Potential sweetening agents of plant origin. 13. An intensely sweet dihydroflavonol derivative based on a natural product lead compound

1988 ◽  
Vol 31 (6) ◽  
pp. 1250-1253 ◽  
Author(s):  
N. P. Dhammika Nanayakkara ◽  
Raouf A. Hussain ◽  
John M. Pezzuto ◽  
D. Doel Soejarto ◽  
A. Douglas Kinghorn
Molecules ◽  
2019 ◽  
Vol 24 (13) ◽  
pp. 2355 ◽  
Author(s):  
Yang Xu ◽  
Fang Wang ◽  
Hongye Guo ◽  
Shihan Wang ◽  
Shuling Ni ◽  
...  

Natural products play an important role in drug discovery. This work employed a natural product 1-methylhydantoin as the lead compound to develop novel dual-active drugs. 1-Methylhydantoin was isolated from Oviductus Ranae, which is a traditional Chinese medicine that has been used for tussive and inflammation treatment for a long time. An in silico study screened the more active 1-methylhydantoin derivatives. Antitussive assessment indicated that the newly synthesized agent had similar bioactivity with the natural product. An anti-inflammatory model used xylene induced ear edema model. At the same dosage (100 mg/Kg), the newly prepared agent had an inhibition rate 53.18% which was much higher than that of the lead compound (22.69%). The results might be ascribed to the cyclooxygenases-1 (COX-1) and cyclooxygenases-2 (COX-2) selectivity, and the fitness of the compound, and the binding pocket. The anti-particulate matter (PM 2.5) acute pneumonia was evaluated through an in vivo model constructed by nasal instillation with PM 2.5 suspension. The results of the above models suggested that this novel agent had remarkable antitussive, anti-inflammatory, and anti-PM 2.5 acute pneumonia activities.


2020 ◽  
Author(s):  
Yuvixza Lizarme-Salas ◽  
Alexandra Daryl Ariawan ◽  
Ranjala Ratnayake ◽  
Hendrik Luesch ◽  
Angela Finch ◽  
...  

Piperine, a natural product derived from peppercorns, has a variety of biological activities that make it an attractive lead compound for medicinal chemistry. However, piperine has some problematic physicochemical properties including poor aqueous solubility and a susceptibility to UV-induced degradation. In this work, we designed an analog of piperine in which the central conjugated hydrocarbon chain is replaced with a vicinal difluoroalkane moiety. We show that this fluorinated analog of piperine has superior physicochemical properties, and it also has higher potency and selectivity towards one particular drug target, acetylcholinesterase. This work highlights the potential usefulness of the threo-difluoroalkane motif as a surrogate for E-alkenes in medicinal chemistry.


1988 ◽  
Vol 42 (2) ◽  
pp. 267-283 ◽  
Author(s):  
R. A. Hussain ◽  
A. D. Klnghorn ◽  
D. D. Soejarto

1993 ◽  
Vol 41 (8) ◽  
pp. 1305-1310 ◽  
Author(s):  
Enrique. Vasquez ◽  
William. Jakinovich ◽  
N. P. Dhammika. Nanayakkara ◽  
Raouf A. Hussain ◽  
Myung Sook. Chung ◽  
...  

Molecules ◽  
2017 ◽  
Vol 22 (6) ◽  
pp. 915 ◽  
Author(s):  
Hélène Carreyre ◽  
Grégoire Carré ◽  
Maurice Ouedraogo ◽  
Clarisse Vandebrouck ◽  
Jocelyn Bescond ◽  
...  

1983 ◽  
Vol 37 (1) ◽  
pp. 71-79 ◽  
Author(s):  
D. D. Soejarto ◽  
C. M. Compadre ◽  
P. J. Medon ◽  
S. K. Kamath ◽  
A. D. Kinghorn

1990 ◽  
Vol 44 (2) ◽  
pp. 174-182 ◽  
Author(s):  
R. A. Hussain ◽  
L. J. Poveda ◽  
J. M. Pezzuto ◽  
D. D. Soejarto ◽  
A. D. Kinghorn

1982 ◽  
Vol 45 (5) ◽  
pp. 590-599 ◽  
Author(s):  
Djaja D. Soejarto ◽  
A. Douglas Kinghorn ◽  
Norman R. Farnsworth

1991 ◽  
Vol 464 ◽  
pp. 213-219 ◽  
Author(s):  
Fekadu Fullas ◽  
Jinwoong Kim ◽  
Cesar M. Compadre ◽  
A. Douglas Kinghorn

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