1-hexadecyl-2-acetyl-glycero-3-phosphocholine has been researched along with framycetin in 6 studies
Studies (1-hexadecyl-2-acetyl-glycero-3-phosphocholine) | Trials (1-hexadecyl-2-acetyl-glycero-3-phosphocholine) | Recent Studies (post-2010) (1-hexadecyl-2-acetyl-glycero-3-phosphocholine) | Studies (framycetin) | Trials (framycetin) | Recent Studies (post-2010) (framycetin) |
---|---|---|---|---|---|
9,156 | 187 | 552 | 8,151 | 460 | 653 |
Protein | Taxonomy | 1-hexadecyl-2-acetyl-glycero-3-phosphocholine (IC50) | framycetin (IC50) |
---|---|---|---|
30S ribosomal protein S6 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S7 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L15 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L10 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L11 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L7/L12 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L19 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L1 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L20 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L27 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L28 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L29 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L31 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L31 type B | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L32 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L33 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L34 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L35 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L36 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S10 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S11 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S12 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S13 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S16 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S18 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S19 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S20 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S2 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S3 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S4 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S5 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S8 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S9 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L13 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L14 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L16 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L23 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S15 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L17 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L21 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L30 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L6 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S14 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S17 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S1 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L18 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L2 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L3 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L24 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L4 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L22 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L5 | Escherichia coli K-12 | 0.032 | |
30S ribosomal protein S21 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L25 | Escherichia coli K-12 | 0.032 | |
50S ribosomal protein L36 2 | Escherichia coli K-12 | 0.032 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (16.67) | 18.7374 |
1990's | 5 (83.33) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chau, LY | 1 |
Kawaguchi, H; Sawa, H; Yasuda, H | 1 |
Holmsen, H; Tysnes, OB; Verhoeven, AJ | 1 |
Alkon, DL; Inoue, H; Kouchi, T; Sakakibara, M; Yoshioka, T | 1 |
Caplan, MS; Hsueh, W; Huang, W; MacKendrick, W; Sun, XM; Tien, J | 1 |
Faili, A; Hatmi, M; Randon, J; Vargaftig, BB | 1 |
6 other study(ies) available for 1-hexadecyl-2-acetyl-glycero-3-phosphocholine and framycetin
Article | Year |
---|---|
Protein kinase C is not involved in the desensitization of platelet activating factor receptor in rabbit platelets.
Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Animals; Blood Platelets; Cell Membrane; Guanosine Triphosphate; Inositol Phosphates; Isoquinolines; Kinetics; Neomycin; Piperazines; Platelet Activating Factor; Platelet Membrane Glycoproteins; Protein Kinase C; Rabbits; Receptors, Cell Surface; Receptors, G-Protein-Coupled; Tetradecanoylphorbol Acetate | 1991 |
Mechanism of increased angiotensin-converting enzyme activity stimulated by platelet-activating factor.
Topics: Angiotensin I; Angiotensin II; Animals; Calcium; Cattle; Cells, Cultured; Endothelium; Neomycin; Peptidyl-Dipeptidase A; Platelet Activating Factor; Pulmonary Artery; Type C Phospholipases | 1990 |
Neomycin inhibits agonist-stimulated polyphosphoinositide metabolism and responses in human platelets.
Topics: Blood Platelets; Collagen; Humans; In Vitro Techniques; Inositol Phosphates; Neomycin; Phosphatidylinositol Phosphates; Phosphatidylinositols; Platelet Activating Factor; Platelet Aggregation; Thrombin | 1987 |
Induction of photoresponse by the hydrolysis of polyphosphoinositides in the Hermissenda type B photoreceptor.
Topics: 1-Methyl-3-isobutylxanthine; Animals; Cyclic AMP; Cyclic GMP; Guanosine 5'-O-(3-Thiotriphosphate); Guanosine Diphosphate; Hydrolysis; Inositol 1,4,5-Trisphosphate; Kinetics; Lithium Chloride; Models, Biological; Neomycin; Phosphatidylinositol 4,5-Diphosphate; Phosphatidylinositol Phosphates; Photoreceptor Cells, Invertebrate; Platelet Activating Factor; Pyrimidinones; Snails; Spermine; Thiazoles; Thionucleotides; Type C Phospholipases | 1994 |
Endogenous bacterial toxins are required for the injurious action of platelet-activating factor in rats.
Topics: Analysis of Variance; Animals; Bacterial Toxins; Drug Therapy, Combination; Endotoxins; Intestines; Male; Metronidazole; Necrosis; Neomycin; Platelet Activating Factor; Polymyxin B; Rats; Rats, Sprague-Dawley; Shock; Specific Pathogen-Free Organisms | 1995 |
Carrageenan-induced activation of human platelets is dependent on the phospholipase C pathway.
Topics: Blood Platelets; Carrageenan; Dose-Response Relationship, Drug; Enzyme Activation; Humans; In Vitro Techniques; Inositol Phosphates; Neomycin; Platelet Activating Factor; Platelet Activation; Platelet Aggregation; Type C Phospholipases | 1993 |