38470-67-6Relevant academic research and scientific papers
Indole chalcones: Design, synthesis, in vitro and in silico evaluation against Mycobacterium tuberculosis
Joji, Annu,Kannan, Tharanikkarasu,Mani, Maheswaran,Ramesh, Deepthi,Sethumadhavan, Aiswarya,Vijayakumar, Balaji Gowrivel
supporting information, (2020/05/01)
Indole chalcones were designed and synthesized as a promising set of compounds against H37Rv strain of Mycobacterium tuberculosis. Within this library of compounds, (E)-1-(furan-3-yl)-3-(1H-indol-3-yl)prop-2-en-1-one (18), (E)-3-(1H-indol-3-yl)
Synthesis and antioxidant activity of a new class of pyrazolyl indoles, thiazolyl pyrazolyl indoles
Ummadi, Nagarjuna,Gundala, Sravya,Venkatapuram, Padmavathi,Adivireddy, Padmaja
, p. 1574 - 1584 (2017/06/05)
A new class of bis and tris heterocycles–pyrazolyl indoles and thiazolyl pyrazolyl indoles were prepared from the Michael acceptor (E)-3-(1H-indol-3-yl)-1-arylprop-2-en-1-ones by ultrasound irradiation technique and tested for antioxidant activity. The th
Synthesis of substituted indole derivatives as a new class of antimalarial agents
Agarwal, Anu,Srivastava, Kumkum,Puri,Chauhan, Prem M.S.
, p. 3133 - 3136 (2007/10/03)
A series of substituted indole derivatives were synthesized and evaluated for their in vitro antimalarial activity against P. falciparum. Out of the 24 compounds synthesized six compounds have shown MIC of 1 μg/mL. These compounds are in vitro several fol
Anti-inflammatory, analgesic and antipyretic 4,6-disubstituted 3-cyano- 2-aminopyridines
Manna, Fedele,Chimenti, Franco,Bolasco, Adriana,Bizzarri, Bruna,Filippelli, Walter,Filippelli, Amelia,Gagliardi, Luigi
, p. 245 - 254 (2007/10/03)
4,6-diaryl and 4,6-aryl-indolyl substituted 3-cyano-2-aminopyridines were synthesized and submitted to evaluation for their anti-inflammatory, analgesic and antipyretic activity. The electronegativity of the substituents and their displacement on the 4- o
