Page last updated: 2024-09-02

quinone methide and tamoxifen

quinone methide has been researched along with tamoxifen in 8 studies

Compound Research Comparison

Studies
(quinone methide)
Trials
(quinone methide)
Recent Studies (post-2010)
(quinone methide)
Studies
(tamoxifen)
Trials
(tamoxifen)
Recent Studies (post-2010) (tamoxifen)
374023220,6302,2276,256

Protein Interaction Comparison

ProteinTaxonomyquinone methide (IC50)tamoxifen (IC50)
5-hydroxytryptamine receptor 4Cavia porcellus (domestic guinea pig)0.46
Serine/threonine-protein kinase D3Homo sapiens (human)1
Bile salt export pumpHomo sapiens (human)10
Epidermal growth factor receptorHomo sapiens (human)3.553
Estrogen receptorHomo sapiens (human)0.9266
Receptor tyrosine-protein kinase erbB-2Homo sapiens (human)2.949
Protein kinase C gamma typeHomo sapiens (human)1
Protein kinase C beta typeHomo sapiens (human)1
Tyrosine-protein kinase LckHomo sapiens (human)8.033
Tyrosine-protein kinase FynHomo sapiens (human)1.195
Progesterone receptorHomo sapiens (human)0.1288
Aldo-keto reductase family 1 member B1Rattus norvegicus (Norway rat)1.472
Muscarinic acetylcholine receptor M2Homo sapiens (human)7.793
Muscarinic acetylcholine receptor M4Homo sapiens (human)4.817
ATP-dependent translocase ABCB1Homo sapiens (human)6.4
Muscarinic acetylcholine receptor M5Homo sapiens (human)2.585
Alpha-2A adrenergic receptorHomo sapiens (human)1.935
Adenosine receptor A3Homo sapiens (human)3.701
Muscarinic acetylcholine receptor M1Homo sapiens (human)2.829
Steroid hormone receptor ERR1Homo sapiens (human)0.2
Angiotensin-converting enzymeOryctolagus cuniculus (rabbit)0.967
Beta-3 adrenergic receptorHomo sapiens (human)7.703
Alpha-1B adrenergic receptorRattus norvegicus (Norway rat)3.701
Protein kinase C alpha typeHomo sapiens (human)1
Alpha-2B adrenergic receptorHomo sapiens (human)3.518
Muscarinic acetylcholine receptor M3Homo sapiens (human)2.974
Substance-K receptorHomo sapiens (human)3.67
D(1A) dopamine receptorHomo sapiens (human)8.502
Prostaglandin G/H synthase 1Homo sapiens (human)4.391
Sodium-dependent noradrenaline transporter Homo sapiens (human)1.472
Thromboxane-A synthase Homo sapiens (human)0.916
Protein kinase C eta typeHomo sapiens (human)1
Histamine H2 receptorHomo sapiens (human)9.396
Alpha-1D adrenergic receptorHomo sapiens (human)4.982
5-hydroxytryptamine receptor 2AHomo sapiens (human)4.801
5-hydroxytryptamine receptor 2CHomo sapiens (human)0.46
Adenosine receptor A2aHomo sapiens (human)7.099
Sodium-dependent serotonin transporterHomo sapiens (human)2.334
D(3) dopamine receptorHomo sapiens (human)1.072
5-hydroxytryptamine receptor 2BHomo sapiens (human)2.084
Protein kinase C iota typeHomo sapiens (human)1
Alpha-1A adrenergic receptorRattus norvegicus (Norway rat)3.701
5-hydroxytryptamine receptor 6Homo sapiens (human)2.679
Estrogen-related receptor gammaHomo sapiens (human)0.0622
Sodium-dependent dopamine transporter Homo sapiens (human)1.841
Protein kinase C epsilon typeHomo sapiens (human)1
Protein kinase C theta typeHomo sapiens (human)1
Protein kinase C zeta typeHomo sapiens (human)1
Protein kinase C delta typeHomo sapiens (human)1
Potassium voltage-gated channel subfamily H member 2Homo sapiens (human)1.2759
Platelet-activating factor acetylhydrolaseHomo sapiens (human)0.904
3-beta-hydroxysteroid-Delta(8),Delta(7)-isomeraseHomo sapiens (human)0.012
Serine/threonine-protein kinase D1Homo sapiens (human)1
Nuclear receptor subfamily 3 group C member 3 Bos taurus (cattle)0.967
Estrogen receptor betaHomo sapiens (human)0.7809
Sigma non-opioid intracellular receptor 1Homo sapiens (human)0.021
7-dehydrocholesterol reductaseHomo sapiens (human)0.012

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (12.50)18.2507
2000's4 (50.00)29.6817
2010's3 (37.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Beland, FA; Marques, MM1
Bolton, JL; Fan, PW; Zhang, F1
Bolton, JL; Fan, PW1
Bolton, JL; van Breemen, RB; Yang, Y; Yao, D; Yu, L; Zhang, F1
Bolton, JL; Burdette, JE; Li, Y; Liu, X; Pisha, E; Tonetti, DA; Yao, D; Yao, J1
Amatore, C; Buriez, O; Frapart, YM; Hamels, D; Hillard, EA; Jaouen, G; Labbé, E; Mansuy, D; Messina, P; Top, S; Vessières, A1
D'Agostino, J; Hollenberg, PF; Sridar, C1
Bindoli, A; Citta, A; Folda, A; Jaouen, G; Lee, HZ; Leong, WK; Rigobello, MP; Salmain, M; Scalcon, V; Top, S; Vessières, A1

Other Studies

8 other study(ies) available for quinone methide and tamoxifen

ArticleYear
Identification of tamoxifen-DNA adducts formed by 4-hydroxytamoxifen quinone methide.
    Carcinogenesis, 1997, Volume: 18, Issue:10

    Topics: Animals; Chromatography, High Pressure Liquid; DNA Adducts; Indolequinones; Indoles; Quinones; Salmon; Spectrometry, Mass, Fast Atom Bombardment; Tamoxifen

1997
4-Hydroxylated metabolites of the antiestrogens tamoxifen and toremifene are metabolized to unusually stable quinone methides.
    Chemical research in toxicology, 2000, Volume: 13, Issue:1

    Topics: Animals; Antineoplastic Agents, Hormonal; Breast Neoplasms; Cytochrome P-450 Enzyme System; Estrogen Receptor Modulators; Female; Glutathione; Humans; Hydroxylation; Indolequinones; Indoles; Mass Spectrometry; Oxidation-Reduction; Quinones; Rats; Rats, Sprague-Dawley; Tamoxifen; Toremifene; Tumor Cells, Cultured

2000
Bioactivation of tamoxifen to metabolite E quinone methide: reaction with glutathione and DNA.
    Drug metabolism and disposition: the biological fate of chemicals, 2001, Volume: 29, Issue:6

    Topics: Antineoplastic Agents, Phytogenic; Biotransformation; DNA; DNA Adducts; Glutathione; Indolequinones; Indoles; Microsomes, Liver; Quinones; Spectrum Analysis; Tamoxifen

2001
Synthesis and reactivity of potential toxic metabolites of tamoxifen analogues: droloxifene and toremifene o-quinones.
    Chemical research in toxicology, 2001, Volume: 14, Issue:12

    Topics: Animals; Antineoplastic Agents; Benzoquinones; Breast Neoplasms; Cell Survival; Deoxyribonucleosides; DNA Adducts; Female; Glutathione; Indolequinones; Indoles; Microsomes, Liver; Quinones; Rats; Rats, Sprague-Dawley; Spectrometry, Mass, Electrospray Ionization; Tamoxifen; Toremifene; Tumor Cells, Cultured

2001
Antiestrogenic and DNA damaging effects induced by tamoxifen and toremifene metabolites.
    Chemical research in toxicology, 2003, Volume: 16, Issue:7

    Topics: Binding, Competitive; Breast Neoplasms; Catechols; Cell Line, Tumor; Cell Survival; Comet Assay; DNA Damage; Drug Screening Assays, Antitumor; Estradiol; Estrogen Receptor Modulators; Female; Humans; Indolequinones; Quinones; Receptors, Estrogen; Tamoxifen; Toremifene

2003
Deciphering the activation sequence of ferrociphenol anticancer drug candidates.
    Chemistry (Weinheim an der Bergstrasse, Germany), 2012, May-21, Volume: 18, Issue:21

    Topics: Antineoplastic Agents; Drug Screening Assays, Antitumor; Electron Spin Resonance Spectroscopy; Female; Ferrous Compounds; Humans; Indolequinones; Models, Molecular; Molecular Structure; Oxidation-Reduction; Tamoxifen

2012
Bioactivation of the cancer chemopreventive agent tamoxifen to quinone methides by cytochrome P4502B6 and identification of the modified residue on the apoprotein.
    Drug metabolism and disposition: the biological fate of chemicals, 2012, Volume: 40, Issue:12

    Topics: Anticarcinogenic Agents; Antineoplastic Agents, Hormonal; Apoproteins; Aryl Hydrocarbon Hydroxylases; Biotransformation; Cytochrome P-450 CYP2B6; Glutathione; Humans; Hydroxylation; Indolequinones; Microsomes, Liver; Oxidoreductases, N-Demethylating; Tamoxifen

2012
Osmocenyl-tamoxifen derivatives target the thioredoxin system leading to a redox imbalance in Jurkat cells.
    Journal of inorganic biochemistry, 2016, Volume: 160

    Topics: Antineoplastic Agents; Cell Death; Coordination Complexes; Ferrous Compounds; Gene Expression; Glutathione; Humans; Indolequinones; Jurkat Cells; Membrane Potential, Mitochondrial; Mitochondria; Organometallic Compounds; Osmium; Oxidation-Reduction; Oxidative Stress; Peroxiredoxin III; Reactive Oxygen Species; Tamoxifen; Thioredoxin Reductase 1; Thioredoxins

2016