Page last updated: 2024-08-24

dehydroabietylamine and abietic acid

dehydroabietylamine has been researched along with abietic acid in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aicher, TD; Brand, LJ; Damon, RE; Gao, J; Kaplan, EL; Koletar, J; Mann, WR; Shetty, SS; Vinluan, CC1
Connelly, M; Fatima, I; Gautam, LN; González, MA; Ling, T; Miranda-Carboni, G; Rivas, F; Tran, M; Wood, RK1
Gowda, DC; Gowda, R; Inamdar, GS; Kuzu, OF; Rangappa, KS; Robertson, GP; Sadashiva, MP; Wu, X1

Other Studies

3 other study(ies) available for dehydroabietylamine and abietic acid

ArticleYear
Triterpene and diterpene inhibitors of pyruvate dehydrogenase kinase (PDK).
    Bioorganic & medicinal chemistry letters, 1999, Aug-02, Volume: 9, Issue:15

    Topics: Administration, Oral; Animals; Blood Glucose; Diabetes Mellitus, Experimental; Disease Models, Animal; Diterpenes; Mice; Protein Kinase Inhibitors; Protein Kinases; Protein Serine-Threonine Kinases; Pyruvate Dehydrogenase Acetyl-Transferring Kinase; Rats; Rats, Sprague-Dawley; Structure-Activity Relationship; Triterpenes

1999
(+)-Dehydroabietylamine derivatives target triple-negative breast cancer.
    European journal of medicinal chemistry, 2015, Sep-18, Volume: 102

    Topics: Abietanes; Antineoplastic Agents, Phytogenic; Apoptosis; Biological Products; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Discovery; Drug Screening Assays, Antitumor; Female; Humans; MCF-7 Cells; Molecular Structure; Stereoisomerism; Structure-Activity Relationship; Triple Negative Breast Neoplasms

2015
A non-cytotoxic N-dehydroabietylamine derivative with potent antimalarial activity.
    Experimental parasitology, 2015, Volume: 155

    Topics: Abietanes; Antimalarials; Benzamides; Benzothiazoles; Cell Line; Cell Line, Tumor; Diamines; Dose-Response Relationship, Drug; Erythrocytes; Fibroblasts; Fluorescent Dyes; Humans; Inhibitory Concentration 50; Organic Chemicals; Plasmodium falciparum; Quinolines; Structure-Activity Relationship

2015