Drugs Information:
Tamsulosin
Basic Information
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| ID | DDInter1745 | |
| Drug Type | small molecule | |
| Molecular Formula | C20H28N2O5S | |
| Molecular Weight | 408.512 | |
| CAS Number | 106133-20-4 | |
| Description | Tamsulosin is a selective alpha-1A and alpha-1B adrenoceptor antagonist that exerts its greatest effect in the prostate and bladder, where these receptors are most common.[Label] It is indicated for the treatment of signs and symptoms of benign prostatic hypertrophy.[Label] Antagonism of these receptors leads to relaxation of smooth muscle in the prostate and detrusor muscles in the bladder, allowing for better urinary flow.[Label] Other alpha-1 adrenoceptor antagonists developed in the 1980s were less selective and more likely to act on the smooth muscle of blood vessels, resulting in hypotension.[A178351] Tamsulosin was first approved by the FDA on April 15, 1997.[L6238] | |
| ATC Classification | G04CA52 G04CA02 G01AE10 G04CA54 G04CA53 | |
| IUPAC Name | 5-[(2R)-2-{[2-(2-ethoxyphenoxy)ethyl]amino}propyl]-2-methoxybenzene-1-sulfonamide | |
| InChI | DRHKJLXJIQTDTD-OAHLLOKOSA-N | |
| Canonical SMILES | CCOC1=CC=CC=C1OCCN[C@H](C)CC1=CC(=C(OC)C=C1)S(N)(=O)=O | |
| Useful Links | DrugBank ChEBI PubChem Substance KEGG Compound ChemSpider BindingDB PharmGKB Therapeutic Targets Database Guide to Pharmacology Wikipedia ChEMBL ZINC | |
Interactions with
Tamsulosin
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Interactions with compound preparation
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