342421-15-2Relevant articles and documents
Antineoplastic Agents. 585. Isolation of Bridelia ferruginea Anticancer Podophyllotoxins and Synthesis of 4-Aza-podophyllotoxin Structural Modifications
Pettit, George R.,Searcy, Justin D.,Tan, Rui,Cragg, Gordon M.,Melody, Noeleen,Knight, John C.,Chapuis, Jean-Charles
, p. 507 - 518 (2016)
Cytotoxic constituents of the terrestrial plant Bridelia ferruginea were isolated using bioactivity-guided fractionation, which revealed the presence of the previously known deoxypodophyllotoxin (1), isopicrodeoxypodophyllotoxin (2), β-peltatin (3), β-pel
Identification of the first inhibitor of the GBP1:PIM1 interaction. Implications for the development of a new class of anticancer agents against paclitaxel resistant cancer cells
Andreoli, Mirko,Persico, Marco,Kumar, Ajay,Orteca, Nausicaa,Kumar, Vineet,Pepe, Antonella,Mahalingam, Sakkarapalayam,Alegria, Antonio E.,Petrella, Lella,Sevciunaite, Laima,Camperchioli, Alessia,Mariani, Marisa,Di Dato, Antonio,Novellino, Ettore,Scambia, Giovanni,Malhotra, Sanjay V.,Ferlini, Cristiano,Fattorusso, Caterina
, p. 7916 - 7932 (2014/12/10)
Class III β-tubulin plays a prominent role in the development of drug resistance to paclitaxel by allowing the incorporation of the GBP1 GTPase into microtubules. Once in the cytoskeleton, GBP1 binds to prosurvival kinases such as PIM1 and initiates a sig
Dihydrofuro[3,4-b]quinolin-1-one compounds
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, (2008/06/13)
The invention relates to compound of formula (I): wherein: represents a single or double bond, R0represents hydrogen or hydroxy or alkoxy, R1and R2, which are identical or different, each represents hydrogen or halogen or alkyl, alkoxy, hydroxy, polyhaloalkyl, nitro or optionally substituted amino or ?wherein m represents an integer such that 1≦m≦4, or form together with the carbon atoms carrying them an aromatic or non-aromatic, mono- or bi-cyclic group having from 5 to 12 ring members and optionally containing 1 or 2 hetero atoms selected from O, S and N, R3represents hydrogen or aryl, heteroaryl, cycloalkyl, optionally substituted alkyl or a group of formula COR7wherein R7represents aryl, optionally substituted alkyl, optionally substituted amino or OR10wherein R10represents aryl or optionally substituted alkyl, X represents oxygen or sulphur or —CH2— or —CH2—CH2—, Ar represents aryl, heteroaryl or arylalkyl, its optical isomers, its hydrates, solvates, and also its addition salts with a pharmaceutically acceptable acid. Medicinal products containing the same are useful in the treatment of cancer.