LEADER 04258nam 22007695 450 001 9910733706403321 005 20200704034936.0 010 $a1-299-33667-1 010 $a3-7091-1312-1 024 7 $a10.1007/978-3-7091-1312-7 035 $a(CKB)2670000000337172 035 $a(EBL)1083120 035 $a(OCoLC)828794572 035 $a(SSID)ssj0000878595 035 $a(PQKBManifestationID)11476020 035 $a(PQKBTitleCode)TC0000878595 035 $a(PQKBWorkID)10850659 035 $a(PQKB)10001456 035 $a(DE-He213)978-3-7091-1312-7 035 $a(MiAaPQ)EBC1083120 035 $a(PPN)168331446 035 $a(EXLCZ)992670000000337172 100 $a20130217d2013 u| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 14$aThe Chemistry of Mycotoxins /$fby Stefan Bräse, Franziska Gläser, Carsten Kramer, Stephanie Lindner, Anna M. Linsenmeier, Kye-Simeon Masters, Anne C. Meister, Bettina M. Ruff, Sabilla Zhong 205 $a1st ed. 2013. 210 1$aVienna :$cSpringer Vienna :$cImprint: Springer,$d2013. 215 $a1 online resource (303 p.) 225 1 $aProgress in the Chemistry of Organic Natural Products,$x2191-7043 ;$v97 300 $aDescription based upon print version of record. 311 $a3-7091-1746-1 311 $a3-7091-1311-3 320 $aIncludes bibliographical references and indexes. 327 $aAflatoxins -- Citrinin -- Ergot alkaloids -- Fumonisins -- Ochratoxins -- Trichothecenes -- (Thio)diketopiperazines -- Alternaria metabolites -- Skyrins -- Xanthones -- Cytochalasans -- Peptidic mycotoxins. 330 $aThe biological activity of mycotoxins ranges from weak and/or sometimes positive effects, such as antibacterial activity (see penicillin derivatives derived from Penicillium strains) to strong mutagenic (e. g. aflatoxins, patulin), carcinogenic (e. g. aflatoxins), teratogenic, neurotoxic (e. g. ochratoxins), nephrotoxic (e. g. fumonisins, citrinin), hepatotoxic, and immunotoxic (e. g. ochratoxins, diketopiperazines) activity. Nowadays, many laboratories around the world are specialized in the detection of mycotoxins in food products and contaminated material found in housing. In this volume, a focus on the most important classes of mycotoxins is provided and their chemistry of the last ten years is discussed. In each Section, the individual biological impact is outlined. Sections are arranged according to mycotoxin classes (e. g. aflatoxins) and/or structural classes (e. g. resorcinyl lactones, diketopiperazines). The biology of mycotoxins is also described. 410 0$aProgress in the Chemistry of Organic Natural Products,$x2191-7043 ;$v97 606 $aOrganic chemistry 606 $aPharmacology 606 $aPharmacy 606 $aOrganic Chemistry$3https://scigraph.springernature.com/ontologies/product-market-codes/C19007 606 $aPharmacology/Toxicology$3https://scigraph.springernature.com/ontologies/product-market-codes/B21007 606 $aPharmacy$3https://scigraph.springernature.com/ontologies/product-market-codes/F00008 615 0$aOrganic chemistry. 615 0$aPharmacology. 615 0$aPharmacy. 615 14$aOrganic Chemistry. 615 24$aPharmacology/Toxicology. 615 24$aPharmacy. 676 $a615.19005 676 $a615.9/52/92 700 $aBräse$b Stefan$4aut$4http://id.loc.gov/vocabulary/relators/aut$0856039 702 $aGläser$b Franziska$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aKramer$b Carsten$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aLindner$b Stephanie$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aLinsenmeier$b Anna M$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aMasters$b Kye-Simeon$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aMeister$b Anne C$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aRuff$b Bettina M$4aut$4http://id.loc.gov/vocabulary/relators/aut 702 $aZhong$b Sabilla$4aut$4http://id.loc.gov/vocabulary/relators/aut 906 $aBOOK 912 $a9910733706403321 996 $aThe Chemistry of Mycotoxins$93397853 997 $aUNINA