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C16 and C17 substituted derivatives of pregnenolone and progesterone as inhibitors of 17α-hydroxylase-C17,20-lyase: Synthesis and biological evaluationHAIDAR, Samer; HARTMANN, Rolf W.Archiv der Pharmazie (Weinheim). 2002, Vol 335, Num 11-12, pp 526-534, issn 0365-6233, 9 p.Article

17β-HSD2 inhibitors for the treatment of osteoporosis: Identification of a promising scaffoldWETZEL, Marie; MARCHAIS-OBERWINKLER, Sandrine; HARTMANN, Rolf W et al.Bioorganic & medicinal chemistry. 2011, Vol 19, Num 2, pp 807-815, issn 0968-0896, 9 p.Article

Prediction of protein-protein interaction inhibitors by chemoinformatics and machine learning methodsNEUGEBAUER, Alexander; HARTMANN, Rolf W; KLEIN, Christian D et al.Journal of medicinal chemistry (Print). 2007, Vol 50, Num 19, pp 4665-4668, issn 0022-2623, 4 p.Article

Discovery of inhibitors of MCF-7 tumor cell adhesion to endothelial cells and investigation on their mode of actionBILD, Thomas; JOSE, Joachim; HARTMANN, Rolf W et al.Archiv der Pharmazie (Weinheim). 2004, Vol 337, Num 12, pp 687-694, issn 0365-6233, 8 p.Article

Development of a simple and rapid assay for the evaluation of inhibitors of human 17α-hydroxylase-C17,20-lyase (P450c17) by coexpression of P450c17 with NADPH-cytochrome-P450-reductase in Escherichia coliEHMER, Peter B; JOSE, Joachim; HARTMANN, Rolf W et al.Journal of steroid biochemistry and molecular biology. 2000, Vol 75, Num 1, pp 57-63, issn 0960-0760Article

Development and evaluation of a pharmacophore model for inhibitors of aldosterone synthase (CYP11B2)ULMSCHNEIDER, Sarah; NEGRI, Matthias; VOETS, Marieke et al.Bioorganic & medicinal chemistry letters (Print). 2006, Vol 16, Num 1, pp 25-30, issn 0960-894X, 6 p.Article

Synthesis and evaluation of 2'-substituted 4-(4'-carboxy- or 4'-carboxymethylbenzylidene)-n-acylpiperidines: Highly potent and in vivo active steroid 5α-reductase type 2 inhibitorsPICARD, Franck; BARASSIN, Stephan; MOKHTARIAN, Armand et al.Journal of medicinal chemistry (Print). 2002, Vol 45, Num 16, pp 3406-3417, issn 0022-2623Article

Stable expression of human 5α-reductase type II in COS1 cells due to chromosomal gene integration : a novel tool for inhibitor identificationREICHERT, Wolfgang; MICHEL, Armin; HARTMANN, Rolf W et al.Journal of steroid biochemistry and molecular biology. 2001, Vol 78, Num 3, pp 275-284, issn 0960-0760Article

Design and synthesis of 1,3,5-trisubstituted 1,2,4-triazoles as CYP enzyme inhibitorsAL-SOUD, Yaseen A; HEYDEL, Michael; HARTMANN, Rolf W et al.Tetrahedron letters. 2011, Vol 52, Num 48, issn 0040-4039, 6307, 6372-6375 [5 p.]Article

Evaluation of 4'-substituted bicyclic pyridones as non-steroidal inhibitors of steroid 5α-reductaseMCCARTHY, Anna R; HARTMANN, Rolf W; ABELL, Andrew D et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 13, pp 3603-3607, issn 0960-894X, 5 p.Article

Protein-dynamics of the putative HCV receptor CD81 large extracellular loopNEUGEBAUER, Alexander; KLEIN, Christian D. P; HARTMANN, Rolf W et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 7, pp 1765-1769, issn 0960-894X, 5 p.Article

Discovery of selective CYP11B2 (aldosterone synthase) inhibitors for the therapy of congestive heart failure and myocardial fibrosisHARTMANN, Rolf W; MÜLLER, Ursula; EHMER, Peter B et al.European journal of medicinal chemistry. 2003, Vol 38, Num 4, pp 363-366, issn 0223-5234, 4 p.Conference Paper

Synthesis of 6-or 4-functionalized indoles via a reductive cyclization approach and evaluation as aromatase inhibitorsLEZE, Marie-Pierre; PALUSCZAK, Anja; HARTMANN, Rolf W et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 16, pp 4713-4715, issn 0960-894X, 3 p.Article

Discovery of a new class of bicyclic substituted hydroxyphenylmethanones as 17β-hydroxysteroid dehydrogenase type 2 (17β-HSD2) inhibitors for the treatment of osteoporosisWETZEL, Marie; GARGANO, Emanuele M; HINSBERGER, Stefan et al.European journal of medicinal chemistry. 2012, Vol 47, pp 1-17, issn 0223-5234, 17 p.Article

Influence of DNA Template Choice on Transcription and Inhibition of Escherichia coli RNA PolymeraseHAUPENTHAL, Joerg; HÜSECKEN, Kristina; NEGRI, Matthias et al.Antimicrobial agents and chemotherapy. 2012, Vol 56, Num 8, pp 4536-4539, issn 0066-4804, 4 p.Article

Steroidal carbonitriles as potential aromatase inhibitorsYADAV, Mange Ram; SABALE, Prafulla M; GIRIDHAR, Rajani et al.Steroids. 2012, Vol 77, Num 8-9, pp 850-857, issn 0039-128X, 8 p.Article

Methyl esters of N-(Dicyclohexyl)acetyl-piperidine-4- (benzylidene-4-carboxylic acids) as drugs and prodrugs : A new strategy for dual inhibition of 5α-Reductase type 1 and type 2STREIBER, Martina; PICARD, Franck; SCHERER, Christiane et al.Journal of pharmaceutical sciences. 2005, Vol 94, Num 3, pp 473-480, issn 0022-3549, 8 p.Article

Synthesis and evaluation of a dimer of 2-(4-pyridylmethyl)-1-indanone as a novel nonsteroidal aromatase inhibitorGUPTA, Ranju; DHARAM PAUL JINDAL; JIT, Birinder et al.Archiv der Pharmazie (Weinheim). 2004, Vol 337, Num 7, pp 398-401, issn 0365-6233, 4 p.Article

Preparation and pharmacological profile of 7-(α-azolylbenzyl)-1H-indoles and indolines as new aromatase inhibitorsMARCHAND, Pascal; LE BORGNE, Marc; PALZER, Martina et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 9, pp 1553-1555, issn 0960-894X, 3 p.Article

Development of a test system for inhibitors of human aldosterone synthase (CYP11B2): screening in fission yeast and evaluation of selectivity in V79 cellsEHMER, Peter B; BUREIK, Matthias; BERNHARDT, Rita et al.Journal of steroid biochemistry and molecular biology. 2002, Vol 81, Num 2, pp 173-179, issn 0960-0760Article

N-(Pyridin-3-yl)benzamides as selective inhibitors of human aldosterone synthase (CYP11B2)ZIMMER, Christina; HAFNER, Marieke; ZENDER, Michael et al.Bioorganic & medicinal chemistry letters (Print). 2011, Vol 21, Num 1, pp 186-190, issn 0960-894X, 5 p.Article

Synthesis of amidinohydrazones and evaluation of their inhibitory effect towards aldosterone synthase (CYP11B2) and the formation of selected steroidsVOETS, Marieke; MÜLLER-VIEIRA, Ursula; MARCHAIS-OBERWINKLER, Sandrine et al.Archiv der Pharmazie (Weinheim). 2004, Vol 337, Num 7, pp 411-416, issn 0365-6233, 6 p.Article

Synthesis and evaluation of novel steroidal oxime inhibitors of P450 17 (17α-hydroxylase/C17-20-lyase) and 5α-reductase types 1 and 2HARTMANN, Rolf W; HECTOR, Markus; HAIDAR, Samer et al.Journal of medicinal chemistry (Print). 2000, Vol 43, Num 22, pp 4266-4277, issn 0022-2623Article

New Insights into the Bacterial RNA Polymerase Inhibitor CBR703 as a Starting Point for Optimization as an Anti-Infective AgentWEIXING ZHU; HAUPENTHAL, Jörg; GROH, Matthias et al.Antimicrobial agents and chemotherapy. 2014, Vol 58, Num 7, pp 4242-4245, issn 0066-4804, 4 p.Article

Enantiomeric resolution of some human aldosterone synthase [CYP 11 B2] inhibitors on derivatized polysaccharide chiral stationary phasesABOUL-ENEIN, Hassan Y; HEFNAWY, Mohamed M; EHMER, Peter B et al.Journal of separation science. 2003, Vol 26, Num 15-16, pp 1455-1458, issn 1615-9306, 4 p.Article

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