About: Piotr Przybylski

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Polish pharmaceutical scientist

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) Polish pharmaceutical scientist (en) polski naukowiec (nauki farmaceutyczne, nauki chemiczne chemia organiczna) (pl)
rdfs:label	Piotr Przybylski (en) Piotr Przybylski (pl) Piotr Przybylski (sl) Piotr Przybylski (ast) Piotr Przybylski (es) Piotr Przybylski (nl)
skos:prefLabel	Piotr Przybylski (en) Piotr Przybylski (pl) Piotr Przybylski (sl) Piotr Przybylski (ast) Piotr Przybylski (es) Piotr Przybylski (nl)
name	Piotr Przybylski (en) Piotr Przybylski (pl) Piotr Przybylski (sl) Piotr Przybylski (ast) Piotr Przybylski (es) Piotr Przybylski (nl)
Polish scientist ID (deprecated)	wds:Q43148729-381d58e3-4aa9-714b-fee8-0afb90b95697
Polish scientist ID (deprecated)	124595
Scopus author ID	wds:Q43148729-9E9913D9-4C52-478F-B5C8-8062175C2C45
Scopus author ID	6701517479
given name	wds:Q43148729-68BCA7BD-0428-4BBD-8C78-D9BB08E362AD
given name	Piotr
instance of	wds:Q43148729-9BE26690-4CAB-476E-94CA-70482515E4A4
instance of	Homo sapiens
doctoral student	wds:Q43148729-8E7B7D1C-6294-4AF0-BF4F-4B0A687DDB50
interested in	wds:Q43148729-9A1B0A40-DE89-424A-A4C0-028DE56C5637
doctoral student	Krystian Pyta
interested in	organic chemistry
occupation	wds:Q43148729-59BA01EE-D9B2-4BBB-8145-7FF40C21F389
employer	wds:Q43148729-C3A406F4-8C25-42C4-BF38-3BBFA73ED430
sex or gender	wds:Q43148729-F3129E2C-7ABF-49ED-9DB7-E2FF4AB1EEA0
academic degree	wds:Q43148729-4AC5F8F5-F148-4CEA-8D38-DB76C04D4E01 wds:Q43148729-64E98AA2-F6E7-4F7E-B301-8B1EB7442574 wds:Q43148729-661AC33C-F96C-4862-AFB3-23035A56876B
family name	wds:Q43148729-F08E1B0F-DD7E-4425-B07C-931B69A28AA8
occupation	researcher
employer	Adam Mickiewicz University in Poznań
sex or gender	male
academic degree	professor doctorate habilitation
family name	Przybylski
ORCID iD	wds:Q43148729-EAA1B4B4-7E84-4C75-90F5-C50B00F17DD8
ORCID iD	https://orcid.org/0000-0001-8072-5877
ORCID iD	0000-0001-8072-5877
is about of	https://pl.wikipedia.org/wiki/Piotr_Przybylski_(chemik) https://www.wikidata.org/wiki/Special:EntityData/Q43148729
is author of	Biological Properties of Schiff Bases and Azo Derivatives of Phenols Kinetic studies of complexation reaction of polyoxaalkyl phosphates with Fe(III) in ethanol 1H- and 13C-NMR, FTIR, UV-VIS, ESI-MS, and PM5 studies as well as emission properties of a new Schiff base of gossypol with 5-methoxytryptamine and a new hydrazone of gossypol with dansylhydrazine. Fragmentation pathways of new aza derivatives of 16-membered macrolide antibiotic--analog of Josamycin investigated by ESI and FAB mass spectrometric methods. X-ray, FT-IR, ESI MS and PM5 studies of Schiff base of gossypol with allylamine and its complexes with alkali metal cations and perchlorate anion Crystal structure of Schiff base derivative of gossypol with 3,6,9-trioxa-decylamine Synthesis, Antibacterial, and Anticancer Evaluation of Novel Spiramycin-Like Conjugates Containing C(5) Triazole Arm. 16-Membered Macrolide Lactone Derivatives Bearing a Triazole-Functionalized Arm at the Aglycone C13 Position as Antibacterial and Anticancer Agents. 1H NMR, FT-IR and MS studies and PM5 semiempirical calculations of complexes between the Schiff base of gossypol with 2-(aminomethyl)-15-crown-5 and Ca2+, Pb2+ and Ba2+ cations Schiff base of gossypol with 3,6,9-trioxa-decylamine complexes with monovalent cations studied by mass spectrometry, (1)H-NMR, FTIR, and PM5 semiempirical methods. Antifungal activity of alkyl and heterocyclic aza-derivatives of gossypol as well as their complexes with NaClO4 against Fusarium oxysporum f. sp. lupini. Spectroscopic studies and PM5 semiempirical calculations of new Schiff bases of gossypol with polyoxaalkylamines. Cascade reactions as efficient and universal tools for construction and modification of 6-, 5-, 4- and 3-membered sulfur heterocycles of biological relevance Conversion of leucomycin-A3 antibiotic into novel triazole analogues via regio- and diastereoselective SN1′ substitution with allylic rearrangement and 1,3-dipolar cycloaddition of CuAAC type Synthesis, structure and antimicrobial evaluation of a new gossypol triazole conjugates functionalized with aliphatic chains and benzyloxy groups Impact of metal cation complexation and protonation on tautomeric and resonance forms of the oxaalkyl Schiff bases derived from 5-substituted salicylaldehyde and 2-hydroxy-1-naphthlaldehyde MALDI-TOF tandem mass spectrometric analysis of novel aza-analogues of semi-synthetic ansamycin antibiotic - rifampicin Spectroscopic and theoretical studies of the protonation of N-(5-nitrosalicylidene)-ethylamine X-ray, spectroscopic and computational studies of the tautomeric structure of a new hydrazone of 5-nitrosalicylaldehyde with indole-3-acetic hydrazide Synthesis, crystal structures and antibacterial activity studies of aza-derivatives of phytoalexin from cotton plant – gossypol CP/MAS spectroscopy in the determination of the tautomeric forms of gossypol, its Schiff bases and hydrazones in the solid state Monensin A benzyl ester and its complexes with monovalent metal cations studied by spectroscopic, mass spectrometry and semiempirical methods Multinuclear NMR, FT-IR, ESI MS studies and PM5 semiempirical calculations of new ethylene glycol ester of lasalocid acid and their complexes with K+ cation The Schiff base of gossypol with 2-(aminomethyl)-18-crown-6 complexes and H+, Li+, Na+, K+, Rb+, Cs+ cations studied by ESI MS, 1H NMR, FT-IR and PM5 semiempirical methods Complexes of Schiff base of gossypol with 5-hydroxy-3-oxapentylamine and some monovalent cations studied by ESI MS as well as PM5 semiempirical methods Spectroscopic studies of Schiff bases of 2,2′-dihydroxybiphenyl-3-carbaldehyde and para substituted anilines Spectroscopic study and PM5 semiempirical calculations of tautomeric forms of gossypol Schiff base with n-butylamine in the solid state and in the solution Spectroscopic studies and PM3 semiempirical calculations of Schiff bases of gossypol withL-amino acid methyl esters Spectroscopic studies and PM5 semiempirical calculations of new Schiff bases of gossypol with amino derivatives of crown ethers Spectroscopic studies of new Schiff and Schiff–Mannich bases of ortho-derivatives of 4-bromophenol The Schiff base of gossypol with 2-(aminomethyl)-15-crown-5 complexes with monovalent cations studied by MS,1H NMR, FT-IR and PM5 semiempirical methods Spectroscopic and semiempirical studies of gossypol complexes with Fe2+ and Fe3+ cations Modifications and Biological Activity of Natural and Semisynthetic 16-Membered Macrolide Antibiotics 14- and 15-membered lactone macrolides and their analogues and hybrids: structure, molecular mechanism of action and biological activity Synthesis and antibacterial activity of new N-alkylammonium and carbonate-triazole derivatives within desosamine of 14- and 15-membered lactone macrolides Synthesis and antimicrobial properties of monensin A esters

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