Page last updated: 2024-09-04

cd 437 and adapalene

cd 437 has been researched along with adapalene in 3 studies

Compound Research Comparison

Studies
(cd 437)
Trials
(cd 437)
Recent Studies (post-2010)
(cd 437)
Studies
(adapalene)
Trials
(adapalene)
Recent Studies (post-2010) (adapalene)
134026448150225

Protein Interaction Comparison

ProteinTaxonomycd 437 (IC50)adapalene (IC50)
60 kDa heat shock protein, mitochondrialHomo sapiens (human)2.3
10 kDa heat shock protein, mitochondrialHomo sapiens (human)2.3
60 kDa chaperonin Escherichia coli3.6
10 kDa chaperonin Escherichia coli3.6

Research

Studies (3)

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

Authors

AuthorsStudies
Bernardon, JM; Charpentier, B; Eustache, J; Martin, B; Michel, S; Millois, C; Shroot, B1
Bhuiyan, M; Chao, WR; Dawson, MI; Farhana, L; Feng, GS; Fontana, JA; Han, YH; Hobbs, PD; Jiang, T; Jong, L; Macchiarulo, A; Nuti, R; Pang, Y; Patel, B; Pellicciari, R; Su, Y; Tautz, L; Waleh, N; Xia, Z; Xue, LP; Ye, M; Zhang, XK1
Arlabosse, JM; Bouix-Peter, C; Chambon, S; Chantalat, L; Daver, S; Dumais, L; Duvert, G; Feret, A; Ouvry, G; Pascau, J; Portal, T; Raffin, C; Rodeville, N; Soulet, C; Tabet, S; Talano, S; Thoreau, E1

Other Studies

3 other study(ies) available for cd 437 and adapalene

ArticleYear
Synthesis, structure-affinity relationships, and biological activities of ligands binding to retinoic acid receptor subtypes.
    Journal of medicinal chemistry, 1995, Dec-22, Volume: 38, Issue:26

    Topics: Animals; Cell Differentiation; Magnetic Resonance Spectroscopy; Mice; Receptors, Retinoic Acid; Recombinant Proteins; Retinoic Acid Receptor alpha; Retinoic Acid Receptor gamma; Retinoids; Structure-Activity Relationship; Teratocarcinoma; Tretinoin; Tumor Cells, Cultured

1995
Adamantyl-substituted retinoid-derived molecules that interact with the orphan nuclear receptor small heterodimer partner: effects of replacing the 1-adamantyl or hydroxyl group on inhibition of cancer cell growth, induction of cancer cell apoptosis, and
    Journal of medicinal chemistry, 2008, Sep-25, Volume: 51, Issue:18

    Topics: Adamantane; Antineoplastic Agents; Apoptosis; Cell Division; Cell Line, Tumor; Cinnamates; Dimerization; Enzyme Inhibitors; Humans; Models, Molecular; Neoplasms; Protein Tyrosine Phosphatase, Non-Receptor Type 11

2008
Structure-based design of Trifarotene (CD5789), a potent and selective RARγ agonist for the treatment of acne.
    Bioorganic & medicinal chemistry letters, 2018, 06-01, Volume: 28, Issue:10

    Topics: Acne Vulgaris; Dose-Response Relationship, Drug; Drug Design; Humans; Molecular Docking Simulation; Molecular Structure; Receptors, Retinoic Acid; Retinoic Acid Receptor gamma; Retinoids; Structure-Activity Relationship

2018
chemdatabank.com