| 1 |
Zhai Z, Huang Y, Zhang Y, Zhao L, Li W. Clinical Research Progress of Small Molecule Compounds Targeting Nrf2 for Treating Inflammation-Related Diseases. Antioxidants (Basel) 2022;11:1564. [PMID: 36009283 DOI: 10.3390/antiox11081564] [Reference Citation Analysis]
|
| 2 |
Patel S, Challagundla N, Rajput RA, Mishra S. Design, synthesis, characterization and anticancer activity evaluation of deoxycholic acid-chalcone conjugates. Bioorg Chem 2022;127:106036. [PMID: 35878450 DOI: 10.1016/j.bioorg.2022.106036] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
|
| 3 |
Ilić M, Pastor K, Marković J, Grbović L, Jovanović-Šanta S, Mitrović I, Trivunović Z, Ačanski M. Feasibility study of separation and purification of bile acid derivatives by HPLC on C18 and F5 columns. Steroids 2022;:109074. [PMID: 35787835 DOI: 10.1016/j.steroids.2022.109074] [Reference Citation Analysis]
|
| 4 |
Yang R, Du C, Cao T, Wang G, Jiang X, Gao J, Lin T, Sun C, Ding R, Tian W, Chen H. Synthesis and Anti-Hepatoma Activities of U12 Derivatives Arresting G0/G1 Phase and Inducing Apoptosis by PI3K/AKT/mTOR Pathway. Pharmaceuticals 2022;15:107. [DOI: 10.3390/ph15010107] [Reference Citation Analysis]
|
| 5 |
Wang Z, Qiang X, Peng Y, Wang Y, Zhao Q, He D. Design and synthesis of bile acid derivatives and their activity against colon cancer. RSC Med Chem 2022. [DOI: 10.1039/d2md00220e] [Reference Citation Analysis]
|
| 6 |
Ruiz-Gaspà S, Guañabens N, Jurado S, Dubreuil M, Combalia A, Peris P, Monegal A, Parés A. Bile acids and bilirubin effects on osteoblastic gene profile. Implications in the pathogenesis of osteoporosis in liver diseases. Gene 2020;725:144167. [PMID: 31639434 DOI: 10.1016/j.gene.2019.144167] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 1.8] [Reference Citation Analysis]
|
| 7 |
Ruiz-gaspà S, Guañabens N, González SJ, Dubreuil M, Combalia A, Peris P, Monegal A, Parés A. Bile acids and bilirubin effects on osteoblastic gene profile. Implications in the pathogenesis of osteoporosis in liver diseases.. [DOI: 10.1101/705871] [Reference Citation Analysis]
|
| 8 |
Sassi K, Nury T, Zarrouk A, Sghaier R, Khalafi-Nezhad A, Vejux A, Samadi M, Aissa-Fennira FB, Lizard G. Induction of a non-apoptotic mode of cell death associated with autophagic characteristics with steroidal maleic anhydrides and 7β-hydroxycholesterol on glioma cells. J Steroid Biochem Mol Biol 2019;191:105371. [PMID: 31034873 DOI: 10.1016/j.jsbmb.2019.04.020] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
|
| 9 |
Luo G, Qian Z, Qiu R, You Q, Xiang H. Lipid reducing activity of novel cholic acid (CA) analogs: Design, synthesis and preliminary mechanism study. Bioorg Chem 2018;80:396-407. [PMID: 29986186 DOI: 10.1016/j.bioorg.2018.07.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
|
| 10 |
Salomatina OV, Popadyuk II, Zakharenko AL, Zakharova OD, Fadeev DS, Komarova NI, Reynisson J, Arabshahi HJ, Chand R, Volcho KP, Salakhutdinov NF, Lavrik OI. Novel Semisynthetic Derivatives of Bile Acids as Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Molecules 2018;23:E679. [PMID: 29562592 DOI: 10.3390/molecules23030679] [Cited by in Crossref: 20] [Cited by in F6Publishing: 21] [Article Influence: 4.0] [Reference Citation Analysis]
|
| 11 |
Agarwal DS, Singh RP, Lohitesh K, Jha PN, Chowdhury R, Sakhuja R. Synthesis and evaluation of bile acid amides of $$\alpha $$ α -cyanostilbenes as anticancer agents. Mol Divers 2018;22:305-21. [DOI: 10.1007/s11030-017-9797-9] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
|
| 12 |
Popadyuk II, Markov AV, Babich VO, Salomatina OV, Logashenko EB, Zenkova MA, Salakhutdinov NF. Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: Synthesis and evaluation of anti-proliferative activity. Bioorg Med Chem Lett 2017;27:3755-9. [PMID: 28688958 DOI: 10.1016/j.bmcl.2017.06.072] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
|
| 13 |
Bjedov S, Jakimov D, Pilipović A, Poša M, Sakač M. Antitumor activity of newly synthesized oxo and ethylidene derivatives of bile acids and their amides and oxazolines. Steroids 2017;120:19-25. [DOI: 10.1016/j.steroids.2017.01.008] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
|
| 14 |
Mao S, Chen H, Yu L, Lv F, Xing Y, Liu T, Xie J, Tang J, Yi Z, Yang F. Novel 3,4- seco bile acid diamides as selective anticancer proliferation and migration agents. European Journal of Medicinal Chemistry 2016;122:574-83. [DOI: 10.1016/j.ejmech.2016.04.055] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
|
| 15 |
Singh AK, Bhardwaj JK, Olival A, Kumar Y, Podder A, Maheshwari A, Agrawal R, Latha N, Singh BK, Tomás H, Rodrigues J, Kishan R, Rupini B, Rathi B. Design, synthesis and biological evaluation of Arylpiperazine-based novel Phthalimides: Active inducers of testicular germ cell apoptosis. J Chem Sci 2016;128:1245-63. [DOI: 10.1007/s12039-016-1122-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
|
| 16 |
Faustino C, Serafim C, Rijo P, Reis CP. Bile acids and bile acid derivatives: use in drug delivery systems and as therapeutic agents. Expert Opinion on Drug Delivery 2016;13:1133-48. [DOI: 10.1080/17425247.2016.1178233] [Cited by in Crossref: 72] [Cited by in F6Publishing: 63] [Article Influence: 10.3] [Reference Citation Analysis]
|
| 17 |
Agarwal DS, Anantaraju HS, Sriram D, Yogeeswari P, Nanjegowda SH, Mallu P, Sakhuja R. Synthesis, characterization and biological evaluation of bile acid-aromatic/heteroaromatic amides linked via amino acids as anti-cancer agents. Steroids 2016;107:87-97. [PMID: 26748355 DOI: 10.1016/j.steroids.2015.12.022] [Cited by in Crossref: 23] [Cited by in F6Publishing: 19] [Article Influence: 2.9] [Reference Citation Analysis]
|
| 18 |
Hwang SR, Kim IJ, Park JW. Formulations of deoxycholic for therapy: a patent review (2011 – 2014). Expert Opinion on Therapeutic Patents 2015;25:1423-40. [DOI: 10.1517/13543776.2016.1102888] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
|
