Unsubstituted Phenols
eMolecules 693288-97-0 | Medchem Express | CPPHA | 5mg | 446264375 | HY-14612 | MFCD12912405 | 406.82 | C22H15ClN2O4
Medchem Express | CPPHA | 5mg | 446264375 | HY-14612 | 693288-97-0 | MFCD12912405 | 406.820 | C22H15ClN2O4
Medchemexpress LLC Ko 143 | 461054-93-3 | MFCD19053160 | 99.9% | 469.57 g·mol⁻¹ | C26H35N3O5 | 50 MG
Ko 143 is a potent, selective inhibitor of the ATP-binding cassette subfamily G member 2 (ABCG2/BCRP) used as a research reagent to investigate transporter-mediated drug efflux and multidrug resistance. It exhibits nanomolar activity in biochemical and cell-based assays and shows substantial selectivity versus other transporters. Supplied as a research-grade small molecule for laboratory use only.
- Potent ABCG2 inhibition at nanomolar concentrations.
- High selectivity over P-gp and MRP-1.
- Suitable for studies of transporter activity and drug resistance.
- Supplied in milligram quantities for laboratory experiments.
- Stable as powder when stored appropriately at low temperature.
Medchemexpress LLC Eltrombopag-13C4 | 1217230-31-3 | C2113C4H22N4O4 | 1 MG
Eltrombopag-13C4 (SB-497115-13C4) is 13C-labeled Z-Eltrombopag. Z-Eltrombopag is an orally active thrombopoietin-receptor non-peptide agonist with platelet-stimulating activity for the study of chronic immune thrombocytopenia. Eltrombopag also has strong inhibitory effects on multidrug-resistant Staphylococcus aureus and can induce apoptosis in liver cancer cells.
- Used as a tracer.
- Functions as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Acts as an orally active thrombopoietin-receptor non-peptide agonist.
- Exhibits platelet-stimulating activity, useful for studying chronic immune thrombocytopenia.
- Demonstrates strong inhibitory effects on multidrug-resistant Staphylococcus aureus.
- Induces apoptosis in liver cancer cells.
Medchemexpress LLC ML-109 | 1186649-91-1 | 99.0% | 523.58 | 50 MG
ML-109 is identified as a potent and full agonist of the thyroid stimulating hormone receptor (TSHR), exhibiting an EC50 of 40 nM. While being surprisingly stable under neutral and basic conditions with a half-life of approximately 16 hours, it degrades at lower pH levels, with a half-life of about 3 hours. It shows no activity at FSHR or LHCGR.
- Potent and full thyroid stimulating hormone receptor (TSHR) agonist
- EC50 of 40 nM for TSHR
- No activity at FSHR or LHCGR
- Stable at neutral and basic conditions (t1/2 of ~16 h)
Medchemexpress LLC Ko 143 | 461054-93-3 | MFCD19053160 | 100.0% | 469.6 g/mol | C26H35N3O5 | 1 ML
Potent, selective ABCG2 (BCRP) inhibitor used to probe transporter function and multidrug resistance. Shows over 200-fold selectivity versus P-gp and MRP-1; supplied as a 10 mM solution in 1 mL for laboratory use.
- Potent and selective ABCG2 (BCRP) inhibitor for transporter studies.
- Displays greater than 200-fold selectivity over P-gp and MRP-1.
- Supplied as a 10 mM solution in 1 mL for convenient dosing.
- Molecular weight 469.6 g/mol and formula C26H35N3O5.
- CAS number 461054-93-3 for unambiguous identification.
eMolecules 863774-58-7 | Medchem Express | Dimethylenastron | 5mg | 446270566 | HY-19944 | MFCD09264157 | 302.39 | C16H18N2O2S
Medchem Express | Dimethylenastron | 5mg | 446270566 | HY-19944 | 863774-58-7 | MFCD09264157 | 302.390 | C16H18N2O2S
eMolecules 69839-83-4 | Medchem Express | Didox | 5mg | 446269827 | HY-19387 | MFCD01667810 | 169.136 | C7H7NO4
Medchem Express | Didox | 5mg | 446269827 | HY-19387 | 69839-83-4 | MFCD01667810 | 169.136 | C7H7NO4
eMolecules 10537-47-0 | Medchem Express | Tyrphostin A9 | 50mg | 446265839 | HY-15511 | MFCD00209853 | 282.387 | C18H22N2O
Medchem Express | Imatinib-d8 | 1mg | 791206451 | HY-15463S | 1092942-82-9 | 501.664 | C29H31N7O
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eMolecules Building Block Tool
Medchemexpress LLC IKK-16 hydrochloride | 1186195-62-9 | MFCD09971091 | 100.0% | 520.09 g·mol⁻¹ | C28H30ClN5OS | 5 MG
IKK-16 hydrochloride is the hydrochloride salt form of a selective IκB kinase (IKK) inhibitor used in research to modulate NF-κB signaling pathways. It is provided as a characterized research reagent for biochemical and cellular studies where inhibition of IKK is required.
- Selective inhibition of IκB kinase to modulate NF-κB signaling.
- Suitable for biochemical and cellular assays.
- High reported purity for reliable experimental results.
- Hydrochloride salt form improves solubility in common solvents.
- Available in small quantities for research workflows.
Sigma Aldrich Fine Chemicals Biosciences Phenol natural, 97%, FG | 108-95-2 | MFCD00002143 |
Phenol natural, 97%, FG | Purity: 97% | Mol Wt: 94.11 | 108-95-2 | MFCD00002143 |
Enzo Life Sciences Tyrphostin 47 (RG-50864) (AG-213) (5mg). CAS: 122520-86-9
A potent inhibitor of EGF receptor kinase activity (IC50‘s:EGFR = 2.4 µM, PDGFR = 3.5 µM, p210bcr-abl=5.9 µM, insulin receptor = 640 µM). Purity: ≥99% (TLC). Solubility: Soluble at 20 mg/ml in 100% ethanol or DMSO. Long Term Storage: -20°C.
Selleck Chemical LLC 2 6-Dihydroxybenzoic acid
2 6-Dihydroxybenzoic acid ( -resorcylic acid 2-Carboxyresorcinol 2 6-Resorcylic acid) is a phenolic compound which is known to have poor biological performance such as DPPH scavenging activity and microbial growth inhibition
Medchemexpress LLC Taxifolin 7-O-α-L-rhamnoside | 137592-12-2 | 20 MG
Taxifolin 7-O-rhamnoside (Taxifolin 7-O-α-L-rhamnoside) is a flavonoid isolated from *Hypericum japonicum*. It is intended for research use only.
- Purity: 98.13%
- Appearance: Solid, off-white to light yellow
- Molecular weight: 450.39
- Formula: C21H22O11
- Soluble in DMSO at 125 mg/mL
- Storage: 4°C, protected from light
- In solvent, -80°C for 6 months or -20°C for 1 month (protect from light)