about
Structure and antimicrobial properties of monensin A and its derivatives: summary of the achievementsSpectroscopic and semiempirical studies of a proton channel formed by the methyl ester of monensin A.Monensin A acid complexes as a model of electrogenic transport of sodium cation.Polyether ionophores-promising bioactive molecules for cancer therapy.Antiproliferative activity of salinomycin and its derivatives.In vitro activity of salinomycin and monensin derivatives against Trypanosoma bruceiDifferences in Antiproliferative Activity Between Salinomycin-AZT Conjugates Obtained via 'Click' and Esterification Reactions.Synthesis, antiproliferative activity and molecular docking of Colchicine derivatives.Anti-proliferative activity of Monensin and its tertiary amide derivatives.Synthesis and antiproliferative activity of new bioconjugates of Salinomycin with amino acid esters.Synthesis and biological activity of salinomycin conjugates with floxuridine.Synthesis, antiproliferative and antibacterial evaluation of C-ring modified colchicine analogues.Synthesis, anticancer and antibacterial activity of salinomycin N-benzyl amides.Synthesis, antiproliferative and antibacterial activity of new amides of salinomycin.Synthesis, cytotoxicity and antibacterial activity of new esters of polyether antibiotic - salinomycin.One-pot synthesis and cytotoxicity studies of new Mannich base derivatives of polyether antibiotic--lasalocid acid.Angiogenesis and cancer stem cells: New perspectives on therapy of ovarian cancer.Salinomycin: a new cancer drug candidate.Synthesis and Antiproliferative Activity of Silybin Conjugates with Salinomycin and Monensin.Structural characterization and antibacterial activity against clinical isolates of Staphylococcus of N-phenylamide of monensin A and its 1:1 complexes with monovalent cations.Reinvestigation of the structure of monensin A phenylurethane sodium salt based on X-ray crystallographic and spectroscopic studies, and its activity against hospital strains of methicillin-resistant S. epidermidis and S. aureus.Synthesis, FT-IR, ¹H, ¹³CNMR, ESI MS and PM5 studies of a new Mannich base of polyether antibiotic - Lasalocid acid and its complexes with Li⁺, Na⁺ and K⁺ cations.Synthesis and antimicrobial properties of monensin A esters.Monensin A methyl ester complexes with Li+, Na+, and K+ cations studied by ESI-MS, 1H- and 13C-NMR, FTIR, as well as PM5 semiempirical method.Spectroscopic, mass spectrometry, and semiempirical investigation of a new ester of Monensin A with ethylene glycol and its complexes with monovalent metal cations.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.Trypanosoma brucei: trypanocidal and cell swelling activities of lasalocid acid.FT-IR, 1H, 13C NMR, ESI-MS and semiempirical investigation of the structures of Monensin phenyl urethane complexes with the sodium cation.Synthesis and antimicrobial activity of amide derivatives of polyether antibiotic-salinomycin.Salinomycin derivatives exhibit activity against primary acute lymphoblastic leukemia (ALL) cells in vitro.Electrogenic and nonelectrogenic ion fluxes across lipid and mitochondrial membranes mediated by monensin and monensin ethyl ester.Spectroscopic studies of the equilibrium between complexes of lasalocid acid with propargylamine and metal cations.Tertiary amides of Salinomycin: A new group of antibacterial agents against Bacillus anthracis and methicillin-resistant Staphylococcus epidermidis.Synthesis, crystal structures and antibacterial activity studies of aza-derivatives of phytoalexin from cotton plant – gossypolEI MS and ESI MS studies of the bisesquiterpene from cotton seeds—Gossypol and its Aza-derivativesX-ray Crystallographic, FT-IR, and Density Functional Theory Studies of the Salt Formed between Dipicrylamine and 1,5,7-Triazabicyclo[4.4.0]dec-1-eneSalinomycin – a breakthrough in the treatment of ovarian cancer?Antiproliferative Activity and Molecular Docking of Novel Double-Modified Colchicine DerivativesCytotoxic and trypanocidal activities of cinchona alkaloid derivativesStructural and antimicrobial studies of a new N-phenylamide of monensin A complex with sodium chloride
P50
Q21284778-1A1423E4-47E3-443D-BCDE-64085505DDDEQ31051123-691E4EC3-E8CF-4723-840D-38E47BCB23C9Q34260582-BE4839BA-5893-4075-A489-E0CBF9519273Q34643914-E0B7BF8B-2B93-454D-9098-3301590A2D2DQ34644181-CC8B494C-98C1-45C0-A899-E77C90C8E121Q37149494-5716D4A3-29BD-4D75-9219-7EAD04B5D1DAQ38750367-C5508E32-EE6C-41E7-BCF3-F2CD045AB9FCQ38801044-0C95BFA5-95FE-40FF-B46A-EFBB0A5CDD20Q38838139-CD69AFD4-62F8-4F04-90E9-A56E84E631C9Q38854403-67A9B197-2DB8-40C4-896D-B972D396C066Q38913829-0D95FAE9-5DE5-4798-8D80-B0D72F041608Q38936505-C1A849A3-7001-49ED-B1B5-3672F84ED3DAQ38937356-1E7E1EAC-006F-4DB9-9CB2-FA63146B469BQ39015403-C52F3EB7-D00C-442C-A9ED-75511C37BED1Q39018082-CD69B690-0B7F-4671-A292-D426F394D752Q39112810-1F2D79B5-85E0-4556-875F-CCB505E15397Q39399146-005FAB32-1995-4ED6-A7F4-2A434A8429A8Q39432450-4ADAEB12-851B-43DD-B91E-0C7542133B8CQ42826454-8265CC51-669E-42C0-90B6-A7157AF0CF60Q43004831-73CAD588-FC26-4A44-866D-37004C7F85A7Q43640881-A057396D-B0AC-4A84-904E-25E3C9E8E3B4Q45095937-356A234D-F3E3-48F9-835C-50EB91710106Q46675104-9A32C48A-977D-452F-B8A3-92F0D6265B97Q46823743-ED635C85-1648-4037-BAEE-B20CDC82F313Q46976762-D4C9B197-4E9F-4E9B-BDE9-877DE45CF5CDQ46991306-E42A45DA-E27A-45F3-9208-0187F6C8F3FEQ47133878-03DF3BF1-B257-4231-86A2-D2BD18FE314AQ48017659-A62D54F0-7285-4CB3-9FF5-2B1F093C19F7Q48153044-E0F76B77-37C4-4671-8263-5EA674826E7CQ49790835-A8003998-6DE5-45B6-9408-3A5F5ED82EB0Q51665807-34020096-9F9D-427B-BF7B-2FF5C397D8BCQ52865242-2041D810-9A46-44C4-A7BA-166F8B5988F1Q53536204-61FB37A7-1A4A-4B1F-B7F0-D48130F26E7CQ57587300-F5E9E146-B803-4CFA-998B-28B0DC251A71Q57587307-81F9C2FB-6FE5-48EE-AD2B-EEDDD666170FQ57628654-3BB673C8-2D4F-4F76-A297-0A87E75588AAQ58424224-892E724D-9206-426A-AA6F-7BB807A6B8AAQ58547427-AE1388CB-7E8F-476C-96B6-2F96A0E6532BQ58854966-2D2F1E04-76B2-4236-ACD8-95689F437786Q59666209-1A0A8C5E-9C21-4774-9693-6E014E64C735
P50
description
Polish biochemist
@en
Pools onderzoeker
@nl
bithchemiceoir Polannach
@ga
investigador polacu
@ast
polnischer Forscher
@de
polski biochemik
@pl
name
Adam Huczyński
@ast
Adam Huczyński
@ca
Adam Huczyński
@cs
Adam Huczyński
@de
Adam Huczyński
@en
Adam Huczyński
@es
Adam Huczyński
@fr
Adam Huczyński
@ga
Adam Huczyński
@gl
Adam Huczyński
@hr
type
label
Adam Huczyński
@ast
Adam Huczyński
@ca
Adam Huczyński
@cs
Adam Huczyński
@de
Adam Huczyński
@en
Adam Huczyński
@es
Adam Huczyński
@fr
Adam Huczyński
@ga
Adam Huczyński
@gl
Adam Huczyński
@hr
altLabel
Adam Huczynski
@en
Adam Włodzimierz Huczyński
@pl
prefLabel
Adam Huczyński
@ast
Adam Huczyński
@ca
Adam Huczyński
@cs
Adam Huczyński
@de
Adam Huczyński
@en
Adam Huczyński
@es
Adam Huczyński
@fr
Adam Huczyński
@ga
Adam Huczyński
@gl
Adam Huczyński
@hr
P1053
D-9450-2011
P1153
12786082600
56431093300
P1412
P1559
Adam Huczyński
@pl
P21
P27
P31
P3124
P3829
P496
0000-0003-4770-215X