Three dimensional model of severe acute respiratory syndrome coronavirus helicase ATPase catalytic domain and molecular design of severe acute respiratory syndrome coronavirus helicase inhibitors.Spectroscopic, potentiometric and quantum-mechanical studies of S-(-)-nicotine complexes with Cu(II) ion.In search of excited-state proton transfer in the lumichrome dimer in the solid state: theoretical and experimental approach.New type of bonding formed from an overlap between pi aromatic and pi C=O molecular orbitals stabilizes the coexistence in one molecule of the ionic and neutral meso-ionic forms of imidazopyridine.Generation of Low-Dimensional Architectures through the Self-Assembly of Pyromellitic Diimide Derivatives.Unusual ion UO(4)(-) formed upon collision induced dissociation of [UO(2)(NO(3))(3)](-), [UO(2)(ClO(4))(3)](-), [UO(2)(CH(3)COO)(3)](-) ions.Screening of a chemical library reveals novel PXR-activating pharmacologic compounds.Can Google Searches Predict the Popularity and Harm of Psychoactive Agents?Selectivity of major isoquinoline alkaloids from Chelidonium majus towards telomeric G-quadruplex: A study using a transition-FRET (t-FRET) assay.Experimental and theoretical studies on fluvastatin primary photoproduct formation.Synthesis and anticancer activity of some 5-fluoro-2'-deoxyuridine phosphoramidates.Quantum-chemical, NMR, FT IR, and ESI MS studies of complexes of colchicine with Zn(II).Synthesis and anticancer activity of 5'-chloromethylphosphonates of 3'-azido-3'-deoxythymidine (AZT).Naphthalimides Selectively Inhibit the Activity of Bacterial, Replicative DNA Ligases and Display Bactericidal Effects against Tubercle Bacilli.Mechanism of activation of an immunosuppressive drug: azathioprine. Quantum chemical study on the reaction of azathioprine with cysteine.Detailed mechanism of squalene epoxidase inhibition by terbinafine.Quantum chemical studies on substitution effects within silyl group in the silylative coupling of olefins.Probing the shapes of chiral bis-(o-naphthalimidobenzoyl) systems using X-ray and circular dichroism methods.DFT study on hydroxy acid-lactone interconversion of statins: the case of atorvastatin.Modeling of purine derivatives transport across cell membranes based on their partition coefficient determination and quantum chemical calculations.Syn- and anti-conformations of 5'-deoxy- and 5'-O-methyl-uridine 2',3'-cyclic monophosphate.Ground- and excited-state double proton transfer in lumichrome/acetic acid system: theoretical and experimental approach.Relationship between structure and photoinitiating abilities of selected bromide salts of 2-oxo-2,3-dihydro-1H-imidazo[1,2-a]pyridine (IMP): influence of the solvent and the substitution in benzaldehyde on the course of its reaction with IMP.Microwave-assisted one-pot synthesis of new ionic iridium complexes of [Ir(bzq)2(N^N)]+A- type and their selected electroluminescent properties.IA, database of known ligands of aminoacyl-tRNA synthetases.Methyl group transfer upon gas phase decomposition of protonated methyl benzoate and similar compounds.In silico prediction of SARS protease inhibitors by virtual high throughput screening.Antioxidant and cytotoxic activity of new di- and polyamine caffeine analogues.Highly selective synthesis of substituted (E)-alkenylsilatranes via catalytic trans-silylation and mechanistic implications.X-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-eneA new 2,6-di(anthracen-9-yl)pyridine ligand and its complexes with Ag(I) ions: Synthesis, structure and photocatalytic activityThe amide protonation of (–)-N-benzoylcytisine in its perchlorate saltsDemethoxycurcumin-Metal Complexes: Fragmentation and Comparison with Curcumin-Metal Complexes, as Studied by ESI-MS/MSEffect of fluorine substitution of the β-ketoiminate ancillary ligand on photophysical properties and electroluminescence ability of new iridium(iii) complexesIntramolecular hydrogen exchange prior to methanol loss from protonated methyl benzoates bearing different ring substituents under CID conditionsUnexpected formation of [M]2+ from [M+CuCl+H]2+ ions under CID conditions, where M is a molecule of 3,5-bis(2,2’-bipyridin-4-ylethynyl)benzoic acid or its methyl esterInfluence of O/S/Se Exchange on the Stability of 1,3,4-Selana(Thia/Oxa)Diazole-Palladium Complexes as Studied by Electrospray Ionization Mass SpectrometrySelf-Assembly and Characterization of Homo- and Heterodinuclear Complexes of Zinc(II) and Lanthanide(III) Ions with a Tridentate Schiff-Base LigandQuantum-chemical studies of homoleptic iridium(III) complexes in OLEDs: fac versus mer isomersSynthesis and Characterization of Rod Like Nano-sized Cobaltammine Complexes as Textile Dyeing Agents
P50
Q30356850-1C00F2B8-3A17-4F2D-AE34-B7E29D51B63DQ30784855-2D85B695-84EA-4326-8A13-9FABFEB157BFQ30812390-79BBC506-EA41-49E8-BA93-30E428A16650Q33249706-D5736143-5EFA-4C19-9652-2D5A0736CEDFQ33619617-5AC156E3-9A35-4156-9A03-D5F521370FBDQ33647604-0CA5D6F6-9E7E-4E29-AEDB-59A244072107Q35470873-B0E44BE9-8E02-41B7-9F51-B71D261E5780Q36674560-6C8144C4-31C7-4F9D-8B90-3FF6D374F6F8Q38288204-3F2E456B-DCCF-4D54-AA09-558A6F83CF0EQ38709033-565C3295-88CA-46C1-961B-CE8379A01191Q38778648-EA353565-A9FB-4F8F-BEFB-BFACBAB3F735Q38891935-CF733CF7-DCAD-4F40-A5B6-FFB5F46D214BQ39468629-E7B7BFDC-DA6F-4EAD-9171-C8D0E5F8376FQ40371811-EF4FE98E-20CC-454B-AE91-D125BE646E00Q43654083-E452A310-F8A7-4B46-8DC7-C2955002A541Q44098212-45597884-B4E0-438F-AF04-A08BAEF16252Q45927188-880FF1FC-E0AB-4E13-8D08-B1FF74827097Q46155996-8A4B7F02-E194-4B0C-9915-822BED4F0016Q46198618-ECA10FCA-CEC3-4389-92AA-A4AB235133FAQ46563204-31EA4E78-A18D-43A5-8047-FEF8DF123305Q46678978-F63FF9B8-F2B9-4739-883F-8C809EF6D1A7Q46860390-D9E1BBA4-C61A-4E85-926C-16473A300FD0Q46910305-CCB9D456-9A67-4185-A899-6E73ACB9EA2DQ47957757-F0B9789B-71AF-4A82-AC11-2AE69F67E7A3Q48593386-9EE52F4C-3A9C-4F10-8282-D499607869E1Q50020193-D8BC0E39-E233-457C-8E12-4DBBD4EE16C5Q51916292-A90125BD-AD80-4B35-8588-62570F86BE8DQ52580033-D7756A1C-63C7-4E10-8F98-989EAB3AB303Q52695553-2D11AF40-EBD1-47D0-8F68-AFE346EA3CF3Q57628654-27770D88-2153-4094-8CF4-C70B3F23C3E2Q58885552-B3EB53BB-C39D-4F89-B6EB-4ACB4E1AA43AQ58921096-373412A3-7555-48AF-8CB8-D02A834F717BQ59021080-4AC2AB96-2791-4863-BE85-41F0826EAF6FQ60547551-5F708D76-4FE7-4C7B-9470-55863DB4A590Q60547552-98A4DF0B-666A-4D71-A2C6-A9846DE35F30Q60547569-85DBD272-AC70-4C96-968D-387EBC557B4AQ60547588-60C6BAE1-8384-4951-942B-6A457E85241BQ64007374-9EF71D6F-AFCD-4892-8EED-DFD9632549F1Q64007377-C3B144C5-F47C-4CD3-AC42-8F56AB6B68D8Q64007378-EFF6FC93-558B-4CCF-95C5-77C678437751
P50
description
Polish chemist
@en
Poola keemik
@et
Pools onderzoeker
@nl
ceimiceoir Polannach
@ga
chimist polonez
@ro
chimiste polonais
@fr
investigador polacu
@ast
kimist polak
@sq
polnischer Forscher
@de
polski chemik
@pl
name
Marcin Hoffmann
@ast
Marcin Hoffmann
@ca
Marcin Hoffmann
@de
Marcin Hoffmann
@en
Marcin Hoffmann
@es
Marcin Hoffmann
@fr
Marcin Hoffmann
@ga
Marcin Hoffmann
@it
Marcin Hoffmann
@nl
Marcin Hoffmann
@pl
type
label
Marcin Hoffmann
@ast
Marcin Hoffmann
@ca
Marcin Hoffmann
@de
Marcin Hoffmann
@en
Marcin Hoffmann
@es
Marcin Hoffmann
@fr
Marcin Hoffmann
@ga
Marcin Hoffmann
@it
Marcin Hoffmann
@nl
Marcin Hoffmann
@pl
altLabel
Marcin Maciej Hoffmann
@pl
prefLabel
Marcin Hoffmann
@ast
Marcin Hoffmann
@ca
Marcin Hoffmann
@de
Marcin Hoffmann
@en
Marcin Hoffmann
@es
Marcin Hoffmann
@fr
Marcin Hoffmann
@ga
Marcin Hoffmann
@it
Marcin Hoffmann
@nl
Marcin Hoffmann
@pl
P214
P1053
A-9877-2012
P1207
n2014008087
P1412
P1695
P1960
6p-9FNMAAAAJ
P21
P214
P27
P31
P3124
P496
0000-0002-1729-977X
P569
1972-10-02T00:00:00Z
P734
P7859
viaf-306420790