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Ritodrine, formerly sold under the brand name Yutopar among others, is a tocolytic drug used to stop premature labor. It was withdrawn from the US market, according to the FDA Orange Book. It was available in oral tablets or as an injection and was typically used as the hydrochloride salt.
The analysis highlights Community, Culture and Applications as prominent areas in the source structure around Ritodrine.
Source areas are shown by the number of related topics found in each part of the analysis. Use smaller areas too: they can reveal specialized angles and content gaps.
Smaller areas are not necessarily less important. They contain fewer connections in this analysis and can be useful for finding specialized angles or coverage gaps.
High-confidence facts extracted from structured source data. Use them as anchors for further research.
Browse the complete topic structure, not only the most central items. Less prominent entities and concepts can reveal missing angles, specialized context and useful research gaps. Each item opens a new analysis centered on that subject.
Deeper signals for content research, entity SEO and topical coverage. The plain-language headings explain what each technical view is useful for.
The extracted context around Ritodrine shows recurring relationship patterns in the source. For example, Ritodrine → BANMTooltip British Approved Name, BANTooltip British Approved Name, DCFTooltip Dénomination Commune Française, DU-21220, In, INNTooltip International Nonproprietary Name, It, Name, Pre-Par, The, USANTooltip United States Adopted, Utopar, Yutopar Another extracted example is Ritodrine → Adrenergic, In, It, Most, The. Use these groups to spot repeated connection types before inspecting the individual relationships.
Use these terms to understand the vocabulary surrounding the topic, not as a checklist for keyword stuffing.
drug receptor used also name β2-adrenergic approved united states medical yutopar names among others labor side effects hydrochloride salt us
TTTA extracted 51 structured relationships around Ritodrine. Examples in this analysis include Ritodrine → 3D model (JSmol) → Interactive image and Ritodrine → AHFS/Drugs.com → Micromedex Detailed Consumer Information. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Ritodrine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Ritodrine | AHFS/Drugs.com | Micromedex Detailed Consumer Information | 1.00 | infobox |
| Ritodrine | ATC code | G02CA01 (WHO) | 1.00 | infobox |
| Ritodrine | CAS Number | 26652-09-5 Y | 1.00 | infobox |
| Ritodrine | ChEMBL | ChEMBL785 Y | 1.00 | infobox |
| Ritodrine | ChemSpider | 30971 Y | 1.00 | infobox |
| Ritodrine | CompTox Dashboard (EPA) | DTXSID7048534 | 1.00 | infobox |
| Ritodrine | DrugBank | DB00867 Y | 1.00 | infobox |
| Ritodrine | ECHA InfoCard | 100.043.512 | 1.00 | infobox |
| Ritodrine | Elimination half-life | 1.7–2.6 hours | 1.00 | infobox |
| Ritodrine | Formula | C17H21NO3 | 1.00 | infobox |
| Ritodrine | IUPHAR/BPS | 7294 | 1.00 | infobox |
| Ritodrine | KEGG | D02359 Y | 1.00 | infobox |
| Ritodrine | Legal status | US: Discontinued | 1.00 | infobox |
| Ritodrine | Metabolism | Hepatic, metabolites are inactive | 1.00 | infobox |
| Ritodrine | Molar mass | 287.359 g·mol−1 | 1.00 | infobox |
| Ritodrine | Other names | DU-21220; 4-Hydroxy-β-hydroxy-N-(4-hydroxyphenylethyl)amphetamine; N-(4-Hydroxyphenylethyl)-4-hydroxynorephedrine | 1.00 | infobox |
| Ritodrine | Pronunciation | /ˈraɪtoʊdriːn/ RY-toh-dreen | 1.00 | infobox |
| Ritodrine | Protein binding | ~56% | 1.00 | infobox |
| Ritodrine | PubChem CID | 33572 | 1.00 | infobox |
| Ritodrine | Routes of administration | By mouth, parenteral | 1.00 | infobox |
| Ritodrine | Trade names | Pre-Par, Utopar, Yutopar | 1.00 | infobox |
| Ritodrine | UNII | I0Q6O6740J | 1.00 | infobox |
The concept neighborhoods around Ritodrine bring nearby vocabulary together. In this analysis, examples include Name, Approved and States. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Ritodrine, one of the stronger structural bridges in this analysis connects Ritodrine with Side effects. Bridges highlight paths between different parts of the map and can reveal research angles that are easy to miss in a flat list.
TTTA analyzes the structure around Ritodrine to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as Community, Culture & Applications, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — Ritodrine · EN edition · Analysis: TopicsToTalkAbout