1 |
Brandes B, Hoenke S, Schultz C, Deigner HP, Csuk R. Converting bile acids into mitocans. Steroids 2023;189:109148. [PMID: 36414156 DOI: 10.1016/j.steroids.2022.109148] [Reference Citation Analysis]
|
2 |
Kaur KK, K. Allahbadia GN, Singh M. Mode of Actions of Bile Acids in Avoidance of Colorectal Cancer Development; and their Therapeutic Applications in Cancers - A Narrative Review. J Pharm Nutr Sci 2022;12:35-53. [DOI: 10.29169/1927-5951.2022.12.04] [Reference Citation Analysis]
|
3 |
Shansky Y, Bespyatykh J. Bile Acids: Physiological Activity and Perspectives of Using in Clinical and Laboratory Diagnostics. Molecules 2022;27. [PMID: 36431930 DOI: 10.3390/molecules27227830] [Reference Citation Analysis]
|
4 |
Rocha Aguiar G, Leda Gomes de Lemos T, Braz-Filho R, Marques da Fonseca A, Silva Marinho E, Vasconcelos Ribeiro PR, Marques Canuto K, Queiroz Monte FJ. Synthesis and in silico study of chenodeoxycholic acid and its analogues as an alternative inhibitor of spike glycoprotein of SARS-CoV-2. J Biomol Struct Dyn 2022;:1-15. [PMID: 36218138 DOI: 10.1080/07391102.2022.2133010] [Reference Citation Analysis]
|
5 |
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]
|
6 |
Jang JY, Im E, Choi YH, Kim ND. Mechanism of Bile Acid-Induced Programmed Cell Death and Drug Discovery against Cancer: A Review. IJMS 2022;23:7184. [DOI: 10.3390/ijms23137184] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
|
7 |
Huang J, Chen Y, Guo Y, Bao M, Hong K, Zhang Y, Hu W, Lei J, Liu Y, Xu X. Synthesis of dihydrofuran-3-one and 9,10-phenanthrenequinone hybrid molecules and biological evaluation against colon cancer cells as selective Akt kinase inhibitors. Mol Divers 2022. [PMID: 35751771 DOI: 10.1007/s11030-022-10458-w] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
|
8 |
Patel S, Bariya D, Mishra R, Mishra S. Bile Acid-based Receptors and Their Applications in Recognition. Steroids 2022. [DOI: 10.1016/j.steroids.2022.108981] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
|
9 |
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]
|
10 |
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]
|
11 |
Zhang RH, Guo HY, Deng H, Li J, Quan ZS. Piperazine skeleton in the structural modification of natural products: a review. J Enzyme Inhib Med Chem 2021;36:1165-97. [PMID: 34080510 DOI: 10.1080/14756366.2021.1931861] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
|
12 |
di Gregorio MC, Cautela J, Galantini L. Physiology and Physical Chemistry of Bile Acids. Int J Mol Sci 2021;22:1780. [PMID: 33579036 DOI: 10.3390/ijms22041780] [Cited by in Crossref: 21] [Cited by in F6Publishing: 24] [Article Influence: 10.5] [Reference Citation Analysis]
|
13 |
Bariya D, Anand V, Mishra S. Recent advances in the bile acid based conjugates/derivatives towards their gelation applications. Steroids 2021;165:108769. [PMID: 33207227 DOI: 10.1016/j.steroids.2020.108769] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
|
14 |
Mishra R, Mishra S. Updates in bile acid-bioactive molecule conjugates and their applications. Steroids 2020;159:108639. [DOI: 10.1016/j.steroids.2020.108639] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 5.7] [Reference Citation Analysis]
|
15 |
Mishra S, Patel S. Design, Synthesis, and Anti-bacterial Activity of Novel Deoxycholic Acid- Amino Alcohol Conjugates. MC 2020;16:385-91. [DOI: 10.2174/1573406415666190206231002] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
|
16 |
Huang R, Li Z, Li C, Wang G, Yan P, Peng L, Wang J, Zhu X, Hu P, Zhang J, Chang Z, Huang Z, Cheng L, Zhang J. Germ Cell-Specific Gene 1-Like Protein Regulated by Splicing Factor CUGBP Elav-Like Family Member 5 and Primary Bile Acid Biosynthesis are Prognostic in Glioblastoma Multiforme. Front Genet 2019;10:1380. [PMID: 32117422 DOI: 10.3389/fgene.2019.01380] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
|
17 |
Marchesi E, Chinaglia N, Capobianco ML, Marchetti P, Huang TE, Weng HC, Guh JH, Hsu LC, Perrone D, Navacchia ML. Dihydroartemisinin-Bile Acid Hybridization as an Effective Approach to Enhance Dihydroartemisinin Anticancer Activity. ChemMedChem 2019;14:779-87. [PMID: 30724466 DOI: 10.1002/cmdc.201800756] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 3.7] [Reference Citation Analysis]
|
18 |
Chanquia SN, Ripani E, Baldessari A, García Liñares G. Bile acids: Lipase-catalyzed synthesis of new hyodeoxycholic acid derivatives. Steroids 2018;140:45-51. [PMID: 30217787 DOI: 10.1016/j.steroids.2018.09.004] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
|
19 |
Baldessari A, García Liñares G. Lipase-Catalyzed Acetylation and Esterification of Bile Acids. Methods Mol Biol 2018;1835:337-50. [PMID: 30109661 DOI: 10.1007/978-1-4939-8672-9_18] [Reference Citation Analysis]
|
20 |
Al-masoudi NA, Sami A, Abdul-rida NA, Fortscher M. New cholic acid analogs: synthesis and 17β-hydroxydehydrogenase (17β-HSD) inhibition activity. Zeitschrift für Naturforschung B 2018;73:211-223. [DOI: 10.1515/znb-2018-0192] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
|
21 |
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]
|
22 |
Laskowska AK, Puszko AK, Sosnowski P, Różycki K, Kosson P, Matalińska J, Durlik M, Misicka A. Opioid Tripeptides Hybridized with trans-1-Cinnamylpiperazine as Proliferation Inhibitors of Pancreatic Cancer Cells in Two- and Three-Dimensional in vitro Models. ChemMedChem 2017;12:1637-44. [PMID: 28834399 DOI: 10.1002/cmdc.201700453] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
|
23 |
Popadyuk II, Markov AV, Morozova EA, Babich VO, Salomatina OV, Logashenko EB, Zenkova MA, Tolstikova TG, Salakhutdinov NF. Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position. Steroids 2017;127:1-12. [PMID: 28887170 DOI: 10.1016/j.steroids.2017.08.016] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
|
24 |
Kozanecka-Okupnik W, Jasiewicz B, Pospieszny T, Matuszak M, Mrówczyńska L. Haemolytic activity of formyl- and acetyl-derivatives of bile acids and their gramine salts. Steroids 2017;126:50-6. [PMID: 28711706 DOI: 10.1016/j.steroids.2017.07.003] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
|
25 |
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]
|
26 |
Cateni F, Zacchigna M, Procida G, Zilic J, Cordone A, Zanfardino A, Varcamonti M. Cholane and Lanostane Derivatives: Antimicrobial Evaluation. ChemistrySelect 2016;1:4856-4860. [DOI: 10.1002/slct.201600556] [Reference Citation Analysis]
|
27 |
Wen G, Qu X, Wang D, Chen X, Tian X, Gao F, Zhou X. Recent advances in design, synthesis and bioactivity of paclitaxel-mimics. Fitoterapia 2016;110:26-37. [DOI: 10.1016/j.fitote.2016.02.010] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 3.1] [Reference Citation Analysis]
|
28 |
Chen W, Chen X, Zhou S, Zhang H, Wang L, Xu J, Hu X, Yin W, Yan G, Zhang J. Design and synthesis of polyhydroxy steroids as selective inhibitors against AKR1B10 and molecular docking. Steroids 2016;110:1-8. [PMID: 26968129 DOI: 10.1016/j.steroids.2016.03.004] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
|
29 |
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]
|
30 |
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]
|
31 |
García Liñares G, Antonela Zígolo M, Simonetti L, Longhi SA, Baldessari A. Enzymatic synthesis of bile acid derivatives and biological evaluation against Trypanosoma cruzi. Bioorganic & Medicinal Chemistry 2015;23:4804-14. [DOI: 10.1016/j.bmc.2015.05.035] [Cited by in Crossref: 16] [Cited by in F6Publishing: 18] [Article Influence: 2.0] [Reference Citation Analysis]
|
32 |
Santos JAD, Polonini HC, Suzuki ÉY, Raposo NR, da Silva AD. Synthesis of conjugated bile acids/azastilbenes as potential antioxidant and photoprotective agents. Steroids 2015;98:114-21. [DOI: 10.1016/j.steroids.2015.03.009] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
|
33 |
Sanka Loganathachetti D, Muthuraman S. Biomedical potential of natural products derived through metagenomic approaches. RSC Adv 2015;5:101200-101213. [DOI: 10.1039/c5ra20116k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
|
34 |
Huang Y, Yao Q, Cui J, Gan C, Huang Q, Su B, Zhou A. Syntheses of lactam derivatives of chenodeoxycholic acid and in vitro antiproliferative activity. Chem Res Chin Univ 2014;30:605-13. [DOI: 10.1007/s40242-014-4003-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
|
35 |
Brossard D, Lechevrel M, El Kihel L, Quesnelle C, Khalid M, Moslemi S, Reimund JM. Synthesis and biological evaluation of bile carboxamide derivatives with pro-apoptotic effect on human colon adenocarcinoma cell lines. Eur J Med Chem 2014;86:279-90. [PMID: 25173827 DOI: 10.1016/j.ejmech.2014.07.080] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 2.0] [Reference Citation Analysis]
|
36 |
Bansal R, Acharya PC. Man-Made Cytotoxic Steroids: Exemplary Agents for Cancer Therapy. Chem Rev 2014;114:6986-7005. [DOI: 10.1021/cr4002935] [Cited by in Crossref: 72] [Cited by in F6Publishing: 77] [Article Influence: 8.0] [Reference Citation Analysis]
|
37 |
Májer F, Sharma R, Mullins C, Keogh L, Phipps S, Duggan S, Kelleher D, Keely S, Long A, Radics G, Wang J, Gilmer JF. New highly toxic bile acids derived from deoxycholic acid, chenodeoxycholic acid and lithocholic acid. Bioorganic & Medicinal Chemistry 2014;22:256-68. [DOI: 10.1016/j.bmc.2013.11.029] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 2.0] [Reference Citation Analysis]
|
38 |
Patiño Cano LP, Bartolotta SA, Casanova NA, Siless GE, Portmann E, Schejter L, Palermo JA, Carballo MA. Isolation of acetylated bile acids from the sponge Siphonochalina fortis and DNA damage evaluation by the comet assay. Steroids 2013;78:982-6. [PMID: 23791668 DOI: 10.1016/j.steroids.2013.05.020] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.6] [Reference Citation Analysis]
|
39 |
Huang Y, Cui J, Chen S, Gan C, Yao Q, Lin Q. Synthesis and antiproliferative activity of C-homo-lactam derivatives of 7-deoxycholic acid. Bioorganic & Medicinal Chemistry Letters 2013;23:2265-7. [DOI: 10.1016/j.bmcl.2012.08.064] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
|
40 |
Perrone D, Bortolini O, Fogagnolo M, Marchesi E, Mari L, Massarenti C, Navacchia ML, Sforza F, Varani K, Capobianco ML. Synthesis and in vitro cytotoxicity of deoxyadenosine–bile acid conjugates linked with 1,2,3-triazole. New J Chem 2013;37:3559. [DOI: 10.1039/c3nj00513e] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
|
41 |
Ren J, Wang Y, Wang J, Lin J, Wei K, Huang R. Synthesis and antitumor activity of N-sulfonyl-3,7-dioxo-5β-cholan-24-amides, ursodeoxycholic acid derivatives. Steroids 2013;78:53-8. [DOI: 10.1016/j.steroids.2012.09.009] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.7] [Reference Citation Analysis]
|
42 |
Barrasa JI, Olmo N, Lizarbe MA, Turnay J. Bile acids in the colon, from healthy to cytotoxic molecules. Toxicol In Vitro. 2013;27:964-977. [PMID: 23274766 DOI: 10.1016/j.tiv.2012.12.020] [Cited by in Crossref: 110] [Cited by in F6Publishing: 117] [Article Influence: 10.0] [Reference Citation Analysis]
|
43 |
Tu Z, Ma Y, Tian J, Li H, Akers W, Achilefu S, Gu Y. Estrogen receptor β potentiates the antiproliferative effect of raloxifene and affects the cell migration and invasion in HCT-116 colon cancer cells. J Cancer Res Clin Oncol. 2012;138:1091-1103. [PMID: 22398780 DOI: 10.1007/s00432-011-1145-3] [Cited by in Crossref: 19] [Cited by in F6Publishing: 23] [Article Influence: 1.7] [Reference Citation Analysis]
|
44 |
Huang Y, Cui J, Chen S, Gan C, Zhou A. Synthesis and antiproliferative activity of some steroidal lactams. Steroids 2011;76:1346-50. [DOI: 10.1016/j.steroids.2011.06.013] [Cited by in Crossref: 24] [Cited by in F6Publishing: 20] [Article Influence: 2.0] [Reference Citation Analysis]
|