tramadol has been researched along with bisindolylmaleimide i in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kaibara, M; Minami, K; Murasaki, O; Shiga, Y; Shigematsu, A; Shiraishi, M; Uezono, Y | 1 |
| Minami, K; Ogata, J; Okamoto, T; Shigematsu, A; Shiraishi, M; Ueta, Y; Uezono, Y | 1 |
| Horishita, T; Minami, K; Ogata, J; Okamoto, T; Shigematsu, A; Shiraishi, M; Uezono, Y | 1 |
| Minami, K; Ogata, J; Uezono, Y; Yokoyama, T | 1 |
4 other study(ies) available for tramadol and bisindolylmaleimide i
| Article | Year |
|---|---|
The inhibitory effects of tramadol on muscarinic receptor-induced responses in Xenopus oocytes expressing cloned M(3) receptors.
Topics: Acetylcholine; Analgesics, Opioid; Animals; Cloning, Molecular; Female; GTP-Binding Protein alpha Subunits, Gq-G11; Heterotrimeric GTP-Binding Proteins; Indoles; Isoflurane; Maleimides; Muscarinic Antagonists; Oocytes; Quinuclidinyl Benzilate; Receptor, Muscarinic M3; Receptors, Muscarinic; RNA, Complementary; Tramadol; Xenopus | 2002 |
The inhibitory effects of ketamine and pentobarbital on substance p receptors expressed in Xenopus oocytes.
Topics: Aluminum Compounds; Anesthetics, Intravenous; Animals; Chloride Channels; Depression, Chemical; DNA, Complementary; Enzyme Activation; Enzyme Inhibitors; Excitatory Amino Acid Antagonists; Female; Fluorides; GABA Modulators; Indoles; Ketamine; Maleimides; Microinjections; Oocytes; Pentobarbital; Propofol; Protein Kinase C; Rats; Receptors, Neurokinin-1; Tramadol | 2003 |
The tramadol metabolite, O-desmethyl tramadol, inhibits 5-hydroxytryptamine type 2C receptors expressed in Xenopus Oocytes.
Topics: Animals; Female; In Vitro Techniques; Indoles; Maleimides; Oocytes; Protein Kinase C; Receptor, Serotonin, 5-HT2C; Serotonin; Serotonin 5-HT2 Receptor Antagonists; Tramadol; Xenopus laevis | 2006 |
The tramadol metabolite O-desmethyl tramadol inhibits substance P-receptor functions expressed in Xenopus oocytes.
Topics: Analgesics, Opioid; Animals; Chloride Channels; Indoles; Maleimides; Neurokinin-1 Receptor Antagonists; Oocytes; Protein Kinase Inhibitors; Receptors, Neurokinin-1; Substance P; Tramadol; Xenopus | 2011 |