Evaluating cholinesterases inhibition by BAC and DDAC biocides: A combined experimental and theoretical approach

Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have b...

Full description

Saved in:
Bibliographic Details
Published inBiochimica et biophysica acta. Biomembranes Vol. 1868; no. 12; p. 130726
Main Authors Mouawad, Lynn, Esque, Jeremy, André, Isabelle, Istamboulie, Georges, Catanante, Gaëlle, Noguer, Thierry
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.12.2024
Elsevier
Subjects
Online AccessGet full text
ISSN0304-4165
1872-8006
0005-2736
1872-8006
1879-2642
DOI10.1016/j.bbagen.2024.130726

Cover

Abstract Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases. •A rapid colorimetric microplate test was developed to study cholinesterase inhibition by quaternary ammonium biocides.•4 different enzymes were tested including 3 acetylcholinesterases and 1 butyrylcholinesterase.•In silico molecular docking allowed confirmation of the results obtained by enzymatic methods.
AbstractList Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases.
Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases.Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases.
Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of biocides are quaternary ammonium compounds (QAs), notably benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC), which have been shown to inhibit cholinesterases. This study aims to evaluate the effect of these biocides towards different cholinesterases using both enzyme inhibition and molecular docking experiments. Acetylcholinesterase (AChE) from Drosophila melanogaster (DM-AChE), Electrophorus electricus (EE-AChE), bovine erythrocytes (BE-AChE) and butyrylcholinesterase from horse serum (BChE) were selected for this study. Using a colorimetric assay, all these enzymes were shown to be inhibited in a competitive form by both biocides, BAC and DDAC, with the exception of DM-AChE, which was inhibited in a non-competitive manner by BAC. Molecular docking experiments enabled to identify structural determinants involved in the different modes of inhibition observed. More particularly, our results suggest that non-competitive inhibition of DM-AChE by BAC could be related to the binding of the inhibitor into a more extended active site compared to other cholinesterases. •A rapid colorimetric microplate test was developed to study cholinesterase inhibition by quaternary ammonium biocides.•4 different enzymes were tested including 3 acetylcholinesterases and 1 butyrylcholinesterase.•In silico molecular docking allowed confirmation of the results obtained by enzymatic methods.
ArticleNumber 130726
Author André, Isabelle
Mouawad, Lynn
Esque, Jeremy
Noguer, Thierry
Catanante, Gaëlle
Istamboulie, Georges
Author_xml – sequence: 1
  givenname: Lynn
  surname: Mouawad
  fullname: Mouawad, Lynn
  organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France
– sequence: 2
  givenname: Jeremy
  surname: Esque
  fullname: Esque, Jeremy
  organization: Toulouse Biotechnology Institute, TBI, Université de Toulouse, CNRS, INRAE, INSA, 31077 Toulouse, France
– sequence: 3
  givenname: Isabelle
  surname: André
  fullname: André, Isabelle
  organization: Toulouse Biotechnology Institute, TBI, Université de Toulouse, CNRS, INRAE, INSA, 31077 Toulouse, France
– sequence: 4
  givenname: Georges
  surname: Istamboulie
  fullname: Istamboulie, Georges
  organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France
– sequence: 5
  givenname: Gaëlle
  surname: Catanante
  fullname: Catanante, Gaëlle
  email: gaelle.catanante@univ-perp.fr
  organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France
– sequence: 6
  givenname: Thierry
  surname: Noguer
  fullname: Noguer, Thierry
  email: noguer@univ-perp.fr
  organization: Biosensors Analysis Environment Group (BAE-LBBM), Université de Perpignan Via Domitia, 66860 Perpignan, France
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39433227$$D View this record in MEDLINE/PubMed
https://insa-toulouse.hal.science/hal-04757302$$DView record in HAL
BookMark eNqFkUuP0zAUhS00iOkM_AOEsoRFil-Jk1kglc4LqRIbWFs39u3EVWoXO62Yf49DhlmwAG_sa33n6OqcC3Lmg0dC3jK6ZJTVH3fLroMH9EtOuVwyQRWvX5AFaxQvG0rrM7KggspSsro6Jxcp7Wg-VVu9IueilUJwrhbkcHOC4Qij8w-F6cPgPKYRIyRMhfO969zogi-6x-Lzal2At8X1dX50LhhnMV0Vq8KEfZdltsCfB4xuj36E4Tc69hgijs5M8-EQA5j-NXm5hSHhm6f7kny_vfm2vi83X---rFeb0kjJx1KKZsub2poGWNWB2VYUuWkBha0VA0YNMIbGQiWbWraGdzVTVFmrqlZUyohL8mH27WHQh7wWxEcdwOn71UZPf1SqSgnKTyyz72c2r_jjmAPQe5cMDgN4DMekBWMta4XiNKPvntBjt0f77Pwn0QzIGTAxpBRx-4wwqqfi9E7PxempOD0Xl2VXf8mMG2HKfozghv-JP81izIGeHEadjENv0LqIZtQ2uH8b_AI2I7S9
CitedBy_id crossref_primary_10_3390_bios15010026
Cites_doi 10.1016/0014-5793(90)81522-P
10.1016/j.cbi.2010.01.042
10.1042/BJ20071551
10.3390/molecules26082276
10.1021/bi300955k
10.1002/j.1460-2075.1996.tb00864.x
10.1016/0006-2952(61)90145-9
10.1093/nar/28.1.304
10.1016/S0047-6374(01)00309-8
10.1016/j.bios.2007.06.022
10.1093/bioinformatics/btq066
10.1046/j.1365-2672.92.5s1.12.x
10.1016/j.bioorg.2018.10.035
10.1016/0006-2952(73)90196-2
10.1016/j.fct.2021.112064
10.1093/protein/8.2.127
10.1093/jimb/kuab074
10.1080/10643389.2021.1889284
10.1002/jcc.21256
10.1074/jbc.272.52.33045
10.1074/jbc.M210241200
10.1111/j.1742-4658.2009.06957.x
10.1021/ja106820e
10.1016/j.pharmthera.2014.11.011
10.1021/bi000210o
10.1126/science.1678899
10.1002/jcc.21334
10.1042/bj3290329
10.1002/prot.20264
ContentType Journal Article
Copyright 2024 Elsevier B.V.
Copyright © 2024 Elsevier B.V. All rights reserved.
Distributed under a Creative Commons Attribution 4.0 International License
Copyright_xml – notice: 2024 Elsevier B.V.
– notice: Copyright © 2024 Elsevier B.V. All rights reserved.
– notice: Distributed under a Creative Commons Attribution 4.0 International License
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
1XC
VOOES
DOI 10.1016/j.bbagen.2024.130726
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
Hyper Article en Ligne (HAL)
Hyper Article en Ligne (HAL) (Open Access)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE

MEDLINE - Academic

Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
Biology
EISSN 1872-8006
1879-2642
ExternalDocumentID oai_HAL_hal_04757302v1
39433227
10_1016_j_bbagen_2024_130726
S0304416524001697
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
--K
--M
.~1
0R~
1B1
1RT
1~.
1~5
23N
3O-
4.4
457
4G.
53G
5GY
5RE
5VS
7-5
71M
8P~
9JM
AACTN
AAEDT
AAEDW
AAHBH
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AAQXK
AAXKI
AAXUO
ABEFU
ABFNM
ABGSF
ABMAC
ABUDA
ABXDB
ACDAQ
ACIUM
ACRLP
ADBBV
ADEZE
ADMUD
ADUVX
AEBSH
AEHWI
AEKER
AFJKZ
AFKWA
AFTJW
AFXIZ
AGHFR
AGRDE
AGUBO
AGYEJ
AHHHB
AIEXJ
AIKHN
AITUG
AJOXV
AKRWK
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
ASPBG
AVWKF
AXJTR
AZFZN
BKOJK
BLXMC
CS3
EBS
EFJIC
EJD
EO8
EO9
EP2
EP3
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYGXN
G-2
G-Q
GBLVA
HLW
HVGLF
HZ~
IHE
J1W
KOM
LX3
M41
MO0
N9A
O-L
O9-
OAUVE
OHT
OZT
P-8
P-9
PC.
Q38
R2-
ROL
RPZ
SBG
SCC
SDF
SDG
SDP
SES
SEW
SPCBC
SSU
SSZ
T5K
UQL
WH7
WUQ
XJT
XPP
~G-
AATTM
AAYWO
AAYXX
ABWVN
ACRPL
ACVFH
ADCNI
ADNMO
AEIPS
AEUPX
AFPUW
AGCQF
AGQPQ
AGRNS
AIGII
AIIUN
AKBMS
AKYEP
ANKPU
APXCP
BNPGV
CITATION
SSH
CGR
CUY
CVF
ECM
EIF
NPM
7X8
ACLOT
EFKBS
EFLBG
~HD
1XC
6J9
AABNK
IXB
OK1
RSU
VOOES
ID FETCH-LOGICAL-c442t-438f286dc8a15bacf50e2c9ae3d671a10ca11ecda548649c2b61707dd759357c3
IEDL.DBID .~1
ISSN 0304-4165
1872-8006
0005-2736
IngestDate Fri Sep 12 12:31:23 EDT 2025
Sat Sep 27 22:57:08 EDT 2025
Fri May 30 10:59:47 EDT 2025
Thu Apr 24 22:58:40 EDT 2025
Tue Jul 01 00:22:20 EDT 2025
Sat Nov 09 16:00:11 EST 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 12
Keywords Enzyme kinetics
Biocides
Molecular docking
Cholinesterases
molecular docking
biocides
enzyme kinetics
Language English
License Copyright © 2024 Elsevier B.V. All rights reserved.
Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c442t-438f286dc8a15bacf50e2c9ae3d671a10ca11ecda548649c2b61707dd759357c3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0001-6280-4109
0000-0001-7987-7945
0000-0002-5786-848X
0000-0002-1394-5404
OpenAccessLink https://insa-toulouse.hal.science/hal-04757302
PMID 39433227
PQID 3119193720
PQPubID 23479
ParticipantIDs hal_primary_oai_HAL_hal_04757302v1
proquest_miscellaneous_3119193720
pubmed_primary_39433227
crossref_primary_10_1016_j_bbagen_2024_130726
crossref_citationtrail_10_1016_j_bbagen_2024_130726
elsevier_sciencedirect_doi_10_1016_j_bbagen_2024_130726
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-12-01
PublicationDateYYYYMMDD 2024-12-01
PublicationDate_xml – month: 12
  year: 2024
  text: 2024-12-01
  day: 01
PublicationDecade 2020
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Biochimica et biophysica acta. Biomembranes
PublicationTitleAlternate Biochim Biophys Acta Gen Subj
PublicationYear 2024
Publisher Elsevier B.V
Elsevier
Publisher_xml – name: Elsevier B.V
– name: Elsevier
References Yung-Chi, Prusoff (bb0175) 1973; 22
Sharma (bb0010) 2019; 20
Nicolet, Lockridge, Masson, Fontecilla-Camps, Nachon (bb0195) 2003; 278
Maillard (bb0065) 2005; 1
Doctor, Chapman, Christner, Deal, De La Hoz, Gentry, Ogert, Rush, Smyth, Wolfe (bb0140) 1990; 266
Li, Schopfer, Masson, Lockridge (bb0145) 2008; 411
Jones, Joshi (bb0075) 2021; 26
Darboux, Barthalay, Piovant, Hipeau-Jacquotte (bb0130) 1996; 15
Simon, Massoulié (bb0135) 1997; 272
Sehnal, Svobodová Vařeková, Berka, Pravda, Navrátilová, Banáš, Ionescu, Otyepka, Koča (bb0200) 2013
Dvir, Silman, Harel, Rosenberry, Sussman (bb0025) 2010; 187
Čadež, Kolić, Šinko, Kovarik (bb0060) 2021
Rosenberry, Brazzolotto, Macdonald, Wandhammer, Trovaslet-Leroy, Darvesh, Nachon (bb0210) 2017
Russell (bb0070) 2002; 92
Bairoch (bb0150) 2000; 28
Trott, Olson (bb0155) 2010; 31
Fox, Kelly, Humphreys, Waigh, Lu, McBain (bb0080) 2022; 49
Marcel, Palacios, Pertuy, Masson, Fournier (bb0045) 1998; 329
European Food Safety Authority, (EFSA). Evaluation of monitoring data on residues of didecyldimethylammonium chloride (DDAC) and benzalkonium chloride (BAC). Available online
Delaune, Alsayouri (bb0165) 2022
Hanwell, Curtis, Lonie, Vandermeersch, Zurek, Hutchison (bb0125) 2012
Lockridge (bb0030) 2015; 148
Mallender, Szegletes, Rosenberry (bb0055) 2000; 39
Bourne, Radić, Taylor, Marchot (bb0105) 2010; 132
Pelley (bb0170) 2012
Talesa (bb0005) 2001; 122
Zhang, Skolnick (bb0185) 2004; 57
Silver (bb0020) 1974; 36
Pietsch, Christian, Inhester, Petzold, Gütschow (bb0050) 2009; 276
Lockridge, Quinn, Radić (bb0015) 2023
Santé publique Sécurite de la chaine alimentaire Environement. Risque et danger.
Xu, Zhang (bb0190) 2010; 26
(accessed on 7 December 2023).
(accessed 24 March 2024).
Wallace, Laskowski, Thornton (bb0205) 1995; 8
Tanoli, Ramzan, Hassan, Sadiq, Jan Saeed, Khan, Ullah, Ahmad, Bibi, Mahmood, Rashid (bb0110) 2019; 83
Macdonald, Martin, Rosenberry, Darvesh (bb0040) 2012; 51
Hwang, Jeong, Jung, Nam, Lim (bb0095) 2021; 150
Barber, Hartmann (bb0100) 2022; 52
Morris, Huey, Lindstrom, Sanner, Belew, Goodsell, Olson (bb0160) 2009; 30
Nachon, Rosenberry, Silman, Sussman (bb0180) 2020
Sussman, Harel, Frolow, Atomic, Goldman, Toker, Silman (bb0035) 1991; 253
Istamboulie, Andreescu, Marty, Noguer (bb0120) 2007; 23
Ellman, Courtney, Andres, Featherstone (bb0115) 1961; 7
Simon (10.1016/j.bbagen.2024.130726_bb0135) 1997; 272
Lockridge (10.1016/j.bbagen.2024.130726_bb0015) 2023
Trott (10.1016/j.bbagen.2024.130726_bb0155) 2010; 31
Dvir (10.1016/j.bbagen.2024.130726_bb0025) 2010; 187
Sharma (10.1016/j.bbagen.2024.130726_bb0010) 2019; 20
Wallace (10.1016/j.bbagen.2024.130726_bb0205) 1995; 8
10.1016/j.bbagen.2024.130726_bb0090
Čadež (10.1016/j.bbagen.2024.130726_bb0060) 2021
10.1016/j.bbagen.2024.130726_bb0085
Maillard (10.1016/j.bbagen.2024.130726_bb0065) 2005; 1
Darboux (10.1016/j.bbagen.2024.130726_bb0130) 1996; 15
Zhang (10.1016/j.bbagen.2024.130726_bb0185) 2004; 57
Nicolet (10.1016/j.bbagen.2024.130726_bb0195) 2003; 278
Morris (10.1016/j.bbagen.2024.130726_bb0160) 2009; 30
Silver (10.1016/j.bbagen.2024.130726_bb0020) 1974; 36
Sussman (10.1016/j.bbagen.2024.130726_bb0035) 1991; 253
Talesa (10.1016/j.bbagen.2024.130726_bb0005) 2001; 122
Ellman (10.1016/j.bbagen.2024.130726_bb0115) 1961; 7
Hanwell (10.1016/j.bbagen.2024.130726_bb0125) 2012
Hwang (10.1016/j.bbagen.2024.130726_bb0095) 2021; 150
Nachon (10.1016/j.bbagen.2024.130726_bb0180) 2020
Lockridge (10.1016/j.bbagen.2024.130726_bb0030) 2015; 148
Sehnal (10.1016/j.bbagen.2024.130726_bb0200) 2013
Yung-Chi (10.1016/j.bbagen.2024.130726_bb0175) 1973; 22
Pietsch (10.1016/j.bbagen.2024.130726_bb0050) 2009; 276
Li (10.1016/j.bbagen.2024.130726_bb0145) 2008; 411
Doctor (10.1016/j.bbagen.2024.130726_bb0140) 1990; 266
Xu (10.1016/j.bbagen.2024.130726_bb0190) 2010; 26
Barber (10.1016/j.bbagen.2024.130726_bb0100) 2022; 52
Istamboulie (10.1016/j.bbagen.2024.130726_bb0120) 2007; 23
Jones (10.1016/j.bbagen.2024.130726_bb0075) 2021; 26
Macdonald (10.1016/j.bbagen.2024.130726_bb0040) 2012; 51
Tanoli (10.1016/j.bbagen.2024.130726_bb0110) 2019; 83
Marcel (10.1016/j.bbagen.2024.130726_bb0045) 1998; 329
Fox (10.1016/j.bbagen.2024.130726_bb0080) 2022; 49
Bourne (10.1016/j.bbagen.2024.130726_bb0105) 2010; 132
Pelley (10.1016/j.bbagen.2024.130726_bb0170) 2012
Mallender (10.1016/j.bbagen.2024.130726_bb0055) 2000; 39
Russell (10.1016/j.bbagen.2024.130726_bb0070) 2002; 92
Bairoch (10.1016/j.bbagen.2024.130726_bb0150) 2000; 28
Delaune (10.1016/j.bbagen.2024.130726_bb0165) 2022
Rosenberry (10.1016/j.bbagen.2024.130726_bb0210) 2017
References_xml – volume: 276
  start-page: 2292
  year: 2009
  end-page: 2307
  ident: bb0050
  article-title: Kinetics of inhibition of acetylcholinesterase in the presence of acetonitrile
  publication-title: FEBS J.
– volume: 15
  start-page: 4835
  year: 1996
  end-page: 4843
  ident: bb0130
  article-title: The structure-function relationships in drosophila neurotactin show that cholinesterasic domains may have adhesive properties
  publication-title: EMBO J.
– volume: 30
  start-page: 2785
  year: 2009
  end-page: 2791
  ident: bb0160
  article-title: AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility
  publication-title: J. Comput. Chem.
– volume: 26
  start-page: 889
  year: 2010
  end-page: 895
  ident: bb0190
  article-title: How significant is a protein structure similarity with TM-score = 0.5?
  publication-title: Bioinformatics
– reference: Santé publique Sécurite de la chaine alimentaire Environement. Risque et danger.
– reference: . (accessed 24 March 2024).
– start-page: 4
  year: 2012
  ident: bb0125
  article-title: Avogadro: an advanced semantic chemical editor, visualization, and analysis platform
  publication-title: Aust. J. Chem.
– volume: 52
  start-page: 2691
  year: 2022
  end-page: 2719
  ident: bb0100
  article-title: Benzalkonium chloride: a systematic review of its environmental entry through wastewater treatment, potential impact, and mitigation strategies
  publication-title: Crit. Rev. Environ. Sci. Technol.
– volume: 31
  start-page: 455
  year: 2010
  end-page: 461
  ident: bb0155
  article-title: AutoDock vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
  publication-title: J. Comput. Chem.
– volume: 272
  start-page: 33045
  year: 1997
  end-page: 33055
  ident: bb0135
  article-title: Cloning and expression of acetylcholinesterase from electrophorus: splicing pattern of the 3′ exons in vivo and in transfected mammalian cells
  publication-title: J. Biol. Chem.
– volume: 278
  start-page: 41141
  year: 2003
  end-page: 41147
  ident: bb0195
  article-title: Crystal structure of human butyrylcholinesterase and of its complexes with substrate and products
  publication-title: J. Biol. Chem.
– start-page: 22
  year: 2017
  ident: bb0210
  article-title: Comparison of the binding of reversible inhibitors to human butyrylcholinesterase and acetylcholinesterase: a crystallographic, kinetic and calorimetric study
  publication-title: Molecules
– volume: 39
  start-page: 7753
  year: 2000
  end-page: 7763
  ident: bb0055
  article-title: Acetylthiocholine binds to Asp74 at the peripheral site of human acetylcholinesterase as the first step in the catalytic pathway
  publication-title: Biochemistry
– volume: 7
  start-page: 88
  year: 1961
  end-page: 95
  ident: bb0115
  article-title: A new and rapid colorimetric determination of acetylcholinesterase activity
  publication-title: Biochem. Pharmacol.
– volume: 8
  start-page: 127
  year: 1995
  end-page: 134
  ident: bb0205
  article-title: LIGPLOT: a program to generate schematic diagrams of protein-ligand interactions
  publication-title: Protein Eng.
– volume: 51
  start-page: 7046
  year: 2012
  end-page: 7053
  ident: bb0040
  article-title: Probing the peripheral site of human butyrylcholinesterase
  publication-title: Biochemistry
– volume: 187
  start-page: 10
  year: 2010
  end-page: 22
  ident: bb0025
  article-title: Acetylcholinesterase: from 3D structure to function
  publication-title: Chem. Biol. Interact.
– volume: 253
  start-page: 872
  year: 1991
  end-page: 879
  ident: bb0035
  article-title: Structure of acetylcholinesterase from torpedo californica: a prototypic acetylcholine-binding protein
  publication-title: Science
– volume: 150
  year: 2021
  ident: bb0095
  article-title: Skin irritation and inhalation toxicity of biocides evaluated with reconstructed human epidermis and airway models
  publication-title: Food Chem. Toxicol.
– year: 2023
  ident: bb0015
  article-title: Esterases, Reference Module in Biomedical Sciences
– start-page: 5
  year: 2013
  ident: bb0200
  article-title: MOLE 2.0: advanced approach for analysis of biomacromolecular channels
  publication-title: J. Chemother.
– volume: 1
  start-page: 307
  year: 2005
  end-page: 320
  ident: bb0065
  article-title: Antimicrobial biocides in the healthcare environment: efficacy, usage, policies, and perceived problems
  publication-title: Ther. Clin. Risk Manag.
– volume: 266
  start-page: 123
  year: 1990
  end-page: 127
  ident: bb0140
  article-title: Complete amino acid sequence of fetal bovine serum acetylcholinesterase and its comparison in various regions with other cholinesterases
  publication-title: FEBS Lett.
– volume: 132
  start-page: 18292
  year: 2010
  end-page: 18300
  ident: bb0105
  article-title: Conformational remodeling of femtomolar inhibitor-acetylcholinesterase complexes in the crystalline state
  publication-title: J. Am. Chem. Soc.
– volume: 23
  start-page: 506
  year: 2007
  end-page: 512
  ident: bb0120
  article-title: Highly sensitive detection of organophosphorus insecticides using magnetic microbeads and genetically engineered acetylcholinesterase
  publication-title: Biosens. Bioelectron.
– volume: 20
  start-page: 1479
  year: 2019
  end-page: 1487
  ident: bb0010
  article-title: Cholinesterase inhibitors as Alzheimer’s therapeutics (review)
  publication-title: Mol. Med. Rep.
– volume: 26
  start-page: 2276
  year: 2021
  ident: bb0075
  article-title: Biocide use in the antimicrobial era: a review
  publication-title: Molecules
– reference: European Food Safety Authority, (EFSA). Evaluation of monitoring data on residues of didecyldimethylammonium chloride (DDAC) and benzalkonium chloride (BAC). Available online :
– start-page: 29
  year: 2012
  end-page: 37
  ident: bb0170
  article-title: 4 - enzymes and energetics
  publication-title: Elsevier’s Integrated Review Biochemistry
– start-page: 25
  year: 2020
  ident: bb0180
  article-title: A second look at the crystal structures of
  publication-title: Molecules
– volume: 411
  start-page: 425
  year: 2008
  end-page: 432
  ident: bb0145
  article-title: Lamellipodin proline rich peptides associated with native plasma butyrylcholinesterase tetramers
  publication-title: Biochem. J.
– volume: 36
  start-page: 426
  year: 1974
  end-page: 447
  ident: bb0020
  article-title: The biology of cholinesterases
  publication-title: Front. Biol.
– start-page: 11
  year: 2021
  ident: bb0060
  article-title: Assessment of four organophosphorus pesticides as inhibitors of human acetylcholinesterase and butyrylcholinesterase
  publication-title: Sci. Rep.
– year: 2022
  ident: bb0165
  article-title: Physiology, Noncompetitive Inhibitor,
– volume: 22
  start-page: 3099
  year: 1973
  end-page: 3108
  ident: bb0175
  article-title: Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
  publication-title: Biochem. Pharmacol.
– volume: 57
  start-page: 702
  year: 2004
  end-page: 710
  ident: bb0185
  article-title: Scoring function for automated assessment of protein structure template quality
  publication-title: Proteins
– volume: 92
  start-page: 121
  year: 2002
  end-page: 135
  ident: bb0070
  article-title: Introduction of biocides into clinical practice and the impact on antibiotic-resistant bacteria
  publication-title: J. Appl. Microbiol.
– volume: 329
  start-page: 329
  year: 1998
  end-page: 334
  ident: bb0045
  article-title: Two invertebrate acetylcholinesterases show activation followed by inhibition with substrate concentration
  publication-title: Biochem. J.
– volume: 28
  start-page: 304
  year: 2000
  end-page: 305
  ident: bb0150
  article-title: The ENZYME database in 2000
  publication-title: Nucleic Acids Res.
– volume: 49
  year: 2022
  ident: bb0080
  article-title: Assessing the risk of resistance to cationic biocides incorporating realism-based and biophysical approaches
  publication-title: J. Ind. Microbiol. Biotechnol.
– volume: 83
  start-page: 336
  year: 2019
  end-page: 347
  ident: bb0110
  article-title: Design, synthesis and bioevaluation of tricyclic fused ring system as dual binding site acetylcholinesterase inhibitors
  publication-title: Bioorg. Chem.
– volume: 122
  start-page: 1961
  year: 2001
  end-page: 1969
  ident: bb0005
  article-title: Acetylcholinesterase in Alzheimer’s disease
  publication-title: Mech. Ageing Dev.
– reference: (accessed on 7 December 2023).
– volume: 148
  start-page: 34
  year: 2015
  end-page: 46
  ident: bb0030
  article-title: Review of human butyrylcholinesterase structure, function, genetic variants, history of use in the clinic, and potential therapeutic uses
  publication-title: Pharmacol. Ther.
– volume: 266
  start-page: 123
  year: 1990
  ident: 10.1016/j.bbagen.2024.130726_bb0140
  article-title: Complete amino acid sequence of fetal bovine serum acetylcholinesterase and its comparison in various regions with other cholinesterases
  publication-title: FEBS Lett.
  doi: 10.1016/0014-5793(90)81522-P
– volume: 187
  start-page: 10
  year: 2010
  ident: 10.1016/j.bbagen.2024.130726_bb0025
  article-title: Acetylcholinesterase: from 3D structure to function
  publication-title: Chem. Biol. Interact.
  doi: 10.1016/j.cbi.2010.01.042
– volume: 411
  start-page: 425
  year: 2008
  ident: 10.1016/j.bbagen.2024.130726_bb0145
  article-title: Lamellipodin proline rich peptides associated with native plasma butyrylcholinesterase tetramers
  publication-title: Biochem. J.
  doi: 10.1042/BJ20071551
– volume: 26
  start-page: 2276
  year: 2021
  ident: 10.1016/j.bbagen.2024.130726_bb0075
  article-title: Biocide use in the antimicrobial era: a review
  publication-title: Molecules
  doi: 10.3390/molecules26082276
– ident: 10.1016/j.bbagen.2024.130726_bb0085
– volume: 51
  start-page: 7046
  year: 2012
  ident: 10.1016/j.bbagen.2024.130726_bb0040
  article-title: Probing the peripheral site of human butyrylcholinesterase
  publication-title: Biochemistry
  doi: 10.1021/bi300955k
– volume: 15
  start-page: 4835
  year: 1996
  ident: 10.1016/j.bbagen.2024.130726_bb0130
  article-title: The structure-function relationships in drosophila neurotactin show that cholinesterasic domains may have adhesive properties
  publication-title: EMBO J.
  doi: 10.1002/j.1460-2075.1996.tb00864.x
– start-page: 22
  year: 2017
  ident: 10.1016/j.bbagen.2024.130726_bb0210
  article-title: Comparison of the binding of reversible inhibitors to human butyrylcholinesterase and acetylcholinesterase: a crystallographic, kinetic and calorimetric study
  publication-title: Molecules
– volume: 7
  start-page: 88
  year: 1961
  ident: 10.1016/j.bbagen.2024.130726_bb0115
  article-title: A new and rapid colorimetric determination of acetylcholinesterase activity
  publication-title: Biochem. Pharmacol.
  doi: 10.1016/0006-2952(61)90145-9
– volume: 28
  start-page: 304
  year: 2000
  ident: 10.1016/j.bbagen.2024.130726_bb0150
  article-title: The ENZYME database in 2000
  publication-title: Nucleic Acids Res.
  doi: 10.1093/nar/28.1.304
– start-page: 25
  year: 2020
  ident: 10.1016/j.bbagen.2024.130726_bb0180
  article-title: A second look at the crystal structures of drosophila melanogaster acetylcholinesterase in complex with tacrine derivatives provides insights concerning catalytic intermediates and the design of specific insecticides
  publication-title: Molecules
– start-page: 5
  year: 2013
  ident: 10.1016/j.bbagen.2024.130726_bb0200
  article-title: MOLE 2.0: advanced approach for analysis of biomacromolecular channels
  publication-title: J. Chemother.
– volume: 122
  start-page: 1961
  year: 2001
  ident: 10.1016/j.bbagen.2024.130726_bb0005
  article-title: Acetylcholinesterase in Alzheimer’s disease
  publication-title: Mech. Ageing Dev.
  doi: 10.1016/S0047-6374(01)00309-8
– volume: 23
  start-page: 506
  year: 2007
  ident: 10.1016/j.bbagen.2024.130726_bb0120
  article-title: Highly sensitive detection of organophosphorus insecticides using magnetic microbeads and genetically engineered acetylcholinesterase
  publication-title: Biosens. Bioelectron.
  doi: 10.1016/j.bios.2007.06.022
– volume: 26
  start-page: 889
  year: 2010
  ident: 10.1016/j.bbagen.2024.130726_bb0190
  article-title: How significant is a protein structure similarity with TM-score = 0.5?
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btq066
– volume: 92
  start-page: 121
  year: 2002
  ident: 10.1016/j.bbagen.2024.130726_bb0070
  article-title: Introduction of biocides into clinical practice and the impact on antibiotic-resistant bacteria
  publication-title: J. Appl. Microbiol.
  doi: 10.1046/j.1365-2672.92.5s1.12.x
– volume: 83
  start-page: 336
  year: 2019
  ident: 10.1016/j.bbagen.2024.130726_bb0110
  article-title: Design, synthesis and bioevaluation of tricyclic fused ring system as dual binding site acetylcholinesterase inhibitors
  publication-title: Bioorg. Chem.
  doi: 10.1016/j.bioorg.2018.10.035
– year: 2022
  ident: 10.1016/j.bbagen.2024.130726_bb0165
– volume: 22
  start-page: 3099
  year: 1973
  ident: 10.1016/j.bbagen.2024.130726_bb0175
  article-title: Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction
  publication-title: Biochem. Pharmacol.
  doi: 10.1016/0006-2952(73)90196-2
– start-page: 29
  year: 2012
  ident: 10.1016/j.bbagen.2024.130726_bb0170
  article-title: 4 - enzymes and energetics
– volume: 150
  year: 2021
  ident: 10.1016/j.bbagen.2024.130726_bb0095
  article-title: Skin irritation and inhalation toxicity of biocides evaluated with reconstructed human epidermis and airway models
  publication-title: Food Chem. Toxicol.
  doi: 10.1016/j.fct.2021.112064
– volume: 8
  start-page: 127
  year: 1995
  ident: 10.1016/j.bbagen.2024.130726_bb0205
  article-title: LIGPLOT: a program to generate schematic diagrams of protein-ligand interactions
  publication-title: Protein Eng.
  doi: 10.1093/protein/8.2.127
– volume: 49
  year: 2022
  ident: 10.1016/j.bbagen.2024.130726_bb0080
  article-title: Assessing the risk of resistance to cationic biocides incorporating realism-based and biophysical approaches
  publication-title: J. Ind. Microbiol. Biotechnol.
  doi: 10.1093/jimb/kuab074
– volume: 52
  start-page: 2691
  year: 2022
  ident: 10.1016/j.bbagen.2024.130726_bb0100
  article-title: Benzalkonium chloride: a systematic review of its environmental entry through wastewater treatment, potential impact, and mitigation strategies
  publication-title: Crit. Rev. Environ. Sci. Technol.
  doi: 10.1080/10643389.2021.1889284
– volume: 36
  start-page: 426
  year: 1974
  ident: 10.1016/j.bbagen.2024.130726_bb0020
  article-title: The biology of cholinesterases
  publication-title: Front. Biol.
– volume: 30
  start-page: 2785
  year: 2009
  ident: 10.1016/j.bbagen.2024.130726_bb0160
  article-title: AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility
  publication-title: J. Comput. Chem.
  doi: 10.1002/jcc.21256
– ident: 10.1016/j.bbagen.2024.130726_bb0090
– volume: 272
  start-page: 33045
  year: 1997
  ident: 10.1016/j.bbagen.2024.130726_bb0135
  article-title: Cloning and expression of acetylcholinesterase from electrophorus: splicing pattern of the 3′ exons in vivo and in transfected mammalian cells
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.272.52.33045
– volume: 278
  start-page: 41141
  year: 2003
  ident: 10.1016/j.bbagen.2024.130726_bb0195
  article-title: Crystal structure of human butyrylcholinesterase and of its complexes with substrate and products
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M210241200
– volume: 20
  start-page: 1479
  year: 2019
  ident: 10.1016/j.bbagen.2024.130726_bb0010
  article-title: Cholinesterase inhibitors as Alzheimer’s therapeutics (review)
  publication-title: Mol. Med. Rep.
– volume: 276
  start-page: 2292
  year: 2009
  ident: 10.1016/j.bbagen.2024.130726_bb0050
  article-title: Kinetics of inhibition of acetylcholinesterase in the presence of acetonitrile
  publication-title: FEBS J.
  doi: 10.1111/j.1742-4658.2009.06957.x
– volume: 132
  start-page: 18292
  year: 2010
  ident: 10.1016/j.bbagen.2024.130726_bb0105
  article-title: Conformational remodeling of femtomolar inhibitor-acetylcholinesterase complexes in the crystalline state
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja106820e
– start-page: 4
  year: 2012
  ident: 10.1016/j.bbagen.2024.130726_bb0125
  article-title: Avogadro: an advanced semantic chemical editor, visualization, and analysis platform
  publication-title: Aust. J. Chem.
– volume: 148
  start-page: 34
  year: 2015
  ident: 10.1016/j.bbagen.2024.130726_bb0030
  article-title: Review of human butyrylcholinesterase structure, function, genetic variants, history of use in the clinic, and potential therapeutic uses
  publication-title: Pharmacol. Ther.
  doi: 10.1016/j.pharmthera.2014.11.011
– volume: 39
  start-page: 7753
  year: 2000
  ident: 10.1016/j.bbagen.2024.130726_bb0055
  article-title: Acetylthiocholine binds to Asp74 at the peripheral site of human acetylcholinesterase as the first step in the catalytic pathway
  publication-title: Biochemistry
  doi: 10.1021/bi000210o
– volume: 1
  start-page: 307
  year: 2005
  ident: 10.1016/j.bbagen.2024.130726_bb0065
  article-title: Antimicrobial biocides in the healthcare environment: efficacy, usage, policies, and perceived problems
  publication-title: Ther. Clin. Risk Manag.
– start-page: 11
  year: 2021
  ident: 10.1016/j.bbagen.2024.130726_bb0060
  article-title: Assessment of four organophosphorus pesticides as inhibitors of human acetylcholinesterase and butyrylcholinesterase
  publication-title: Sci. Rep.
– year: 2023
  ident: 10.1016/j.bbagen.2024.130726_bb0015
– volume: 253
  start-page: 872
  year: 1991
  ident: 10.1016/j.bbagen.2024.130726_bb0035
  article-title: Structure of acetylcholinesterase from torpedo californica: a prototypic acetylcholine-binding protein
  publication-title: Science
  doi: 10.1126/science.1678899
– volume: 31
  start-page: 455
  year: 2010
  ident: 10.1016/j.bbagen.2024.130726_bb0155
  article-title: AutoDock vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
  publication-title: J. Comput. Chem.
  doi: 10.1002/jcc.21334
– volume: 329
  start-page: 329
  year: 1998
  ident: 10.1016/j.bbagen.2024.130726_bb0045
  article-title: Two invertebrate acetylcholinesterases show activation followed by inhibition with substrate concentration
  publication-title: Biochem. J.
  doi: 10.1042/bj3290329
– volume: 57
  start-page: 702
  year: 2004
  ident: 10.1016/j.bbagen.2024.130726_bb0185
  article-title: Scoring function for automated assessment of protein structure template quality
  publication-title: Proteins
  doi: 10.1002/prot.20264
SSID ssj0000595
ssj0016425
Score 2.464262
Snippet Disinfectant biocides are chemicals that are heavily used for disinfection purposes in households, hospitals, and agrifood industry. The most common type of...
SourceID hal
proquest
pubmed
crossref
elsevier
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 130726
SubjectTerms Acetylcholinesterase - metabolism
Animals
Benzalkonium Compounds - chemistry
Benzalkonium Compounds - pharmacology
Biochemistry, Molecular Biology
Biocides
Butyrylcholinesterase - chemistry
Butyrylcholinesterase - metabolism
Cattle
Cholinesterase Inhibitors - chemistry
Cholinesterase Inhibitors - pharmacology
Cholinesterases
Disinfectants - pharmacology
Drosophila melanogaster - drug effects
Drosophila melanogaster - enzymology
Electrophorus
Enzyme kinetics
Erythrocytes - drug effects
Erythrocytes - enzymology
Horses
Life Sciences
Molecular docking
Molecular Docking Simulation
Quaternary Ammonium Compounds - chemistry
Quaternary Ammonium Compounds - pharmacology
Title Evaluating cholinesterases inhibition by BAC and DDAC biocides: A combined experimental and theoretical approach
URI https://dx.doi.org/10.1016/j.bbagen.2024.130726
https://www.ncbi.nlm.nih.gov/pubmed/39433227
https://www.proquest.com/docview/3119193720
https://insa-toulouse.hal.science/hal-04757302
Volume 1868
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVESC
  databaseName: Baden-Württemberg Complete Freedom Collection (Elsevier)
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0016425
  issn: 0304-4165
  databaseCode: GBLVA
  dateStart: 20110101
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: Baden-Württemberg Complete Freedom Collection (Elsevier)
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000595
  issn: 0304-4165
  databaseCode: GBLVA
  dateStart: 20110101
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: Elsevier SD Complete Freedom Collection [SCCMFC]
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0016425
  issn: 0304-4165
  databaseCode: ACRLP
  dateStart: 20241001
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: Elsevier SD Complete Freedom Collection [SCCMFC]
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000595
  issn: 0304-4165
  databaseCode: ACRLP
  dateStart: 19950118
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: ScienceDirect Freedom Collection 2013
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0016425
  issn: 0304-4165
  databaseCode: .~1
  dateStart: 19950101
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: ScienceDirect Freedom Collection 2013
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000595
  issn: 0304-4165
  databaseCode: .~1
  dateStart: 19950101
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: ScienceDirect Freedom Collection Journals
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0016425
  issn: 0304-4165
  databaseCode: AIKHN
  dateStart: 20240601
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVESC
  databaseName: ScienceDirect Freedom Collection Journals
  customDbUrl:
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000595
  issn: 0304-4165
  databaseCode: AIKHN
  dateStart: 19950118
  isFulltext: true
  titleUrlDefault: https://www.sciencedirect.com
  providerName: Elsevier
– providerCode: PRVLSH
  databaseName: Elsevier Journals
  customDbUrl:
  mediaType: online
  eissn: 1872-8006
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0000595
  issn: 0304-4165
  databaseCode: AKRWK
  dateStart: 19640113
  isFulltext: true
  providerName: Library Specific Holdings
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Zb9QwEB6VVgheEC3XclRuxWvYTXyteQtpqy1UVVWo1DfLV2gQSlfsFqkv_HY8cbIUCVSpTznkHPI3GY_jb74BeEuFrym1NLNT5zNGQ55ZI3zmjRLB8KCk71i-x2J2xj6e8_M1qIZcGKRV9r4_-fTOW_dnxn1vjudNM_6Mi3oxnODIgsyFwoxyVP-KNv3u1x-aRwwfeFpJYBm2HtLnOo6XtfGjRRXUgmFZZIkSC_8enu5dIE_yf0FoNxgdPIZHfRRJyvSim7AW2i24n-pKXm_Bg2oo4_YE5vu9nnf7laCrQ5o7Zh0vwoI07UVjO84WsdfkQ1kR03qytxd3bBNR82HxnpQk9k2cPwdPbpYD6JreSIMkgzr5Uzg72P9SzbK-zELmGCuWEaBpXUyFd1OTc2tczSehcMoE6oXMTT5xJs-D8yZObgRTrrAo4i69l1xRLh19BuvtZRteADExHKgLJNooy2x0hoxabgT-D609U3YEdOhd7XoNciyF8V0PZLNvOmGiEROdMBlBtrpqnjQ4bmkvB-D0X7ak4zBxy5W7EefVQ1B6e1YeaTw3YZJHb1j8zEewM5iBjljiAotpw-XVQlNUy1NY92cEz5N9rO5FFSrFFfLlnV_uFTzEo8SleQ3ryx9X4U2MiJZ2uzP5bdgoq9OjE9wefpod_wbF_gnu
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LT9wwEB7BogouFaWvbUvrVr1Gu4lf697SBRTKdi8FiZvlVyBVFVbsUol_X08eC5WokHqLHDuxPM54HH_zfQCfqfAlpZYmduJ8wmhIE2uET7xRIhgelPQNyncuijP27Zyfb8C0z4VBWGXn-1uf3njrrmTUjeZoUVWjH3ioF8MJjijIVCi5CVuMR588gK38-KSY3zlk3oivYP0EG_QZdA3My9r43SIRasZQGVkiy8LDK9TmJUIl_xWHNuvR0S487QJJkrd9fQYbod6DJ6205O0ebE97JbfnsDjsKL3rC4LeDpHumHi8DEtS1ZeVbWBbxN6Sr_mUmNqTg4N4YatoOB-WX0hO4vDELXTw5L4iQFP1XiYk6QnKX8DZ0eHptEg6pYXEMZatoo0mZTYR3k1Myq1xJR-HzCkTqBcyNenYmTQNzpu4vxFMucwij7v0XnJFuXT0JQzqqzq8BmJiRFBmiLVRltnoDxm13Aj8JVp6puwQaD-62nU05KiG8Uv3eLOfurWJRpvo1iZDSNatFi0NxyP1ZW84_dd00nGleKTlp2jn9UuQfbvIZxrLxkzy6BCz3-kQPvbTQEdb4hmLqcPVzVJTJMxTKP0zhFft_Fg_iyoki8vkm__u3AfYLk6_z_TseH7yFnbwTguteQeD1fVN2I8B0sq-7z6AP3kvCwQ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Evaluating+cholinesterases+inhibition+by+BAC+and+DDAC+biocides%3A+A+combined+experimental+and+theoretical+approach&rft.jtitle=Biochimica+et+biophysica+acta.+General+subjects&rft.au=Mouawad%2C+Lynn&rft.au=Esque%2C+Jeremy&rft.au=Andr%C3%A9%2C+Isabelle&rft.au=Istamboulie%2C+Georges&rft.date=2024-12-01&rft.issn=1872-8006&rft.eissn=1872-8006&rft.volume=1868&rft.issue=12&rft.spage=130726&rft_id=info:doi/10.1016%2Fj.bbagen.2024.130726&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0304-4165&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0304-4165&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0304-4165&client=summon