Semi-synthetic transformations of ajugasterone C (1), poststerone
By A Mystery Man Writer
Description
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Ecdysteroids as defensive chemicals - ScienceDirect
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.researchgate.net/publication/378400098/figure/fig2/AS:11431281225376161@1708692928248/Reactive-oxygen-species-ROS-measurement-in-human-brain-microvascular-endothelial-cells_Q320.jpg)
Máté VÁGVÖLGYI, Research Fellow, Ph.D., University of Szeged, Szeged, Institute of Pharmacognosy
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.researchgate.net/publication/360749787/figure/fig5/AS:1158809343008817@1653293085651/Effects-of-dietary-CHO-on-a-molting-frequency-MF-b-total-molting-times-c_Q320.jpg)
Semi-synthetic transformations of ajugasterone C (1), poststerone (8)
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.frontiersin.org/files/MyHome%20Article%20Library/552088/552088_Thumb_400.jpg)
Frontiers Squalenoylated Nanoparticle Pro-Drugs of Adjuvant Antitumor 11α-Hydroxyecdysteroid 2,3-Acetonides Act as Cytoprotective Agents Against Doxorubicin and Paclitaxel
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.frontiersin.org/files/Articles/552088/fphar-11-552088-HTML/image_m/fphar-11-552088-g001.jpg)
Frontiers Squalenoylated Nanoparticle Pro-Drugs of Adjuvant Antitumor 11α-Hydroxyecdysteroid 2,3-Acetonides Act as Cytoprotective Agents Against Doxorubicin and Paclitaxel
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.researchgate.net/publication/365850039/figure/fig1/AS:11431281184166807@1693236106611/Principal-component-analysis-PCA-of-Diaphanosoma-celebensis-exposed-to-control-MP-Hg_Q320.jpg)
Identification on Daily Mortality Cause of Larvae in Treatment A1 (0 mg
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://i1.rgstatic.net/publication/312934201_Backstabbing_P-gp_Side-Chain_Cleaved_Ecdysteroid_23-Dioxolanes_Hyper-Sensitize_MDR_Cancer_Cells_to_Doxorubicin_without_Efflux_Inhibition/links/588f316faca272fa50e1972d/largepreview.png)
PDF) Backstabbing P-gp: Side-Chain Cleaved Ecdysteroid 2,3-Dioxolanes Hyper-Sensitize MDR Cancer Cells to Doxorubicin without Efflux Inhibition
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.researchgate.net/publication/371551682/figure/tbl2/AS:11431281167852321@1686757260419/Chemical-yields-of-substituted-N-benzoylthioureas-3a-l_Q320.jpg)
Tamás Gáti's research works Semmelweis University, Budapest (SOTE) and other places
Effect on proliferation (A) and viability (B) in the A431 cancer cell
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://ars.els-cdn.com/content/image/1-s2.0-S0065280622000169-f02-01-9780323952644.jpg)
Ecdysteroids as defensive chemicals - ScienceDirect
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.researchgate.net/profile/Hoang-Vu-11/publication/378147505/figure/tbl1/AS:11431281223398200@1707740277530/Cytotoxicity-of-ecdysteroids-1-5_Q320.jpg)
8 normal web of Trichonephila clavipes9 cocoon of H. bicolor attached
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.researchgate.net/publication/357572340/figure/fig2/AS:11431281089360033@1665540393807/Structures-of-furanoecdysteroids-3-6-isolated-from-A-bidentata_Q320.jpg)
Ecdysteroids: isolation, chemical transformations, and biological activity
![Semi-synthetic transformations of ajugasterone C (1), poststerone](https://www.mdpi.com/microbiolres/microbiolres-13-00071/article_deploy/html/images/microbiolres-13-00071-g001-550.jpg)
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