Results 51 to 60 of about 728 (182)
Extraction of rotenoids from Derris elliptica using supercritical CO2
, 2018 BACKGROUND: Supercritical (SC)-CO2 extraction of rotenoids from Derris elliptica roots was proposed using fractional separation of the extracts and operating at increasing pressure. RESULTS: The best processing conditions were found at 200 bar, 40 °C and Mariarosa Scognamiglio, Ernesto Reverchon, Lucia Baldino, Reverchon, Ernesto, Scognamiglio, Mariarosa, Baldino, Lucia +5 morecore +1 more sourceFrom MS1 to Structure: A Van Krevelen–DBE–Aromaticity‐Based Framework for Annotating Specialized Metabolites via High‐Resolution Mass Spectrometry
Rapid Communications in Mass Spectrometry, Volume 39, Issue 24, 30 December 2025.ABSTRACT Rationale
Classifying specialized metabolites in untargeted metabolomics remains a major challenge, particularly when relying solely on high‐resolution mass spectrometry (HRMS) data at the MS1 level. Traditional approaches using Van Krevelen diagrams often lack sufficient resolution to distinguish structurally similar metabolite classes ...Nerilson M. Lima, Luana A. Pereira, Lucas S. Tironi, Matheus P. G. do Carmo, Milbya L. Costa, Renato A. Oliveira, Salva Asghar, Vinicius Fortes da Silva +7 morewiley +1 more sourceRotenone and Rotenoids in Cubè Resins, Formulations and Residues on Olives
, 2004 Rotenone and rotenoids (deguelin, β-rotenolone (12aβ -hydroxyrotenone), tephrosin (12aβ-hydroxydeguelin), 12aα -hydroxyrotenone, and dehydrorotenone) were determined in cubè resins and formulations.TUBEROSO, CARLO IGNAZIO GIOVANNI, ANGIONI, ALBERTO, CABRAS P., MELIS, MARINELLA, CABRAS M, CABIZZA M +5 morecore +1 more sourceThe Concise Guide to PHARMACOLOGY 2025/26: G protein‐coupled receptors
British Journal of Pharmacology, Volume 182, Issue S1, Page S24-S151, December 2025.The Concise Guide to Pharmacology 2025/26 marks the seventh edition in this series of biennial publications in the British Journal of Pharmacology. Presented in landscape format, the guide provides a comparative overview of the pharmacology of drug target families. The concise nature of the Concise Guide refers to the style of presentation, being clear,Stephen P. H. Alexander, Anthony P. Davenport, Eamonn Kelly, Alasdair J. Gibb, Alistair A. Mathie, Chloe J. Peach, Emma L. Veale, Jane F. Armstrong, Elena Faccenda, Simon D. Harding, Christopher Southan, Jamie A. Davies, Maria Pia Abbracchio, George R. Abraham, Alexander Agoulnik, Wayne Alexander, Khaled Al‐hosaini, Magnus Bäck, Jillian G. Baker, Nicholas M. Barnes, Ross Bathgate, Jean‐Martin Beaulieu, Annette G. Beck‐Sickinger, Maik Behrens, Kirstie A. Bennett, Kenneth E. Bernstein, Bernhard Bettler, Nigel J. M. Birdsall, Victoria A. Blaho, Pascal Bonaventure, Francois Boulay, Corinne Bousquet, Hans Bräuner‐Osborne, Andrew J. Brown, Geoffrey Burnstock, Marta Busnelli, Girolamo Caló, Vanni Caruso, Justo P. Castaño, Kevin J. Catt, Stefania Ceruti, Paul Chazot, Nan Chiang, Bice Chini, Arthur Christopoulos, Jerold Chun, Antonia Cianciulli, Olivier Civelli, Lucie H. Clapp, Réjean Couture, Helen M. Cox, Zsolt Csaba, Claes Dahlgren, Frank M. Dautzenberg, Gordon Dent, Steven D. Douglas, Pascal Dournaud, Margarita L. Dubocovich, Satoru Eguchi, Emanuel Escher, Edward J. Filardo, Tung Fong, Huamei Fu Forsman, Marta Fumagalli, Raul R. Gainetdinov, Michael L. Garelja, Marc de Gasparo, Florence Gbahou, Craig Gerard, Marvin Gershengorn, Michelle Glass, David E. Gloriam, Fernand Gobeil, Theodore L. Goodfriend, Cyril Goudet, Lukas Grätz, Karen J. Gregory, Christian Gruber, Andrew L. Gundlach, Jörg Hamann, Julien Hanson, Deborah S. Hartman, Richard L. Hauger, Debbie L. Hay, Akos Heinemann, Laura Heitman, Deron R. Herr, Morley D. Hollenberg, Nicholas D. Holliday, Birgitte Holst, Mastgugu Horiuchi, Daniel Hoyer, László Hunyady, Ahsan Husain, Adriaan P. IJzerman, Tadashi Inagami, Paul A. Insel, Kenneth A. Jacobson, Laura H. Jacobson, Robert T. Jensen, Ralf Jockers, Deepa Jonnalagadda, Sadashiva Karnik, Klemens Kaupmann, Jacqueline Kemp, Charles Kennedy, Yasuyuki Kihara, Julia Kinsolving, Takio Kitazawa, Pawel Kozielewicz, Hans‐Jürgen Kreienkamp, Jyrki P. Kukkonen, Luxmichan Laishram, Tobias Langenhan, Christopher J. Langmead, Dan Larhammar, Katie Leach, Davide Lecca, John D. Lee, Susan E. Leeman, Jérôme Leprince, Rob Leurs, Xaria X. Li, Ines Liebscher, Stephen J. Lolait, Amelie Lupp, Robyn Macrae, Janet J. Maguire, Davide Malfacini, Maurice Manning, Davide Marangon, Kirill Martemyanov, Jean Mazella, Craig A. McArdle, Shlomo Melmed, Martin C. Michel, Laurence J. Miller, Vincenzo Mitolo, Bernard Mouillac, Christa E. Müller, Philip M. Murphy, Jean‐Louis Nahon, Richard R. Neubig, Tony Ngo, Xavier Norel, Duuamene Nyimanu, Anne‐Marie O’Carroll, Stefan Offermanns, Maria Antonietta Panaro, Marc Parmentier, Nicole Perry‐Hauser, Roger G. Pertwee, Jean‐Philippe Pin, Eric R. Prossnitz, Helena Chengxue Qin, Mark Quinn, Stefano Raffaele, Rithwik Ramachandran, Manisha Ray, Rainer K. Reinscheid, Alejandro Romeral Buzón, Philippe Rondard, Mette M. Rosenkilde, G. Enrico Rovati, Chiara Ruzza, Gareth J. Sanger, Nicole Scholz, Torsten Schöneberg, Gunnar Schulte, Stefan Schulz, Deborah L. Segaloff, Charles N. Serhan, Arun K. Shukla, Khuraijam Dhanachandra Singh, Craig M. Smith, Nicola J. Smith, Claudia Stäubert, Leigh A. Stoddart, Yukihiko Sugimoto, Roger Summers, Valerie P. Tan, David M. Thal, Walter ( Wally) Thomas, Pieter B. M. W. M. Timmermans, Kalyan Tirupula, Lawrence Toll, Giovanni Tulipano, Hamiyet Unal, Thomas Unger, Celine Valant, Patrick Vanderheyden, David Vaudry, Hubert Vaudry, Joseph G. Verbalis, Jean‐Pierre Vilardaga, Christopher S. Walker, Ji Ming Wang, Donald T. Ward, Hans‐Jürgen Wester, Gary B. Willars, Tom Lloyd Williams, Trent M. Woodruff, Huixian Wu, Cheng Yang, Chengcan Yao, Richard D. Ye, Nathan Zaidman +206 morewiley +1 more sourceIsoflavones and Rotenoids from the Leaves of Millettia oblata ssp. teitensis
, 2017 A new isoflavone, 8-prenylmilldrone (1), and four
new rotenoids, oblarotenoids A−D (2−5), along with nine known
compounds (6−14), were isolated from the CH2Cl2/CH3OH
(1:1) extract of the leaves of Millettia oblata ssp.Deyou, Tsegaye,, Pelletier, J., Heydenreich, Matthias (Dr.), Yenesew, A., Erdelyi, Mate,, Gruhonjic, Amra, Gruhonjic, Amra,, Deyou, Tsegaye, Tsegaye Deyou, Amra Gruhonjic, Koch, Andreas (Dr.), Marco, M., Erdélyi, Máté, Fangfang Pan, Matthias Heydenreich, Abiy Yenesew, Makungu Marco, Derese, Solomon, Máté Erdélyi, Paul A. Fitzpatrick, Fitzpatrick, Paul A.,, Solomon Derese, Rissanen, Kari, Jerry Pelletier, Koch, A., Koch, Andreas, Kari Rissanen, Marco, Makungu, Heydenreich, Matthias, Pan, Fangfang, Derese, S., Andreas Koch, Rissanen, K., Pan, F. F., Fitzpatrick, Paul A, Heydenreich, M., Pelletier, Jerry, Yenesew, Abiy, Fitzpatrick, Paul A. +38 morecore +1 more sourceStructural Elucidation and Chemical Conversion of Amorphispironone, a Novel Spironone from Amorpha fruticosa, to Rotenoids.
, 1993 To search for possible antiumor promoters, we carried out an investigation of the leaves of Amorpha fruticosa L. (Leguminosae). The novel spironone type rotenoid, amorphispironone (1), isolated together with four known rotenoids, tephrosin (2 ...Li, Leping, Terada, Hiroki, Ito, Kazuo, Konoshima, Takao, Haruna, Mitsumasa, Wang, Hui Kang, Lee, Kuo Hsiung, Kokumai, Midori, Kozuka, Mutsuo, Estes, James R. +9 morecore +2 more sourcesIn silico (Eco)toxicology and molecular docking of halogenated and oxygenated rotenoid derivatives
, 2023 The rotenoids are compounds widely disseminated in the agro-industrial and chemical-pharmacological sectors due to their structural constitution and versatility in biological activities, however, these present toxic activity for fish. Thus, the objective Sousa, Damião Sampaio de, Mendes, Francisco Rogênio da Silva, Marinho, Emmanuel Silva, Belarmino, Anthony Barbosa, Oliveira, Victor Moreira de, Marinho, Gabrielle Silva +5 morecore +2 more sources