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Filtered Search Results
Medchemexpress LLC Brilaroxazine | 1239729-06-6 | 98.8% | 450.36 g/mol | C22H25Cl2N3O3 | 5 MG
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Brilaroxazine (RP5063) is an investigational atypical antipsychotic and serotonin-dopamine system modulator supplied for research use. It is offered as a purified solid and as a DMSO solution, intended for preclinical pharmacology, receptor profiling, and in vitro studies.
- Investigational atypical antipsychotic and dopamine/5-HT modulator.
- High purity (98.8%).
- Chemical formula C22H25Cl2N3O3; molecular weight 450.36 g/mol.
- Available as solid and as a 10 mM solution in DMSO.
- Suitable for receptor binding, pharmacology, and preclinical studies.
- Offered in small research pack sizes, including 5 mg.
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Medchemexpress LLC HY-112721 10mg Medchemexpress, FDI-6 CAS:313380-27-7 Purity:>98%
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Medchemexpress, HY-112721 10mg FDI-6 CAS:313380-27-7 FDI-6 is an inhibitor of FOXM1. FDI-6 binds directly to FOXM1 protein, to displace FOXM1 from genomic targets in MCF-7 breast cancer cells, and induce concomitant transcriptional down-regulation. 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 Dp-c-4 (EGFR PARP dual-targeting PROTAC) | 00-00-0 | 98.2% | 1450.93 | C72H78ClF2N15O14 | 5 MG
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DP-C-4 is a Cereblon-based dual PROTAC that induces simultaneous degradation of EGFR and PARP in vitro, showing dose-dependent effects in cellular assays (1-50 μM; 24 h). It is intended for research into targeted protein degradation and dual-target therapeutic strategies, supplied as a high-purity solid with specific storage and solubility recommendations.
- High purity: 98.15%.
- Dual-target activity: degrades EGFR and PARP simultaneously.
- Validated in cell assay: dose-dependent degradation in SW1990 cells (1-50 μM; 24 h).
- Appearance: light yellow to green yellow solid.
- Solubility: DMSO 12 mg/mL; may require ultrasonic agitation.
- Storage: -80°C under nitrogen; stock solution stable up to 6 months.
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Medchemexpress LLC CCR2 antagonist 3 | 1380100-86-6 | 99.9% | 308.39 | C17H25FN2O2 | 10 MG
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CCR2 antagonist 3 is a small-molecule antagonist of the chemokine receptor CCR2 supplied for research use. It is suitable for in vitro and preclinical studies probing CCR2-mediated signaling and inflammatory responses.
- Antagonist of chemokine receptor CCR2.
- High purity (>99.9% by HPLC).
- Molecular weight 308.39 g·mol⁻¹; formula C17H25FN2O2.
- White to off-white solid powder.
- Supplied as 10 mg.
- Recommended storage: powder -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (6 months) or -20°C (1 month).
- Intended for research use only; not for human or clinical use.
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eMolecules 2201048-82-8 | Medchem Express | Zagociguat | 5mg | 721309664 | HY-145607 | 362.292 | C16H10F4N6
Ambeed | 2-Butoxy-5-methylphenylboronic acid | 100mg | 632174613 | A558883 | 480438-72-0 | MFCD04974068 | 208.060 | C11H17BO3
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Medchemexpress LLC SB 239063 | 193551-21-2 | >99.2% | 368.40 | 1 ML
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SB 239063 is a potent, selective, and orally active p38 MAPK inhibitor. It exhibits an IC50 of 44 nM for recombinant purified human p38α and has equipotent inhibitory activity against p38α and p38β. This compound does not affect p38γ or p38δ. It demonstrates anti-asthma activity and can be utilized to enhance memory impaired due to aging or medical conditions like Alzheimer's Disease (AD), as it can penetrate the blood-brain barrier (BBB).
- Potent, selective, and orally active p38 MAPK inhibitor.
- Exhibits equipotent inhibitory activity against p38α and p38β.
- Demonstrates anti-asthma activity.
- Can enhance memory.
- Penetrates the blood-brain barrier (BBB).
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Medchemexpress LLC HY-124422 50mg Medchemexpress, Pentacosanoic acid CAS:506-38-7 Purity:>98%
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Medchemexpress, HY-124422 50mg Pentacosanoic acid CAS:506-38-7 Pentacosanoic acid is a 25-carbon long-chain saturated fatty acid. Pentacosanoic is a conjugate acid of a pentacosanoate. 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-103028 10mg Medchemexpress, GSK962 CAS:2049872-86-6 Purity:>98%
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Medchemexpress, HY-103028 10mg GSK962 CAS:2049872-86-6 GSK962 is an inactive enantiomer of GSK963 and can be used to confirm on-target effects. 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 Palacaparib | 2756333-39-6 | 98.3% | C21H22F2N6O2 | 10MG
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Palacaparib is a CNS-penetrant, selective PARP1 inhibitor supplied for research use. It potently inhibits and traps PARP1 at sites of single-strand DNA breaks and is used in preclinical studies of homologous recombination-deficient cancers and other advanced solid malignancies.
- CNS-penetrant PARP1 inhibitor.
- High selectivity for PARP1 over other PARP family members.
- Potent inhibition and trapping of PARP1 at single-strand breaks.
- High purity (98.3%).
- Supplied as a powder with defined cold-storage recommendations.
- For research use only.
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eMolecules 1393653-34-3 | Medchem Express | Narmafotinib | 5mg | 705861150 | HY-145652 | 527.592 | C28H32F3N5O2
Ambeed | 3-Bromo-2-chloro-6-(difluoromethyl)pyridine | 50mg | 666598643 | A660455 | 1805221-46-8 | MFCD25477647 | 242.450 | C6H3BrClF2N
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Medchemexpress LLC Golgicide A-1 | 1394285-49-4 | 99.9% | 284.3 g/mol | C17H14F2N2 | 10 MG
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Golgicide A-1 (GCA-1) is the cis-diastereomer of Golgicide A supplied as a research reagent. It is described by the manufacturer as a less active isomer of Golgicide A and is reported to weakly inhibit mosquito reproduction. The material is intended for laboratory research use and is provided with supporting analytical documentation.
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Medchemexpress LLC HY-101845 5mg Medchemexpress, FITM CAS:932737-65-0 Purity:>98%
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Medchemexpress, HY-101845 5mg FITM CAS:932737-65-0 FITM is a negative allosteric modulator of mGlu1 receptor with a Ki of 2.5 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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Medchemexpress LLC HY-119093 10mg Medchemexpress, Halopemide CAS:59831-65-1 Purity:>98%
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Medchemexpress, HY-119093 10mg Halopemide CAS:59831-65-1 Halopemide is a potent phospholipase D (PLD) inhibitor, with IC50s of 220 and 310 nM for human PLD1 and PLD2, respectively. Halopemid is a dopamine receptors antagonist, and acts a psychotropic agent. 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 PD-1-IN-24 (compound 1) | 2360909-50-6 | 98.1% | C27H26F3NO3 | 10MG
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PD-1-IN-24 (compound 1) is a small-molecule, orally active PD-1 inhibitor used in preclinical immunology and oncology research. It modulates the PD-1/PD-L1 immune checkpoint pathway and has documented in vivo activity. The compound is provided as a powder or as DMSO solutions, and is supplied with analytical documentation including molecular formula C27H26F3NO3, molecular weight 469.50, and typical purity around 98.1%.
- Orally active small-molecule PD-1 inhibitor.
- Validated for PD-1/PD-L1 pathway modulation in preclinical models.
- Supplied as powder and ready-to-use DMSO solution formats.
- High supplied purity (~98.1%) for reproducible results.
- Available in multiple sizes suitable for screening and in vivo dosing.
- Accompanied by safety data sheet and technical datasheet documentation.
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Accela Chembio Inc 1-bromo-4-chloro-2-fluorobenzene | 100g | 1996-29-8 | MFCD00079708 | 97+% | D: 1.678 | Shelf Life: 1260 Days | Light Sensitive
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1-bromo-4-chloro-2-fluorobenzene | 100g | 1996-29-8 | MFCD00079708 | 97+% | D: 1.678 | Shelf Life: 1260 Days | Light Sensitive
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