Page last updated: 2024-09-04

levofloxacin and vinblastine

levofloxacin has been researched along with vinblastine in 8 studies

Compound Research Comparison

Studies
(levofloxacin)
Trials
(levofloxacin)
Recent Studies (post-2010)
(levofloxacin)
Studies
(vinblastine)
Trials
(vinblastine)
Recent Studies (post-2010) (vinblastine)
4,3465812,209243077

Protein Interaction Comparison

ProteinTaxonomylevofloxacin (IC50)vinblastine (IC50)
Tubulin alpha-1A chainSus scrofa (pig)1.1
Tubulin beta chainSus scrofa (pig)1.1
Tubulin beta-4A chainHomo sapiens (human)0.8233
CholinesteraseHomo sapiens (human)2.1
ATP-dependent translocase ABCB1Mus musculus (house mouse)8
Tubulin beta chainHomo sapiens (human)0.8233
ATP-dependent translocase ABCB1Homo sapiens (human)6
Tubulin alpha-3C chainHomo sapiens (human)0.8233
Cytochrome P450 2D6Homo sapiens (human)0.6
Polyunsaturated fatty acid lipoxygenase ALOX15Oryctolagus cuniculus (rabbit)5.037
Alpha-2B adrenergic receptorRattus norvegicus (Norway rat)2.1
Alpha-2C adrenergic receptorRattus norvegicus (Norway rat)2.1
Alpha-2A adrenergic receptorRattus norvegicus (Norway rat)2.1
Thromboxane-A synthase Homo sapiens (human)1.87
Tubulin alpha-1B chainHomo sapiens (human)0.8233
Tubulin alpha-4A chainHomo sapiens (human)0.8233
Tubulin beta-4B chainHomo sapiens (human)0.8233
Tubulin beta-3 chainHomo sapiens (human)0.8233
Tubulin beta-2A chainHomo sapiens (human)0.8233
Beta-tubulin Leishmania donovani1
Tubulin beta-8 chainHomo sapiens (human)0.8233
Tubulin beta-2B chainBos taurus (cattle)0.65
Tubulin alpha-3E chainHomo sapiens (human)0.8233
Tubulin alpha-1A chainHomo sapiens (human)0.8233
Similar to alpha-tubulin isoform 1 Bos taurus (cattle)0.65
Similar to alpha-tubulin isoform 1 Bos taurus (cattle)0.65
Tubulin alpha-1C chainHomo sapiens (human)0.8233
Tubulin beta-6 chainHomo sapiens (human)0.8233
Tubulin beta-2B chainHomo sapiens (human)0.8233
Tubulin beta-1 chainHomo sapiens (human)0.8233

Research

Studies (8)

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

Authors

AuthorsStudies
Gibbons, S; Kaatz, GW; Zloh, M1
Lombardo, F; Obach, RS; Waters, NJ1
Chupka, J; El-Kattan, A; Feng, B; Miller, HR; Obach, RS; Troutman, MD; Varma, MV1
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
Chang, G; El-Kattan, A; Miller, HR; Obach, RS; Rotter, C; Steyn, SJ; Troutman, MD; Varma, MV1
Benet, LZ; Brouwer, KL; Chu, X; Dahlin, A; Evers, R; Fischer, V; Giacomini, KM; Hillgren, KM; Hoffmaster, KA; Huang, SM; Ishikawa, T; Keppler, D; Kim, RB; Lee, CA; Niemi, M; Polli, JW; Sugiyama, Y; Swaan, PW; Tweedie, DJ; Ware, JA; Wright, SH; Yee, SW; Zamek-Gliszczynski, MJ; Zhang, L1
Glen, RC; Lowe, R; Mitchell, JB1

Reviews

1 review(s) available for levofloxacin and vinblastine

ArticleYear
Membrane transporters in drug development.
    Nature reviews. Drug discovery, 2010, Volume: 9, Issue:3

    Topics: Animals; Computer Simulation; Decision Trees; Drug Approval; Drug Discovery; Drug Evaluation, Preclinical; Drug Interactions; Humans; Membrane Transport Proteins; Mice; Mice, Knockout; Prescription Drugs

2010

Other Studies

7 other study(ies) available for levofloxacin and vinblastine

ArticleYear
Inhibitors of multidrug resistance (MDR) have affinity for MDR substrates.
    Bioorganic & medicinal chemistry letters, 2004, Feb-23, Volume: 14, Issue:4

    Topics: Anti-Bacterial Agents; Antineoplastic Agents; ATP Binding Cassette Transporter, Subfamily B; Biological Transport; Cell Membrane; Drug Resistance, Microbial; Drug Resistance, Multiple; Ligands; Models, Molecular

2004
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
    Drug metabolism and disposition: the biological fate of chemicals, 2008, Volume: 36, Issue:7

    Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding

2008
Physicochemical determinants of human renal clearance.
    Journal of medicinal chemistry, 2009, Aug-13, Volume: 52, Issue:15

    Topics: Humans; Hydrogen Bonding; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Kidney; Metabolic Clearance Rate; Molecular Weight

2009
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
Physicochemical space for optimum oral bioavailability: contribution of human intestinal absorption and first-pass elimination.
    Journal of medicinal chemistry, 2010, Feb-11, Volume: 53, Issue:3

    Topics: Administration, Oral; Biological Availability; Humans; Intestinal Absorption; Pharmaceutical Preparations

2010
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