Cresols
Medchemexpress LLC Moracin p | 102841-46-3 | 99.6% | 326.34 | C19H18O5 | 10 MG
Moracin P is a 2-arylbenzofuran isolated from Mori Cortex Radicis. It inhibits hypoxia-inducible factor (HIF-1), reduces oxygen-glucose deprivation (OGD)-induced reactive oxygen species (ROS), and demonstrates neuroprotective and anti-inflammatory effects - suitable for in vitro and in vivo research applications.
- Demonstrates HIF-1 inhibitory activity.
- Reduces ROS production in OGD models.
- Exhibits neuroprotective effects.
- Shows anti-inflammatory activity.
- High purity (≈99.6%) and solid form; highly soluble in DMSO (≥100 mg/mL).
- Stability: store protected from light at 4°C; in solution store at -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC o,p'-DDE (2,4'-DDE) | 3424-82-6 | >=95.0% | 50 MG
o,p'-DDE (2,4'-DDE) is an organochlorine pesticide metabolite and degradation product of DDT commonly used as an analytical standard and in toxicological and environmental research.
- Metabolite of DDT commonly used as an analytical standard
- CAS number 3424-82-6
- Molecular formula C14H8Cl4, molecular weight 318.03 g/mol
- Provided as a small solid package suitable for laboratory use
- Purity not specified on product page; check Certificate of Analysis for lot-specific purity
Medchemexpress LLC Serpin A3N Mouse P 5ug
Recombinant mouse Serpin A3N protein produced in Pichia pastoris and purified with an N-terminal 6xHis tag. Supplied as a small-quantity aliquot suitable for biochemical assays, protease inhibition studies, and antibody validation in in vitro applications.
- Recombinant mouse origin for species-specific studies.
- Expressed in Pichia pastoris for eukaryotic expression characteristics.
- N-terminal 6xHis tag enables affinity purification and detection.
- Supplied in a 5 μg aliquot for low-volume assays and pilot experiments.
- Suitable for protease inhibition assays, biochemical characterization, and antibody validation.
TARGETMOL CHEMICALS INC E/Z-BIX02188 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BIX02188 is a specific MEK5 inhibitor (IC50 4.3 nM) also inhibits ERK5 catalytic activity (IC50 810 nM) and does not inhibit closely related kinases MEK1/2 JNK2 and ERK2. purity: 99%
![Medchemexpress LLC 1-[5-(2,4-difluorophenyl)sulfanyl-4-nitrothiophen-2-yl]ethanone | 1247819-59-5 | MFCD22580421 | ≥98.0% | 315.32 g·mol-1 | C12H7F2NO3S2 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000222915.png-250.jpg)
Medchemexpress LLC 1-[5-(2,4-difluorophenyl)sulfanyl-4-nitrothiophen-2-yl]ethanone | 1247819-59-5 | MFCD22580421 | ≥98.0% | 315.32 g·mol-1 | C12H7F2NO3S2 | 5 MG
A cell-permeable small-molecule inhibitor of the deubiquitinating enzyme ubiquitin-specific protease 7 (USP7) that also inhibits USP47. It is used in biochemical and cell-based studies to probe deubiquitination pathways; reported EC50 values are 8.01 μM for USP7 and 8.74 μM for USP47. Molecular formula C12H7F2NO3S2; molecular weight 315.32 g·mol-1; CAS 1247819-59-5.
- Cell-permeable small-molecule inhibitor of USP7 and USP47 (EC50 8.01 μM and 8.74 μM).
- Suitable for biochemical and cell-based deubiquitination assays.
- Reported activity values support use in target validation and pathway studies.
- Provided in small research quantities for laboratory experiments (1-10 mg).
- Molecular formula C12H7F2NO3S2 and molecular weight 315.32 g·mol-1.
eMolecules 4770-43-8 | 7-Methoxyindoline hydrochloride | MFCD11506101 | 1g
Ambeed | (2-((Furan-2-ylmethyl)amino)pyrimidin-5-yl)boronic acid | 100mg | 752810273 | A1677289 | | 219.010 | C9H10BN3O3
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Medchemexpress LLC 4-(dimethylamino)benzaldehyde | 100-10-7 | MFCD00003381 | 99.9% | 149.19 g/mol | C9H11NO | 250g
p-Dimethylaminobenzaldehyde (4-Dimethylaminobenzaldehyde) can be used as a chromogenic reagent or as an absorbent agent for heavy metal ions[1][2]
Cayman Chemical 4-hydroxy Nebivolol hydrochl
A major metabolite of nebivolol; formed by the hydroxylation of nebivolol by CYP2D6
Selleck Chemical LLC 740 Y-P
740 Y-P (PDGFR 740Y-P 740YPDGFR) is a cell-permeable phosphopeptide activator of PI3K