Page last updated: 2024-09-05

lapatinib and vorinostat

lapatinib has been researched along with vorinostat in 13 studies

Compound Research Comparison

Studies
(lapatinib)
Trials
(lapatinib)
Recent Studies (post-2010)
(lapatinib)
Studies
(vorinostat)
Trials
(vorinostat)
Recent Studies (post-2010) (vorinostat)
1,9193051,4422,5291811,840

Protein Interaction Comparison

ProteinTaxonomylapatinib (IC50)vorinostat (IC50)
Chain A, Histone deacetylase-like amidohydrolaseAlcaligenaceae bacterium FB1880.95
Chain A, Histone deacetylase-like amidohydrolaseAlcaligenaceae bacterium FB1880.95
Histone deacetylase 8Schistosoma mansoni1.3147
Histone deacetylase Rattus norvegicus (Norway rat)0.165
Gli1Mus musculus (house mouse)2.23
nuclear receptor subfamily 0 group B member 1Homo sapiens (human)0.7472
cystic fibrosis transmembrane conductance regulatorHomo sapiens (human)1.55
Histone deacetylase 1Mus musculus (house mouse)0.1121
Histone deacetylase 3Homo sapiens (human)0.3382
Bromodomain-containing protein 4Homo sapiens (human)0.2644
Nuclear receptor corepressor 1Homo sapiens (human)0.0382
Epidermal growth factor receptorHomo sapiens (human)0.456
Tubulin alpha-1A chainSus scrofa (pig)1.5
Tubulin beta chainSus scrofa (pig)1.5
AlbuminHomo sapiens (human)0.1072
Leukotriene A-4 hydrolaseHomo sapiens (human)4.66
Cytochrome P450 2C8Homo sapiens (human)0.0903
Cytochrome P450 2D6Homo sapiens (human)0.011
Cytochrome P450 2C9 Homo sapiens (human)0.24
Androgen receptorRattus norvegicus (Norway rat)0.1582
Alpha-1B adrenergic receptorRattus norvegicus (Norway rat)2.8
5-hydroxytryptamine receptor 1ARattus norvegicus (Norway rat)0.053
Cannabinoid receptor 1Rattus norvegicus (Norway rat)0.116
Alpha-1D adrenergic receptorRattus norvegicus (Norway rat)2.8
Leukotriene A-4 hydrolaseMus musculus (house mouse)6.15
Cytochrome P450 2C19Homo sapiens (human)0.042
Prostaglandin G/H synthase 2Homo sapiens (human)0.13
Delta-type opioid receptorHomo sapiens (human)7.2
Alpha-1A adrenergic receptorRattus norvegicus (Norway rat)2.8
Histamine H2 receptorCavia porcellus (domestic guinea pig)7.2
Histone deacetylase 4Homo sapiens (human)0.6096
Glutamate receptor ionotropic, NMDA 2BRattus norvegicus (Norway rat)0.086
Potassium voltage-gated channel subfamily H member 2Homo sapiens (human)0.322
Platelet-activating factor acetylhydrolaseHomo sapiens (human)0.1
Histone deacetylase 1Homo sapiens (human)0.2701
Histone deacetylase 1Rattus norvegicus (Norway rat)0.165
Histone deacetylase Rattus norvegicus (Norway rat)0.165
Sigma non-opioid intracellular receptor 1Cavia porcellus (domestic guinea pig)0.07
ReninMacaca fascicularis (crab-eating macaque)0.067
Histone deacetylase 3Rattus norvegicus (Norway rat)0.165
Histone deacetylase-like amidohydrolaseAlcaligenaceae bacterium FB1881
Histone deacetylase Plasmodium falciparum 3D70.1
Histone deacetylase 7Homo sapiens (human)0.6115
Histone deacetylase 2Homo sapiens (human)0.3746
HD2 type histone deacetylase HDA106 Zea mays0.2227
Polyamine deacetylase HDAC10Homo sapiens (human)0.4211
Histone deacetylase 11 Homo sapiens (human)0.5235
Carboxypeptidase B2Homo sapiens (human)0.362
Histone deacetylase 7Rattus norvegicus (Norway rat)0.165
Histone deacetylase 6 Rattus norvegicus (Norway rat)0.165
Histone deacetylase 4Rattus norvegicus (Norway rat)0.165
Histone deacetylase 8Homo sapiens (human)0.9141
Histone deacetylase 6Homo sapiens (human)0.2634
Histone deacetylase 9Homo sapiens (human)0.5614
Histone deacetylase 5Homo sapiens (human)0.5926
Histone deacetylase Plasmodium falciparum (malaria parasite P. falciparum)0.0945
Nuclear receptor corepressor 2Homo sapiens (human)0.0905
Histone deacetylase 6Mus musculus (house mouse)0.3742
Histone deacetylase Zea mays0.029

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's11 (84.62)24.3611
2020's2 (15.38)2.80

Authors

AuthorsStudies
Bao, R; Cai, X; Forrester, J; Lai, CJ; Qian, C; Qu, H; Wang, J; Yin, L; Zhai, HX1
Baer, T; Beckers, T; Ciossek, T; Eichhorn, E; Mahboobi, S; Maier, T; Pongratz, H; Sellmer, A; Winkler, M1
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ1
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K1
Chen, S; Chen, YZ; Ding, C; Hu, G; Jiang, Y; Li, L; Tan, C; Zhang, C; Zhang, W1
Jadhav, A; Kerns, E; Nguyen, K; Shah, P; Sun, H; Xu, X; Yan, Z; Yu, KR1
Ajenjo, N; Albarrán, MI; Bischoff, JR; Blanco-Aparicio, C; Cebriá, A; Cebrián, D; Cuadrado-Urbano, M; García, AB; García-Serelde, B; Gómez de la Oliva, CA; Gómez-Casero, E; González Cantalapiedra, E; Hernández, AI; Klett, J; Martínez-González, S; Oyarzabal, J; Pastor, J; Rabal, O; Rodríguez-Arístegui, S; Varela, C1
Kabir, M; Kerns, E; Nguyen, K; Shah, P; Sun, H; Wang, Y; Xu, X; Yu, KR1
Liu, Y; Xu, Z; Zhao, SJ1
Abuo-Rahma, GEA; Badr, M; Bass, AKA; El-Zoghbi, MS; Mohamed, MFA; Nageeb, EM1
Kabir, M; Kerns, E; Neyra, J; Nguyen, K; Nguyễn, ÐT; Shah, P; Siramshetty, VB; Southall, N; Williams, J; Xu, X; Yu, KR1
Beck, JF; Kurtze, I; Sonnemann, J1
Geng, P; Lin, F; Wang, S; Wu, C; Zhang, Q; Zhang, X; Zhou, Y; Zou, H1

Reviews

3 review(s) available for lapatinib and vorinostat

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
1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships.
    European journal of medicinal chemistry, 2019, Dec-01, Volume: 183

    Topics: Antineoplastic Agents; Humans; Molecular Structure; Neoplasms; Structure-Activity Relationship; Triazoles

2019
Comprehensive review for anticancer hybridized multitargeting HDAC inhibitors.
    European journal of medicinal chemistry, 2021, Jan-01, Volume: 209

    Topics: Androgen Antagonists; Animals; Antineoplastic Agents; Benzimidazoles; Cyclic Nucleotide Phosphodiesterases, Type 5; Daunorubicin; Doxorubicin; fms-Like Tyrosine Kinase 3; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Molecular Targeted Therapy; Morpholines; Nicotinamide Phosphoribosyltransferase; Nitric Oxide; Pyrimidines; Quinazolines; Structure-Activity Relationship; Transcription Factors

2021

Other Studies

10 other study(ies) available for lapatinib and vorinostat

ArticleYear
Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer.
    Journal of medicinal chemistry, 2010, Mar-11, Volume: 53, Issue:5

    Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Growth Processes; Enzyme Inhibitors; ErbB Receptors; Female; HeLa Cells; Hep G2 Cells; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Mice; Mice, Nude; Neoplasms; Quinazolines; Receptor, ErbB-2; Structure-Activity Relationship; Xenograft Model Antitumor Assays

2010
Novel chimeric histone deacetylase inhibitors: a series of lapatinib hybrides as potent inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), and histone deacetylase activity.
    Journal of medicinal chemistry, 2010, Dec-23, Volume: 53, Issue:24

    Topics: Acetylation; Acrylamides; Antineoplastic Agents; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Screening Assays, Antitumor; ErbB Receptors; Histone Deacetylase Inhibitors; Histones; Humans; Isoenzymes; Lapatinib; Quinazolines; Receptor, ErbB-2; Stereoisomerism; Structure-Activity Relationship

2010
Identification of potent Yes1 kinase inhibitors using a library screening approach.
    Bioorganic & medicinal chemistry letters, 2013, Aug-01, Volume: 23, Issue:15

    Topics: Binding Sites; Cell Line; Cell Survival; Drug Design; Humans; Hydrogen Bonding; Molecular Docking Simulation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-yes; Small Molecule Libraries; Structure-Activity Relationship

2013
Synthesis and investigation of novel 6-(1,2,3-triazol-4-yl)-4-aminoquinazolin derivatives possessing hydroxamic acid moiety for cancer therapy.
    Bioorganic & medicinal chemistry, 2017, 01-01, Volume: 25, Issue:1

    Topics: Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Drug Design; Drug Screening Assays, Antitumor; Green Fluorescent Proteins; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Molecular Docking Simulation; Quinazolines; Receptor, ErbB-2; Structure-Activity Relationship; Triazoles

2017
Highly predictive and interpretable models for PAMPA permeability.
    Bioorganic & medicinal chemistry, 2017, 02-01, Volume: 25, Issue:3

    Topics: Artificial Intelligence; Caco-2 Cells; Cell Membrane Permeability; Humans; Models, Biological; Organic Chemicals; Regression Analysis; Support Vector Machine

2017
Discovery of novel triazolo[4,3-b]pyridazin-3-yl-quinoline derivatives as PIM inhibitors.
    European journal of medicinal chemistry, 2019, Apr-15, Volume: 168

    Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Discovery; Drug Screening Assays, Antitumor; Humans; Molecular Structure; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-pim-1; Pyridazines; Quinolines; Structure-Activity Relationship; Triazoles

2019
Predictive models of aqueous solubility of organic compounds built on A large dataset of high integrity.
    Bioorganic & medicinal chemistry, 2019, 07-15, Volume: 27, Issue:14

    Topics: Drug Discovery; Organic Chemicals; Pharmaceutical Preparations; Solubility

2019
Retrospective assessment of rat liver microsomal stability at NCATS: data and QSAR models.
    Scientific reports, 2020, 11-26, Volume: 10, Issue:1

    Topics: Animals; Computer Simulation; Databases, Factual; Drug Discovery; High-Throughput Screening Assays; Liver; Machine Learning; Male; Microsomes, Liver; National Center for Advancing Translational Sciences (U.S.); Pharmaceutical Preparations; Quantitative Structure-Activity Relationship; Rats; Rats, Sprague-Dawley; Retrospective Studies; United States

2020
KRAS-mutated non-small cell lung cancer cells are responsive to either co-treatment with erlotinib or gefitinib and histone deacetylase inhibitors or single treatment with lapatinib.
    Oncology reports, 2011, Volume: 25, Issue:4

    Topics: Adenocarcinoma; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Carcinoma, Non-Small-Cell Lung; Cell Proliferation; Erlotinib Hydrochloride; Flow Cytometry; Gefitinib; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Lapatinib; Lung Neoplasms; Membrane Potential, Mitochondrial; Mutation; Proto-Oncogene Proteins; Proto-Oncogene Proteins p21(ras); Quinazolines; ras Proteins; Tumor Cells, Cultured; Vorinostat

2011
Pharmacokinetic interaction study combining lapatinib with vorinostat in rats.
    Pharmacology, 2015, Volume: 95, Issue:3-4

    Topics: Animals; Antineoplastic Agents; Drug Interactions; Hydroxamic Acids; Lapatinib; Male; Quinazolines; Rats, Sprague-Dawley; Vorinostat

2015