918892-30-5Relevant academic research and scientific papers
A Structure-based Design Approach for Generating High Affinity BRD4 D1-Selective Chemical Probes
Cui, Huarui,Divakaran, Anand,Hoell, Zachariah J.,Ellingson, Mikael O.,Scholtz, Cole R.,Zahid, Huda,Johnson, Jorden A.,Griffith, Elizabeth C.,Gee, Clifford T.,Lee, Amani L.,Khanal, Shalil,Shi, Ke,Aihara, Hideki,Shah, Vijay H.,Lee, Richard E.,Harki, Daniel A.,Pomerantz, William C. K.
, p. 2342 - 2360 (2022/01/27)
Chemical probes for epigenetic proteins are essential tools for dissecting the molecular mechanisms for gene regulation and therapeutic development. The bromodomain and extra-terminal (BET) proteins are master transcriptional regulators. Despite promising
The base-free van Leusen reaction of cyclic imines on water: Synthesis of N-fused imidazo 6,11-dihydro β-carboline derivatives
Satyam, Killari,Murugesh,Suresh, Surisetti
, p. 5234 - 5238 (2019/06/07)
Construction of imidazoles has been demonstrated on water under base-free conditions. The reaction of dihydro β-carboline imines and p-toluenesulfonylmethyl isocyanides furnished the corresponding substituted N-fused imidazo 6,11-dihydro β-carboline derivatives in very good yields under ambient conditions. The use of deuterium oxide (D2O) as a solvent enabled the incorporation of deuterium isotopes in the imidazole ring.
Design, Synthesis, and Biological Evaluation of New 1-(Aryl-1 H-pyrrolyl)(phenyl)methyl-1 H-imidazole Derivatives as Antiprotozoal Agents
Saccoliti, Francesco,Madia, Valentina Noemi,Tudino, Valeria,De Leo, Alessandro,Pescatori, Luca,Messore, Antonella,De Vita, Daniela,Scipione, Luigi,Brun, Reto,Kaiser, Marcel,M?ser, Pascal,Calvet, Claudia M.,Jennings, Gareth K.,Podust, Larissa M.,Pepe, Giacomo,Cirilli, Roberto,Faggi, Cristina,Di Marco, Annalise,Battista, Maria Rosaria,Summa, Vincenzo,Costi, Roberta,Di Santo, Roberto
, p. 1330 - 1347 (2019/02/24)
We have designed and synthesized a series of new imidazole-based compounds structurally related to an antiprotozoal agent with nanomolar activity which we identified recently. The new analogues possess micromolar activities against Trypanosoma brucei rhod
COMPOUNDS FOR THE TREATMENT OF RESPIRATORY DISEASES
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Page/Page column 75; 74, (2018/11/26)
The present invention relates to new compounds that are useful in the prevention or treatment of respiratory diseases, such as asthma, to the preparation of the compounds, and to compositions including the compounds. The present invention also relates to the use of the compounds, as well as compositions including the compounds, in treating or preventing respiratory diseases.
LXR MODULATORS
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, (2014/09/29)
The present invention provides compounds of Formula I: and pharmaceutically acceptable salts or solvates thereof, as modulators of liver X receptors (LXR), compositions comprising any of such novel compounds, methods of using these compounds or compositions as medicaments for prevention or treatment of diseases or disorders related to liver X receptor (LXR), as well as methods of preparing these LXR modulators and using them in the manufacture of medicaments.
Synthesis, biological evaluation, and molecular modeling studies of novel heterocyclic compounds as anti-proliferative agents
Chaudhary, Anurag,Sharma,Bhardwaj, Gautam,Jain, Vaibhav,Bharatam,Shrivastav, Birendra,Roy
, p. 5654 - 5669 (2013/11/06)
Two novel series of heterocyclic compounds have been synthesized. In first series, isatin was allowed to react with substituted aromatic/cyclic carbonyl compounds to get desired mannich bases (2a-e). In second series, 4,5-disubstituted oxazoles (6a-p) wer
