Nucleosides, Nucleotides and Nucleic Acids, volume 20, issue 9, pages 1691-1704
SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES
1
a Cancer Research Campaign Centre for Cancer Therapeutics at the Institute of Cancer Research , 15 Cotswold Road, Sutton, Surrey, SM2 5NG, UK
|
2
b Cancer Research Campaign Centre for Cancer Therapeutics at the Institute of Cancer Research , 15 Cotswold Road, Sutton, Surrey, SM2 5NG, UK
|
Publication type: Journal Article
Publication date: 2001-09-30
Quartile SCImago
Q3
Quartile WOS
Q4
SJR: 0.262
CiteScore: 2.6
Impact factor: 1.1
ISSN: 15257770, 15322335
Biochemistry
General Medicine
Genetics
Molecular Medicine
Abstract
Derivatives of 2'-deoxyuridine in which the 5'-OH group is replaced by a 2,3,6-trifluoro-5-hydroxy-4-nitrophenoxy or a 4-carboxy-2,3,6-trifluoro-5-hydroxyphenoxy group have been prepared for evaluation as possible dUTP analogues. They showed a weak ability to displace radiolabelled dUTP from a dUTP-binding antiserum. The corresponding compounds lacking the three fluorine substituents were prepared for comparison.
Top-30
Journals
|
1
2
|
|
|
Journal of Medicinal Chemistry
2 publications, 22.22%
|
|
|
Nucleosides, Nucleotides and Nucleic Acids
2 publications, 22.22%
|
|
|
ChemMedChem
1 publication, 11.11%
|
|
|
ChemInform
1 publication, 11.11%
|
|
|
Chemical Reviews
1 publication, 11.11%
|
|
|
Russian Chemical Reviews
1 publication, 11.11%
|
|
|
1
2
|
Publishers
|
1
2
3
|
|
|
American Chemical Society (ACS)
3 publications, 33.33%
|
|
|
Wiley
2 publications, 22.22%
|
|
|
Taylor & Francis
2 publications, 22.22%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 11.11%
|
|
|
1
2
3
|
- We do not take into account publications without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Marriott J. H. et al. SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES // Nucleosides, Nucleotides and Nucleic Acids. 2001. Vol. 20. No. 9. pp. 1691-1704.
GOST all authors (up to 50)
Copy
Marriott J. H., AHERNE G. W., Hardcastle A., JARMAN M. SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES // Nucleosides, Nucleotides and Nucleic Acids. 2001. Vol. 20. No. 9. pp. 1691-1704.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1081/ncn-100105905
UR - https://doi.org/10.1081/ncn-100105905
TI - SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES
T2 - Nucleosides, Nucleotides and Nucleic Acids
AU - Marriott, Jonathan H
AU - AHERNE, G. WYNNE
AU - Hardcastle, Anthea
AU - JARMAN, MICHAEL
PY - 2001
DA - 2001/09/30
PB - Taylor & Francis
SP - 1691-1704
IS - 9
VL - 20
SN - 1525-7770
SN - 1532-2335
ER -
Cite this
BibTex
Copy
@article{2001_Marriott,
author = {Jonathan H Marriott and G. WYNNE AHERNE and Anthea Hardcastle and MICHAEL JARMAN},
title = {SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES},
journal = {Nucleosides, Nucleotides and Nucleic Acids},
year = {2001},
volume = {20},
publisher = {Taylor & Francis},
month = {sep},
url = {https://doi.org/10.1081/ncn-100105905},
number = {9},
pages = {1691--1704},
doi = {10.1081/ncn-100105905}
}
Cite this
MLA
Copy
Marriott, Jonathan H., et al. “SYNTHESIS OF CERTAIN 2′-DEOXYURIDINE DERIVATIVES CONTAINING SUBSTITUTED PHENOXY GROUPS ATTACHED TO C-5′; EVALUATION AS POTENTIAL dUTP ANALOGUES.” Nucleosides, Nucleotides and Nucleic Acids, vol. 20, no. 9, Sep. 2001, pp. 1691-1704. https://doi.org/10.1081/ncn-100105905.