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Filtered Search Results
Cayman Chemical NGaminoLArginine hydrochlori
Inhibits nNOS, iNOS, and eNOS (Ki = 0.3, 3, and 2.5 μM, respectively); can be used both in cell culture and in vivo
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Medchemexpress LLC RS 67333 hydrochloride | 168986-60-5 | 99.7% | 389.36 g/mol | C19H30Cl2N2O2 | 50 MG
RS 67333 hydrochloride is the hydrochloride salt of a selective partial agonist of the 5-HT4 (serotonin) receptor. Supplied as a solid research reagent, it is used in neuroscience studies of 5-HT4 receptor pharmacology, neuroprotection, and related pathways. For research use only.
- Selective partial agonist of 5-HT4 receptor.
- High purity (99.7%).
- Supplied as a solid suitable for in vitro and in vivo studies.
- Stable when stored sealed at 4°C, away from moisture.
- Available in small laboratory quantities for research applications.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000364449 ZZW-115 HYDROCHLORI 5MG
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Medchemexpress LLC Hypidone hydrochloride | 1339058-04-6 | 99.7% | 334.84 g/mol | C18H23ClN2O2 | 100 MG
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Hypidone hydrochloride is the hydrochloride salt of a research compound with potent serotonergic activity. It functions as a selective serotonin (5-HT) uptake inhibitor and a 5-HT1A receptor agonist, and has demonstrated oral activity in animal models of depression. Supplied as a powder for laboratory research use only; not for human or clinical use.
- High purity suitable for research applications.
- Dual mechanism: serotonin uptake inhibition and 5-HT1A receptor agonism.
- Demonstrated oral activity in animal depression models.
- Available in multiple pack sizes including small research quantities.
- Recommended sealed storage away from moisture; in solvent store at -80°C for long term.
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Selleck Chemical LLC OTS964-5mg
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OTS964 is a potent TOPK inhibitor with high affinity and selectivity and IC50 value is 28 nM. OTS964 is also a potent inhibitor of the cyclin-dependent kinase CDK11 with Kd of 40 nM. OTS964 treatment activates autophagy in glioma cells and induces apoptosis of human lung cancer cells in mouse xenografts.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000411131 TACRINE HYDROCHLORI 10MM 1ML
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eMolecules 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one | 569646-79-3 | MFCD16990622 | 100mg
Toronto Research Chemicals | 4-(3-ethoxy-4-hydroxyphenyl)butan-2-one | 100mg | 601595350 | E677460 | | 569646-79-3 | MFCD16990622 | 208.257 | C12H16O3
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Matrix Scientific 2,4-DICHLORO-6-AMINOPHENOL2-10
2,4-dichloro-6-aminophenol Mf C6h5cl2no Mw 178.02 Cas 527-62-8 Mdl MFCD00035766
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eMolecules Ambeed / 55-(Perfluoropropane-22-diyl)bis(isobenzofuran-13-dione) / 1g / 490493560 / A110372 / / 1107-00-2 / MFCD00039143 / 444.241 / C19H6F6O6
Ambeed / 55-(Perfluoropropane-22-diyl)bis(isobenzofuran-13-dione) / 1g / 490493560 / A110372 / / 1107-00-2 / MFCD00039143 / 444.241 / C19H6F6O6
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5000411769 NEFOPAM HYDROCHLORI 100MG
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Ambeed 2 1Aminocyclohexyl acetic acid
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2-(1-Aminocyclohexyl)acetic acid, 37631-92-8, 95%
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5000362084 DI-PAL-MTO 5MG
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Medchemexpress LLC Delapril hydrochloride | 83435-67-0 | 98.0% | 489.00 g·mol⁻¹ | C26H33ClN2O5 | 1 ML
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Delapril hydrochloride is the hydrochloride salt of delapril, an angiotensin-converting enzyme (ACE) inhibitor used in cardiovascular research and preclinical studies. The compound is provided both as a ready-to-use 10 mM solution in DMSO (1 mL) and in solid quantities. Typical reported purity is 98.0% and the molecular weight is 489.00 g·mol⁻¹. Store and handle according to supplier safety data.
- ACE inhibitor used in cardiovascular research.
- Available as 10 mM solution in DMSO (1 mL) and as solid quantities.
- High reported purity, 98.0%.
- Molecular weight 489.00 g·mol⁻¹.
- CAS number 83435-67-0 for unambiguous identification.
- Store solid at 4°C; store solution frozen for long-term stability.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000398730 OXYTOCIN PARALLEL DI 1MG
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Apexbio Technology LLC Clemizole hydrochloride 1163-36-6 10mM (in 1mL DMSO)
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Clemizole hydrochloride is a histamine H1 receptor antagonist reported to inhibit hepatitis C virus (HCV) replication by targeting the viral NS4B protein a component essential for viral RNA replication Clemizole demonstrates antiviral activity in vitro against HCV genotype 2a subgenomic replicons exhibiting an IC50 value around 8 mM When combined with HCV protease inhibitors (such as VX950 or SCH503034) clemizole displays synergistic antiviral effects In contrast additive antiviral effects occur in combination with interferon ribavirin or polymerase inhibitors Clemizole is utilized in research contexts aimed at evaluating its efficacy potential antiviral combinations metabolism pathways and pharmacokinetics relevant to its consideration as a therapeutic candidate for HCV infection
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