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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H22N6O4
Molecular Weight 446.4586
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(DEOXYGUANOSIN-8-YL)-2-AMINOFLUORENE

SMILES

NC1=NC(=O)C2=C(N1)N([C@H]3C[C@H](O)[C@@H](CO)O3)C(NC4=CC=C5C(CC6=CC=CC=C56)=C4)=N2

InChI

InChIKey=RMYQNJYFBAYPNG-RCCFBDPRSA-N
InChI=1S/C23H22N6O4/c24-22-27-20-19(21(32)28-22)26-23(29(20)18-9-16(31)17(10-30)33-18)25-13-5-6-15-12(8-13)7-11-3-1-2-4-14(11)15/h1-6,8,16-18,30-31H,7,9-10H2,(H,25,26)(H3,24,27,28,32)/t16-,17+,18+/m0/s1

HIDE SMILES / InChI

Molecular Formula C23H22N6O4
Molecular Weight 446.4586
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Genetic and epigenetic changes in rat preneoplastic liver tissue induced by 2-acetylaminofluorene.
2008-03
Probing the thermodynamics of aminofluorene-induced translesion DNA synthesis by differential scanning calorimetry.
2007-10-10
Examination of the long-range effects of aminofluorene-induced conformational heterogeneity and its relevance to the mechanism of translesional DNA synthesis.
2007-03-09
Conformation-specific recognition of carcinogen-DNA adduct in escherichia coli nucleotide excision repair.
2007-01
Mutagenic properties of 3-(deoxyguanosin-N2-yl)-2-acetylaminofluorene, a persistent acetylaminofluorene-derived DNA adduct in mammalian cells.
2004-11-30
Mutagenic events in Escherichia coli and mammalian cells generated in response to acetylaminofluorene-derived DNA adducts positioned in the Nar I restriction enzyme site.
2002-12-03
Translesional synthesis past acetylaminofluorene-derived DNA adducts catalyzed by human DNA polymerase kappa and Escherichia coli DNA polymerase IV.
2001-12-18
1Alpha,25-dihydroxyvitamin D3 inhibits hepatic chromosomal aberrations, DNA strand breaks and specific DNA adducts during rat hepatocarcinogenesis.
2001-07
Influence of flanking sequence context on the mutagenicity of acetylaminofluorene-derived DNA adducts in mammalian cells.
2001-03-27
Gene- and tissue-specificity of mutation in Big Blue rats treated with the hepatocarcinogen N-hydroxy-2-acetylaminofluorene.
2001
Comparison of hprt and lacI mutant frequency with DNA adduct formation in N-hydroxy-2-acetylaminofluorene-treated Big Blue rats.
2001
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:09:44 GMT 2025
Edited
by admin
on Mon Mar 31 19:09:44 GMT 2025
Record UNII
1D7E8EIA7K
Record Status Validated (UNII)
Record Version
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Name Type Language
N-(DEOXYGUANOSIN-8-YL)-2-AMINOFLUORENE
Systematic Name English
AMINOFLUORENE-DG
Preferred Name English
DG-8-AF
Common Name English
GUANOSINE, 2'-DEOXY-8-(9H-FLUOREN-2-YLAMINO)-
Systematic Name English
Code System Code Type Description
PUBCHEM
135562692
Created by admin on Mon Mar 31 19:09:44 GMT 2025 , Edited by admin on Mon Mar 31 19:09:44 GMT 2025
PRIMARY
CHEBI
75814
Created by admin on Mon Mar 31 19:09:44 GMT 2025 , Edited by admin on Mon Mar 31 19:09:44 GMT 2025
PRIMARY
MESH
C031838
Created by admin on Mon Mar 31 19:09:44 GMT 2025 , Edited by admin on Mon Mar 31 19:09:44 GMT 2025
PRIMARY
EPA CompTox
DTXSID60993823
Created by admin on Mon Mar 31 19:09:44 GMT 2025 , Edited by admin on Mon Mar 31 19:09:44 GMT 2025
PRIMARY
FDA UNII
1D7E8EIA7K
Created by admin on Mon Mar 31 19:09:44 GMT 2025 , Edited by admin on Mon Mar 31 19:09:44 GMT 2025
PRIMARY
CAS
73051-69-1
Created by admin on Mon Mar 31 19:09:44 GMT 2025 , Edited by admin on Mon Mar 31 19:09:44 GMT 2025
PRIMARY