Benzenoids
Medchemexpress LLC o,p'-DDE (2,4'-dichlorodiphenyldichloroethylene) | 3424-82-6 | 25 MG
o,p'-DDE (2,4'-DDE) is an organochlorine pesticide metabolite and degradation product of DDT supplied as an analytical reference standard for environmental and toxicology research. It is provided in small vial quantities suitable for laboratory analytical workflows.
- Used as an analytical standard for environmental and toxicology analysis.
- Metabolite and degradation product of DDT.
- Chemical formula C14H8Cl4.
- Molecular weight 318.03 g/mol.
- Available in small vial sizes including 25 mg for lab-scale analyses.
- Refer to the product datasheet for exact purity and handling instructions.
Cambridge Isotope Laboratories 2 3 7 8-Tetrabromodibenzo-p-dioxin (13C12 99%) 5 ug/mL in nonane 4 x 1 2 mL
2 3 7 8-Tetrabromodibenzo-p-dioxin (13C12 99%) 5 ug/mL in nonane 4 x 1 2 mL
Medchemexpress LLC Animal-Free KGF-2/FG 10ug
KGF-2/FGF-10 proteins coordinate embryonic development regulate cell proliferation and differentiation and are indispensable in branching morphogenesis This multifunctional protein may aid in wound healing Animal-Free KGF-2/FGF-10 Protein Human (His) is the recombinant human-derived animal-FreeKGF-2/FGF-10 protein expressed by E coli with C-His C-His labeled tag This product is for cell culture use only
Medchemexpress LLC Ethanone, 1-[5-[(2,4-difluorophenyl)thio]-4-nitro-2-thienyl]- | 1247819-59-5 | 98.4% | 315.32 | 25 MG
P 22077 is a cell-permeable ubiquitin-specific protease 7 (USP7) inhibitor that also inhibits USP47. It demonstrates antiproliferative activity against human HCT116 cells and reduces the viability of neuroblastoma cells. The compound increases p53 activity, induces apoptosis in p53 wild-type and HDM2-expressing neuroblastoma cells, and enhances the cytotoxic effects of Dox and VP-16. In vivo, it exhibits potent antitumor activities in xenograft mouse models.
- Cell-permeable ubiquitin-specific protease 7 (USP7) inhibitor
- Inhibits USP47
- Exhibits antiproliferative activity against human HCT116 cells
- Reduces cell viability of neuroblastoma cells
- Increases p53 activity and induces apoptosis in p53 wild-type cells
- Enhances cytotoxic effect of Dox and VP-16 on neuroblastoma cells
- Shows potent antitumor activities in xenograft mouse models
Medchemexpress LLC Histone H1-derived Peptide | 889112-06-5 | 99.9% | 1252.51 | 10 MG
Histone H1-derived Peptide is a phosphopeptide whose peptide substrates contain a sequence in accordance with the optimal recognition motif for CDK. It can be used for detecting CDK1-cyclinB1 enzyme activity.
- Phosphopeptide designed for CDK activity detection
- Contains sequence matching optimal recognition motif for CDK
- Used for detecting CDK1-cyclinB1 enzyme activity
Medchemexpress LLC PfLDH P. falciparum 10ug | 10ug
The pfHPRT (Plasmodium falciparum hypoxanthine-guanine phosphoribosyltransferase) protein is a member of the LDH/MDH (lactate dehydrogenase/malate dehydrogenase) superfamily It plays a crucial role in the purine metabolism salvage pathway of the malaria-causing parasite Plasmodium falciparum PfLDH Protein P falciparum (His) is the recombinant PfLDH protein expressed by E coli with C-His labeled tag
Medchemexpress LLC 5'-ODMT cEt N-Bz A Phosphoramidite (amidite) | 1197033-19-4 | >98.5% | 899.97 | 25 MG
This nucleoside phosphoramidite monomer is used for synthesizing locked nucleic acid (LNA) analog oligonucleotides, acting as a building block for antisense oligonucleotides (ASOs) to target complementary RNA sequences. Its 2',4'-constrained ethyl (cEt) modification enhances hybridization affinity and mismatch discrimination with RNA, improving oligonucleotides' resistance to exonuclease digestion and enabling gene expression regulation.
- Synthesizes locked nucleic acid (LNA) analog oligonucleotides.
- Enhances RNA hybridization affinity and mismatch discrimination.
- Improves oligonucleotide resistance to exonuclease digestion.
- Facilitates RNase H-dependent mRNA degradation.
- Used in antisense drug development and gene research.
- Improves qPCR probe/primer stability and melting temperature.
Medchemexpress LLC P-CAB agent 2 hydrochloride | 2209911-80-6 | C22H26ClFN2O4S | 1 ML
P-CAB agent 2 hydrochloride is a potent and orally active potassium-competitive acid blocker and a gastric acid secretion inhibitor. It inhibits H+/K+-ATPase activity with an IC50 value of <100 nM. It also inhibits the hERG potassium channel with an IC50 value of 18.69 μM. This agent shows no acute toxicity and inhibits histamine-induced gastric acid secretion.
- Potent and orally active potassium-competitive acid blocker.
- Inhibits gastric acid secretion.
- Inhibits H+/K+-ATPase activity with an IC50 value of <100 nM.
- Inhibits hERG potassium channel with an IC50 value of 18.69 μM.
- Shows no acute toxicity.
- Effectively inhibits histamine-induced gastric acid secretion.
Medchemexpress LLC P-CAB agent 2 hydrochloride | 2209911-80-6 | MFCD18878621 | C22H26ClFN2O4S | 25 MG
P-CAB agent 2 hydrochloride is a potent and orally active potassium-competitive acid blocker and a gastric acid secretion inhibitor. It inhibits H+/K+-ATPase activity with an IC50 value of <100 nM. It also inhibits the hERG potassium channel with an IC50 value of 18.69 μM. This compound shows no acute toxicity and inhibits histamine-induced gastric acid secretion.
- Potent and orally active potassium-competitive acid blocker
- Gastric acid secretion inhibitor
- Inhibits H+/K+-ATPase activity with an IC50 value of <100 nM
- Inhibits the hERG potassium channel with an IC50 value of 18.69 μM
- Shows no acute toxicity
- Inhibits histamine-induced gastric acid secretion
Medchemexpress LLC P-ethylhydratropic acid | 3585-52-2 | 99.5% | 178.23 g·mol-1 | C11H14O2 | 10 MG
p-Ethylhydratropic acid is an identified impurity of ibuprofen supplied as an analytical reference standard for impurity profiling and method development.
- impurity of ibuprofen used for analytical reference and profiling.
- cas number 3585-52-2.
- molecular formula c11h14o2 and molecular weight 178.23 g·mol-1.
- high purity by hplc (≈99.5%).
- common package sizes: 5 mg, 10 mg.
- storage: store at room temperature (3 years); in solvent -80°C (2 years), -20°C (1 year).
- intended for research use only; not for human use.
TARGETMOL CHEMICALS INC P 22077 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. P 22077 (P22077) is an inhibitor of ubiquitin-specific protease USP7 with EC50 of 8.6 uM. It also inhibits the closely related USP47. purity: 98%
Medchemexpress LLC P-selectin Mouse B 20ug
P-selectin is a Ca(2 )-dependent receptor on myeloid cells that specifically binds to carbohydrates on neutrophils and monocytes It mediates interactions between activated endothelial cells or platelets and leukocytes by recognizing sialic acid-Lewis X P-selectin Protein Mouse (Biotinylated HEK293 Avi-His) is the recombinant mouse-derived P-selectin protein expressed by HEK293 with C-Avi C-6 His labeled tag