| Weight | 302.329 g/mol |
|---|---|
| Formula | C20H14O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
BPDE (55097-80-8, 58917-67-2)
Score:
#1736 in Physics
,
#2056 in Biochemistry
,
#4283 in Biology
,
#5402 in Chemistry
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- Protection by quercetin and quercetin-rich fruit juice against induction of oxidative DNA damage and formation of BPDE-DNA adducts in human lymphocytes. (Mutation Research-genetic Toxicology and Environmental Mutagenesis, 2005)
- Mutability of p53 hotspot codons to benzo(a)pyrene diol epoxide (BPDE) and the frequency of p53 mutations in nontumorous human lung. (Cancer Research, 2001)
- Translesion synthesis by human DNA polymerase on a DNA template containing a single stereoisomer of dG-(+)- or dG-(-)-anti-N2-BPDE (7,8-dihydroxy-anti-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene) (Biochemistry, 2002)
- DNA Polymerase Is Specifically Required for Recovery from the Benzo[a]pyrene-Dihydrodiol Epoxide (BPDE)-induced S-phase Checkpoint (Journal of Biological Chemistry, 2005)
- Arsenite and its biomethylated metabolites interfere with the formation and repair of stable BPDE-induced DNA adducts in human cells and impair XPAzf and Fpg. (DNA Repair, 2003)
- Effect of dna repair gene polymorphisms on BPDE-DNA adducts in human lymphocytes (International Journal of Cancer, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C3C(=C1)C=CC4=C3C(=CC5=C4C6C(O6)C(C5O)O)C=C2
-
InChIKeyDQEPMTIXHXSFOR-UHFFFAOYSA-N
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