Anzahl der Einträge in dieser Kategorie: 105.
Scheuerer, Simon,
Motlova, Lucia,
Schäker-Hübner, Linda,
Sellmer, Andreas,
Feller, Felix,
Ertl, Fabian J.,
Koch, Pierre ![ORCID 0000-0003-4620-4650](/images/orcid_16x16.gif)
,
Hansen, Finn K.,
Barinka, Cyril und
Mahboobi, Siavosh ![ORCID 0000-0002-4528-6538](/images/orcid_16x16.gif)
(2024)
Biological and structural investigation of tetrahydro-β-carboline-based selective HDAC6 inhibitors with improved stability.
European Journal of Medicinal Chemistry 276, S. 116676.
Nagl, Martin,
Moennich, Denise,
Rosier, Niklas ![ORCID 0000-0003-2835-7928](/images/orcid_16x16.gif)
,
Schihada, Hannes,
Sirbu, Alexei,
Konar, Nergis,
Reyes-Resina, Irene,
Navarro, Gemma,
Franco, Rafael,
Kolb, Peter,
Annibale, Paolo und
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
(2023)
Fluorescent Tools for the Imaging of Dopamine D2‐Like Receptors.
ChemBioChem.
Rosier, Niklas ![ORCID 0000-0003-2835-7928](/images/orcid_16x16.gif)
,
Moennich, Denise,
Nagl, Martin,
Schihada, Hannes,
Sirbu, Alexei,
Konar, Nergis,
Reyes-Resina, Irene,
Navarro, Gemma,
Franco, Rafael,
Kolb, Peter,
Annibale, Paolo und
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
(2023)
Shedding Light on the D1‐Like Receptors: A Fluorescence‐Based Toolbox for Visualization of the D1 and D5 Receptors.
ChemBioChem.
Winkler, René ![ORCID 0000-0002-7570-0242](/images/orcid_16x16.gif)
,
Mägdefrau, Ann-Sophie,
Piskor, Eva-Maria,
Kleemann, Markus,
Beyer, Mandy,
Linke, Kevin,
Hansen, Lisa,
Schaffer, Anna-Maria ![ORCID 0000-0002-2561-0820](/images/orcid_16x16.gif)
,
Hoffmann, Marina E. ![ORCID 0000-0002-5381-3043](/images/orcid_16x16.gif)
,
Poepsel, Simon ![ORCID 0000-0002-8304-4062](/images/orcid_16x16.gif)
,
Heyd, Florian,
Beli, Petra,
Möröy, Tarik,
Mahboobi, Siavosh,
Krämer, Oliver H. und
Kosan, Christian
(2022)
Targeting the MYC interaction network in B-cell lymphoma via histone deacetylase 6 inhibition.
Oncogene 41 (40), S. 4560-4572.
Singh, Gurpreet,
Liu, Peng,
Yao, Katherine R.,
Strasser, Jessica M.,
Hlynialuk, Chris,
Leinonen-Wright, Kailee,
Teravskis, Peter J.,
Choquette, Jessica M.,
Ikramuddin, Junaid,
Bresinsky, Merlin,
Nelson, Kathryn M.,
Liao, Dezhi,
Ashe, Karen H.,
Walters, Michael A. und
Pockes, Steffen
(2022)
Caspase-2 Inhibitor Blocks Tau Truncation and Restores Excitatory Neurotransmission in Neurons Modeling FTDP-17 Tauopathy.
ACS Chemical Neuroscience 13 (10), S. 1549-1557.
Volltext nicht vorhanden.
Beyer, Mandy,
Henninger, Sven J.,
Haehnel, Patricia S.,
Mustafa, Al-Hassan M. ![ORCID 0000-0002-4453-2573](/images/orcid_16x16.gif)
,
Gurdal, Ece ![ORCID 0000-0003-1064-8639](/images/orcid_16x16.gif)
,
Schubert, Bastian,
Christmann, Markus,
Sellmer, Andreas ![ORCID 0000-0002-4752-2418](/images/orcid_16x16.gif)
,
Mahboobi, Siavosh,
Drube, Sebastian,
Sippl, Wolfgang,
Kindler, Thomas und
Krämer, Oliver H.
(2022)
Identification of a highly efficient dual type I/II FMS-like tyrosine kinase inhibitor that disrupts the growth of leukemic cells.
Cell Chemical Biology 29 (3), 398-411.e4.
Volltext nicht vorhanden.
Szczepańska, Katarzyna,
Podlewska, Sabina,
Dichiara, Maria,
Gentile, Davide,
Patamia, Vincenzo,
Rosier, Niklas,
Mönnich, Denise,
Ruiz Cantero, Ma Carmen,
Karcz, Tadeusz,
Łażewska, Dorota,
Siwek, Agata,
Pockes, Steffen,
Cobos, Enrique J.,
Marrazzo, Agostino,
Stark, Holger,
Rescifina, Antonio,
Bojarski, Andrzej J.,
Amata, Emanuele und
Kieć-Kononowicz, Katarzyna
(2022)
Structural and Molecular Insight into Piperazine and Piperidine Derivatives as Histamine H3 and Sigma-1 Receptor Antagonists with Promising Antinociceptive Properties.
ACS Chemical Neuroscience 13 (1), S. 1-15.
Volltext nicht vorhanden.
Wachholz, Vanessa,
Mustafa, Al-Hassan M.,
Zeyn, Yanira,
Henninger, Sven J.,
Beyer, Mandy,
Dzulko, Melanie,
Piée-Staffa, Andrea,
Brachetti, Christina,
Haehnel, Patricia S.,
Sellmer, Andreas,
Mahboobi, Siavosh,
Kindler, Thomas,
Brenner, Walburgis,
Nikolova, Teodora und
Krämer, Oliver H.
(2021)
Inhibitors of class I HDACs and of FLT3 combine synergistically against leukemia cells with mutant FLT3.
Archives of Toxicology 96 (1), S. 177-193.
Grätz, Lukas,
Laasfeld, Tõnis,
Allikalt, Anni ![ORCID 0000-0002-3056-3088](/images/orcid_16x16.gif)
,
Gruber, Corinna G.,
Pegoli, Andrea,
Tahk, Maris-Johanna,
Tsernant, Mari-Liis,
Keller, Max und
Rinken, Ago
(2021)
BRET- and fluorescence anisotropy-based assays for real-time monitoring of ligand binding to M2 muscarinic acetylcholine receptors.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 1868 (3), S. 118930.
Volltext nicht vorhanden.
Gergs, Ulrich,
Büxel, Maren L.,
Bresinsky, Merlin,
Kirchhefer, Uwe,
Fehse, Charlotte,
Höring, Carina,
Hofmann, Britt,
Marušáková, Margaréta,
Čináková, Aneta,
Schwarz, Rebecca,
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
und
Neumann, Joachim
(2021)
Cardiac Effects of Novel Histamine H2 Receptor Agonists.
Journal of Pharmacology and Experimental Therapeutics 379 (3), S. 223-234.
Volltext nicht vorhanden.
Szczepańska, Katarzyna ![ORCID 0000-0002-6110-9400](/images/orcid_16x16.gif)
,
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
,
Podlewska, Sabina,
Höring, Carina,
Mika, Kamil,
Latacz, Gniewomir,
Bednarski, Marek,
Siwek, Agata ![ORCID 0000-0001-5321-9266](/images/orcid_16x16.gif)
,
Karcz, Tadeusz,
Nagl, Martin,
Bresinsky, Merlin,
Mönnich, Denise,
Seibel, Ulla,
Kuder, Kamil J. ![ORCID 0000-0003-3077-5539](/images/orcid_16x16.gif)
,
Kotańska, Magdalena,
Stark, Holger,
Elz, Sigurd und
Kieć-Kononowicz, Katarzyna
(2021)
Structural modifications in the distal, regulatory region of histamine H3 receptor antagonists leading to the identification of a potent anti-obesity agent.
European Journal of Medicinal Chemistry 213, S. 113041.
Volltext nicht vorhanden.
Grätz, Lukas,
Tropmann, Katharina,
Bresinsky, Merlin,
Müller, Christoph,
Bernhardt, Günther ![ORCID 0000-0001-6491-9874](/images/orcid_16x16.gif)
und
Pockes, Steffen
(2020)
NanoBRET binding assay for histamine H2 receptor ligands using live recombinant HEK293T cells.
Scientific Reports 10, S. 13288.
Sellmer, Andreas,
Pilsl, Bernadette,
Beyer, Mandy,
Pongratz, Herwig,
Wirth, Lukas,
Elz, Sigurd,
Dove, Stefan,
Henninger, Sven Julian,
Spiekermann, Karsten,
Polzer, Harald,
Klaeger, Susan,
Kuster, Bernhard,
Böhmer, Frank D.,
Fiebig, Heinz-Herbert,
Krämer, Oliver H. und
Mahboobi, Siavosh
(2020)
A series of novel aryl-methanone derivatives as inhibitors of FMS-like tyrosine kinase 3 (FLT3) in FLT3-ITD-positive acute myeloid leukemia.
European Journal of Medicinal Chemistry 193, S. 112232.
Volltext nicht vorhanden.
Schihada, Hannes ![ORCID 0000-0002-1889-1636](/images/orcid_16x16.gif)
,
Ma, Xiaoyuan,
Zabel, Ulrike,
Vischer, Henry F.,
Schulte, Gunnar ![ORCID 0000-0002-2700-7013](/images/orcid_16x16.gif)
,
Leurs, Rob,
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
und
Lohse, Martin J. ![ORCID 0000-0002-0599-3510](/images/orcid_16x16.gif)
(2020)
Development of a Conformational Histamine H3 Receptor Biosensor for the Synchronous Screening of Agonists and Inverse Agonists.
ACS Sensors 5 (6), S. 1734-1742.
Volltext nicht vorhanden.
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
,
Wifling, David ![ORCID 0000-0002-1370-2138](/images/orcid_16x16.gif)
,
Keller, Max,
Buschauer, Armin ![ORCID 0000-0002-9709-1433](/images/orcid_16x16.gif)
und
Elz, Sigurd
(2018)
Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H2 Receptor Agonists.
ACS Omega 2018 (3), S. 2865-2882.
Leonhardt, Michel,
Sellmer, Andreas ![ORCID 0000-0002-4752-2418](/images/orcid_16x16.gif)
,
Krämer, Oliver H.,
Dove, Stefan,
Elz, Sigurd,
Kraus, Birgit,
Beyer, Mandy und
Mahboobi, Siavosh
(2018)
Design and biological evaluation of tetrahydro-β-carboline derivatives as highly potent histone deacetylase 6 (HDAC6) inhibitors.
European Journal of Medicinal Chemistry 152, S. 329-357.
Volltext nicht vorhanden.
Ridinger, Johannes,
Koeneke, Emily,
Kolbinger, Fiona R.,
Koerholz, Katharina,
Mahboobi, Siavosh,
Hellweg, Lars,
Gunkel, Nikolas,
Miller, Aubry K.,
Peterziel, Heike,
Schmezer, Peter,
Hamacher-Brady, Anne ![ORCID 0000-0001-5042-1338](/images/orcid_16x16.gif)
,
Witt, Olaf und
Oehme, Ina
(2018)
Dual role of HDAC10 in lysosomal exocytosis and DNA repair promotes neuroblastoma chemoresistance.
Scientific Reports 8 (1).
Volltext nicht vorhanden.
Pons, Miriam,
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,
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(2018)
Human platelet lysate as validated replacement for animal serum to assess chemosensitivity.
ALTEX.
Volltext nicht vorhanden.
Stojanovic, N.,
Hassan, Z.,
Wirth, M.,
Wenzel, P.,
Beyer, M.,
Schäfer, C.,
Brand, P.,
Kroemer, A.,
Stauber, R. H.,
Schmid, R. M.,
Arlt, A.,
Sellmer, A.,
Mahboobi, S.,
Rad, R.,
Reichert, M.,
Saur, D.,
Krämer, O. H. und
Schneider, G.
(2017)
HDAC1 and HDAC2 integrate the expression of p53 mutants in pancreatic cancer.
Oncogene 36 (13), S. 1804-1815.
Volltext nicht vorhanden.
Tsitsipatis, Dimitrios,
Jayavelu, Ashok Kumar,
Müller, Jörg P.,
Bauer, Reinhard,
Schmidt-Arras, Dirk,
Mahboobi, Siavosh,
Schnöder, Tina M.,
Heidel, Florian und
Böhmer, Frank D.
(2017)
Synergistic killing of FLT3ITD-positive AML cells by combined inhibition of tyrosine-kinase activity and N-glycosylation.
Oncotarget 8 (16).
Volltext nicht vorhanden.
Naporra, Franziska,
Gobleder, Susanne,
Wittmann, Hans-Joachim,
Spindler, Julia,
Bodensteiner, Michael,
Bernhardt, Günther,
Hübner, Harald,
Gmeiner, Peter,
Elz, Sigurd und
Strasser, Andrea
(2016)
Dibenzo[b,f][1,4]oxazepines and dibenzo[b,e]oxepines: Influence of the chlorine substitution pattern on the pharmacology at the H1R, H4R, 5-HT2AR and other selected GPCRs.
Pharmacological Research 113, S. 610-625.
(Im Druck)
Volltext nicht vorhanden.
Hammer, Sebastian,
Gobleder, Susanne,
Naporra, Franziska,
Wittmann, Hans-Joachim,
Elz, Sigurd,
Heinrich, Markus ![ORCID 0000-0001-7113-2025](/images/orcid_16x16.gif)
und
Strasser, Andrea
(2016)
2,4-Diaminopyrimidines as dual ligands at the histamine H1 and H4 receptor - H1/H4-receptor selectivity.
Bioorganic & Medicinal Chemistry Letters 26, S. 292-300.
Volltext nicht vorhanden.
Naporra, Franziska,
Gobleder, Susanne,
Wittmann, Hans-Joachim,
Spindler, Julia,
Bodensteiner, Michael,
Bernhardt, Günther,
Hübner, Harald,
Gmeiner, Peter ![ORCID 0000-0002-4127-197X](/images/orcid_16x16.gif)
,
Elz, Sigurd und
Strasser, Andrea
(2016)
Dibenzo[ b , f ][1,4]oxazepines and dibenzo[ b , e ]oxepines: Influence of the chlorine substitution pattern on the pharmacology at the H 1 R, H 4 R, 5-HT 2A R and other selected GPCRs.
Pharmacological Research 113, S. 610-625.
Volltext nicht vorhanden.
Baumeister, Paul,
Erdmann, Daniela,
Biselli, Sabrina,
Kagermeier, Nicole,
Elz, Sigurd,
Bernhardt, Günther und
Buschauer, Armin
(2015)
3HUR-DE257: Development of a tritium-labeled squaramide-type selective histamine H2 receptor antagonist.
ChemMedChem 10 (1), S. 83-93.
Volltext nicht vorhanden.
Darras, Fouad,
Pockes, Steffen ![ORCID 0000-0002-2211-9868](/images/orcid_16x16.gif)
,
Huang, Guozheng,
Wehle, Sarah,
Strasser, Andrea,
Wittmann, Hans-Joachim,
Nimczick, Martin,
Sotriffer, Christoph und
Decker, Michael
(2014)
Synthesis, biological evaluation, and computational studies of tri- and tetracyclic nitrogen-bridgehead compounds as potent dual-acting AChE inhibitors and hH3 receptor antagonists.
ACS Chemical Neuroscience 5 (3), S. 225-242.
Volltext nicht vorhanden.
Geyer, Roland,
Igel, Patrick,
Kaske, Melanie,
Elz, Sigurd und
Buschauer, Armin
(2014)
Synthesis, SAR and selectivity of 2-acyl- and 2-cyano-1-hetarylalkyl-guanidines at the four histamine receptor subtypes: a bioisosteric approach.
MedChemComm 5 (1), S. 72-81.
Volltext nicht vorhanden.
Birnkammer, Tobias,
Spickenreither, Anja,
Brunskole, Irena,
Lopuch, Miroslaw,
Kagermeier, Nicole,
Bernhardt, Günther,
Dove, Stefan,
Seifert, Roland,
Elz, Sigurd und
Buschauer, Armin
(2012)
The bivalent ligand approach leads to highly potent and selective acylguanidine-type histamine H2 receptor agonists.
Journal of Medicinal Chemistry 55 (3), S. 1147-1160.
Volltext nicht vorhanden.
Ghorai, Prasanta,
Kraus, Anja,
Birnkammer, Tobias,
Geyer, Roland,
Bernhardt, Günther,
Dove, Stefan,
Seifert, Roland,
Elz, Sigurd und
Buschauer, Armin
(2010)
Chiral N(G)-acylated hetarylpropylguanidine-type histamine H2 receptor agonists do not show significant stereoselectivity.
Bioorganic & Medicinal Chemistry Letters 20 (10), S. 3173-3176.
Volltext nicht vorhanden.
Igel, Patrick,
Schneider, Erich,
Schnell, David,
Elz, Sigurd,
Seifert, Roland und
Buschauer, Armin
(2009)
N(G)-Acylated imidazolylpropylguanidines as potent histamine H4 receptor agonists: selectivity by variation of the N(G)-substituent.
Journal of Medicinal Chemistry 52 (8), S. 2623-2627.
Volltext nicht vorhanden.
Kraus, Anja,
Ghorai, Prasanta,
Birnkammer, Tobias,
Schnell, David,
Elz, Sigurd,
Seifert, Roland,
Dove, Stefan,
Bernhardt, Günther und
Buschauer, Armin
(2009)
N(G)-Acylated aminothiazolylpropylguanidines as potent and selective histamine H2 receptor agonists.
ChemMedChem 4 (2), S. 232-240.
Volltext nicht vorhanden.
Mahboobi, Siavosh,
Dove, Stefan,
Sellmer, Andreas,
Winkler, Matthias,
Eichhorn, Emerich,
Pongratz, Herwig,
Ciossek, Thomas,
Baer, Thomas,
Maier, Thomas und
Beckers, Thomas
(2009)
Design of chimeric histone deacetylase- and tyrosine kinase-inhibitors: a series of imatinib hybrides as potent inhibitors of wild-type and mutant BCR-ABL, PDGF-Rbeta, and histone deacetylases.
Journal of medicinal chemistry 52 (8), S. 2265-79.
Volltext nicht vorhanden.
Ghorai, Prasanta,
Kraus, Anja,
Keller, Max,
Götte, Carsten,
Igel, Patrick,
Schneider, Erich,
Schnell, David,
Bernhardt, Günther,
Dove, Stefan,
Zabel, Manfred,
Elz, Sigurd,
Seifert, Roland und
Buschauer, Armin
(2008)
Acylguanidines as bioisosteres of guanidines: N(G)-acylated imidazolylpropylguanidines, a new class of histamine H2 receptor agonists.
Journal of Medicinal Chemistry 51 (22), S. 7193-7204.
Volltext nicht vorhanden.
Mahboobi, Siavosh,
Sellmer, Andreas,
Eswayah, Asma,
Elz, Sigurd,
Uecker, Andrea und
Böhmer, Frank-D.
(2008)
Inhibition of PDGFR tyrosine kinase activity by a series of novel N-(3-(4-(pyridin-3-yl)-1H-imidazol-2-ylamino)phenyl)amides: a SAR study on the bioisosterism of pyrimidine and imidazole.
European journal of medicinal chemistry 43 (7), S. 1444-1453.
Volltext nicht vorhanden.
Mahboobi, Siavosh,
Uecker, A.,
Cénac, C.,
Sellmer, A.,
Eichhorn, E.,
Elz, Sigurd,
Böhmer, F.-D. und
Dove, Stefan
(2007)
Inhibition of FLT3 and PDGFR tyrosine kinase activity by bis(benzo[b]furan-2-yl)methanones.
Bioorganic & medicinal chemistry 15 (5), S. 2187-2197.
Volltext nicht vorhanden.
Xie, Sheng-Xue,
Kraus, Anja,
Ghorai, Prasanta,
Ye, Qi-Zhuang,
Elz, Sigurd,
Buschauer, Armin und
Seifert, Roland
(2006)
N1-(3-Cyclohexylbutanoyl)-N2-[3-(1H-imidazol-4-
yl)propyl]guanidine (UR-AK57), a Potent Partial Agonist for the Human Histamine H1- and H2- Receptors.
Journal of Pharmacology and Experimental Therapeutics 317 (3), S. 1262-1268.
Zugang zum Volltext eingeschränkt.
Mahboobi, Siavosh,
Uecker, A.,
Sellmer, A.,
Cénac, C.,
Höcher, H.,
Pongratz, H.,
Hufsky, H.,
Trümpler, A.,
Sicker, M.,
Heidel, F.,
Fischer, T.,
Stocking, C.,
Elz, Sigurd,
Böhmer, F.-D. und
Dove, Stefan
(2006)
Novel bis-(1H-indol-2-yl)-methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase.
Journal of Medicinal Chemistry 49 (11), S. 3101-3115.
Volltext nicht vorhanden.
Li, Liantao,
Kracht, Julia,
Peng, Shiqi,
Bernhardt, Günther,
Elz, Sigurd und
Buschauer, Armin
(2003)
Synthesis and pharmacological activity of fluorescent histamine H2 receptor antagonists related to potentidine,.
Bioorganic & Medicinal Chemistry Letters 13 (10), 0960-894.
Volltext nicht vorhanden.
Böhmer, F. D.,
Karagyozov, L.,
Uecker, A.,
Serve, H.,
Botzki, A.,
Mahboobi, Siavosh und
Dove, Stefan
(2003)
A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP-site inhibitor STI-571.
The Journal of Biological Chemistry 278 (7), S. 5148-5155.
Volltext nicht vorhanden.
Seifert, Roland,
Wenzel-Seifert, Katharina,
Bürckstümmer, Tilmann,
Pertz, Heinz H.,
Schunack, Walter,
Dove, Stefan,
Buschauer, Armin und
Elz, Sigurd
(2003)
Multiple differences in agonist and antagonist pharmacology between human and guinea pig histamine H1-receptor,.
Journal of Pharmacology and Experimental Therapeutics 305, S. 1104-1115.
Volltext nicht vorhanden.
Mahboobi, Siavosh,
Teller, S.,
Pongratz, H.,
Hufsky, H.,
Sellmer, A.,
Botzki, Alexander,
Uecker, A.,
Beckers, T.,
Baasner, S.,
Schächtele, C.,
Überall, F.,
Kassack, M. U.,
Dove, Stefan und
Böhmer, F.-D.
(2002)
Bis(1H-2-indolyl)methanones as a novel class of inhibitors of the platelet-derived growth factor receptor kinase.
Journal of Medicinal Chemistry 45 (5), S. 1002-1018.
Volltext nicht vorhanden.
Mayer, Klaus K.,
Dove, Stefan,
Pongratz, Herwig,
Ertan, M. und
Wiegrebe, Wolfgang
(1998)
Electron impact induced fragmentation of 4-aryl-4,6,7,8-tetrahydro-1H,3H-quinazolinone-2,5-diones.
Heterocycles 48 (6), S. 1169-1183.
Volltext nicht vorhanden.
Mahboobi, Siavosh,
Dove, Stefan,
Bednarski, P. J.,
Kuhr, S.,
Burgemeister, Thomas und
Schollmeyer, D.
(1997)
X-Ray Crystal Structure of Woodinine and Conformational Analysis by Means of Semiempirical and 1H-NMR Methods.
Journal of Natural Products-Copublished with the Am. Soc. of Pharmacognosy 60 (6), S. 587-591.
Volltext nicht vorhanden.
Hirschfeld, Jürgen,
Buschauer, Armin,
Elz, Sigurd,
Schunack, Walter,
Ruat, Martial,
Traiffort, Elisabeth und
Schwartz, Jean-Charles
(1992)
Iodoaminopotentidine and related compounds: a new class of ligands with high affinity and selectivity for the histamine H_2-receptor.
Journal of Medicinal Chemistry 35, S. 2231-2238.
Volltext nicht vorhanden.
Buschauer, Armin,
Schickaneder, Helmut,
Elz, Sigurd,
Schunack, Walter,
Szelenyi, Istvan,
Baumann, Gert und
Ahrens, K.-H.
(1986)
Guanidinderivate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel.
Patentanmeldung P 35 12 084.3 (2.4.1985), Offenlegungsschrift DE 35 12 084 A.
Volltext nicht vorhanden.
Schunack, Walter,
Buschauer, Armin,
Büyüktimkim, Servet,
Dziuron, Peter,
Elz, Sigurd,
Gerhardt, Günter,
Lebenstedt, Ernst,
Lennartz, Hans-Gerd,
Schwarz, Siegfried,
Spitzhoff, Margrit und
Steffens, Robert
(1985)
2. Histamine agonists - chemistry and structure-activity relationships.
In:
Dahlbom, R. und
Nilsson, J. L. G., (eds.)
VIIIth International Symposium on Medicinal Chemistry.
Swedish Pharmaceutical Press, Stockholm, S. 169-182.
Volltext nicht vorhanden.
Buschauer, Armin,
Schickaneder, Helmut,
Schunack, Walter,
Elz, Sigurd,
Szelenyi, Istvan,
Baumann, Gert und
Ahrens, K.-H.
(1985)
Imidazolylalkylguanidine, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel.
Patentanmeldung 85 114 205.9 (12.11.1985), Eur. Pat. Appl. EP 0 199 845 (5.11.1986).
Volltext nicht vorhanden.
Elz, Sigurd,
Buschauer, Armin,
Dräger, M. und
Schunack, Walter
(1983)
Darstellung, Eigenschaften und Kristallstruktur der N-[2-(4,5,6,7-Tetrahydro-2-benzimidazolyl)ethyl]phthalamidsäure.
Z. Naturforsch. 38b, S. 1203-1207.
Volltext nicht vorhanden.
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