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Results: 1-12 |
Results: 12
Synthesis and study of a cyclic angiotensin II antagonist analogue revealsthe role of pi-pi* interactions in the C-terminal aromatic residue for agonist activity and its structure resemblance with AT(1) non-peptide antagonists
Authors: Polevaya, L Mavromoustakos, T Zoumboulakis, P Grdadolnik, SG Roumelioti, P Giatas, N Mutule, I Keivish, T Vlahakos, DV Iliodromitis, EK Kremastinos, DT Matsoukas, J
Citation: L. Polevaya et al., Synthesis and study of a cyclic angiotensin II antagonist analogue revealsthe role of pi-pi* interactions in the C-terminal aromatic residue for agonist activity and its structure resemblance with AT(1) non-peptide antagonists, BIO MED CH, 9(6), 2001, pp. 1639-1647
Design and structure-activity relationship of thrombin inhibitors with an azaphenylalanine scaffold: Potency and selectivity enhancements via P2 optimization
Authors: Zega, A Mlinsek, G Sepic, P Grdadolnik, SG Solmajer, T Tschopp, TB Steiner, B Kikelj, D Urleb, U
Citation: A. Zega et al., Design and structure-activity relationship of thrombin inhibitors with an azaphenylalanine scaffold: Potency and selectivity enhancements via P2 optimization, BIO MED CH, 9(10), 2001, pp. 2745-2756
Structure elucidation and conformational properties of a novel bioactive clerodane diterpene using a combination of high field NMR spectroscopy, computational analysis and X-ray diffraction
Authors: Kolocouris, A Mavromoustakos, T Demetzos, C Terzis, A Grdadolnik, SG
Citation: A. Kolocouris et al., Structure elucidation and conformational properties of a novel bioactive clerodane diterpene using a combination of high field NMR spectroscopy, computational analysis and X-ray diffraction, BIOORG MED, 11(6), 2001, pp. 837-840
A simple stereoselective one pot conversion of compounds with a dimethylaminomethylene group into enol esters
Authors: Selic, L Jukic, L Sorsak, G Grdadolnik, SG Stanovnik, B
Citation: L. Selic et al., A simple stereoselective one pot conversion of compounds with a dimethylaminomethylene group into enol esters, SYN COMMUN, 31(11), 2001, pp. 1743-1752
Influence of chirality of the preceding acyl moiety on the cis/trans ratioof the proline peptide bond
Authors: Breznik, M Grdadolnik, SG Giester, G Leban, I Kikelj, D
Citation: M. Breznik et al., Influence of chirality of the preceding acyl moiety on the cis/trans ratioof the proline peptide bond, J ORG CHEM, 66(21), 2001, pp. 7044-7050
The synthesis and transformations of 2-[2-ethoxycarbonyl-2-(2-pyridinyl)ethenyl]amino-3-dimethylaminopropenoates. The synthesis of substituted beta-amino-alpha,beta-didehydro-alpha-amino acid derivatives
Authors: Jukic, L Recnik, S Grdadolnik, SG Svete, J Stanovnik, B
Citation: L. Jukic et al., The synthesis and transformations of 2-[2-ethoxycarbonyl-2-(2-pyridinyl)ethenyl]amino-3-dimethylaminopropenoates. The synthesis of substituted beta-amino-alpha,beta-didehydro-alpha-amino acid derivatives, J HETERO CH, 38(4), 2001, pp. 859-868
Improved method for intracellular pH determination in filamentous fungi
Authors: Legisa, M Grdadolnik, SG
Citation: M. Legisa et Sg. Grdadolnik, Improved method for intracellular pH determination in filamentous fungi, ACTA CHIM S, 47(3), 2000, pp. 389-400
Ethyl 2-(2-acetyl-2-ethoxycarbonyl-1-ethenyl)amino-3-dimethylaminopropenoate in the synthesis of heterocyclic systems. The synthesis of substituted 3-aminoazolo- and -azinopyrimidinones, pyridopyridinones and pyranones
Authors: Toplak, R Zucchiati, M Grdadolnik, SG Stanovnik, B
Citation: R. Toplak et al., Ethyl 2-(2-acetyl-2-ethoxycarbonyl-1-ethenyl)amino-3-dimethylaminopropenoate in the synthesis of heterocyclic systems. The synthesis of substituted 3-aminoazolo- and -azinopyrimidinones, pyridopyridinones and pyranones, HETEROCYCLE, 50(2), 1999, pp. 853-866
The synthesis of methyl 2-(benzyloxycarbonyl)amino-3-dimethylaminopropenoate. The synthesis of trisubstituted pyrroles, 3-amino-2H-pyran-2-ones, fused 2H-pyran-2-ones and 4H-pyridin-4-ones
Authors: Toplak, R Svete, J Stanovnik, B Grdadolnik, SG
Citation: R. Toplak et al., The synthesis of methyl 2-(benzyloxycarbonyl)amino-3-dimethylaminopropenoate. The synthesis of trisubstituted pyrroles, 3-amino-2H-pyran-2-ones, fused 2H-pyran-2-ones and 4H-pyridin-4-ones, J HETERO CH, 36(1), 1999, pp. 225-235
Methyl (Z)-2-[(benzyloxycarbonyl)amino]-3-dimethylaminopropenoate in the synthesis of heterocyclic systems. Synthesis of (benzyloxycarbonyl)amino substituted fused pyrimidinones
Authors: Toplak, R Svete, J Grdadolnik, SG Stanovnik, B
Citation: R. Toplak et al., Methyl (Z)-2-[(benzyloxycarbonyl)amino]-3-dimethylaminopropenoate in the synthesis of heterocyclic systems. Synthesis of (benzyloxycarbonyl)amino substituted fused pyrimidinones, COLL CZECH, 64(2), 1999, pp. 177-189
The synthesis of ethyl 2-(2-cyano-2-ethoxycarbonylethenyl)amino-3-dimethylaminopropenoate. The synthesis of substituted aminoazolo-, aminoazionpyrimidinones and 2H-1-benzopyran-2-ones
Authors: Selic, L Grdadolnik, SG Stanovnik, B
Citation: L. Selic et al., The synthesis of ethyl 2-(2-cyano-2-ethoxycarbonylethenyl)amino-3-dimethylaminopropenoate. The synthesis of substituted aminoazolo-, aminoazionpyrimidinones and 2H-1-benzopyran-2-ones, HETEROCYCLE, 49, 1998, pp. 133-142
The synthesis of ethyl 2-[(2,2-dibenzoyl)ethenyl]amino-3-dimethylaminopropenoate and its application to the synthesis of fused 3-aminopyran-2-ones and 3-aminoazolo- and -azinopyrimidin-4(4H)-ones
Authors: Sorsak, G Grdadolnik, SG Stanovnik, B
Citation: G. Sorsak et al., The synthesis of ethyl 2-[(2,2-dibenzoyl)ethenyl]amino-3-dimethylaminopropenoate and its application to the synthesis of fused 3-aminopyran-2-ones and 3-aminoazolo- and -azinopyrimidin-4(4H)-ones, J HETERO CH, 35(6), 1998, pp. 1275-1279
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