5 BROMO 1 [ETHYL(2' O ACETYL 3' O BENZYL 5',6'DIDEOXY 5' N 4 NITROBENZOYLAMINO BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
5 BROMO 1 [ETHYL(2' O ACETYL 5',6' DIDEOXY 3' O METHYL 5' N 4 NITROBENZOYLAMINO ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
5 BROMO 1 [ETHYL(2' O ACETYL 5',6' DIDEOXY 3' O METHYL 5' N 4 NITROBENZOYLAMINO BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
5 BROMO 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 5',6' DIDEOXY 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
5 BROMO 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 5',6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
6 [2 (DIMETHYLAMINO)ETHYLAMINO] 3 HYDROXY 7H INDENO[2,1 C]QUINOLIN 7 ONE;
6 AZA 1 [ETHYL (2' O ACETYL 3' O BENZYL 5',6' DIDEOXY 5' N 4 NITROBENZOYLAMINO BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 3' O BENZYL 5' N 3 CHLOROBENZOYLAMINO 5',6' DIDEOXY ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL]URACIL;
6 AZA 1 [ETHYL(2' O ACETYL 3' O BENZYL 5' N 3 CHLOROBENZOYLAMINO 5',6' DIDEOXY BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL]URACIL;
6 AZA 1 [ETHYL(2' O ACETYL 5' N 3 CHLOROBENZOYLAMINO 5',6' DIDEOXY 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5' N 3 CHLOROBENZOYLAMINO 5',6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5' N 4 NITROBENZOYLAMINO 5' 6' DIDEOXY 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL]URACIL;
6 AZA 1 [ETHYL(2' O ACETYL 5' N 4 NITROBENZOYLAMINO 5' 6' DIDEOXY 3' O METHYL ALPHA DEXTRO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5' N 4 NITROBENZOYLAMINO 5' 6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5' N 4 NITROBENZOYLAMINO 5' 6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL]URACIL;
6 AZA 1 [ETHYL(2' O ACETYL 5' N BENZYLAMINO 5',6' DIDEOXY 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5' N BENZYLAMINO 5',6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5' N CYCLOPROPYLAMINO 5',6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
6 AZA 1 [ETHYL(2' O ACETYL 5',6' DIDEOXY 5' N FURYLAMINO 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5',6' DIDEOXY 5' N FURYLAMINO 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(2' O ACETYL 5',6' DIDEOXY 5' N HEXADECYLAMINO 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 3' O BENZYL 5',6' DIDEOXY BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 3' O BENZYL 5',6' DIDEOXY BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
6 AZA 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 5',6' DIDEOXY 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 5',6' DIDEOXY 3' O METHYL ALPHA DEXTRO GLUCO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
6 AZA 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 5',6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]THYMINE;
6 AZA 1 [ETHYL(5' N ACETYLAMINO 2' O ACETYL 5',6' DIDEOXY 3' O METHYL BETA LEVO IDO HEPTO 1',4' FURANURONAT 1' YL)]URACIL;
DNA TOPOISOMERASE (ATP HYDROLYSING);
ISOMERASE INHIBITOR;
NUCLEOSIDE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
ARTICLE;
BIOLOGICAL ACTIVITY;
BRUGIA MALAYI;
CATALYSIS;
CONTROLLED STUDY;
DNA SYNTHESIS;
DRUG EFFECT;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
FILARIA;
HYDROLYSIS;
NONHUMAN;
POLYMERIZATION;
SILYLATION;
ACETATES;
AMMONIA;
CATALYSIS;
DNA TOPOISOMERASES, TYPE II;
HYDROLYSIS;
METHANOL;
NUCLEOSIDES;
PYRIMIDINES;
TIN COMPOUNDS;
Nucleoside Analogs: Chemistry, Biology and Medical Applications, Nato Advanced Studies Series: Series A, Life Sciences. Walker, R.T., Clercque, D.E., Eckstein, F., Eds.; Plenum Press: New York, 1979; Vol. 26.
Site specific incorporation of 6-azauridine into the genomic HDV ribozyme active site
Oyelere, A.K.; Strobel, S.A. Site specific incorporation of 6-azauridine into the genomic HDV ribozyme active site. Nucleosides Nucleotides Nucleic Acids 2001, 20, 1851-1858.
Synthetic nucleosides and nucleotides. XXI. On the synthesis and biological evaluations of 2′-deoxy-alpha-D-ribofuranosyl nucleosides and nucleotides
Yamaguchi, T.; Saneyoshi, M. Synthetic nucleosides and nucleotides. XXI. On the synthesis and biological evaluations of 2′-deoxy-alpha-D- ribofuranosyl nucleosides and nucleotides. Chem. Pharm. Bull. 1984, 32, 1441-1450.
Conformational parameters of the carbohydrate moieties of α-arabinonucleosides
Ekiel, I.; Darzynkiewics, E.; Shugar, D. Conformational parameters of the carbohydrate moieties of α-arabinonucleosides. Carbohydr. Res. 1981, 92, 21-36.
Enzymatic incorporation of a new base pair in to DNA and RNA extends the genetic alphabet
Piccirilli, J.A.; Krauch, T.; Moroney, S.E.; Benner, S.A. Enzymatic incorporation of a new base pair in to DNA and RNA extends the genetic alphabet. Nature 1990, 343, 33-35.
A thiamidine triphosphate shape analog lacking Watson-Crick pairing ability isreplicated with high sequence selectivity
Moran, S.A.; Ren, R.X.F.; Kool, E.T. A thiamidine triphosphate shape analog lacking Watson-Crick pairing ability isreplicated with high sequence selectivity. Proc. Natl. Acad. Sci. U. S. A. 1997, 94, 10506-10508.
Varied molecular interactions at the active sites of several DNA polymers: Nonpolar nucleoside isosters as probes
Morales, J.C.; Kool, E.T. Varied molecular interactions at the active sites of several DNA polymers: nonpolar nucleoside isosters as probes. J. Am. Chem. Soc. 2000, 122, 1001-1004.
Efforts towards expansion of genetic alphabet: Information storage and replication with unnatural hydrophobic base pairs
Ogawa, A.K.; Wu, Y.; McMinn, D.L.; Liu, J.; Schultz, P.G.; Romesberg, F.E. Efforts towards expansion of genetic alphabet: information storage and replication with unnatural hydrophobic base pairs. J. Am. Chem. Soc. 2000, 122, 3274-3276.
Solution structure of a nonpolar, non-hydrogen bonded base pair surrogat in DNA
Guckian, K.M.; Krugh, T.R.; Kool, E.T. Solution structure of a nonpolar, non-hydrogen bonded base pair surrogat in DNA. J. Am. Chem. Soc. 2000, 122, 6841-6843.
General synthesis of pyrimidine-C-5-nucleosides related to pseudouridine. Synthsis of 5-(β-D-ribofuranosyl) isocytosine (pseudoisocytidine), 5-(β-D-ribofuranosyl)-2-thio uracil (2-thiopseudouridine) and 5-(β-D-ribofuranosyl) uracil (pseudouridine)
Chu, C.K.; Wempen, I.; Watanabe, K.A.; Fox, J.J. General synthesis of pyrimidine-C-5-nucleosides related to pseudouridine. Synthsis of 5-(β-D-ribofuranosyl) isocytosine (pseudoisocytidine), 5-(β-D- ribofuranosyl)-2-thio uracil (2-thiopseudouridine) and 5-(β-D- ribofuranosyl) uracil (pseudouridine). J. Org. Chem. 1976, 41, 2793-2801.
Stereocontrolled synthesis of heterocyclic-C-nucleosides, protecting group effect and molecular modelling studies
Guianvarc'h, D.; Fourrey, J.L.; Dau, M.E.T.H.; Guerineau, V. Stereocontrolled synthesis of heterocyclic-C-nucleosides, protecting group effect and molecular modelling studies. J. Org. Chem. 2002, 67, 3724-3729.
Fluoro nucleosides, isothiocyanato-C-nucleoside and thiouridine di-C-nucleosides via cyclic sulpahates
Fuentes, J.; Angulo, M.; Pradera, M.A. Fluoro nucleosides, isothiocyanato-C-nucleoside and thiouridine di-C-nucleosides via cyclic sulpahates. J. Org. Chem 2002, 67, 2577-2583.
Conformational parameters of the carbohydrate moieties of α-arabino nucleosides
Ekeil, I.; Darzynkiewics, E.; Shugar, D. Conformational parameters of the carbohydrate moieties of α-arabino nucleosides. Carbohydr. Res. 1981, 92, 21-36.
DNA topoisomerases as targets for the anticancer drug TAS-103: Primary cellular target and DNA cleavage enhancement
Byl, J.A.W.; Fortune, J.M.; Burden, D.A.; Nitiss, J.L.; Utsugi, T.; Yamada, Y.; Osheroff, N. DNA topoisomerases as targets for the anticancer drug TAS-103: primary cellular target and DNA cleavage enhancement. Biochemistry 1999, 38 (47), 15573-15579.
(1999)Biochemistry, vol.38, Issue.47, pp. 15573-15579