LEADER 04600nam 2201441z- 450 001 9910557109903321 005 20231214132852.0 035 $a(CKB)5400000000040948 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/69151 035 $a(EXLCZ)995400000000040948 100 $a20202105d2020 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aAdvances in Plant Alkaloid Research 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2020 215 $a1 electronic resource (278 p.) 311 $a3-03943-172-2 311 $a3-03943-173-0 330 $aPlant alkaloids are critical components of modern medicine and pharmaceuticals. These compounds are also becoming increasingly important for industrial uses as part of the green chemistry revolution. This Special Issue will focus on the molecular advances being made in understanding how such a large and diverse class of compounds are made by plants and how metabolic engineering advances are increasing the overall yield of crucial precursors. 606 $aResearch & information: general$2bicssc 606 $aBiology, life sciences$2bicssc 610 $acanthin-6-one 610 $aPicrolemma huberi 610 $aSimaroubaceae 610 $aantiplasmodial activity 610 $aSarcococca hookeriana 610 $asarchookloides A?C 610 $asteroidal alkaloid 610 $acytotoxicity 610 $aRhodophiala 610 $aalkaloids 610 $amolecular docking 610 $aAChE 610 $aBuChE 610 $aGC-MS 610 $aMahonia imbricata 610 $aBerberidaceae 610 $aisoquinoline alkaloid 610 $amahimbrine A 610 $ahedgehog signaling 610 $aVeratrum californicum 610 $acyclopamine 610 $aHPLC-MS 610 $aShh-Light II cells 610 $ahalogencyclopropane 610 $adichlorocarbene 610 $aepoxidation 610 $avindoline 610 $acatharanthine 610 $adimer alkaloids 610 $avindoline trimer 610 $aRuta graveolens 610 $aphotosystem II 610 $aChl a fluorescence 610 $aHill reaction inhibitors 610 $aacridone alkaloids 610 $abenzylisoquinoline alkaloids 610 $acytochrome P450 monooxygenase 610 $amedicinal properties 610 $amethyltransferase 610 $aNelumbo nucifera 610 $anorcoclaurine synthase 610 $asacred lotus 610 $astereochemistry 610 $aAristotelia chilensis Molina Stuntz 610 $avascular activity 610 $aendothelium-independent 610 $aindole alkaloid 610 $a8-oxo-9-dihydromakomakine 610 $avoltage-dependent calcium channels 610 $aCatharanthus roseus 610 $acambial meristematic cells 610 $aAspergillus flavus 610 $aterpenoid indole alkaloids 610 $abiosynthesis 610 $aBuxaceae 610 $aBorago officinalis 610 $aCrassocephalum 610 $aCopper-dependent diamine oxidase 610 $aGynura bicolor 610 $aHomospermidine synthase 610 $aLolium perenne 610 $aNecic acids 610 $aNecine bases 610 $aPyrrolizidine alkaloid biosynthesis 610 $aSenecionine 610 $atropane alkaloids 610 $ascopolamine 610 $acocaine 610 $acalystegine 610 $achemistry 610 $apharmacology 610 $abiotechnological production 610 $aErythroxylaceae 610 $aErythroxylum coca 610 $anext generation sequencing 610 $atraditional medicine 610 $abioprospecting 610 $atropane 610 $alate-stage functionalization 610 $asulfinate 610 $aDiversinateTM 610 $anatural product 610 $amedicinal chemistry 610 $apapaverine 610 $ascaffold 610 $alibrary 610 $abiodiscovery 610 $aSwinglea glutinosa 610 $adereplication 610 $aacridones 610 $aphenylacrylamides 615 7$aResearch & information: general 615 7$aBiology, life sciences 700 $aD'Auria$b John C$4edt$01307049 702 $aD'Auria$b John C$4oth 906 $aBOOK 912 $a9910557109903321 996 $aAdvances in Plant Alkaloid Research$93028655 997 $aUNINA