| Year |
Citation |
Score |
| 2015 |
Fournier D, Ciobanu L, Poirier D. A Sequential Dual Cleavage of the Arylsulfamate Linker to Provide Both Sulfamate and Phenol Derivatives Chemistry Journal of Moldova. 10: 68-76. DOI: 10.19261/Cjm.2015.10(2).09 |
0.543 |
|
| 2007 |
Cantin L, Faucher FR, Couture JF, De Jésus-Tran KP, Legrand P, Ciobanu LC, Fréchette Y, Labrecque R, Singh SM, Labrie F, Breton R. Structural characterization of the human androgen receptor ligand-binding domain complexed with EM5744, a rationally designed steroidal ligand bearing a bulky chain directed toward helix 12 Journal of Biological Chemistry. 282: 30910-30919. PMID 17711855 DOI: 10.1074/Jbc.M705524200 |
0.308 |
|
| 2006 |
Ciobanu LC, Poirier D. Synthesis of libraries of 16beta-aminopropyl estradiol derivatives for targeting two key steroidogenic enzymes. Chemmedchem. 1: 1249-59. PMID 16986200 DOI: 10.1002/Cmdc.200600071 |
0.659 |
|
| 2004 |
Maltais R, Tremblay MR, Ciobanu LC, Poirier D. Steroids and combinatorial chemistry. Journal of Combinatorial Chemistry. 6: 443-56. PMID 15244402 DOI: 10.1021/Cc030118M |
0.637 |
|
| 2003 |
Ciobanu LC, Luu-The V, Martel C, Labrie F, Poirier D. Inhibition of estrone sulfate-induced uterine growth by potent nonestrogenic steroidal inhibitors of steroid sulfatase. Cancer Research. 63: 6442-6. PMID 14559834 |
0.609 |
|
| 2003 |
Ciobanu LC, Poirier D. Solid-phase parallel synthesis of 17alpha-substituted estradiol sulfamate and phenol libraries using the multidetachable sulfamate linker. Journal of Combinatorial Chemistry. 5: 429-40. PMID 12857111 DOI: 10.1021/Cc020115U |
0.641 |
|
| 2003 |
Ciobanu LC, Boivin RP, Luu-The V, Poirier D. 3Beta-sulfamate derivatives of C19 and C21 steroids bearing a t-butylbenzyl or a benzyl group: synthesis and evaluation as non-estrogenic and non-androgenic steroid sulfatase inhibitors. Journal of Enzyme Inhibition and Medicinal Chemistry. 18: 15-26. PMID 12751816 DOI: 10.1080/1475636031000069282 |
0.621 |
|
| 2002 |
Poirier D, Ciobanu LC, Bérubé M. A multidetachable sulfamate linker successfully used in a solid-phase strategy to generate libraries of sulfamate and phenol derivatives. Bioorganic & Medicinal Chemistry Letters. 12: 2833-8. PMID 12270157 DOI: 10.1016/S0960-894X(02)00637-6 |
0.61 |
|
| 2002 |
Ciobanu LC, Luu-The V, Poirier D. Nonsteroidal compounds designed to mimic potent steroid sulfatase inhibitors. The Journal of Steroid Biochemistry and Molecular Biology. 80: 339-53. PMID 11948019 DOI: 10.1016/S0960-0760(02)00024-9 |
0.624 |
|
| 2001 |
Ciobanu LC, Boivin RP, Luu-The V, Poirier D. Synthesis and steroid sulphatase inhibitory activity of C19- and C21-steroidal derivatives bearing a benzyl-inhibiting group. European Journal of Medicinal Chemistry. 36: 659-71. PMID 11600235 DOI: 10.1016/S0223-5234(01)01262-4 |
0.619 |
|
| 2000 |
Ciobanu LC, Maltais R, Poirier D. The sulfamate functional group as a new anchor for solid-phase organic synthesis Organic Letters. 2: 445-8. PMID 10814347 DOI: 10.1021/Ol990381P |
0.627 |
|
| 1999 |
Ciobanu LC, Boivin RP, Luu-The V, Labrie F, Poirier D. Potent inhibition of steroid sulfatase activity by 3-O-sulfamate 17alpha-benzyl(or 4'-tert-butylbenzyl)estra-1,3,5(10)-trienes: combination of two substituents at positions C3 and c17alpha of estradiol. Journal of Medicinal Chemistry. 42: 2280-6. PMID 10377235 DOI: 10.1021/Jm980677L |
0.621 |
|
| 1999 |
Poirier D, Ciobanu LC, Maltais R. Steroid sulfatase inhibitors Expert Opinion On Therapeutic Patents. 9: 1083-1099. DOI: 10.1517/13543776.9.8.1083 |
0.643 |
|
| Show low-probability matches. |