Page last updated: 2024-10-15

n(7)-hydroxyethylguanine

Cross-References

ID SourceID
PubMed CID135484986
CHEMBL ID123765
SCHEMBL ID48362
MeSH IDM0107549

Synonyms (25)

Synonym
53498-52-5
54408-44-5
nsc637506
nsc-637506
2-amino-7-(2-hydroxyethyl)-7h-purin-6-ol
2-amino-7-(2-hydroxyethyl)purin-6-ol
NCI60_012421
CHEMBL123765
FT-0669617
2-amino-7-(2-hydroxyethyl)-3h-purin-6-one
6h-purin-6-one, 2-amino-1,7-dihydro-7-(2-hydroxyethyl)-
2-amino-1,7-dihydro-7-(2-hydroxyethyl)-6h-purin-6-one
n(7)-hydroxyethylguanine
n7-(2-hydroxyethyl)guanine
7-(2-hydroxyethyl)guanine
MLS004491913
smr003288855
SCHEMBL48362
AKOS022644956
DTXSID10201703
2-amino-7-(2-hydroxy-ethyl)-1,7-dihydro-purin-6-one
2-amino-7-(2-hydroxyethyl)-6,7-dihydro-1h-purin-6-one
Q26840964
2-amino-7-(2-hydroxyethyl)-1h-purin-6(7h)-one
2-amino-7-(2-hydroxyethyl)-1h-purin-6-one

Dosage Studied

ExcerptReference
" Dose-response relationships for 7-HEG were nonlinear in both mice and rats, with the alkylating efficiency of ETO increasing at high exposures."( Molecular dosimetry of ethylene oxide: formation and persistence of 7-(2-hydroxyethyl)guanine in DNA following repeated exposures of rats and mice.
Fennell, TR; Prevost, V; Shuker, DE; Skopek, TR; Swenberg, JA; Upton, PB; Walker, VE, 1992
)
" The dose-response curves for 7-HEG in rat tissues were linear between 10 and 100 ppm ETO and increased in slope above 100 ppm."( Molecular dosimetry of DNA and hemoglobin adducts in mice and rats exposed to ethylene oxide.
Fennell, TR; MacNeela, JP; Swenberg, JA; Upton, PB; Walker, VE, 1993
)
" Quantification results are shown for 7HEG after calf thymus DNA and blood exposure to various doses of EO, in both cases obtaining clear dose-response relationships."( High-performance liquid chromatography/electrospray mass spectrometry for the analysis of modified bases in DNA: 7-(2-hydroxyethyl)guanine, the major ethylene oxide-DNA adduct.
De Pauw, E; Laurent, C; Leclercq, L, 1997
)
" 7-HEG exhibited tissue- and species-specific dose-response relationships in EO-exposed animals."( Molecular dosimetry of endogenous and ethylene oxide-induced N7-(2-hydroxyethyl) guanine formation in tissues of rodents.
Ranasinghe, A; Swenberg, JA; Upton, PB; Walker, VE; Wu, KY, 1999
)
" For mutagenesis and other genotoxicity endpoints, the dose-response reflects the molecular dose of each type of DNA adduct, cell proliferation, as well as endogenous factors that lead to mutagenesis such as the formation and repair of endogenous DNA adducts."( DNA adducts: effects of low exposure to ethylene oxide, vinyl chloride and butadiene.
Ham, A; Koc, H; Morinello, E; Ranasinghe, A; Swenberg, JA; Tretyakova, N; Upton, PB; Wu, K, 2000
)
" The major objectives of this study were: (a) to determine the formation and persistence of N7-HEG adducts in liver DNA of adult male rats exposed to 0, 50, 100 and 200 ppm by inhalation (4 weeks, 5 days/week, 6 h/day) and (b) to assess dose-response relationships for Hprt gene mutations and various types of chromosomal changes in splenic lymphocytes."( Formation of DNA adducts and induction of mutagenic effects in rats following 4 weeks inhalation exposure to ethylene oxide as a basis for cancer risk assessment.
Boogaard, PJ; Ehrenberg, LG; Natarajan, AT; Tates, AD; Törnqvist, MA; van Sittert, NJ, 2000
)
" A dose-response relationship was established, indicating that the adduct formation increases with the exposure level."( Quantitative detection of N(7)-(2-hydroxyethyl)guanine adducts in DNA using high-performance liquid chromatography/electrospray ionization tandem mass spectrometry.
Chen, SH; Hung, CW; Li, CM; Liao, PC, 2001
)
" We have therefore defined in vivo dose-response relationships over a concentration range relevant to human EO exposures using a dual-isotope approach."( Dose-response relationships for N7-(2-hydroxyethyl)guanine induced by low-dose [14C]ethylene oxide: evidence for a novel mechanism of endogenous adduct formation.
Britton, RG; Brown, K; Farmer, PB; Johnson, GE; Jones, DJ; Marsden, DA; Ognibene, T; Ubick, E, 2009
)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID158514Activity against Plasmodium berghei in mice (Mus musculus)1980Journal of medicinal chemistry, Apr, Volume: 23, Issue:4
Synthesis of potential inhibitors of hypoxanthine-guanine phosphoribosyltransferase for testing as antiprotozoal agents. 1. 7-Substituted 6-oxopurines.
AID93194Ability to inhibit hypoxanthine-guanine phosphoribosyltransferase in crude extracts of H.Ep.-2 cells.1980Journal of medicinal chemistry, Apr, Volume: 23, Issue:4
Synthesis of potential inhibitors of hypoxanthine-guanine phosphoribosyltransferase for testing as antiprotozoal agents. 1. 7-Substituted 6-oxopurines.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (47)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (12.77)18.7374
1990's24 (51.06)18.2507
2000's16 (34.04)29.6817
2010's1 (2.13)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (6.12%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other46 (93.88%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]