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Gestodene, sold under the brand names Femodene and Minulet among others, is a progestin medication which is used in birth control pills for women. It is also used in menopausal hormone therapy. The medication is available almost exclusively in combination with an estrogen. It is taken by mouth.
The analysis highlights History, Community, Culture and Applications as prominent areas in the source structure around Gestodene.
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 Gestodene shows recurring relationship patterns in the source. For example, Gestodene → Asia, Australia, Canada, Colombia, Ecuador, Europe, India, Ireland, It, Japan, Latin America, Mexico, New Zealand, Peru, Portugal, South Africa, South Korea, United Kingdom, United States Another extracted example is Gestodene → Avaden, Avadene, Convaden, Femoden, Femodene, Femodette, Gynera, Harmonet, It, Lindynette, Logest, Meliane, Millinette, Minesse, Minulet, Mirelle, Triadene. 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.
oral use androgenic also menopausal hormone therapy activity levonorgestrel combination progestin pills glucocorticoid effects names contraceptive receptor marketed medication progestogen
TTTA extracted 122 structured relationships around Gestodene. Examples in this analysis include Gestodene → 3D model (JSmol) → Interactive image and Gestodene → AHFS/Drugs.com → International Drug Names. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Gestodene | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Gestodene | AHFS/Drugs.com | International Drug Names | 1.00 | infobox |
| Gestodene | ATC code | G03AA10 (WHO) G03AB06 (WHO) (only combinations with estrogens) | 1.00 | infobox |
| Gestodene | Bioavailability | 96% (87–111%) | 1.00 | infobox |
| Gestodene | CAS Number | 60282-87-3 Y | 1.00 | infobox |
| Gestodene | ChEBI | CHEBI:135323 Y | 1.00 | infobox |
| Gestodene | ChEMBL | ChEMBL1213583 Y | 1.00 | infobox |
| Gestodene | ChemSpider | 2298532 Y | 1.00 | infobox |
| Gestodene | CompTox Dashboard (EPA) | DTXSID6046478 | 1.00 | infobox |
| Gestodene | Drug class | Progestogen; Progestin | 1.00 | infobox |
| Gestodene | DrugBank | DB06730 Y | 1.00 | infobox |
| Gestodene | ECHA InfoCard | 100.056.478 | 1.00 | infobox |
| Gestodene | Elimination half-life | 12–15 hours | 1.00 | infobox |
| Gestodene | Excretion | Urine | 1.00 | infobox |
| Gestodene | Formula | C21H26O2 | 1.00 | infobox |
| Gestodene | KEGG | D04316 Y | 1.00 | infobox |
| Gestodene | Legal status | In general: ℞ (Prescription only) | 1.00 | infobox |
| Gestodene | Melting point | 197.9 °C (388.2 °F) | 1.00 | infobox |
| Gestodene | Metabolism | Liver (reduction, hydroxylation) | 1.00 | infobox |
| Gestodene | Molar mass | 310.437 g·mol−1 | 1.00 | infobox |
| Gestodene | Other names | GSD; SHB-331; δ15-Norgestrel; 15-Dehydronorgestrel; 17-hydroxy-18a-homo-19-nor-17α-pregna-4,15-dien-20-yn-3-one; 17α-Ethynyl-18-methyl-19-nor-δ15-testosterone; 17α-Ethynyl-18-me… | 1.00 | infobox |
| Gestodene | Pregnancy category | X | 1.00 | infobox |
| Gestodene | Protein binding | 98% (64% to SHBGTooltip sex hormone-binding globulin, 34% to albumin, 2% free) | 1.00 | infobox |
| Gestodene | PubChem CID | 3033968 | 1.00 | infobox |
| Gestodene | Routes of administration | By mouth | 1.00 | infobox |
| Gestodene | Trade names | Femodene, Femodette, Gynera, Harmonet, Meliane, Minesse, Minulet, others | 1.00 | infobox |
| Gestodene | UNII | 1664P6E6MI | 1.00 | infobox |
| Gestodene | is a | progestin | 0.90 | text |
| Gestodene | is a | most potent of all of the currently used oral contraceptive progestogens | 0.90 | text |
The concept neighborhoods around Gestodene bring nearby vocabulary together. In this analysis, examples include Oral, Levonorgestrel and Containing. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Gestodene, one of the stronger structural bridges in this analysis connects Gestodene with Overview. 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 Gestodene to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as History, 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 — Gestodene · EN edition · Analysis: TopicsToTalkAbout