Page last updated: 2024-09-03

9-methyl-7-bromoeudistomin d and caffeine

9-methyl-7-bromoeudistomin d has been researched along with caffeine in 12 studies

*Caffeine: A methylxanthine naturally occurring in some beverages and also used as a pharmacological agent. Caffeine's most notable pharmacological effect is as a central nervous system stimulant, increasing alertness and producing agitation. It also relaxes SMOOTH MUSCLE, stimulates CARDIAC MUSCLE, stimulates DIURESIS, and appears to be useful in the treatment of some types of headache. Several cellular actions of caffeine have been observed, but it is not entirely clear how each contributes to its pharmacological profile. Among the most important are inhibition of cyclic nucleotide PHOSPHODIESTERASES, antagonism of ADENOSINE RECEPTORS, and modulation of intracellular calcium handling. [MeSH]

*Caffeine: A methylxanthine naturally occurring in some beverages and also used as a pharmacological agent. Caffeine's most notable pharmacological effect is as a central nervous system stimulant, increasing alertness and producing agitation. It also relaxes SMOOTH MUSCLE, stimulates CARDIAC MUSCLE, stimulates DIURESIS, and appears to be useful in the treatment of some types of headache. Several cellular actions of caffeine have been observed, but it is not entirely clear how each contributes to its pharmacological profile. Among the most important are inhibition of cyclic nucleotide PHOSPHODIESTERASES, antagonism of ADENOSINE RECEPTORS, and modulation of intracellular calcium handling. [MeSH]

Compound Research Comparison

Studies
(9-methyl-7-bromoeudistomin d)
Trials
(9-methyl-7-bromoeudistomin d)
Recent Studies (post-2010)
(9-methyl-7-bromoeudistomin d)
Studies
(caffeine)
Trials
(caffeine)
Recent Studies (post-2010) (caffeine)
160125,5012,3936,825

Protein Interaction Comparison

ProteinTaxonomy9-methyl-7-bromoeudistomin d (IC50)caffeine (IC50)
AcetylcholinesteraseHomo sapiens (human)7.25

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's9 (75.00)18.2507
2000's2 (16.67)29.6817
2010's1 (8.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fang, YI; Ishibashi, M; Kobayashi, J; Kobayashi, M; Momose, K; Nakamura, H; Ohizumi, Y; Seino, A1
Furukawa, K; Ishibashi, M; Kobayashi, J; Kozutsumi, D; Ohizumi, Y; Takahashi, Y1
Furukawa, K; Momose, K; Ohizumi, Y; Yamamoto, M; Yoshikawa, K1
Adachi, M; Fang, YI; Kobayashi, J; Ohizumi, Y1
Furukawa, K; Ishibashi, M; Ishiyama, H; Kobayashi, J; Kozutsumi, D; Ohizumi, Y; Takahashi, Y1
Adachi, M; Fang, Y; Kobayashi, J; Ohizumi, Y; Yamakuni, T1
Adachi, M; Kakubari, M; Ohizumi, Y2
Henmi, S; Imaizumi, Y; Ohizumi, Y; Uyama, Y; Watanabe, M1
Atsuki, K; Imaizumi, Y; Ohi, Y; Ohizumi, Y; Tori, Y; Watanabe, M1
Ahmed, M; Bruton, JD; Frame, M; Furman, BL; Islam, MS; Lemmens, R; Persson-Sjögren, S; Pyne, NJ; Shi, CL; Westerblad, H1
Copello, JA; Diaz-Sylvester, PL; Fleischer, S; Juettner, VV; Lv, Y; Porta, M1

Other Studies

12 other study(ies) available for 9-methyl-7-bromoeudistomin d and caffeine

ArticleYear
9-methyl-7-bromoeudistomin D, a powerful radio-labelable Ca++ releaser having caffeine-like properties, acts on Ca(++)-induced Ca++ release channels of sarcoplasmic reticulum.
    The Journal of pharmacology and experimental therapeutics, 1991, Volume: 256, Issue:3

    Topics: Animals; Binding Sites; Caffeine; Calcium; Calcium Channels; Carbolines; Magnesium; Muscles; Procaine; Rabbits; Ruthenium Red; Ryanodine; Sarcoplasmic Reticulum

1991
4,6-Dibromo-3-hydroxycarbazole (an analogue of caffeine-like Ca2+ releaser), a novel type of inhibitor of Ca(2+)-induced Ca2+ release in skeletal muscle sarcoplasmic reticulum.
    British journal of pharmacology, 1995, Volume: 114, Issue:5

    Topics: Animals; Caffeine; Calcium; Calcium Radioisotopes; Carbazoles; Carbolines; In Vitro Techniques; Ion-Selective Electrodes; Magnesium; Male; Muscle, Skeletal; Procaine; Rabbits; Ruthenium Red; Ryanodine; Sarcoplasmic Reticulum

1995
[3H]9-Methyl-7-bromoeudistomin D, a caffeine-like powerful Ca2+ releaser, binds to caffeine-binding sites distinct from the ryanodine receptors in brain microsomes.
    FEBS letters, 1995, Oct-16, Volume: 373, Issue:3

    Topics: Adenosine Triphosphate; Animals; Binding Sites; Binding, Competitive; Brain; Caffeine; Calcium; Calcium Channels; Carbolines; Cholic Acids; Cyclic GMP; Detergents; Guinea Pigs; Inositol 1,4,5-Trisphosphate; Kinetics; Microsomes; Muscle Proteins; Procaine; Ruthenium Red; Ryanodine; Ryanodine Receptor Calcium Release Channel

1995
High affinity binding of 9-[3H]methyl-7-bromoeudistomin D to the caffeine-binding site of skeletal muscle sarcoplasmic reticulum.
    The Journal of biological chemistry, 1993, Sep-05, Volume: 268, Issue:25

    Topics: Adenosine Triphosphate; Animals; Binding Sites; Binding, Competitive; Caffeine; Calcium; Carbolines; Cell Membrane; Magnesium; Muscles; Procaine; Rabbits; Ruthenium Red; Ryanodine; Sarcoplasmic Reticulum

1993
Structure-activity relationship of bromoeudistomin D, a powerful Ca2+ releaser in skeletal muscle sarcoplasmic reticulum.
    European journal of pharmacology, 1995, Feb-15, Volume: 288, Issue:3

    Topics: Animals; Caffeine; Calcium; Calcium Channels; Carbolines; Male; Muscle Proteins; Muscle, Skeletal; Rabbits; Ryanodine Receptor Calcium Release Channel; Sarcoplasmic Reticulum; Structure-Activity Relationship

1995
Properties of the binding sites of [3H]9-methyl-7-bromoeudistomin D in bovine aortic smooth muscle microsomes.
    The Journal of pharmacy and pharmacology, 1994, Volume: 46, Issue:9

    Topics: Animals; Aorta; Binding Sites; Binding, Competitive; Caffeine; Carbolines; Cattle; Microsomes; Muscle, Smooth, Vascular

1994
Tissue- and subcellular-distribution of the binding site of [3H]9- methyl-7-bromoeudistomin D, a potent caffeine-like Ca2+ releaser, in rabbits.
    The Journal of pharmacy and pharmacology, 1994, Volume: 46, Issue:9

    Topics: Animals; Binding Sites; Binding, Competitive; Caffeine; Calcium; Carbolines; Cell Membrane; Male; Organ Specificity; Rabbits; Subcellular Fractions

1994
The specific binding site of 9-[3H]methyl-7-bromoeudistomin D, a caffeine-like Ca2+ releaser, in liver microsomes in distinct from that in skeletal sarcoplasmic reticulum.
    Biological chemistry Hoppe-Seyler, 1994, Volume: 375, Issue:3

    Topics: Animals; Binding Sites; Caffeine; Calcium; Carbolines; In Vitro Techniques; Male; Microsomes, Liver; Muscles; Nucleotides; Procaine; Rabbits; Sarcoplasmic Reticulum

1994
Effects of 9-methyl-7-bromoeudistomin D (MBED), a powerful Ca2+ releaser, on smooth muscles of the guinea pig.
    Annals of the New York Academy of Sciences, 1993, Dec-20, Volume: 707

    Topics: Animals; Caffeine; Calcium; Carbolines; Guinea Pigs; Ileum; In Vitro Techniques; Membrane Potentials; Mesenteric Arteries; Muscle Contraction; Muscle, Smooth; Muscle, Smooth, Vascular; Patch-Clamp Techniques

1993
Imaging of Ca2+ release by caffeine and 9-methyl-7-bromoeudistomin D and the associated activation of large conductance Ca2+-dependent K+ channels in urinary bladder smooth muscle cells of the guinea pig.
    Japanese journal of pharmacology, 2001, Volume: 85, Issue:4

    Topics: Animals; Caffeine; Calcium; Carbolines; Guinea Pigs; Male; Microscopy, Confocal; Muscle, Smooth; Patch-Clamp Techniques; Phosphodiesterase Inhibitors; Potassium Channels; Urinary Bladder

2001
Ryanodine receptors of pancreatic beta-cells mediate a distinct context-dependent signal for insulin secretion.
    FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2003, Volume: 17, Issue:2

    Topics: 3',5'-Cyclic-AMP Phosphodiesterases; Animals; Caffeine; Calcium; Carbolines; Dose-Response Relationship, Drug; Glucose; Insulin; Insulin Secretion; Islets of Langerhans; Ryanodine Receptor Calcium Release Channel; Signal Transduction; Tumor Cells, Cultured

2003
Eudistomin D and penaresin derivatives as modulators of ryanodine receptor channels and sarcoplasmic reticulum Ca2+ ATPase in striated muscle.
    Molecular pharmacology, 2014, Volume: 85, Issue:4

    Topics: Animals; Caffeine; Calcium; Calcium Channel Agonists; Calcium Channel Blockers; Calcium-Transporting ATPases; Carbolines; In Vitro Techniques; Indole Alkaloids; Lipid Bilayers; Microsomes; Muscle, Skeletal; Myocardium; Protein Binding; Rabbits; Ryanodine Receptor Calcium Release Channel; Sarcoplasmic Reticulum

2014