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1.
Carbohydr Res ; 399: 2-7, 2014 Nov 18.
Article in English | MEDLINE | ID: mdl-25369262

ABSTRACT

Synthesis of sugar based triazolyl azido-alcohols was accomplished via one pot click reaction of glycosyl alkynes with epichlorohydrin in aqueous medium. All the developed triazolyl azido-alcohols were further utilized for the synthesis of bis-triazolyl ethisterone glycoconjugates using CuAAC reaction. The developed triazole-linked ethisterone glycoconjugates would be crucial in androgen receptor pharmacology and chemical biology.


Subject(s)
Ethisterone/chemistry , Ethisterone/chemical synthesis , Glycoconjugates/chemistry , Glycoconjugates/chemical synthesis , Triazoles/chemistry , Molecular Conformation
2.
Steroids ; 80: 71-9, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24316164

ABSTRACT

Numerous deoxy-azido sugars 3 were prepared by the reaction of tosyl/bromo sugars with NaN3 in dry DMF under heating condition. The 1,3-dipolar cycloaddition of deoxy-azido sugars 3 with ethisterone 4 to afford regioselective triazole-linked ethisterone glycoconjugates 5 was investigated in the presence of CuI and DIPEA in dichloromethane or CuSO4·5H2O and sodium ascorbate in aqueous medium. All the developed compounds were characterized by spectroscopic analysis (IR, (1)H &(13)C NMR, and MS spectra). Structure of triazolyl ethisterone glycoconjugate 5a has been further confirmed by its Single Crystal X-ray analysis.


Subject(s)
Click Chemistry , Ethisterone/analogs & derivatives , Glycoconjugates/chemical synthesis , Triazoles/chemical synthesis , Crystallography, X-Ray , Cyclization , Ethisterone/chemical synthesis , Ethisterone/chemistry , Glycoconjugates/chemistry , Models, Molecular , Molecular Conformation , Triazoles/chemistry
3.
ACS Chem Biol ; 7(10): 1693-701, 2012 Oct 19.
Article in English | MEDLINE | ID: mdl-22871957

ABSTRACT

Sustained treatment of prostate cancer with androgen receptor (AR) antagonists can evoke drug resistance, leading to castrate-resistant disease. Elevated activity of the AR is often associated with this highly aggressive disease state. Therefore, new therapeutic regimens that target and modulate AR activity could prove beneficial. We previously introduced a versatile chemical platform to generate competitive and non-competitive multivalent peptoid oligomer conjugates that modulate AR activity. In particular, we identified a linear and a cyclic divalent ethisterone conjugate that exhibit potent anti-proliferative properties in LNCaP-abl cells, a model of castrate-resistant prostate cancer. Here, we characterize the mechanism of action of these compounds utilizing confocal microscopy, time-resolved fluorescence resonance energy transfer, chromatin immunoprecipitation, flow cytometry, and microarray analysis. The linear conjugate competitively blocks AR action by inhibiting DNA binding. In addition, the linear conjugate does not promote AR nuclear localization or co-activator binding. In contrast, the cyclic conjugate promotes AR nuclear localization and induces cell-cycle arrest, despite its inability to compete against endogenous ligand for binding to AR in vitro. Genome-wide expression analysis reveals that gene transcripts are differentially affected by treatment with the linear or cyclic conjugate. Although the divalent ethisterone conjugates share extensive chemical similarities, we illustrate that they can antagonize the AR via distinct mechanisms of action, establishing new therapeutic strategies for potential applications in AR pharmacology.


Subject(s)
Androgen Receptor Antagonists/pharmacology , Ethisterone/analogs & derivatives , Ethisterone/pharmacology , Prostatic Neoplasms, Castration-Resistant/metabolism , Cell Cycle/drug effects , Cell Line, Tumor , Cell Proliferation/drug effects , Ethisterone/chemical synthesis , Gene Expression/drug effects , HEK293 Cells , Humans , Male , Microarray Analysis
4.
J Inorg Biochem ; 105(4): 525-31, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21334280

ABSTRACT

The novel steroidal carrier ligand 17-α-[4'-ethynyl-dimethylbenzylamine]-17-ß-testosterone (ET-dmba 1) and the steroid--C,N-chelate platinum(II) derivatives [Pt(ET-dmba)Cl(L)] (L = DMSO (2) and PTA (3; PTA =1,3,5-triaza-7-phosphaadamantane)) have been prepared. Values of IC(50) were calculated for the new platinum complexes 2 and 3 against a panel of human tumor cell lines representative of ovarian (A2780 and A2780cisR) and breast cancers (T47D). At 48h incubation time complexes 2 and 3 show very low resistance factors (RF of <2) against an A2780 cell line which has acquired resistant to cisplatin and were more active than cisplatin (about 4-fold for 3) in T47D (AR+, AR=androgen receptor). Compound 1 retains a moderate degree of relative binding affinity (RBA=0.94%) for androgen receptors. The cytotoxicity of the non steroidal platinum analogues [Pt(dmba)Cl(L)] (dmba=dimethylbenzylamine; L=DMSO (4) and PTA (5)) has also been studied for comparison purposes. Theoretical calculations at the BP86/def2-TZVP level of theory on complex 3 have been undertaken.


Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Ethisterone/analogs & derivatives , Antineoplastic Agents/chemical synthesis , Cell Line, Tumor , Ethisterone/chemical synthesis , Ethisterone/chemistry , Ethisterone/pharmacology , Humans , Models, Molecular , Organoplatinum Compounds/chemical synthesis , Organoplatinum Compounds/chemistry , Organoplatinum Compounds/pharmacology
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