Aminophenols
TARGETMOL CHEMICALS INC ZM 226600 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ZM 226600 is an ATP-sensitive potassium channel opener with an EC50 value of 500 nM. ZM226600 has an inhibitory effect on spontaneous bladder activity. purity: 100%
Medchemexpress LLC Phenol, 2,4-bis(1,1-dimethylethyl)- | 96-76-4 | MFCD00008828 | 100.0% | 206.33 g/mol | C14H22O | 500 G
2,4-Di-tert-butylphenol (CAS 96-76-4) is a substituted phenol used as a research chemical and chemical intermediate. It has reported antioxidant and anti-inflammatory activities, and is used in studies of nuclear receptor modulation and in the manufacture of antioxidants, UV stabilizers, and related compounds.
- High purity suitable for analytical and research use.
- White to yellow solid for easy handling and storage.
- Exhibits RXRα activation and antioxidant activity in biological assays.
- Useful intermediate for synthesis of antioxidants and UV stabilizers.
- Available in bulk quantities upon request for scale-up and production.
Medchemexpress LLC dTAGV-1 hydrochloride | 2624313-16-0 | 99.8% | C68H91ClN6O14S | 10MG
dTAGV-1 hydrochloride is a selective PROTAC degrader that targets FKBP12F36V-tagged proteins, enabling rapid and tunable protein degradation in cellular and in vivo studies. Supplied as a hydrochloride salt with high reported purity, it is intended for research applications in chemical biology and targeted protein degradation.
- Selective degradation of FKBP12F36V-tagged proteins.
- Effective in cellular and in vivo assays.
- Supplied as hydrochloride salt for improved stability.
- High reported purity suitable for research use.
- Available in small milligram scales for laboratory studies.
- Recommended storage conditions support long-term stability.
Medchemexpress LLC Lavendustin B | 125697-91-8 | MFCD00133446 | 98.0% | 365.38 | C21H19NO5 | 5 MG
Lavendustin B is a small-molecule research reagent that inhibits HIV-1 integrase interaction with LEDGF/p75, functions as an ATP-competitive GLUT1 inhibitor, and exhibits weak tyrosine kinase inhibition. Supplied as a solid for laboratory research use, it is characterized by its CAS number 125697-91-8 and defined molecular properties.
- High purity (98.0%).
- Molecular weight 365.38 g/mol.
- Chemical formula C21H19NO5.
- Available in small milligram quantities suitable for screening and assays.
- Stable as powder when stored at -20°C for long-term storage.
- Suitable for biochemical and cell-based assay applications.
eMolecules Medchem Express / Pinobanksin / 5mg / 769193675 / HY-N3062 / / 548-82-3 / MFCD07784478 / 272.256 / C15H12O5
Medchem Express / Pinobanksin / 5mg / 769193675 / HY-N3062 / / 548-82-3 / MFCD07784478 / 272.256 / C15H12O5