scholarly journals Biotransformation of a potent anabolic steroid, mibolerone, with Cunninghamella blakesleeana, C. echinulata, and Macrophomina phaseolina, and biological activity evaluation of its metabolites

PLoS ONE ◽  
2017 ◽  
Vol 12 (2) ◽  
pp. e0171476 ◽  
Author(s):  
Mahwish Siddiqui ◽  
Malik Shoaib Ahmad ◽  
Atia-tul- Wahab ◽  
Sammer Yousuf ◽  
Narjis Fatima ◽  
...  
Keyword(s):  
Biological Activity ◽  
Anabolic Steroid ◽  
Macrophomina Phaseolina ◽  
Activity Evaluation ◽  
Cunninghamella Blakesleeana

Neocryptolepine: A Promising Indoloisoquinoline Alkaloid with Interesting Biological Activity. Evaluation of the Drug and its Most Relevant Analogs

2015 ◽  
Vol 15 (17) ◽  
pp. 1683-1707 ◽  
Author(s):  
Enrique Larghi ◽  
Andrea Bracca ◽  
Abel Arroyo Aguilar ◽  
Daniel Heredia ◽  
Jorgelina Pergomet ◽  
...  
Keyword(s):  
Biological Activity ◽  
Activity Evaluation

scholarly journals The regio-selective synthesis of 10-hydroxy camptothecin norcantharidin conjugates and their biological activity evaluation in vitro

2018 ◽  
Vol 5 (6) ◽  
pp. 172317 ◽  
Author(s):  
Chang K. Zhao ◽  
Chan Li ◽  
Xian H. Wang ◽  
Yu J. Bao ◽  
Fu H. Yang ◽  
...  
Keyword(s):  
Biological Activity ◽  
Cell Growth ◽  
Cancer Treatment ◽  
Cancer Cell ◽  
Therapeutic Potential ◽  
Selective Synthesis ◽  
Cancer Cell Growth ◽  
Activity Evaluation ◽  
Moderate Yield

A series of conjugates of 10-hydroxy camptothecin (HCPT) with functionalized norcantharidin derivatives were regio-selectively synthesized in the condition of (3-dimethylaminopropyl) ethyl-carbodiimide monohydrochloride in a moderate yield. The synthesized conjugate HCPT pro-drugs can also suppress cancer cell growth in vitro . These conjugated pro-drug constructs possess therapeutic potential as novel bi-functional conjugate platforms for cancer treatment.

Biological activity of Macrophomina phaseolina in soil

1991 ◽  
Vol 23 (5) ◽  
pp. 495-496 ◽  
Author(s):  
D.J. Collins ◽  
T.D. Wyllie ◽  
S.H. Anderson
Keyword(s):  
Biological Activity ◽  
Macrophomina Phaseolina

scholarly journals One Pot Synthesis and Biological Activity Evaluation of Novel Schiff Bases Derived from 2-Hydrazinyl-1,3,4-thiadiazole

2013 ◽  
Vol 61 (2) ◽  
pp. 160-166 ◽  
Author(s):  
Kamaleddin Haj Mohammad Ebrahim Tehrani ◽  
Soroush Sardari ◽  
Vida Mashayekhi ◽  
Marjan Esfahani Zadeh ◽  
Parisa Azerang ◽  
...  
Keyword(s):  
Biological Activity ◽  
Schiff Bases ◽  
One Pot ◽  
Activity Evaluation ◽  
One Pot Synthesis

Design, synthesis and biological activity evaluation of novel conjugated sialic acid and pentacyclic triterpene derivatives as anti-influenza entry inhibitors

MedChemComm ◽  
2016 ◽  
Vol 7 (10) ◽  
pp. 1932-1945 ◽  
Author(s):  
Xu Han ◽  
Yongying Shi ◽  
Longlong Si ◽  
Zibo Fan ◽  
Han Wang ◽  
...  
Keyword(s):  
Influenza Virus ◽  
Biological Activity ◽  
Sialic Acid ◽  
Virus Entry ◽  
Pentacyclic Triterpene ◽  
Design Synthesis ◽  
Entry Inhibitors ◽  
Activity Evaluation ◽  
Virus Entry Inhibitors

A total of 24 novel sialic acid–pentacyclic triterpene conjugates were synthesized and evaluated as anti-influenza virus entry inhibitors.

scholarly journals SYNTHESIS AND BIOLOGICAL ACTIVITY EVALUATION OF SOME DERIVATIVES SYNTHESIZED FROM CURCUMIN AND CURCUMIN ANALOG

2017 ◽  
Vol 126 (1B) ◽  
pp. 127
Author(s):  
Duong Quoc Hoan
Keyword(s):  
Biological Activity ◽  
Acetic Anhydride ◽  
Cell Line ◽  
Cancer Cell ◽  
Condensation Reaction ◽  
Cancer Cell Line ◽  
High Yield ◽  
Curcumin Analog ◽  
Isoxazole Ring ◽  
Activity Evaluation

The acetohydrazides <strong>A5 </strong>containing an isoxazole ring and<strong> B5</strong> containing an indazole ring were synthesized from the corresponding acetohydrazide derivatives with acetic anhydride in about 80% high yield. Also, two acetohydrazones <strong>B6</strong> and <strong>B7</strong> were driven from acetohydrazide <strong>B4</strong> by condensation reaction. Bioactivity testes showed that none of them were active against on bacteria except acetohydrazones  <strong>B7</strong> showing moderate reactivity against KB cancer cell line at <em>IC<sub>50</sub></em> = 57 mg/L.

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