Efficient synthesis of the benzo[a]pyrene metabolic adducts of 2'-deoxyguanosine and 2'-deoxyadenosine and their direct incorporation into DNA.

Abstract:

:A new and efficient method is described for the synthesis in gram quantities of the benzo[a]pyrene (B[a]P) metabolic adducts of 2'-deoxyguanosine (dG) and 2'-deoxyadenosine (dA) substituted, respectively, at the N(2)- and N(6)- positions. When the racemic form of the tris(benzoyloxy)amine 5 (related to the notoriously carcinogenic epoxydiol 2) is coupled with the bromoinosine derivative 6 by means of a Buchwald-Hartwig reaction, the expected pair of diastereomers, 7 and 8, is obtained in high (combined) yield. Selective deblocking of this mixture then gave cleanly the pair of diastereomers 9. These were used in the synthesis of a series of DNA oligomers via their 5'-O-DMT-3'-O-phosphoramidites (10) using standard automated methods. Coupling efficiencies were 94-98% at the point of introduction of the xeno-2'-deoxynucleoside, and in all cases the mixtures of the two diastereomeric oligomers (DMT-off stage) were easily separated by HPLC. By a similar sequence of reactions beginning with 5 and the protected 6-bromopurine 2'-deoxynucleoside 11, it was possible with equal efficiency to introduce the N(6)-modified diastereomers (16) of dA into oligomeric DNA. Circular dichroism measurements were used to establish the fundamental configurations at the xeno-2'-deoxynucleoside site for each of the oligomers. Mass spectral data in both the dG and the dA series confirmed the presence of the xeno-2'-deoxynucleoside in the oligomers. This was complemented by enzymatic degradation of one of the oligomers from each of the series. In both of these cases, after HPLC separation, circular dichroism measurements on the reisolated xenonucleoside also confirmed its presence in the oligomer.

journal_name

Chem Res Toxicol

authors

Johnson F,Bonala R,Tawde D,Torres MC,Iden CR

doi

10.1021/tx0256174

subject

Has Abstract

pub_date

2002-12-01 00:00:00

pages

1489-94

issue

12

eissn

0893-228X

issn

1520-5010

pii

tx0256174

journal_volume

15

pub_type

杂志文章
  • Identification of novel gene targets and putative regulators of arsenic-associated DNA methylation in human urothelial cells and bladder cancer.

    abstract::There is strong epidemiologic evidence linking chronic exposure to inorganic arsenic (iAs) to myriad adverse health effects, including cancer of the bladder. We set out to identify DNA methylation patterns associated with arsenic and its metabolites in exfoliated urothelial cells (EUCs) that originate primarily from t...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx500393y

    authors: Rager JE,Tilley SK,Tulenko SE,Smeester L,Ray PD,Yosim A,Currier JM,Ishida MC,González-Horta Mdel C,Sánchez-Ramírez B,Ballinas-Casarrubias L,Gutiérrez-Torres DS,Drobná Z,Del Razo LM,García-Vargas GG,Kim WY,Zhou YH,Wright

    更新日期:2015-06-15 00:00:00

  • In vivo cadmium mobilization by three novel bis(carbodithioates).

    abstract::Four novel cadmium-chelating agents N,N'di(D-glucosyl)alkanediamine-N,N'-bis(carbodithioates) 4a-e were prepared as disodium salts of the general formula (CH2)n[N(CS2Na)CH2(CHOH)4CH2OH]2, where n = 7, 8, 10, and 12. They were synthesized by the reductive coupling of 2 mol of alpha-D-(+)-glucose (1) with 1 mol of the c...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx950123a

    authors: Singh PK,Jones MM,Kostial K,Blanusa M,Piasek M

    更新日期:1996-01-01 00:00:00

  • Activation of phospholipase A2 in 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine liposomes containing lipid ozonation products.

    abstract::The activation of phospholipase A2 (PLA2) by lipid ozonation products is reported. The principal products from the ozonation of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) are 1-palmitoyl-2-[8-[3(5-octyl-1,2,4-trioxolan-3-yl)octanoyl]--sn-gly cero-3- phosphocholine (PC-Criegee ozonide) and 1-palmitoyl-2-(9...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00039a026

    authors: Salgo MG,Squadrito GL,Pryor WA

    更新日期:1994-05-01 00:00:00

  • A Novel Lipidomics-Based Approach to Evaluating the Risk of Clinical Hepatotoxicity Potential of Drugs in 3D Human Microtissues.

    abstract::The importance of adsorption, distribution, metabolism, excretion, and toxicity (ADMET) analysis is expected to grow substantially due to recent failures in detecting severe toxicity issues of new chemical entities during preclinical/clinical development. Traditionally, safety risk assessment studies for humans have b...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.9b00364

    authors: Goracci L,Valeri A,Sciabola S,Aleo MD,Moritz W,Lichtenberg J,Cruciani G

    更新日期:2020-01-21 00:00:00

  • Systematic toxicity mechanism analysis of proton pump inhibitors: an in silico study.

    abstract::Proton pump inhibitors (PPIs) are extensively used for the treatment of gastric acid-related disorders. PPIs appear to be well tolerated and almost have no short-term side effects. However, the clinical adverse reactions of long-term PPI usage are increasingly reported in recent years. So far, there is no study that e...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx5003782

    authors: Wu D,Qiu T,Zhang Q,Kang H,Yuan S,Zhu L,Zhu R

    更新日期:2015-03-16 00:00:00

  • Cytochrome P450 enzymes involved in acetaminophen activation by rat and human liver microsomes and their kinetics.

    abstract::Acetaminophen (APAP), a commonly used analgesic, is catalyzed by cytochrome P450 (P450) enzymes to a toxic intermediate which can be trapped by glutathione. Using this approach, involvement of enzymes in the activation of APAP and their kinetics were studied. With human liver microsomes, there were three apparent Km v...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00034a019

    authors: Patten CJ,Thomas PE,Guy RL,Lee M,Gonzalez FJ,Guengerich FP,Yang CS

    更新日期:1993-07-01 00:00:00

  • p,p'-DDE induces apoptosis through the modulation of tumor necrosis factor α in PC12 cells.

    abstract::p,p'-DDE, the main metabolite of DDT, is notorious for its persistent and bioaccumulation. It has detrimental effects on the nervous system, while the mechanism is unclear. We sought to investigate the mechanism of p,p'-DDE-induced neurocytic apoptosis in PC12 cells by cytoflow and screen the potential target gene by ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx4003963

    authors: Wang C,Zhang Q,Qian Y,Zhao M

    更新日期:2014-04-21 00:00:00

  • Decomposition rates of isothiocyanate conjugates determine their activity as inhibitors of cytochrome p450 enzymes.

    abstract::Thiol conjugates of isothiocyanates (thiol-ITCs) are metabolites of ITCs formed in the mercapturic acid pathway in mammals. They are effective chemopreventive agents in mouse lung tumor bioassays and in other models. Thiol-ITCs are inhibitors of P450s, but it has not been determined if P450 inhibition is due to conjug...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx010029w

    authors: Conaway CC,Krzeminski J,Amin S,Chung FL

    更新日期:2001-09-01 00:00:00

  • Qualitative analysis of the role of metabolites in inhibitory drug-drug interactions: literature evaluation based on the metabolism and transport drug interaction database.

    abstract::Guidance from the Food and Drug Administration on drug interaction studies does not include a specific section on contributions of metabolites to observed inhibitory drug-drug interactions, and the quantitative role of drug metabolites in inhibitory drug-drug interactions is not presently known. The current work was u...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/tx800491e

    authors: Isoherranen N,Hachad H,Yeung CK,Levy RH

    更新日期:2009-02-01 00:00:00

  • Renal elimination of perfluorocarboxylates (PFCAs).

    abstract::Sex-, species-, and chain length-dependent renal elimination is the hallmark of mammalian elimination of perfluorocarboxylates (PFCAs) and has been extensively studied for almost 30 years. In this review, toxicokinetic data of PFCAs (chain lengths ranging from 4 to 10) in different species are compared with an emphasi...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章,评审

    doi:10.1021/tx200363w

    authors: Han X,Nabb DL,Russell MH,Kennedy GL,Rickard RW

    更新日期:2012-01-13 00:00:00

  • Profiling the reactive metabolites of xenobiotics using metabolomic technologies.

    abstract::A predominant pathway of xenobiotic-induced toxicity is initiated by bioactivation. Characterizing reactive intermediates will provide information on the structure of reactive species, thereby defining a potential bioactivation mechanism. Because most reactive metabolites are not stable, it is difficult to detect them...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx200033v

    authors: Li F,Lu J,Ma X

    更新日期:2011-05-16 00:00:00

  • Nitric oxide produced endogenously is responsible for hypoxia-induced HIF-1α stabilization in colon carcinoma cells.

    abstract::Hypoxia-inducible factor-1α (HIF-1α) is a critical regulator of cellular responses to hypoxia. Under normoxic conditions, the cellular HIF-1α level is regulated by hydroxylation by prolyl hydroxylases (PHDs), ubiquitylation, and proteasomal degradation. During hypoxia, degradation decreases, and its intracellular leve...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx300274a

    authors: Chowdhury R,Godoy LC,Thiantanawat A,Trudel LJ,Deen WM,Wogan GN

    更新日期:2012-10-15 00:00:00

  • In vitro flavon-3-ol oxidation mediated by a B ring hydroxylation pattern.

    abstract::Flavonols are potent naturally occurring antioxidants. Chemical oxidation reactions in combination with modern spectroscopic techniques have been employed to identify oxidized flavonoid products. Although many oxidized derivatives have been generated from commercially available starting materials, few studies have dev...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx034242z

    authors: Krishnamachari V,Levine LH,Zhou C,Paré PW

    更新日期:2004-06-01 00:00:00

  • Structure-activity models for contact sensitization.

    abstract::Allergic contact dermatitis (ACD) is a widespread cause of workers' disabilities. Although some substances found in the workplace are rigorously tested, the potential of the vast majority of chemicals to cause skin sensitization remains unknown. At the same time, exhaustive testing of all chemicals in workplaces is co...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx0497806

    authors: Fedorowicz A,Singh H,Soderholm S,Demchuk E

    更新日期:2005-06-01 00:00:00

  • Bioisosteric Replacement of Amide Group with 1,2,3-Triazoles in Acetaminophen Addresses Reactive Oxygen Species-Mediated Hepatotoxic Insult in Wistar Albino Rats.

    abstract::Acetaminophen (AP) is a popularly recommended over-the-counter analgesic-antipyretic in clinical use. However, the drug is handicapped by the occurrence of hepatotoxic insult following acute ingestion. Consequently, AP-induced hepatotoxicity is often implicated in accidental or suicidal overdose. In the current study,...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.9b00392

    authors: Sahu A,Das D,Sahu P,Mishra S,Sakthivel A,Gajbhiye A,Agrawal R

    更新日期:2020-02-17 00:00:00

  • Bioactivation of lumiracoxib by peroxidases and human liver microsomes: identification of multiple quinone imine intermediates and GSH adducts.

    abstract::Lumiracoxib (Prexige; 2-[(2-fluoro-6-chlorophenyl)amino]-5-methyl-benzeneacetic acid) is a cyclooxygenase-2 selective inhibitor for the symptomatic treatment of osteoarthritis. Recently, the drug has been withdrawn in several countries due to serious liver side effects. Li et al. recently have shown that lumiracoxib i...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx8002356

    authors: Kang P,Dalvie D,Smith E,Renner M

    更新日期:2009-01-01 00:00:00

  • Hepatotoxicity after 3'-hydroxyacetanilide administration to buthionine sulfoximine pretreated mice.

    abstract::The administration of 3'-hydroxyacetanilide, a regioisomer of acetaminophen, to mice failed to produce hepatotoxicity even after the administration of diethyl maleate. In contrast, hepatotoxicity did occur when 3'-hydroxyacetanilide was administered to buthionine sulfoximine pretreated mice. Although the administratio...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00020a014

    authors: Tirmenstein MA,Nelson SD

    更新日期:1991-03-01 00:00:00

  • Fragrance compound geraniol forms contact allergens on air exposure. Identification and quantification of oxidation products and effect on skin sensitization.

    abstract::Fragrances are common causes of contact allergy. Geraniol (trans-3,7-dimethyl-2,6-octadiene-1-ol) is an important fragrance terpene. It is considered a weak contact allergen and is used for fragrance allergy screening among consecutive dermatitis patients. Analogous to other monoterpenes studied, such as limonene and ...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx700017v

    authors: Hagvall L,Bäcktorp C,Svensson S,Nyman G,Börje A,Karlberg AT

    更新日期:2007-05-01 00:00:00

  • Neurotoxic potential and cellular uptake of T-2 toxin in human astrocytes in primary culture.

    abstract::The trichothecene mycotoxin T-2 toxin, which is produced by fungi of the Fusarium species, is a worldwide occurring contaminant of cereal based food and feed. The cytotoxic properties of T-2 toxin are already well described with apoptosis being a major mechanism of action in various cell lines as well as in primary ce...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx3004664

    authors: Weidner M,Lenczyk M,Schwerdt G,Gekle M,Humpf HU

    更新日期:2013-03-18 00:00:00

  • Locating nucleobase lesions within DNA sequences by MALDI-TOF mass spectral analysis of exonuclease ladders.

    abstract::The location of carcinogen-modified nucleobases (DNA adducts) within DNA sequences is a critical factor affecting their promutagenic properties and persistence in DNA. We now report the use of controlled exonuclease digestion followed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MAL...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx010062i

    authors: Tretyakova N,Matter B,Ogdie A,Wishnok JS,Tannenbaum SR

    更新日期:2001-08-01 00:00:00

  • Products and mechanism of the reaction of ozone with phospholipids in unilamellar phospholipid vesicles.

    abstract::While considerable effort has been expended on determining the health effects of exposure to typical urban concentrations of O3, little is known about the chemical events responsible for toxicity. Phospholipids containing unsaturated fatty acids in the cell membranes of lung cells are likely reaction sites for inhaled...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx00025a023

    authors: Santrock J,Gorski RA,O'Gara JF

    更新日期:1992-01-01 00:00:00

  • Role of hydrophobic effects in the reaction of a polynuclear aromatic diol epoxide with oligodeoxynucleotides in aqueous solutions.

    abstract::The need for large-scale direct synthesis of stereochemically defined and site-specific benzo[alpha]pyrenediol epoxide-oligodeoxyribonucleotide adducts for detailed NMR and other biochemical and physicochemical studies has necessitated a better understanding of variables that lead to an enhancement of the reaction yie...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx980006q

    authors: Pirogov N,Shafirovich V,Kolbanovskiy A,Solntsev K,Courtney SA,Amin S,Geacintov NE

    更新日期:1998-04-01 00:00:00

  • Interaction of Cd2+ with Zn finger 3 of transcription factor IIIA: structures and binding to cognate DNA.

    abstract::Finger 3 of transcription factor IIIA of Xenopus laevis was synthesized and constituted with Zn(2+) or Cd(2+). The C-block element of the internal control region of the promoter of the 5S rRNA gene binds to the Zn-F3 and Cd-F3 with dissociation constants of 2.6 x 10(-5) and 1.5 x 10(-4) M, respectively. According to N...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx030057+

    authors: Krepkiy D,Försterling FH,Petering DH

    更新日期:2004-07-01 00:00:00

  • Kinetics of DNA Adducts and Abasic Site Formation in Tissues of Mice Treated with a Nitrogen Mustard.

    abstract::Nitrogen mustards (NM) are an important class of chemotherapeutic drugs used in the treatment of malignant tumors. The accepted mechanism of action of NM is through the alkylation of DNA bases. NM-adducts block DNA replication in cancer cells by forming cytotoxic DNA interstrand cross-links. We previously characterize...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.0c00012

    authors: Chen H,Cui Z,Hejazi L,Yao L,Walmsley SJ,Rizzo CJ,Turesky RJ

    更新日期:2020-04-20 00:00:00

  • Pristine (C60) and hydroxylated [C60(OH)24] fullerene phototoxicity towards HaCaT keratinocytes: type I vs type II mechanisms.

    abstract::The increasing use of fullerene nanomaterials has prompted widespread concern over their biological effects. Herein, we have studied the phototoxicity of gamma-cyclodextrin bicapped pristine C 60 [(gamma-CyD) 2/C 60] and its water-soluble derivative C 60(OH) 24 toward human keratinocytes. Our results demonstrated that...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx800056w

    authors: Zhao B,He YY,Bilski PJ,Chignell CF

    更新日期:2008-05-01 00:00:00

  • Framework for identifying chemicals with structural features associated with the potential to act as developmental or reproductive toxicants.

    abstract::Developmental and reproductive toxicity (DART) end points are important hazard end points that need to be addressed in the risk assessment of chemicals to determine whether or not they are the critical effects in the overall risk assessment. These hazard end points are difficult to predict using current in silico tool...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx400226u

    authors: Wu S,Fisher J,Naciff J,Laufersweiler M,Lester C,Daston G,Blackburn K

    更新日期:2013-12-16 00:00:00

  • Dityrosine cross-linked Abeta peptides: fibrillar beta-structure in Abeta(1-40) is conducive to formation of dityrosine cross-links but a dityrosine cross-link in Abeta(8-14) does not induce beta-structure.

    abstract::Recent reports by Galeazzi and co-workers demonstrated the susceptibility of Abeta(1-42) to undergo dityrosine formation via peroxidase-catalyzed tyrosine cross-linking. We have formed dityrosine cross-links in Abeta(1-40) using these enzymatic conditions as well as a copper-H(2)O(2) method. The efficiency of dityrosi...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx025666g

    authors: Yoburn JC,Tian W,Brower JO,Nowick JS,Glabe CG,Van Vranken DL

    更新日期:2003-04-01 00:00:00

  • Two-Mechanism Model for the Interaction of Etoposide Quinone with Topoisomerase IIα.

    abstract::Topoisomerase II is an essential nuclear enzyme involved in regulating DNA topology to facilitate replication and cell division. Disruption of topoisomerase II function by chemotherapeutic agents is in use as an effective strategy to fight cancer. Etoposide is an anticancer therapeutic that disrupts the catalytic cycl...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/acs.chemrestox.6b00209

    authors: Gibson EG,King MM,Mercer SL,Deweese JE

    更新日期:2016-09-19 00:00:00

  • Identification of 4-S-Cysteinyltetrodotoxin from the liver of the puffer fish, Fugu pardalis, and formation of thiol adducts of tetrodotoxin from 4,9-anhydrotetrodotoxin.

    abstract::The metabolic pathway of tetrodotoxin (TTX), a powerful and specific voltage-gated sodium channel blocker, has not been well-clarified either in TTX-poisoned patients or in puffer fish. 4-S-CysteinylTTX (4-CysTTX) was isolated from the liver of the puffer fish, Fugu pardalis, as the first adduct of TTX with thiol. The...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx050015g

    authors: Yotsu-Yamashita M,Goto A,Nakagawa T

    更新日期:2005-05-01 00:00:00

  • Gamma-radiolysis and hydroxyl radical produce interstrand cross-links in DNA involving thymidine.

    abstract::Interstrand cross-links are minor components of the collection of products formed in DNA by ionizing radiation. Through their formation by other damaging agents, it is known that interstrand cross-links exert significant effects on replication and transcription. The structures of DNA interstrand cross-links produced a...

    journal_title:Chemical research in toxicology

    pub_type: 杂志文章

    doi:10.1021/tx7002307

    authors: Ding H,Greenberg MM

    更新日期:2007-11-01 00:00:00