D1285

2′,3′-Dideoxyadenosin

≥97% (HPLC)

• Synonym(e): ddA
• Empirische Formel (Hill-System): C₁₀H₁₃N₅O₂
• CAS-Nummer: 4097-22-7
• Molekulargewicht: 235.24
• Beilstein: 619924
• EG-Nummer: 223-853-2
• MDL-Nummer: MFCD00010534
• UNSPSC-Code: 41106305
• PubChem Substanz-ID: 24893397
• NACRES: NA.51

Eigenschaften

• Assay: ≥97% (HPLC)
• Form: powder
• Optische Aktivität: [α]/D -28.0±1.0
• mp (Schmelzpunkt): 181-184 °C (lit.)
• Löslichkeit: water: 100 mg/mL, clear, colorless
• Lagertemp.: 2-8°C
• SMILES String: Nc1ncnc2n(cnc12)[C@H]3CC[C@@H](CO)O3
• InChI: 1S/C10H13N5O2/c11-9-8-10(13-4-12-9)15(5-14-8)7-2-1-6(3-16)17-7/h4-7,16H,1-3H2,(H2,11,12,13)/t6-,7+/m0/s1
• InChIKey: WVXRAFOPTSTNLL-NKWVEPMBSA-N
• Angaben zum Gen: human ... DCK(1633)

Beschreibung

Allgemeine Beschreibung

2′,3′-Dideoxyadenosine is a nucleoside analog of deoxyadenosine. On deamination, it is converted to dideoxyinosine. It inhibits adenylyl cyclase and may play a key role in the inhibition of tumor progression. It is a potent inhibitor of reverse transcriptase enzyme of human immunodeficiency virus.

Anwendung

2′,3′-Dideoxyadenosine (ddA), a specific adenylyl cyclase inhibitor, is useful in biological process and pathway studies involving adenylyl cyclase activity and cAMP pool modulation.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 2
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)