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Filtered Search Results
Medchemexpress LLC HY-70003 50mg Medchemexpress, Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 Purity:>98%
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Medchemexpress, HY-70003 50mg Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 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-A0022A 100mg Medchemexpress, Azaphen (dihydrochloride monohydrate) CAS:63302-99-8 Purity:>98%
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Medchemexpress, HY-A0022A 100mg Azaphen (dihydrochloride monohydrate) CAS:63302-99-8 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 Fantofarone | 114432-13-2 | MFCD00867144 | 99.9% | 550.71 g·mol⁻¹ | C31H38N2O5S | 25 MG
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Fantofarone is a potent L-type calcium channel antagonist used as a research reagent to investigate calcium channel pharmacology and related cardiovascular signaling pathways. It is a sulfone-indolizine class compound with molecular formula C31H38N2O5S and a molecular weight of 550.71 g·mol⁻¹. The material is supplied for research use only and is not intended for human or veterinary use.
- Potent L-type calcium channel antagonist for in vitro pharmacology.
- High reported purity suitable for analytical characterization.
- Solid reagent convenient for formulation and dosing in laboratory assays.
- Supplied in small research quantities appropriate for experimental workflows.
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Medchemexpress LLC V-9302 | 1855871-76-9 | 99.5% | 538.68 | 100 MG
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V-9302 is a competitive antagonist of transmembrane glutamine flux. It selectively and potently targets the amino acid transporter ASCT2 (SLC1A5) but not ASCT1, inhibiting ASCT2-mediated glutamine uptake in HEK-293 cells.
- Selectively targets the amino acid transporter ASCT2 (SLC1A5) over ASCT1.
- Inhibits glutamine uptake (IC50=9.6 μM) in HEK-293 cells.
- Pharmacological blockade of ASCT2 leads to attenuated cancer cell growth and proliferation, increases cell death, and increases oxidative stress.
- Prevents tumor growth in HCT-116 and HT29 xenograft models (75 mg/kg; i.p.; daily for 21 days).
- When combined with CB-839, it elicits strong growth inhibition in SNU398 and MHCC97H xenograft models.
- High purity: 99.46%.
- Intended for research use only, not for sale to patients.
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MEDCHEMEXPRESS LLC PFI-4 5MG
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501873670 PFI-4 5MG
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Medchemexpress LLC FR194738 | 204067-52-7 | 99.8% | 476.11 | C27H38ClNO2S | 25 MG
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FR194738 is a small-molecule squalene epoxidase inhibitor for preclinical research. It inhibits squalene epoxidase activity in HepG2 cell homogenates (IC50 = 9.8 nM) and is provided with analytical characterization suitable for biochemical and cellular studies.
- Potent squalene epoxidase inhibitor (IC50 = 9.8 nM).
- Suitable for biochemical and cell-based assays.
- High purity appropriate for analytical applications (~99.8%).
- Characterized by CAS number 204067-52-7 and molecular weight 476.11.
- Available in multiple vial sizes, including 25 mg.
- Supplied with supporting documentation: datasheet, COA, SDS, H NMR, LCMS.
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Medchemexpress LLC ORIC-101 | 10 MG
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ORIC-101 is a highly potent and selective glucocorticoid receptor antagonist, with an EC50 of 5.6 nM. It exhibits anti-cancer activity and is also a click chemistry reagent.
- Highly potent and selective glucocorticoid receptor antagonist
- EC50 of 5.6 nM
- Anti-cancer activity
- Click chemistry reagent
- Contains an Alkyne group
- Can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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eMolecules 54924-78-6 | 5-BROMO-2-ETHOXYBENZAMIDE | AstaTech | MFCD07551819 | 244.088 | C9H10BrNO2 | 95.000 | CCOc1ccc(Br)cc1C(N)=O | 0.1g | 696739802
5-BROMO-2-ETHOXYBENZAMIDE | AstaTech | 54924-78-6 | MFCD07551819 | 244.088 | C9H10BrNO2 | 95.000 | CCOc1ccc(Br)cc1C(N)=O | 0.1g | 696739802
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Medchemexpress LLC TP-004 | 1454299-21-8 | 99.2% | 50 MG
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TP-004 is a small-molecule chemical probe that potently and reversibly inhibits methionine aminopeptidase 2 (MetAP2) with an IC50 of 6 nM. It is supplied as a high-purity research-grade compound for biochemical and cellular studies.
- Potent, reversible MetAP2 inhibitor (IC50 6 nM).
- High purity: 99.2%.
- Molecular weight 363.34 g/mol; formula C17H16F3N5O.
- Supplied as a 50 mg research pack suitable for assay and probe development.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC HY-14545 100mg Medchemexpress, Amisulpride CAS:71675-85-9 Purity:>98%
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Medchemexpress, HY-14545 100mg Amisulpride CAS:71675-85-9 Amisulpride is a dopamine D2/D3 receptor antagonist with Kis of 2.8 and 3.2 nM for human dopamine D2 and D3, 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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Apexbio Technology LLC Mecamylamine hydrochloride 826-39-1 10mg
Mecamylamine hydrochloride (CAS 826-39-1) is an orally active non-selective non-competitive antagonist of nicotinic acetylcholine receptors (nAChRs) capable of crossing the blood-brain barrier It inhibits the amplitude of induced end plate currents at a holding potential of 70 mV with an IC50 of 7 8 M and a Hill coefficient of 1 2 indicating moderate cooperativity In behavioral studies intraperitoneal administration of mecamylamine (0 5 1 mg/kg) in C57BL/6J mice produces antidepressant-like effects in both the tail suspension and forced swim tests effects which are dependent on the 2 and 7 nAChR subunits This compound is widely utilized in neuropsychiatric and neuropharmacological research
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Medchemexpress LLC Zingiberen Newsaponin | 91653-50-8 | 5 MG
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Zingiberen Newsaponin | 91653-50-8 | 5 MG
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Medchemexpress LLC HY-13757A 1g Medchemexpress, Tamoxifen CAS:10540-29-1 Purity:>98%
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Medchemexpress, HY-13757A 1g Tamoxifen CAS:10540-29-1 Tamoxifen (ICI 47699) is an orally active, selective estrogen receptor modulator (SERM) which blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells[2][3]. Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.1 µM and 1.8 µM, respectively[5]. Tamoxifen activates autophagy and induces apoptosis[4]. 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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eMolecules 122-99-6 | 2-Phenoxyethanol | Chem-Impex | MFCD00002857 | 138.166 | C8H10O2 | 99.000 | OCCOc1ccccc1 | 250g | 603112345
2-Phenoxyethanol | Chem-Impex | 122-99-6 | MFCD00002857 | 138.166 | C8H10O2 | 99.000 | OCCOc1ccccc1 | 250g | 603112345
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Medchemexpress LLC Arecaidine hydrochloride | 6018-28-6 | MFCD00051993 | 98.0% | 177.63 g·mol⁻1 | C7H12ClNO2 | 10 MG
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Arecaidine hydrochloride is the hydrochloride salt of arecaidine, a pyridine alkaloid that acts as a GABA uptake inhibitor and a substrate of H+-coupled amino acid transporters. Supplied as a solid for research use, it is listed with high purity and recommended storage conditions.
- Acts as a GABA uptake inhibitor and transporter substrate.
- Molecular formula: C7H12ClNO2.
- Molecular weight: 177.63 g·mol⁻1.
- CAS number: 6018-28-6.
- Purity: 98.0%.
- Appearance: white to light yellow solid.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months) or -20°C (1 month).
- SMILES: O=C(C1=CCCN(C)C1)O.[H]Cl.
- Available in 10 mg pack sizes for research use.
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