Attributes | Values |
---|
rdf:type
| |
Description
| - Benzo[a]pyrene (BaP) belongs to the group of polycyclic aromatic hydrocarbons (PAHs) that have mutagenic and pro-carcinogenic properties. The PAHs compounds are ubiquitous environmental pollutants requiring metabolic activation tohave the carcinogenic properties. The activation steps are mainly presented by hydroxylation and epoxidation of thearomatic system by the group of cytochrome P450 isoenzymes (mainly the P450 1A1 isoenzyme). The epoxy-derivatives of the PAHs molecules are highly reactive electrophiles, able to bind to any primary aminogroup. When sucha molecule is bound to the nucleotide, the structure, as well as natural function, of the nucleic acid is corrupted; thecarcinogenic properties of the BaP molecule take effect in this way. The small molecules, such as benzo[a]pyrene, cannot induce the immunogenic response in animals; therefore it needs to be conjugated to the protein carrier molecule.
- Benzo[a]pyrene (BaP) belongs to the group of polycyclic aromatic hydrocarbons (PAHs) that have mutagenic and pro-carcinogenic properties. The PAHs compounds are ubiquitous environmental pollutants requiring metabolic activation tohave the carcinogenic properties. The activation steps are mainly presented by hydroxylation and epoxidation of thearomatic system by the group of cytochrome P450 isoenzymes (mainly the P450 1A1 isoenzyme). The epoxy-derivatives of the PAHs molecules are highly reactive electrophiles, able to bind to any primary aminogroup. When sucha molecule is bound to the nucleotide, the structure, as well as natural function, of the nucleic acid is corrupted; thecarcinogenic properties of the BaP molecule take effect in this way. The small molecules, such as benzo[a]pyrene, cannot induce the immunogenic response in animals; therefore it needs to be conjugated to the protein carrier molecule. (en)
|
Title
| - Chemical synthesis of benzo[a]pyrene derivatives and their use in development of ELISA method
- Chemical synthesis of benzo[a]pyrene derivatives and their use in development of ELISA method (en)
|
skos:prefLabel
| - Chemical synthesis of benzo[a]pyrene derivatives and their use in development of ELISA method
- Chemical synthesis of benzo[a]pyrene derivatives and their use in development of ELISA method (en)
|
skos:notation
| - RIV/00216224:14310/07:00052274!RIV12-MSM-14310___
|
http://linked.open...avai/riv/aktivita
| |
http://linked.open...avai/riv/aktivity
| |
http://linked.open...vai/riv/dodaniDat
| |
http://linked.open...aciTvurceVysledku
| |
http://linked.open.../riv/druhVysledku
| |
http://linked.open...iv/duvernostUdaju
| |
http://linked.open...titaPredkladatele
| |
http://linked.open...dnocenehoVysledku
| |
http://linked.open...ai/riv/idVysledku
| - RIV/00216224:14310/07:00052274
|
http://linked.open...riv/jazykVysledku
| |
http://linked.open.../riv/klicovaSlova
| - Bioconjugate Benzopyrene MALDI-TOF ELISA Immunization (en)
|
http://linked.open.../riv/klicoveSlovo
| |
http://linked.open...ontrolniKodProRIV
| |
http://linked.open...v/mistoKonaniAkce
| |
http://linked.open...i/riv/mistoVydani
| |
http://linked.open...i/riv/nazevZdroje
| - XI. Pracovní setkání biochemiků a molekulárních biologů, Brno, 31. – 1. února 2007.
|
http://linked.open...in/vavai/riv/obor
| |
http://linked.open...ichTvurcuVysledku
| |
http://linked.open...cetTvurcuVysledku
| |
http://linked.open...vavai/riv/projekt
| |
http://linked.open...UplatneniVysledku
| |
http://linked.open...iv/tvurceVysledku
| - Jílek, Milan
- Prouza, Marek
- Skládal, Petr
- Suchánek, Miloslav
- Přibyl, Jan
|
http://linked.open...vavai/riv/typAkce
| |
http://linked.open.../riv/zahajeniAkce
| |
number of pages
| |
http://purl.org/ne...btex#hasPublisher
| |
https://schema.org/isbn
| |
http://localhost/t...ganizacniJednotka
| |
is http://linked.open...avai/riv/vysledek
of | |