Phenanthrenes and derivatives
Accela Chembio Inc Triphenylene | 25g | 217-59-4 | MFCD00001108 | 97+% | Shelf Life: 900 Days | Light Sensitive
Triphenylene | 25g | 217-59-4 | MFCD00001108 | 97+% | Shelf Life: 900 Days | Light Sensitive
Medchemexpress LLC 6-aminochrysene | 2642-98-0 | MFCD00003699 | 99.7% | 243.30 g/mol | C18H13N | 1 ML
6-Aminochrysene is an aromatic amine (CAS 2642-98-0) supplied as a ready-to-use 10 mM solution in DMSO. Provided in a 1 mL vial for research use, the material is characterized by a defined molecular weight and high purity suitable for biochemical, metabolic, and toxicology studies.
- Ready-to-use 10 mM solution in DMSO.
- Supplied in a 1 mL vial for small-scale experiments.
- High purity (99.7%) suitable for analytical applications.
- Molecular weight 243.30 g/mol for stoichiometric calculations.
- Appropriate for biochemical and metabolic study workflows.
Apexbio Technology LLC PERYLENE D12-100mg
Perylene-d12 (CAS No 1520-96-3) is a deuterated chemical compound used primarily in the field of biomedical research as a tracer in mass spectrometry and as a standard for quantitative analysis Derived from perylene its mechanism of action involves intercalation into DNA and interaction with cellular membranes impacting nucleic acid processes Perylene-d12 exhibits potent in vitro activity typically observed in the nanomolar to low micromolar range It is widely used across various cell models and animal studies particularly in drug screening and toxicology assessments Experimental concentrations typically depend on the specific research design
Sigma Aldrich Fine Chemicals Biosciences Chrysene-d12 98 atom % D | 1719-03-5 | MFCD00134283 | 50MG
Chrysene-d12 98 atom % D | Purity: 99% (CP) | Mol Wt: 240.36 | 1719-03-5 | MFCD00134283 | 50MG
Medchemexpress LLC Aristolochic acid B | 475-80-9 | 311.25 | 5 MG
Aristolochic acid B (Aristolochic Acid II) is an orally active major component of aristolochic acid (AA). It can be isolated from plants of the genus Aristolochica. Aristolochic acid B forms DNA adducts, is mutagenic, and exhibits a greater carcinogenic risk in vivo than Aristolochic acid I.
- Target: DNA alkylator/crosslinker
- Research area: Cancer
- Mechanism: Forms DNA adducts and is mutagenic
- Carcinogenic risk: Exhibits greater carcinogenic risk in vivo than Aristolochic acid I
- Appearance: Solid
- Melting/freezing point: 270-272°C
Medchemexpress LLC SKF 38393 hydrochloride | 62717-42-4 | MFCD00069248 | >98.0% | 291.77 g/mol | C16H18ClNO2 | 200MG
SKF 38393 hydrochloride is the hydrochloride salt of SKF-38393, a selective dopamine D1 receptor agonist with a reported IC50 of approximately 110 nM. Supplied as a research-grade solid analytical standard, it is used for in vitro pharmacology, receptor binding, and analytical assays. Not for human or clinical use.
- Selective D1 receptor agonist, reported IC50 ≈ 110 nM.
- Hydrochloride salt form improves solubility for biological assays.
- Molecular weight 291.77 g/mol.
- Chemical formula C16H18ClNO2.
- Provided as a solid analytical standard suitable for in vitro studies.
- Typical purities reported ≥98% by HPLC from third-party suppliers.
- Not for human or clinical use; for research only.
eMolecules 141-82-2 | Malonic acid | Oakwood Chemical104.061 | C3H4O4 | 99.000 | OC(=O)CC(O)=O | 1g | 603242440
Malonic acid | Oakwood Chemical | 141-82-2104.061 | C3H4O4 | 99.000 | OC(=O)CC(O)=O | 1g | 603242440
Aobchem Triphenylene-2-carbaldehyde | ≥95% | CAS 96404-79-4 | C19H12O | 1g
Triphenylene-2-carbaldehyde | ≥95% | CAS 96404-79-4 | C19H12O | 1g
Medchemexpress LLC 2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(4-hydroxyphenyl)-4-(4-methoxyphenyl)-, (3R,4S)-rel- | 1213777-80-0 | 723112 | 99.6% | C22H20O4 | 25 MG
Triphen diol is a phenol diol derivative known for its excellent anticancer activity against pancreatic cancer and cholangiocarcinoma. It induces pancreatic cell apoptosis through both caspase-mediated and caspase-independent mechanisms, and is intended for research use only.
- Inhibits proliferation of pancreatic cells (IC50 values: 8 μM for HPAC and PANC-1; 0.8 μM for MIAPaCa-2).
- Induces caspase-dependent apoptosis in MIAPaCa-2 and PANC-1 cells (60% early-stage, 30% late-stage).
- Reduces Bcl-2 levels in MIAPaCa-2 and HPAC cell lines.
- Significantly inhibits tumor proliferation in male Balb/c nude mice with MIAPaCa2 cells.
- Shows enhanced efficacy when combined with gemcitabine in vivo.