R9156

Raltitrexed

≥98% (HPLC), solid

• Sinónimos: L-Glutamic acid, N-((5-(((1,4-dihydro-2-methyl-4-oxo-6-quinazolinyl)methyl)methylamino)-2-thienyl)carbonyl), ICI-D-1694, ZD-1694
• Fórmula empírica (notación de Hill): C₂₁H₂₂N₄O₆S
• Número de CAS: 112887-68-0
• Peso molecular: 458.49
• UNSPSC Code: 12352200
• PubChem Substance ID: 329824044
• NACRES: NA.77

Propiedades

• assay: ≥98% (HPLC)
• form: solid
• color: off-white to light yellow
• solubility: H₂O: ≥10 mg/mL; DMSO: ≥40 mg/mL
• originator: AstraZeneca
• storage temp.: 2-8°C
• SMILES string: O=C1NC(C)=NC2=C1C=C(CN(C3=CC=C(C(N[C@H](CCC(O)=O)C(O)=O)=O)S3)C)C=C2

Descripción

Biochem/physiol Actions

Raltitrexed is a folate-based inhibitor of thymidylate synthase (TS) that is rapidly and extensively metabolized to its more potent polyglutamate derivatives. By inhibiting the formation of precursor pyrimidine nucleotides, raltitrexed prevents the formation of DNA and RNA, which are required for the growth and survival of both normal cells and cancer cells.

Features and Benefits

This compound is a featured product for Apoptosis research. Click here to discover more featured Apoptosis products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound was developed by AstraZeneca. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Información de seguridad

• pictograms: GHS06,GHS08
• signalword: Danger
• hcodes: H300,H360
• pcodes: P201 - P301 + P310 + P330
• Hazard Classifications: Acute Tox. 2 Oral - Repr. 1B
• Storage Class: 6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
• wgk_germany: WGK 2
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges