AAAAAA

   
Results: 1-12 |
Results: 12
Synthesis, DNA cleavage, and cytotoxicity of a series of bis(propargylic) sulfone crown ethers
Authors: McPhee, MM Kerwin, SM
Citation: Mm. Mcphee et Sm. Kerwin, Synthesis, DNA cleavage, and cytotoxicity of a series of bis(propargylic) sulfone crown ethers, BIO MED CH, 9(11), 2001, pp. 2809-2818
N-propargyl-2-alkynylbenzothiazolium aza-enediynes: Role of the 2-alkynylbenzothiazolium functionality in DNA cleavage
Authors: Kumar, D David, WM Kerwin, SM
Citation: D. Kumar et al., N-propargyl-2-alkynylbenzothiazolium aza-enediynes: Role of the 2-alkynylbenzothiazolium functionality in DNA cleavage, BIOORG MED, 11(22), 2001, pp. 2971-2974
G-quadruplex DNA binding by a series of carbocyanine dyes
Authors: Kerwin, SM Sun, D Kern, JT Rangan, A Thomas, PW
Citation: Sm. Kerwin et al., G-quadruplex DNA binding by a series of carbocyanine dyes, BIOORG MED, 11(18), 2001, pp. 2411-2414
Evaluation of complexation of metal-mediated DNA-binding drugs to oligonucleotides via electrospray ionization mass spectrometry
Authors: Reyzer, ML Brodbelt, JS Kerwin, SM Kumar, D
Citation: Ml. Reyzer et al., Evaluation of complexation of metal-mediated DNA-binding drugs to oligonucleotides via electrospray ionization mass spectrometry, NUCL ACID R, 29(21), 2001, pp. NIL_9-NIL_20
Inhibition of human telomerase by 7-deaza-2 '-deoxyguanosine nucleoside triphosphate analogs: Potent inhibition by 6-thio-7-deaza-2 '-deoxyguanosine 5 '-triphosphate
Authors: Fletcher, TM Cathers, BE Ravikumar, KS Mamiya, BM Kerwin, SM
Citation: Tm. Fletcher et al., Inhibition of human telomerase by 7-deaza-2 '-deoxyguanosine nucleoside triphosphate analogs: Potent inhibition by 6-thio-7-deaza-2 '-deoxyguanosine 5 '-triphosphate, BIOORG CHEM, 29(1), 2001, pp. 36-55
Synthesis of a phosphoramidate pro-drug of 6-thio-7-deaza-2 '-deoxyguanosine (TDG): a regioselective phosphorylation
Authors: Kumar, D Kanz, B Mamiya, BM Kern, JT Kerwin, SM
Citation: D. Kumar et al., Synthesis of a phosphoramidate pro-drug of 6-thio-7-deaza-2 '-deoxyguanosine (TDG): a regioselective phosphorylation, TETRAHEDR L, 42(4), 2001, pp. 565-567
G-quadruplex DNA as a target for drug design
Authors: Kerwin, SM
Citation: Sm. Kerwin, G-quadruplex DNA as a target for drug design, CUR PHARM D, 6(4), 2000, pp. 441-471
Synthesis of a heterocyclic aza-enediyne and its DNA-cleavage properties
Authors: David, WM Kumar, D Kerwin, SM
Citation: Wm. David et al., Synthesis of a heterocyclic aza-enediyne and its DNA-cleavage properties, BIOORG MED, 10(22), 2000, pp. 2509-2512
G-quadruplexes as targets for drug design
Authors: Hurley, LH Wheelhouse, RT Sun, D Kerwin, SM Salazar, M Fedoroff, OY Han, FX Han, HY Izbicka, E Von Hoff, DD
Citation: Lh. Hurley et al., G-quadruplexes as targets for drug design, PHARM THERA, 85(3), 2000, pp. 141-158
Efficient, Mg2+-dependent photochemical DNA cleavage by the antitumor quinobenzoxazine (S)-A-62176
Authors: Yu, HT Kwok, Y Hurley, LH Kerwin, SM
Citation: Ht. Yu et al., Efficient, Mg2+-dependent photochemical DNA cleavage by the antitumor quinobenzoxazine (S)-A-62176, BIOCHEM, 39(33), 2000, pp. 10236-10246
The conversion of mixed N,O-diacylated 2-aminophenols to 2-substituted benzoxazoles
Authors: DeLuca, MR Taraporewala, IB Kerwin, SM
Citation: Mr. Deluca et al., The conversion of mixed N,O-diacylated 2-aminophenols to 2-substituted benzoxazoles, HETEROCYCLE, 51(5), 1999, pp. 979-982
The novel bis(benzoxazole) cytotoxic natural product UK-1 is a magnesium ion-dependent DNA binding agent and inhibitor of human topoisomerase II
Authors: Reynolds, MB DeLuca, MR Kerwin, SM
Citation: Mb. Reynolds et al., The novel bis(benzoxazole) cytotoxic natural product UK-1 is a magnesium ion-dependent DNA binding agent and inhibitor of human topoisomerase II, BIOORG CHEM, 27(4), 1999, pp. 326-337
Risultati: 1-12 |