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020 _a9789811923203
024 7 _a10.1007/978-981-19-2320-3
_2doi
040 _aES-MaUEC
_bspa
_cES-MaUEC
100 1 _aSpasov, Alexander A
_eautor
_0(orcid)0000-0002-7185-4826
_1https://orcid.org/0000-0002-7185-4826
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
245 1 0 _aPharmacology of Drug Stereoisomers
_cby Alexander A Spasov, Igor N Iezhitsa, Pavel M Vassiliev, Alexander A Ozerov, Renu Agarwal
250 _a1st edition 2022
264 1 _aSingapore
_bSpringer International Publishing
_c2022
300 _a1 recurso en línea (XI, 207 páginas)
_b174 ilustraciones, 6 ilustraciones a color
336 _atexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
347 _aarchivo de texto
_bPDF
490 0 _aProgress in Drug Research
_x2297-4555
_v76
505 0 _aPreface -- General principles of chirality -- Quantitative methods of analysing chirality drugs - Chirality and pharmacokinetics -- Drugs regulating the function of peripheral nervous system -- In silico search for chiral drug compounds.
520 _aThe book is devoted to an important aspect of pharmacology and pharmaceutical chemistry, i.e. the significance of stereoisomerism of drugs for their biological effect from the point of view of their pharmacokinetics, pharmacodynamics and toxicology. The authors review the landmarks in the development of stereochemistry and stereopharmacology. Present-day IUPAC terminology is discussed; general issues of stereoisomerism are considered including separation of racemic mixtures and asymmetric synthesis of isomers, methods of quantifying the isomers of a drug in biological material. The authors put special emphasis on general problems of the influence of stereoisomerism on pharmacological and adverse effects of drugs. A classification of drugs based on stereochemical properties of their isomers is proposed. Possibilities of interaction of stereoisomers in racemic mixtures are discussed. A considerable portion of the book is devoted to pharmacological action of the main groups of drugs whose structure includes asymmetric atoms (that is, drugs with several isomers). Detailed attention is paid to advisability of developing single isomer drugs and to the specifics of their study at the stage of preclinical and clinical trials.
700 1 _aIezhitsa, Igor N
_eautor
_0(orcid)0000-0002-2852-8486
_1https://orcid.org/0000-0002-2852-8486
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
700 1 _aVassiliev, Pavel M
_eautor
_0(orcid)0000-0002-8188-5052
_1https://orcid.org/0000-0002-8188-5052
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
700 1 _aOzerov, Alexander A
_eautor
_0(orcid)0000-0002-4721-0959
_1https://orcid.org/0000-0002-4721-0959
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
700 1 _aAgarwal, Renu
_eautor
_0(orcid)0000-0002-3050-7449
_1https://orcid.org/0000-0002-3050-7449
_4aut
_4http://id.loc.gov/vocabulary/relators/aut
776 0 8 _iPrinted edition:
_z9789811923197
776 0 8 _iPrinted edition:
_z9789811923210
776 0 8 _iPrinted edition:
_z9789811923227
856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1007/978-981-19-2320-3
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942 _2lcc
_cLE
988 _aSpringer_BiomedLife_2022
999 _c393941
_d393941