Page last updated: 2024-09-04

iodoproxyfan and clobenpropit

iodoproxyfan has been researched along with clobenpropit in 6 studies

Compound Research Comparison

Studies
(iodoproxyfan)
Trials
(iodoproxyfan)
Recent Studies (post-2010)
(iodoproxyfan)
Studies
(clobenpropit)
Trials
(clobenpropit)
Recent Studies (post-2010) (clobenpropit)
2502147029

Protein Interaction Comparison

ProteinTaxonomyiodoproxyfan (IC50)clobenpropit (IC50)
Histamine H3 receptorMus musculus (house mouse)0.001
Histamine H3 receptorHomo sapiens (human)0.0011

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's4 (66.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Christiaans, JA; Gynther, J; Kotisaari, S; Kovalainen, JT; Laitinen, JT; Männistö, PT; Tuomisto, L1
Arrang, JM; Ganellin, CR; Ligneau, X; Schunack, W; Schwartz, JC; Sippl, W; Stark, H1
De Esch, IJ; Dean, PM; Hoffmann, M; Leurs, R; Menge, WM; Mills, JE; Nederkoorn, PH; Perkins, TD; Romeo, G; Timmerman, H; Wieland, K1
Hastrup, S; Rimvall, K; Wulff, BS1
Bakker, RA; Leurs, R; Lim, HD; Ling, P; Thurmond, RL; van Rijn, RM1
de Esch, IJ; de Graaf, C; Istyastono, EP; Kooistra, AJ; Leurs, R; Lim, HD; Nijmeijer, S; Roumen, L; van de Stolpe, A; Vischer, HF1

Other Studies

6 other study(ies) available for iodoproxyfan and clobenpropit

ArticleYear
Synthesis and in vitro pharmacology of a series of new chiral histamine H3-receptor ligands: 2-(R and S)-Amino-3-(1H-imidazol-4(5)-yl)propyl ether derivatives.
    Journal of medicinal chemistry, 1999, Apr-08, Volume: 42, Issue:7

    Topics: Animals; Autoradiography; Binding, Competitive; Cerebral Cortex; Corpus Striatum; Histamine Agonists; Histamine Antagonists; Imidazoles; In Vitro Techniques; Ligands; Male; Propylamines; Rats; Rats, Wistar; Receptors, Histamine H3; Stereoisomerism; Structure-Activity Relationship

1999
Different antagonist binding properties of human and rat histamine H3 receptors.
    Bioorganic & medicinal chemistry letters, 2001, Apr-09, Volume: 11, Issue:7

    Topics: Animals; CHO Cells; Cricetinae; Female; Histamine Antagonists; Humans; Imidazoles; Models, Molecular; Protein Binding; Rats; Receptors, Histamine H3; Rhodopsin; Species Specificity

2001
Development of a pharmacophore model for histamine H3 receptor antagonists, using the newly developed molecular modeling program SLATE.
    Journal of medicinal chemistry, 2001, May-24, Volume: 44, Issue:11

    Topics: Animals; Benzyl Compounds; Cerebral Cortex; Guinea Pigs; Histamine Antagonists; Histamine Release; Imidazoles; In Vitro Techniques; Intestines; Ligands; Models, Molecular; Muscle Contraction; Muscle, Smooth; Piperidines; Quantitative Structure-Activity Relationship; Radioligand Assay; Rats; Receptors, Histamine H3; Software

2001
Characteristics of recombinantly expressed rat and human histamine H3 receptors.
    European journal of pharmacology, 2002, Oct-18, Volume: 453, Issue:1

    Topics: Animals; Cell Line; Cloning, Molecular; Histamine Agonists; Histamine Antagonists; Humans; Rats; Receptors, Histamine; Receptors, Histamine H3; Recombination, Genetic

2002
Evaluation of histamine H1-, H2-, and H3-receptor ligands at the human histamine H4 receptor: identification of 4-methylhistamine as the first potent and selective H4 receptor agonist.
    The Journal of pharmacology and experimental therapeutics, 2005, Volume: 314, Issue:3

    Topics: Cell Line; Histamine Agonists; Humans; Imidazoles; Indoles; Isothiuronium; Ligands; Methylhistamines; Piperazines; Radioligand Assay; Receptors, G-Protein-Coupled; Receptors, Histamine; Receptors, Histamine H1; Receptors, Histamine H2; Receptors, Histamine H3; Receptors, Histamine H4

2005
Molecular determinants of ligand binding modes in the histamine H(4) receptor: linking ligand-based three-dimensional quantitative structure-activity relationship (3D-QSAR) models to in silico guided receptor mutagenesis studies.
    Journal of medicinal chemistry, 2011, Dec-08, Volume: 54, Issue:23

    Topics: Cell Line, Tumor; Histamine Antagonists; Humans; Hydrophobic and Hydrophilic Interactions; Imidazoles; Ligands; Models, Molecular; Molecular Conformation; Molecular Dynamics Simulation; Mutagenesis, Site-Directed; Quantitative Structure-Activity Relationship; Receptors, G-Protein-Coupled; Receptors, Histamine; Receptors, Histamine H3; Receptors, Histamine H4; Stereoisomerism; Thiourea

2011