SML4477

Biotin-4-aminophenol, APEX2 Substrate

≥98% (HPLC)

• Synonym(e): (3aS,4S,6aR)-Hexahydro-N-(4-hydroxyphenyl)-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanamide, BP5, N-(4-hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
• Empirische Formel (Hill-System): C₁₆H₂₁N₃O₃S
• CAS-Nummer: 901770-40-9
• Molekulargewicht: 335.42
• UNSPSC Code: 12352200
• Assay: ≥98% (HPLC)
• Form: powder

Eigenschaften

• Quality Segment: 100
• assay: ≥98% (HPLC)
• form: powder
• color: white to beige
• solubility: DMSO: 2 mg/mL, clear
• storage temp.: -10 to -25°C

Beschreibung

Biochem/physiol Actions

Biotin-4-aminophenol (BP5) is a high-reactivity, cell-permeable APEX2 substrate engineered to resolve the spatiotemporal dynamics of cytosolic protein complexes with superior specificity. Mechanistically, BP5 generates short-lived phenoxyl radicals upon H2O2 activation that covalently tag unmodified tyrosine residues while preserving phosphorylated sites (pTyr). Crucially, its elevated reactivity dictates a tighter effective capture radius (<10 nm effective capture) via rapid radical quenching and self-polymerization, thereby eliminating the broad "diffusion cloud" and background noise associated with traditional Biotin-Phenol (BP1). This physiochemical refinement prioritizes the labeling of direct interactors over bystanders, enabling the high-fidelity capture of weak and transient assemblies often lost during cell lysis. Validated against highly dynamic signaling networks—including EGFR adaptors (GRB2, STS1) and the ILK complex—BP5 successfully differentiates interactions indistinguishable by BP1, providing a robust platform for mapping mobile interactomes and protein translocation events at organelle interfaces.

Sicherheitshinweise

• Lagerklasse: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable