-132200 | 518.706 | C30H42N6O2
Ambeed | 46-Dichloro-5-methoxypyrimidine | 10g | 552633648 | A192394 | 5018-38-2 | MFCD00087680 | 179.000 | C5H4Cl2N2O
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Apexbio Technology LLC Canagliflozin(Synonyms: Invokana, TA-7284, JNJ-28431754, Sulisent, Canagliflozin hemihydrate), 100mg, CAS: 842133-18-0.
Canagliflozin (CAS 842133-18-0) is a selective inhibitor of sodium-glucose cotransporter 2 (SGLT2) a transporter responsible for renal glucose reabsorption By inhibiting SGLT2 activity Canagliflozin decreases renal glucose reabsorption resulting in increased urinary glucose excretion In CHO cells expressing human rat or mouse SGLT2 Canagliflozin potently inhibits sodium-dependent glucose uptake with IC50 values of 4 4 3 7 and 2 0 nM respectively Animal studies using db/db mice and Zucker diabetic fatty (ZDF) rats demonstrate dose-dependent reductions in blood glucose as well as decreased respiratory exchange ratio and body weight Canagliflozin is suitable for in vivo research through oral administration
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Medchemexpress LLC C17H11Br2NO2S2 | 893449-38-2 | 99.1% | 485.21 | 10 MG
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PRL-3 Inhibitor I is a potent PRL-3 inhibitor with an IC50 of 0.9 μM. It demonstrates reduced invasion in cell-based assays.
- Potent PRL-3 inhibitor with an IC50 of 0.9 μM.
- Reduces invasion in cell-based assay.
- For research use only.
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Enzo Life Sciences Gefitinib-based PROTAC 3 (5mg). 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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