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Cefoxitin is a second-generation cephamycin antibiotic developed by Merck & Co., Inc. from Cephamycin C in the year following its discovery, 1972. It was synthesized in order to create an antibiotic with a broader spectrum. It is often grouped with the second-generation cephalosporins. Cefoxitin requires a prescription and as of 2010 is sold under the…
The analysis highlights History and Applications as prominent areas in the source structure around Cefoxitin.
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.
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The extracted context around Cefoxitin shows recurring relationship patterns in the source. For example, Cefoxitin → Due, Fernandes, Funsun, Interpretive, Likewise, MRSA, Staphylococcus, United States Another extracted example is Cefoxitin → French Ministry, GI, Health, Hôpitaux, One, Paris, Pharmocokinetic. 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.
bacteria antibiotic spectrum cephamycin bacterial used drug discovery data due antibiotics staphylococcus also sp study may resistance side effects beta-lactamase
TTTA extracted 75 structured relationships around Cefoxitin. Examples in this analysis include Cefoxitin → 3D model (JSmol) → Interactive image and Cefoxitin → AHFS/Drugs.com → Monograph. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Cefoxitin | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Cefoxitin | AHFS/Drugs.com | Monograph | 1.00 | infobox |
| Cefoxitin | ATC code | J01DC01 (WHO) | 1.00 | infobox |
| Cefoxitin | CAS Number | 35607-66-0 Y | 1.00 | infobox |
| Cefoxitin | ChEBI | CHEBI:209807 N | 1.00 | infobox |
| Cefoxitin | ChEMBL | ChEMBL996 N | 1.00 | infobox |
| Cefoxitin | ChemSpider | 389981 Y | 1.00 | infobox |
| Cefoxitin | CompTox Dashboard (EPA) | DTXSID1022764 | 1.00 | infobox |
| Cefoxitin | DrugBank | DB01331 N | 1.00 | infobox |
| Cefoxitin | ECHA InfoCard | 100.047.841 | 1.00 | infobox |
| Cefoxitin | Elimination half-life | 41-59 min | 1.00 | infobox |
| Cefoxitin | Excretion | 85% urine | 1.00 | infobox |
| Cefoxitin | Formula | C16H17N3O7S2 | 1.00 | infobox |
| Cefoxitin | KEGG | D02345 N | 1.00 | infobox |
| Cefoxitin | KEGG | as salt: D00913 N | 1.00 | infobox |
| Cefoxitin | Legal status | AU: S4 (Prescription only) | 1.00 | infobox |
| Cefoxitin | Legal status | UK: POM (Prescription only) | 1.00 | infobox |
| Cefoxitin | Legal status | US: ℞-only | 1.00 | infobox |
| Cefoxitin | License data | US DailyMed: Cefoxitin | 1.00 | infobox |
| Cefoxitin | MedlinePlus | a682737 | 1.00 | infobox |
| Cefoxitin | Melting point | 149 to 150 °C (300 to 302 °F) (dec.) | 1.00 | infobox |
| Cefoxitin | Metabolism | minimal | 1.00 | infobox |
| Cefoxitin | Molar mass | 427.45 g·mol−1 | 1.00 | infobox |
| Cefoxitin | Pregnancy category | AU: B1 | 1.00 | infobox |
| Cefoxitin | PubChem CID | 441199 | 1.00 | infobox |
| Cefoxitin | Routes of administration | Intravenous | 1.00 | infobox |
| Cefoxitin | Trade names | Mefoxin, Renoxitin, others | 1.00 | infobox |
| Cefoxitin | UNII | 6OEV9DX57Y | 1.00 | infobox |
| Cefoxitin | is a | second-generation cephamycin antibiotic developed by Merck | 0.90 | text |
| Cefoxitin | is a | better substrate than imipenem for beta-lactamases | 0.90 | text |
The concept neighborhoods around Cefoxitin bring nearby vocabulary together. In this analysis, examples include Bacteria, Bacterial and Staphylococcus. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Cefoxitin, one of the stronger structural bridges in this analysis connects Cefoxitin with Spectrum of bacterial susceptibility. 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 Cefoxitin to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as History & Applications, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — Cefoxitin · EN edition · Analysis: TopicsToTalkAbout