TY - JOUR A1 - Abdalla, H. A1 - Adam, R. A1 - Aharonian, Felix A. A1 - Benkhali, F. Ait A1 - Angüner, Ekrem Oǧuzhan A1 - Arcaro, C. A1 - Armand, C. A1 - Armstrong, T. A1 - Ashkar, H. A1 - Backes, M. A1 - Baghmanyan, V. A1 - Martins, V. Barbosa A1 - Barnacka, A. A1 - Barnard, M. A1 - Becherini, Y. A1 - Berge, D. A1 - Bernlohr, K. A1 - Bi, B. A1 - Bottcher, M. A1 - Boisson, C. A1 - Bolmont, J. A1 - de Lavergne, M. de Bony A1 - Bordas, Pol A1 - Breuhaus, M. A1 - Brun, F. A1 - Brun, P. A1 - Bryan, M. A1 - Buchele, M. A1 - Bulik, T. A1 - Bylund, T. A1 - Caroff, S. A1 - Carosi, A. A1 - Casanova, Sabrina A1 - Chand, T. A1 - Chandra, S. A1 - Chen, A. A1 - Cotter, G. A1 - Curylo, M. A1 - Mbarubucyeye, J. Damascene A1 - Davids, I. D. A1 - Davies, J. A1 - Deil, C. A1 - Devin, J. A1 - deWilt, P. A1 - Dirson, L. A1 - Djannati-Atai, A. A1 - Dmytriiev, A. A1 - Donath, A. A1 - Doroshenko, V. A1 - Duffy, C. A1 - Dyks, J. A1 - Egberts, Kathrin A1 - Eichhorn, F. A1 - Einecke, S. A1 - Emery, G. A1 - Ernenwein, J. -P. A1 - Feijen, K. A1 - Fegan, S. A1 - Fiasson, A. A1 - de Clairfontaine, G. Fichet A1 - Fontaine, G. A1 - Funk, S. A1 - Fussling, Matthias A1 - Gabici, S. A1 - Gallant, Y. A. A1 - Giavitto, G. A1 - Giunti, L. A1 - Glawion, D. A1 - Glicenstein, J. F. A1 - Gottschall, D. A1 - Grondin, M. -H. A1 - Hahn, J. A1 - Haupt, M. A1 - Hermann, G. A1 - Hinton, J. A. A1 - Hofmann, W. A1 - Hoischen, Clemens A1 - Holch, T. L. A1 - Holler, M. A1 - Horbe, M. A1 - Horns, D. A1 - Huber, D. A1 - Jamrozy, M. A1 - Jankowsky, D. A1 - Jankowsky, F. A1 - Jardin-Blicq, A. A1 - Joshi, V. A1 - Jung-Richardt, I. A1 - Kasai, E. A1 - Kastendieck, M. A. A1 - Katarzynski, K. A1 - Katz, U. A1 - Khangulyan, D. A1 - Khelifi, B. A1 - Klepser, S. A1 - Kluzniak, W. A1 - Komin, Nu. A1 - Konno, R. A1 - Kosack, K. A1 - Kostunin, D. A1 - Kreter, M. A1 - Lamanna, G. A1 - Lemiere, A. A1 - Lemoine-Goumard, M. A1 - Lenain, J. -P. A1 - Levy, C. A1 - Lohse, T. A1 - Lypova, I. A1 - Mackey, J. A1 - Majumdar, J. A1 - Malyshev, D. A1 - Malyshev, D. A1 - Marandon, V. A1 - Marchegiani, P. A1 - Marcowith, Alexandre A1 - Mares, A. A1 - Marti-Devesa, G. A1 - Marx, R. A1 - Maurin, G. A1 - Meintjes, P. J. A1 - Meyer, M. A1 - Mitchell, A. A1 - Moderski, R. A1 - Mohamed, M. A1 - Mohrmann, L. A1 - Montanari, A. A1 - Moore, C. A1 - Morris, P. A1 - Moulin, Emmanuel A1 - Muller, J. A1 - Murach, T. A1 - Nakashima, K. A1 - Nayerhoda, A. A1 - de Naurois, M. A1 - Ndiyavala, H. A1 - Niederwanger, F. A1 - Niemiec, J. A1 - Oakes, L. A1 - O'Brien, Patrick A1 - Odaka, H. A1 - Ohm, S. A1 - Olivera-Nieto, L. A1 - Wilhelmi, E. de Ona A1 - Ostrowski, M. A1 - Oya, I. A1 - Panter, M. A1 - Panny, S. A1 - Parsons, R. D. A1 - Peron, G. A1 - Peyaud, B. A1 - Piel, Q. A1 - Pita, S. A1 - Poireau, V. A1 - Noel, A. Priyana A1 - Prokhorov, D. A. A1 - Prokoph, H. A1 - Puhlhofer, G. A1 - Punch, M. A1 - Quirrenbach, A. A1 - Raab, S. A1 - Rauth, R. A1 - Reichherzer, P. A1 - Reimer, A. A1 - Reimer, O. A1 - Remy, Q. A1 - Renaud, M. A1 - Rieger, F. A1 - Rinchiuso, L. A1 - Romoli, C. A1 - Rowell, G. A1 - Rudak, B. A1 - Ruiz-Velasco, E. A1 - Sahakian, V. A1 - Sailer, S. A1 - Sanchez, D. A. A1 - Santangelo, A. A1 - Sasaki, M. A1 - Scalici, M. A1 - Schussler, F. A1 - Schutte, H. M. A1 - Schwanke, U. A1 - Schwemmer, S. A1 - Seglar-Arroyo, M. A1 - Senniappan, M. A1 - Seyffert, A. S. A1 - Shafi, N. A1 - Shiningayamwe, K. A1 - Simoni, R. A1 - Sinha, A. A1 - Sol, H. A1 - Specovius, A. A1 - Spencer, S. A1 - Spir-Jacob, M. A1 - Stawarz, L. A1 - Sun, L. A1 - Steenkamp, R. A1 - Stegmann, C. A1 - Steinmassl, S. A1 - Steppa, C. A1 - Takahashi, T. A1 - Tavernier, T. A1 - Taylor, A. M. A1 - Terrier, R. A1 - Tiziani, D. A1 - Tluczykont, M. A1 - Tomankova, L. A1 - Trichard, C. A1 - Tsirou, M. A1 - Tuffs, R. A1 - Uchiyama, Y. A1 - van der Walt, D. J. A1 - van Eldik, C. A1 - van Rensburg, C. A1 - van Soelen, B. A1 - Vasileiadis, G. A1 - Veh, J. A1 - Venter, C. A1 - Vincent, P. A1 - Vink, J. A1 - Volk, H. J. A1 - Vuillaume, T. A1 - Wadiasingh, Z. A1 - Wagner, S. J. A1 - Watson, J. A1 - Werner, F. A1 - White, R. A1 - Wierzcholska, A. A1 - Wong, Yu Wun A1 - Yusafzai, A. A1 - Zacharias, M. A1 - Zanin, R. A1 - Zargaryan, D. A1 - Zdziarski, A. A. A1 - Zech, Alraune A1 - Zhu, S. J. A1 - Ziegler, A. A1 - Zorn, J. A1 - Zouari, S. A1 - Zywucka, N. T1 - An extreme particle accelerator in the Galactic plane BT - HESS J1826-130 JF - Astronomy and astrophysics : an international weekly journal N2 - The unidentified very-high-energy (VHE; E > 0.1 TeV) gamma -ray source, HESS J1826-130, was discovered with the High Energy Stereoscopic System (HESS) in the Galactic plane. The analysis of 215 h of HESS data has revealed a steady gamma -ray flux from HESS J1826-130, which appears extended with a half-width of 0.21 degrees +/- 0.02
(stat)degrees
stat degrees +/- 0.05
(sys)degrees sys degrees . The source spectrum is best fit with either a power-law function with a spectral index Gamma = 1.78 +/- 0.10(stat) +/- 0.20(sys) and an exponential cut-off at 15.2
(+5.5)(-3.2) -3.2+5.5 TeV, or a broken power-law with Gamma (1) = 1.96 +/- 0.06(stat) +/- 0.20(sys), Gamma (2) = 3.59 +/- 0.69(stat) +/- 0.20(sys) for energies below and above E-br = 11.2 +/- 2.7 TeV, respectively. The VHE flux from HESS J1826-130 is contaminated by the extended emission of the bright, nearby pulsar wind nebula, HESS J1825-137, particularly at the low end of the energy spectrum. Leptonic scenarios for the origin of HESS J1826-130 VHE emission related to PSR J1826-1256 are confronted by our spectral and morphological analysis. In a hadronic framework, taking into account the properties of dense gas regions surrounding HESS J1826-130, the source spectrum would imply an astrophysical object capable of accelerating the parent particle population up to greater than or similar to 200 TeV. Our results are also discussed in a multiwavelength context, accounting for both the presence of nearby supernova remnants, molecular clouds, and counterparts detected in radio, X-rays, and TeV energies. KW - ISM: supernova remnants KW - ISM: clouds KW - gamma rays: general KW - gamma rays: KW - ISM Y1 - 2020 U6 - https://doi.org/10.1051/0004-6361/202038851 SN - 0004-6361 SN - 1432-0746 VL - 644 PB - EDP Sciences CY - Les Ulis ER - TY - JOUR A1 - Bringmann, Gerhard A1 - Mutanyatta-Comar, Joan A1 - Maksimenka, Katja A1 - Wanjohi, John M. A1 - Heydenreich, Matthias A1 - Brun, Reto A1 - Müller, Werner E. G. A1 - Peter, Martin G. A1 - Midiwo, Jacob O. A1 - Yenesew, Abiy T1 - Joziknipholones A and B : the first dimeric phenylanthraquinones, from the roots of Bulbine frutescens N2 - From the roots of the African plant Bulbine frutescens (Asphodelaceae), two unprecedented novel dimeric phenylanthraquinones, named joziknipholones A and B, possessing axial and centrochirality, were isolated, together with six known compounds. Structural elucidation of the new metabolites was achieved by spectroscopic and chiroptical methods, by reductive cleavage of the central bond between the monomeric phenylanthraquinone and -anthrone portions with sodium dithionite, and by quantum chemical CD calculations. Based on the recently revised absolute axial configuration of the parent phenylanthraquinones, knipholone and knipholone anthrone, the new dimers were attributed to possess the P- configuration (i.e., with the acetyl portions below the anthraquinone plane) at both axes in the case of joziknipholone A, whereas in joziknipholone B, the knipholone part was found to be M-configured. Joziknipholones A and B are active against the chloroquine resistant strain K1 of the malaria pathogen, Plasmodium falciparum, and show moderate activity against murine leukemic lymphoma L5178y cells. Y1 - 2008 UR - http://www3.interscience.wiley.com/journal/26293/home?CRETRY=1&SRETRY=0 SN - 0947-6539 ER - TY - GEN A1 - Bringmann, Gerhard A1 - Mutanyatta-Comar, Joan A1 - Maksimenka, Katja A1 - Wanjohi, John M. A1 - Heydenreich, Matthias A1 - Brun, Reto A1 - Müller, Werner E. G. A1 - Peter, Martin A1 - Midiwo, Jacob O. A1 - Yenesew, Abiy T1 - Joziknipholones A and B : the First Dimeric Phenylanthraquinones, from the Roots of Bulbine frutescens N2 - From the roots of the African plant Bulbine frutescens (Asphodelaceae), two unprecedented novel dimeric phenylanthraquinones, named joziknipholones A and B, possessing axial and centrochirality, were isolated, together with six known compounds. Structural elucidation of the new metabolites was achieved by spectroscopic and chiroptical methods, by reductive cleavage of the central bond between the monomeric phenylanthraquinone and -anthrone portions with sodium dithionite, and by quantum chemical CD calculations. Based on the recently revised absolute axial configuration of the parent phenylanthraquinones, knipholone and knipholone anthrone, the new dimers were attributed to possess the P-configuration (i.e., with the acetyl portions below the anthraquinone plane) at both axes in the case of joziknipholone A, whereas in joziknipholone B, the knipholone part was found to be M-configured. Joziknipholones A and B are active against the chloroquine resistant strain K1 of the malaria pathogen, Plasmodium falciparum, and show moderate activity against murine leukemic lymphoma L5178y cells. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - paper 104 KW - antimalarial activity KW - chirality KW - joziknipholones KW - natural products KW - structure elucidation Y1 - 2008 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-42638 ER -