Synthesis, NoSpherA2 refinement, and noncovalent bonding of abiraterone bromide monohydrate
Author:
Funder
Russian Science Foundation
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Condensed Matter Physics
Link
https://link.springer.com/content/pdf/10.1007/s11224-023-02210-3.pdf
Reference45 articles.
1. Korlyukov AA, Vologzhanina AV, Trzybinski D, Malinska M, Wozniak K (2020) Charge density analysis of abiraterone acetate. Acta Cryst Sect B 76:1018–1026. https://doi.org/10.1107/S2052520620013244
2. Chennuru R, Devarapalli R, Rengaraj P, Srinivas PL, Dey S, Malla Reddy C (2020) Improving solubility of poorly soluble abiraterone acetate by cocrystal design aided by in silico screening. Cryst Growth Des 20:5018–5030. https://doi.org/10.1021/acs.cgd.0c00153
3. Yang Z, Yang Y, Xia M, Dai W, Zhu B, Mei X (2022) Improving the dissolution behaviors and bioavailability of abiraterone acetate via multicomponent crystal forms. Int J Pharm 614:121460. https://doi.org/10.1016/j.ijpharm.2022.121460
4. Sakai Y, Fukami T, Nagaoka M, Hirosawa K, Ichida H, Sato R, Suzuki K, Nakano M, Nakajima M (2021) Arylacetamide deacetylase as a determinant of the hydrolysis and activation of abiraterone acetate in mice and humans. Life Sci 284:119896. https://doi.org/10.1016/j.lfs.2021.119896
5. Silveira RG, Cunha BN, Tenório JC, de Aguiar DVA, da Cruz SP, Vaz BG, Ellena J, Batista AA, Martins FT (2019) A simple alternative to prodrug: the hydrochloride salt monohydrate of the prostate anticancer drug abiraterone. J Mol Struct 1190:165–170. https://doi.org/10.1016/j.molstruc.2019.04.068
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