Page last updated: 2024-09-05

atropine and sertraline

atropine has been researched along with sertraline in 7 studies

Compound Research Comparison

Studies
(atropine)
Trials
(atropine)
Recent Studies (post-2010)
(atropine)
Studies
(sertraline)
Trials
(sertraline)
Recent Studies (post-2010) (sertraline)
26,7111,2591,6973,4801,0281,329

Protein Interaction Comparison

ProteinTaxonomyatropine (IC50)sertraline (IC50)
5-hydroxytryptamine receptor 4Cavia porcellus (domestic guinea pig)1.083
Aldo-keto reductase family 1 member B1Rattus norvegicus (Norway rat)0.9848
Muscarinic acetylcholine receptor M2Homo sapiens (human)2.7675
Muscarinic acetylcholine receptor M4Homo sapiens (human)2.6309
Cytochrome P450 3A4Homo sapiens (human)0.8
Muscarinic acetylcholine receptor M5Homo sapiens (human)0.5073
Alpha-2A adrenergic receptorHomo sapiens (human)0.2888
Cytochrome P450 2D6Homo sapiens (human)1.4
Muscarinic acetylcholine receptor M1Homo sapiens (human)1.2882
Angiotensin-converting enzymeOryctolagus cuniculus (rabbit)8.3173
Alpha-2B adrenergic receptorHomo sapiens (human)0.1814
Alpha-2C adrenergic receptorHomo sapiens (human)4.477
DRattus norvegicus (Norway rat)0.26
D(3) dopamine receptorRattus norvegicus (Norway rat)0.26
Sodium-dependent noradrenaline transporter Homo sapiens (human)0.8783
Sodium-dependent dopamine transporterRattus norvegicus (Norway rat)0.825
D(1B) dopamine receptorRattus norvegicus (Norway rat)0.26
5-hydroxytryptamine receptor 2AHomo sapiens (human)2.7409
5-hydroxytryptamine receptor 2CHomo sapiens (human)1.083
D(4) dopamine receptorRattus norvegicus (Norway rat)0.26
3-oxo-5-alpha-steroid 4-dehydrogenase 2Homo sapiens (human)0.8
Sodium-dependent serotonin transporterHomo sapiens (human)0.0016
Sodium-dependent serotonin transporterRattus norvegicus (Norway rat)0.1743
Melanocortin receptor 5Homo sapiens (human)4.598
Cytochrome P450 2C19Homo sapiens (human)0.655
5-hydroxytryptamine receptor 2BHomo sapiens (human)3.3935
D(2) dopamine receptorRattus norvegicus (Norway rat)0.26
Sodium-dependent dopamine transporter Homo sapiens (human)0.2175
Potassium voltage-gated channel subfamily H member 2Homo sapiens (human)8.3173
Nuclear receptor subfamily 3 group C member 3 Bos taurus (cattle)8.3173
Sigma non-opioid intracellular receptor 1Homo sapiens (human)0.0697
TransporterRattus norvegicus (Norway rat)0.26

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (28.57)29.6817
2010's5 (71.43)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bleich, S; Gulbins, E; Kornhuber, J; Reichel, M; Terfloth, L; Tripal, P; Wiltfang, J1
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A1
Choi, SS; Contrera, JF; Hastings, KL; Kruhlak, NL; Sancilio, LF; Weaver, JL; Willard, JM1
Glen, RC; Lowe, R; Mitchell, JB1
Chen, M; Fang, H; Liu, Z; Shi, Q; Tong, W; Vijay, V1
Cantin, LD; Chen, H; Kenna, JG; Noeske, T; Stahl, S; Walker, CL; Warner, DJ1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1

Reviews

1 review(s) available for atropine and sertraline

ArticleYear
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
    Drug discovery today, 2016, Volume: 21, Issue:4

    Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk

2016

Other Studies

6 other study(ies) available for atropine and sertraline

ArticleYear
Identification of new functional inhibitors of acid sphingomyelinase using a structure-property-activity relation model.
    Journal of medicinal chemistry, 2008, Jan-24, Volume: 51, Issue:2

    Topics: Algorithms; Animals; Cell Line; Cell Line, Tumor; Chemical Phenomena; Chemistry, Physical; Enzyme Inhibitors; Humans; Hydrogen-Ion Concentration; Molecular Conformation; Quantitative Structure-Activity Relationship; Rats; Sphingomyelin Phosphodiesterase

2008
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
    Chemical research in toxicology, 2010, Volume: 23, Issue:1

    Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship

2010
Development of a phospholipidosis database and predictive quantitative structure-activity relationship (QSAR) models.
    Toxicology mechanisms and methods, 2008, Volume: 18, Issue:2-3

    Topics:

2008
Predicting phospholipidosis using machine learning.
    Molecular pharmaceutics, 2010, Oct-04, Volume: 7, Issue:5

    Topics: Animals; Artificial Intelligence; Databases, Factual; Drug Discovery; Humans; Lipidoses; Models, Biological; Phospholipids; Support Vector Machine

2010
FDA-approved drug labeling for the study of drug-induced liver injury.
    Drug discovery today, 2011, Volume: 16, Issue:15-16

    Topics: Animals; Benchmarking; Biomarkers, Pharmacological; Chemical and Drug Induced Liver Injury; Drug Design; Drug Labeling; Drug-Related Side Effects and Adverse Reactions; Humans; Pharmaceutical Preparations; Reproducibility of Results; United States; United States Food and Drug Administration

2011
Mitigating the inhibition of human bile salt export pump by drugs: opportunities provided by physicochemical property modulation, in silico modeling, and structural modification.
    Drug metabolism and disposition: the biological fate of chemicals, 2012, Volume: 40, Issue:12

    Topics: Animals; ATP Binding Cassette Transporter, Subfamily B, Member 11; ATP-Binding Cassette Transporters; Bile Acids and Salts; Cell Line; Chemical and Drug Induced Liver Injury; Humans; Quantitative Structure-Activity Relationship

2012