Page last updated: 2024-09-05

ascididemin and rifampin

ascididemin has been researched along with rifampin in 2 studies

Compound Research Comparison

Studies
(ascididemin)
Trials
(ascididemin)
Recent Studies (post-2010)
(ascididemin)
Studies
(rifampin)
Trials
(rifampin)
Recent Studies (post-2010) (rifampin)
2301020,4681,4996,552

Protein Interaction Comparison

ProteinTaxonomyascididemin (IC50)rifampin (IC50)
Polyunsaturated fatty acid lipoxygenase ALOX15Oryctolagus cuniculus (rabbit)2.949
Caspase-1Homo sapiens (human)8.319
Alpha-synucleinHomo sapiens (human)7.1
Enoyl-[acyl-carrier-protein] reductase [NADH]Mycobacterium tuberculosis H37Rv0.03
DNA-directed RNA polymerase subunit betaMycobacterium tuberculosis H37Rv0.01
Solute carrier organic anion transporter family member 1B3Homo sapiens (human)1.5
Solute carrier organic anion transporter family member 1B1Homo sapiens (human)1.5

Research

Studies (2)

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

Authors

AuthorsStudies
Christiansen, HC; Copp, BR; G Franzblau, S; Lindsay, BS1
Cappoen, D; Claes, P; De Kimpe, N; Huygen, K; Jacobs, J; Mathys, V; Mbala, BM; Mertens, B; Verschaeve, L1

Other Studies

2 other study(ies) available for ascididemin and rifampin

ArticleYear
Identification of heteroarylenamines as a new class of antituberculosis lead molecules.
    Bioorganic & medicinal chemistry letters, 2005, Sep-15, Volume: 15, Issue:18

    Topics: Amines; Antitubercular Agents; Drug Evaluation, Preclinical; Drug Resistance; Inhibitory Concentration 50; Molecular Structure; Mycobacterium tuberculosis; Structure-Activity Relationship

2005
Synthesis and antimycobacterial activity of analogues of the bioactive natural products sampangine and cleistopholine.
    European journal of medicinal chemistry, 2013, Volume: 67

    Topics: Alkaloids; Anthraquinones; Anti-Bacterial Agents; Aza Compounds; Biological Products; Dose-Response Relationship, Drug; Heterocyclic Compounds, 4 or More Rings; Microbial Sensitivity Tests; Molecular Structure; Mycobacterium; Naphthyridines; Structure-Activity Relationship

2013