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10-(2-hydroxyethyl)phenazine
Known as:
10-(2-hydroxyethyl)phenazinium
, 10-HEPH
, N-(2-hydroxyethyl)phenazinium
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
Phenazines
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Direct site-specific cleavage of double-stranded DNA by conjugates of bleomycin A5 with triplex-forming oligonucleotide
A. Pavlova
,
P. Vorobyev
,
V. Zarytova
Russian journal of bioorganic chemistry
2009
Corpus ID: 21316513
Monofunctional conjugates of 15-mer triplex-forming oligonucleotide (TFO) with covalently attached bleomycin A5 residue at the 5…
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1998
1998
[Interaction of derivatives of short oligonucleotides with nucleic acids. VIII. Characteristics of target DNA modification by alkylating oligonucleotide derivatives in tandem complexes].
D. Pyshnyi
,
S. Lokhov
,
E. Ivanova
,
V. Zarytova
Bioorganicheskaia khimiia
1998
Corpus ID: 22610888
The influence of effectors [octanucleotides and their 3',5'-di-N-(2-hydroxyethyl)phenazinium derivatives] on the modification of…
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1997
1997
[Artificial ribonucleases I. Targeted RNA cleavage by 5'-peptidyloligodeoxyribonucleotides containing arginine and leucine residues].
D. Pyshnyi
,
M. Repkova
,
S. Lokhov
,
E. Ivanova
,
Ven'iaminova Ag
,
V. Zarytova
Bioorganicheskaia khimiia
1997
Corpus ID: 26773395
The interaction of DNA and RNA with oligodeoxyribonucleotides and their 3'-terminal N-(2-hydroxyethyl)phenazinium derivatives…
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1993
1993
Oligonucleotide derivatives bearing reactive and stabilizing groups attached to C5 of deoxyuridine.
A. Levina
,
D. R. Tabatadse
,
+4 authors
V. Zarytova
Bioconjugate chemistry
1993
Corpus ID: 41785524
Oligonucleotides bearing an aliphatic amino group at the C5-position of deoxyuridine (ULNH2TCCCA, TULNH2CCCA, ULNH2CCACTT, where…
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1992
1992
Synthesis and high stability of complementary complexes of N-(2-hydroxyethyl)phenazinium derivatives of oligonucleotides.
S. G. Lokhov
,
M. Podyminogin
,
+4 authors
V. Zarytova
Bioconjugate chemistry
1992
Corpus ID: 44613086
Two simple methods for the synthesis of oligonucleotides bearing a N-(2-hydroxyethyl)phenazinium (Phn) residue at the 5'- and/or…
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1992
1992
[Study of the spatial structure of the duplex (Phn-NH(CH2)NH)pd(CCAAACA).pd(TGTTTGGC) with covalently bound 10-(2-hydroxyethyl)phenazine by in aqueous solution by 2D-(1)H-NMR and by limited molecular…
E. Bichenkova
,
L. A. Gorenshteĭn
,
+5 authors
A. Lebedev
Bioorganicheskaia khimiia
1992
Corpus ID: 2509477
Detailed investigation of the spatial structure of duplex (Phn-NH(CH2)2NH) x pd(CCAAACA).pd(TGTTTGGC) having a covalently linked…
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1990
1990
[Effective selective modification of a single-stranded fragment of DNA with alkylating derivatives of short oligodeoxyribonucleotides in the presence of reaction effectors N-(2-hydroxyethyl)phenazine…
V. Zarytova
,
I. V. Kutiavin
,
S. Mamaev
,
M. Podyminogin
Bioorganicheskaia khimiia
1990
Corpus ID: 21778529
Tri-, tetra-, penta- and hexanucleotides bearing a reactive 4-(N-methylamino-N-2-chloroethyl)benzylamide group can effectively…
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1990
1990
The influence of oligonucleotide‐effector on the selectivity of sequence specific modification of 16 S rRNA
M. Zenkova
,
O. Fedorova
,
A. Levina
,
S. Mamaev
,
G. Karpova
FEBS Letters
1990
Corpus ID: 44713046
1990
1990
[Reactive oligonucleotide derivatives containing methylphosphonate groups. V. Increased effectiveness of complementary addressed modification of target DNA by alkylating derivatives of…
Amirkhanov Nv
,
Zarytova Vf
1990
Corpus ID: 88939209
1988
1988
N‐(2‐Hydroxyethyl)phenazinium derivatives of oligonucleotides as effectors of the sequence‐specific modification of nucleic acids with reactive oligonucleotide derivatives
I. Kutyavin
,
M. Podyminogin
,
+5 authors
V. Zarytova
FEBS Letters
1988
Corpus ID: 1169406
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