scholarly journals Structure, Absolute Configuration and Biological Evaluation of a New Labdane Diterpenoid from Jatropha podagrica

2020 ◽  
Vol 14 (5) ◽  
pp. 355-360
Author(s):  
Dongbo Zhang ◽  
Jingao Yu ◽  
Zhen Zhang ◽  
Yanni Liang ◽  
Zhishu Tang ◽  
...  
2019 ◽  
Vol 10 (27) ◽  
pp. 6635-6641 ◽  
Author(s):  
Jian Zhang ◽  
Tianhu Zhao ◽  
Rongwen Yang ◽  
Ittipon Siridechakorn ◽  
Sanshan Wang ◽  
...  

The first total synthesis and isolation of pseudopaline was reported, which allows determination and confirmation of the absolute configuration of the natural product.


2015 ◽  
Vol 69 (1) ◽  
pp. 9-14 ◽  
Author(s):  
Alessio Cimmino ◽  
Gennaro Pescitelli ◽  
Alexander Berestetskiy ◽  
Anna Dalinova ◽  
Denis Krivorotov ◽  
...  

Molecules ◽  
2019 ◽  
Vol 25 (1) ◽  
pp. 158 ◽  
Author(s):  
Yan-Jiao Yin ◽  
Dan-Ling Huang ◽  
Bin Qiu ◽  
Dan Cai ◽  
Jiao-Jiao Zhang ◽  
...  

Five new meroterpenoids, zizhines P-S and U (1−4,7), together with two known meroterpenoids (5 and 6) were isolated from Ganoderma sinensis. Their structures including absolute configurations were assigned by using spectroscopic, computational, and chemical methods. Racemics zizhines P and Q were purified by HPLC on chiral phase. Biological evaluation found that 4, 5 and 6 are cytotoxic toward human cancer cells (A549, BGC-823, Kyse30) with IC50 values in the range of 63.43–80.83 μM towards A549, 59.2 ± 2.73 μM and 64.25 ± 0.37 μM towards BGC-823, 76.28 ± 1.93 μM and 85.42 ± 2.82 μM towards Kyse30.


2019 ◽  
Vol 29 (3) ◽  
pp. 380-382 ◽  
Author(s):  
Miyanou Rosales-Hurtado ◽  
Alexandre Lebeau ◽  
Cyril Bourouh ◽  
Gerardo Cebrian-Torrejon ◽  
Muriel Albalat ◽  
...  

2012 ◽  
Vol 75 (6) ◽  
pp. 1025-1029 ◽  
Author(s):  
Yong-Ming Yan ◽  
Gui-Sheng Wu ◽  
Xiao-Ping Dong ◽  
Lan Shen ◽  
Yan Li ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Ashraf H. Abadi ◽  
Jochen Lehmann ◽  
Gary A. Piazza ◽  
Mohammad Abdel-Halim ◽  
Mohamed S. M. Ali

Two series of fused tetrahydro-β-carboline hydantoin and tetrahydro-β-carboline thiohydantoin derivatives with a pendant 2,4-dimethoxyphenyl at position 5 were synthesized, and chiral carbons at positions 5 and 11a swing from R,R to R,S, S,R, and S,S. The prepared analogues were evaluated for their capacity to inhibit phosphodiesterase 5 (PDE5) isozyme. The R absolute configuration of C-5 in the β-carboline hydantoin derivatives was found to be essential for the PDE5 inhibition. Chiral carbon derived from amino acid even if of the S configuration (L-tryptophan) may lead to equiactive or more active isomers than those derived from amino acid with the R configuration (D-tryptophan). This expands the horizon from which efficient PDE5 inhibitors can be derived and may offer an economic advantage. The thiohydantoin derivatives were less active than their hydantoin congeners.


2008 ◽  
Vol 130 (4) ◽  
pp. 1154-1155 ◽  
Author(s):  
Alexander R. Moise ◽  
Marta Domínguez ◽  
Susana Alvarez ◽  
Rosana Alvarez ◽  
Michael Schupp ◽  
...  

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