Phenols
Medchemexpress LLC Amitifadine hydrochloride | 410074-74-7 | 99.6% | 264.58 | 50 MG
Amitifadine hydrochloride is a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI). It exhibits IC50 values of 12 nM for serotonin, 23 nM for norepinephrine, and 96 nM for dopamine in HEK 293 cells.
- Functions as a triple monoamine reuptake inhibitor, affecting serotonin, norepinephrine, and dopamine reuptake.
- High purity of 99.64%.
- Soluble in DMSO at concentrations ≥ 100 mg/mL and in H2O at 50 mg/mL.
- Studied in clinical trials for major depressive disorder.
- Strictly for research purposes.
eMolecules 65383-58-6 | 4-Ethoxy-3-methoxyphenol | Combi-Blocks | MFCD19301270 | 168.192 | C9H12O3 | 95.000 | CCOc1ccc(O)cc1OC | 1g | 296402175
4-Ethoxy-3-methoxyphenol | Combi-Blocks | 65383-58-6 | MFCD19301270 | 168.192 | C9H12O3 | 95.000 | CCOc1ccc(O)cc1OC | 1g | 296402175
Medchemexpress LLC p-SCN-Bn-DOTA 25mg | 127985-74-4 | 25 MG
p-SCN-Bn-DOTA is a bifunctional chelating agent that combines an isothiocyanate reactive group for covalent protein conjugation with a DOTA macrocycle for stable radiometal chelation. It is used to conjugate radionuclides to antibodies and other biomolecules for radioimaging and radioimmunotherapy applications.
- Bifunctional chelator with an isothiocyanate reactive group for protein conjugation.
- DOTA macrocycle enables stable chelation of radiometals.
- Suitable for antibody conjugation and radioimmunoassays.
- Available as a solid powder, typically supplied in milligram-scale quantities.
- High purity suitable for research applications.
Medchemexpress LLC EM-163 | 1206480-93-4 | 95.0% | 849.88 | 5 MG
EM-163 is a summative BB-Loop analog that can alleviate inflammation and prevent death from toxic shock by targeting the TIR domain of MyD88. It can be used in the study of SEB poisoning (SEB: Staphylococcal enterotoxin B).
- Targets the TIR domain, binding to the protein of the TIR domain and inhibiting the interaction of the TIR-TIR domain.
- Inhibits the production of TNF-α, IFN-γ, IL-2, and IL-1b induced by SEB in human mononuclear cells.
- Effectively inhibits the release of proinflammatory cytokines and delays or avoids death from toxic shock caused by SEB in BALB/c mice.
Medchemexpress LLC GS-443902 trisodium (GS-441524 triphosphate trisodium) | 1355050-21-3 | 100.0% | 597.15 g/mol | C12H13N5Na3O13P3 | 25MG
GS-443902 trisodium is the triphosphate metabolite of remdesivir and a potent inhibitor of viral RNA-dependent RNA polymerases (RdRp). It is used in antiviral research to study polymerase inhibition and remdesivir pharmacology, and is supplied as a high-purity, water-soluble trisodium salt suitable for in vitro and in vivo formulation studies.
- Active triphosphate metabolite of remdesivir
- Inhibits viral RNA-dependent RNA polymerases
- High reported purity for analytical work
- Water soluble; requires ultrasonic for full dissolution
- Suitable for in vitro and in vivo formulation studies
- Requires low-temperature storage and light protection
Medchemexpress LLC Chromotropic acid, disodium salt, dihydrate | 5808-22-0 | MFCD00150612 | >98.5% | 400.29 g·mol⁻¹ | C10H6Na2O8S2 · 2 H2O | 10G
Chromotropic acid disodium dihydrate is the disodium salt dihydrate of chromotropic acid supplied as a light-brown solid powder used as a chromogenic reagent for colorimetric detection and quantification of formaldehyde and other analytical applications. The compound is suitable for research and laboratory analytical chemistry and is provided in multiple laboratory pack sizes.
- Chromogenic reagent for formaldehyde detection.
- Suitable for colorimetric and spectrophotometric assays.
- Available in multiple pack sizes, including 10 g.
- Solid powder, light brown to brown in appearance.
- High assay purity (≥98.5% on anhydrous substance) suitable for analytical use.
- Provided with safety data sheet and product documentation.
Medchemexpress LLC RS100329 hydrochloride | 1215654-26-4 | 99.6% | 462.89 g/mol | C20H26ClF3N4O3 | 100 MG
RS100329 hydrochloride is the hydrochloride salt of a potent and subtype-selective α1A-adrenoceptor antagonist used as a research reagent in receptor pharmacology and selectivity studies. The compound is supplied as a solid, with a reported molecular weight of 462.89 g/mol and high batch-specific purity; consult the certificate of analysis for exact values and handling instructions.
- Potent, selective α1A-adrenoceptor antagonist.
- Hydrochloride salt form for improved stability and handling.
- High purity suitable for in vitro pharmacology (COA available).
- Supplied as a solid for dissolution in common organic solvents.
- Used in receptor binding and functional assays to assess selectivity.
Medchemexpress LLC JNK Inhibitor VIII 10mM 1mL | 894804-07-0 | 10MM 1ML
JNK Inhibitor VIII (TCS JNK 6o) is a c-Jun N-terminal kinases (JNK-1 -2 and -3) inhibitor with Ki values of 2 nM 4 nM 52 nM respectively and has IC50 values of 45 nM and 160 nM for JNK-1 and -2 respectively[1