Double cohesion in structural DNA nanotechnologyProtein backbone engineering as a strategy to advance foldamers toward the frontier of protein-like tertiary structureBN isosteres of indoleCrystallographic studies on the reaction of isopenicillin N synthase with an unsaturated substrate analogueStructure of the parallel-stranded DNA quadruplex d(TTAGGGT)4 containing the human telomeric repeat: evidence for A-tetrad formation from NMR and molecular dynamics simulationsNMR solution structure of dsDNA containing a bicyclic D-arabino-configured nucleotide fixed in an O4'-endo sugar conformationDNA recognition by the anthracycline antibiotic respinomycin D: NMR structure of the intercalation complex with d(AGACGTCT)2Functional and structural characterization of ovine ornithine transcarbamoylase4-Fluorinated L-lysine analogs as selective i-NOS inhibitors: methodology for introducing fluorine into the lysine side chainStructural basis for cyclophellitol inhibition of a beta-glucosidaseRuthenium half-sandwich complexes as protein kinase inhibitors: derivatization of the pyridocarbazole pharmacophore ligandA 1-acetamido derivative of 6-epi-valienamine: an inhibitor of a diverse group of beta-N-acetylglucosaminidasesGlutathione traps formaldehyde by formation of a bicyclo[4.4.1]undecane adductDesign, synthesis and biological evaluation of thrombin inhibitors based on a pyridine scaffoldThe efficiency of C-4 substituents in activating the beta-lactam scaffold towards serine proteases and hydroxide ionProbing the beta-1,3:1,4 glucanase, CtLic26A, with a thio-oligosaccharide and enzyme variantsThe small molecule tool (S)-(−)-blebbistatin: novel insights of relevance to myosin inhibitor designStructural basis for the broad-spectrum inhibition of metallo-beta-lactamases by thiolsInhibitors of the kinase IspE: structure-activity relationships and co-crystal structure analysisSynthesis of (2S)-2-amino-7,8-epoxyoctanoic acid and structure of its metal-bridging complex with human arginase IPotent HIV-1 protease inhibitors incorporating meso-bicyclic urethanes as P2-ligands: structure-based design, synthesis, biological evaluation and protein–ligand X-ray studiesGlycosidase inhibition by ring-modified castanospermine analogues: tackling enzyme selectivity by inhibitor tailoringInhibition of the exo-beta-D-glucosaminidase CsxA by a glucosamine-configured castanospermine and an amino-australine analogueThe crystal structure of an LLL-configured depsipeptide substrate analogue bound to isopenicillin N synthaseNMR structural studies on the covalent DNA binding of a pyrrolobenzodiazepine-naphthalimide conjugateThe first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complexFluorine in medicinal chemistry: β-fluorination of peripheral pyrrolidines attached to acridine ligands affects their interactions with G-quadruplex DNACyclodextrin-mediated crystallization of acid β-glucosidase in complex with amphiphilic bicyclic nojirimycin analoguesRapid preparation of triazolyl substituted NH-heterocyclic kinase inhibitors via one-pot Sonogashira coupling-TMS-deprotection-CuAAC sequenceA potential fortuitous binding of inhibitors of an inverting family GH9 β-glycosidase derived from isofagomineStructural and biochemical analyses reveal how ornithine acetyl transferase binds acidic and basic amino acid substratesSynthesis and biological activity of optimized belactosin C congenersGaining insight into the inhibition of glycoside hydrolase family 20 exo-β-N-acetylhexosaminidases using a structural approachStereoselective synthesis of novel pyrazole derivatives using tert-butansulfonamide as a chiral auxiliarySynthesis and evaluation of novel 3-C-alkylated-Neu5Ac2en derivatives as probes of influenza virus sialidase 150-loop flexibilityA subnanomolar fluorescent probe for protein kinase CK2 interaction studiesThe biolabile 2'-O-pivaloyloxymethyl modification in an RNA helix: an NMR solution structureAromatic thioglycoside inhibitors against the virulence factor LecA from Pseudomonas aeruginosaA structural and dynamic investigation of the inhibition of catalase by nitric oxideInhibition of the family 20 glycoside hydrolase catalytic modules in the Streptococcus pneumoniae exo-β-D-N-acetylglucosaminidase, StrH
P1433
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P1433
description
Wissenschaftliche Fachzeitschrift
@de
czasopismo naukowe
@pl
journal
@en
revista científica
@es
rivista scientifica
@it
vědecký časopis
@cs
wetenschappelijk tijdschrift van Royal Society of Chemistry
@nl
مجلة
@ar
वैज्ञानिक पत्रिका
@hi
英语期刊
@zh
name
Organic & Biomolecular Chemistry
@fr
Organic and Biomolecular Chemistry
@ast
Organic and Biomolecular Chemistry
@da
Organic and Biomolecular Chemistry
@de
Organic and Biomolecular Chemistry
@en
Organic and Biomolecular Chemistry
@es
Organic and Biomolecular Chemistry
@fi
Organic and Biomolecular Chemistry
@it
Organic and Biomolecular Chemistry
@nb
Organic and Biomolecular Chemistry
@nl
type
label
Organic & Biomolecular Chemistry
@fr
Organic and Biomolecular Chemistry
@ast
Organic and Biomolecular Chemistry
@da
Organic and Biomolecular Chemistry
@de
Organic and Biomolecular Chemistry
@en
Organic and Biomolecular Chemistry
@es
Organic and Biomolecular Chemistry
@fi
Organic and Biomolecular Chemistry
@it
Organic and Biomolecular Chemistry
@nb
Organic and Biomolecular Chemistry
@nl
altLabel
Org. Biomol. Chem.
@en
Organic & Biomolecular Chemistry
@en
Organic and Biomolecular Chemistry
@fr
prefLabel
Organic & Biomolecular Chemistry
@fr
Organic and Biomolecular Chemistry
@ast
Organic and Biomolecular Chemistry
@da
Organic and Biomolecular Chemistry
@de
Organic and Biomolecular Chemistry
@en
Organic and Biomolecular Chemistry
@es
Organic and Biomolecular Chemistry
@fi
Organic and Biomolecular Chemistry
@it
Organic and Biomolecular Chemistry
@nb
Organic and Biomolecular Chemistry
@nl
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2003261024
P1156
P1159
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P1476
Organic & Biomolecular Chemistry
@en
P236
P243
P3181
P407
P571
2003-01-01T00:00:00Z