M2070

Merbarone

≥98% (HPLC), solid

• Synonym(e): 5-(N-Phenylcarbamoyl)-2-thiobarbituric acid, NSC-336628
• Empirische Formel (Hill-System): C₁₁H₉N₃O₃S
• CAS-Nummer: 97534-21-9
• Molekulargewicht: 263.27
• NACRES: NA.77
• PubChem Substance ID: 24724534
• UNSPSC Code: 12352200
• MDL number: MFCD00866337
• Assay: ≥98% (HPLC)
• Form: solid

Eigenschaften

• Quality Segment: 200
• assay: ≥98% (HPLC)
• form: solid
• drug control: regulated under CDSA - not available from Sigma-Aldrich Canada
• solubility: DMSO: >5 mg/mL
• storage temp.: 2-8°C
• SMILES string: O=C1NC(=S)NC(=O)C1C(=O)Nc2ccccc2
• InChI: 1S/C11H9N3O3S/c15-8(12-6-4-2-1-3-5-6)7-9(16)13-11(18)14-10(7)17/h1-5,7H,(H,12,15)(H2,13,14,16,17,18)
• InChI key: JARCFMKMOFFIGZ-UHFFFAOYSA-N

Beschreibung

Application

Merbarone has been used to study its effect on the occurrence of DNA lesions.

Biochem/physiol Actions

Thiobarbituric acid with aniline joined by an amide linkage forms merbarone. It is known to prolong cell cycle progression by inducing DNA double strand breaks, retarding S phase and arresting G2 phase. This delays cell entry into mitosis. Merbarone possesses cytotoxic and genotoxic action and promotes endoreduplication. Merbarone has mild antitumor action and is also found to nephrotoxic.

Selective topoisomerase II inhibitor. Blocks topo II-mediated DNA cleavage without stabilizing DNA-topo II-cleavable complexes. Induces apoptosis in CEM cells via caspase 3 dependent mechanism.

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• Was ist los?: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• PSA (Persönliche Schutzausrüstung): Eyeshields, Gloves, type N95 (US)