Benzenoids
Medchemexpress LLC 2-Hydroxyestrone-d4 | 81586-97-2 | 97.9% | 290.39 | 1 MG
2-Hydroxyestrone-d4 is the deuterium-labeled form of 2-Hydroxyestrone. 2-Hydroxyestrone (Catecholestrone) acts as a specific receptor-mediated antiestrogenic agent and is recognized for its anticarcinogenic properties.
- This compound can be used as a tracer.
- This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process.
- Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
Apexbio Technology LLC Closantel Sodium 61438-64-0 10mM (in 1mL DMSO)
Closantel Sodium (CAS 61438-64-0) is a small-molecule inhibitor targeting the KinA/Spo0F two-component signaling system It is designed to inhibit the KinA/Spo0F phosphotransfer interaction thereby interfering with bacterial signal transduction pathways Closantel Sodium exerts its biological activity primarily through inhibition of the KinA/Spo0F phosphotransfer In vitro studies demonstrate inhibitory activity with an IC50 value of approximately 3 8 M Based on these pharmacological properties Closantel Sodium holds research potential in antimicrobial studies particularly for investigating Gram-positive bacterial signaling mechanisms and antibiotic resistance pathways
Apexbio Technology LLC Dextromethorphan hydrobromide 125-69-9 5g
Dextromethorphan hydrobromide is a small-molecule inhibitor targeting neuronal ion channels including voltage-gated Na and Ca channels and antagonizing N-methyl-D-aspartate (NMDA) receptors It is designed to inhibit voltage-gated inward currents and NMDA receptor-induced currents thereby modulating neuronal excitability and neuroprotection pathways Dextromethorphan hydrobromide exerts its biological activity primarily through inhibition of voltage-gated Na and Ca channels and antagonism of NMDA receptors In cultured cortical neurons dextromethorphan hydrobromide demonstrates inhibition of NMDA receptor-induced currents with an IC value of approximately 80 M Based on these pharmacological properties dextromethorphan hydrobromide holds research potential in the investigation of excitotoxicity neuronal injury mechanisms and therapeutic strategies for ischemic or neurodegenerative conditions
Medchemexpress LLC HY-13788A 2mg Medchemexpress, LY 344864 (S-enantiomer) CAS:186544-27-4 Purity:>98%
Medchemexpress, HY-13788A 2mg LY 344864 (S-enantiomer) CAS:186544-27-4 LY 344864 S-enantiomer is the S-enantiomer of LY344864. LY344864 is a 5-HT1F receptor agonist. 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.
eMolecules AstaTech / (R)-1-(35-DICHLOROPHENYL)ETHYLAMINE / 0.25g / 200619803 / SC1347 / 95.000 / 617710-53-9 / MFCD07772552 / 190.070 / C8H9Cl2N
AstaTech / (R)-1-(35-DICHLOROPHENYL)ETHYLAMINE / 0.25g / 200619803 / SC1347 / 95.000 / 617710-53-9 / MFCD07772552 / 190.070 / C8H9Cl2N
eMolecules 4-ETHOXY-3-FLUOROPHENOL | 98121-48-3 | MFCD21984328 | 1g
AstaTech | 4-ETHOXY-3-FLUOROPHENOL | 1g | 571814628 | 36938 | 97.000 | 98121-48-3 | MFCD21984328 | 156.156 | C8H9FO2
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eMolecules Fenretinide | 65646-68-6 | MFCD00792674 | 100mg
Apollo Scientific | Fenretinide | 100mg | 562460510 | BIFK0053 | 99.000 | 65646-68-6 | MFCD00792674 | 391.555 | C26H33NO2
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