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Fórmula empírica (notación de Hill):
C34H24O5
Peso molecular:
512.55
UNSPSC Code:
12171500
PubChem Substance ID:
MDL number:
Servicio técnico
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99-102% (NMR)
Quality Segment
form
solid
shipped in
wet ice
storage temp.
−20°C
SMILES string
O=C1C=CC2=C(c3ccc(OCc4ccccc4)cc3OC2=C1)c5ccccc5C(=O)OCc6ccccc6
InChI
1S/C34H24O5/c35-25-15-17-29-31(19-25)39-32-20-26(37-21-23-9-3-1-4-10-23)16-18-30(32)33(29)27-13-7-8-14-28(27)34(36)38-22-24-11-5-2-6-12-24/h1-20H,21-22H2
InChI key
YZJGKSLPSGPFEV-UHFFFAOYSA-N
Application
DBF is dealkylated by cytochromes P450 (especially CYP2C8, CYP2C9, CYP2C19, and CYP3A) to form a fluorescein ester. Dibenzylfluorescein was reported to be suitable for in vitro assessment of the initial screening of CYP3A4-
mediated drug interactions. The fluorescent fluorescein product can be quantitated after the addition of base, which hydrolyzes the ester and increases the pH for optimal fluorescein fluorescence detection.
mediated drug interactions. The fluorescent fluorescein product can be quantitated after the addition of base, which hydrolyzes the ester and increases the pH for optimal fluorescein fluorescence detection.
DBF is dealkylated by cytochromes P450 (especially CYP2C8, CYP2C9, CYP2C19, and CYP3A) to form a fluorescein ester. The fluorescent fluorescein product can be quantitated after the addition of base, which hydrolyzes the ester and increases the pH for optimal fluorescein fluorescence detection.
Other Notes
Dibenzylfluorescein is light sensitive and should be protected from direct sunlight or UV sources.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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