# monensin

> chemical compound

**Wikidata**: [Q3493048](https://www.wikidata.org/wiki/Q3493048)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Monensin)  
**Source**: https://4ort.xyz/entity/monensin


## References

1. monensin. Global Substance Registration System
2. [CAS Common Chemistry](https://commonchemistry.cas.org/detail?cas_rn=17090-79-8)
3. monensin. PubChem
4. ChEBI release 2020-09-01
5. Gene Ontology release 2019-11-16
6. MONENSIN. ChEMBL
7. Freebase Data Dumps. 2013
8. Monensin. ChemSpider
9. monensin A. ChEBI
10. Insertional Inactivation of Methylmalonyl Coenzyme A (CoA) Mutase and Isobutyryl-CoA Mutase Genes in Streptomyces cinnamonensis: Influence on Polyketide Antibiotic Biosynthesis
11. Role of Crotonyl Coenzyme A Reductase in Determining the Ratio of Polyketides Monensin A and Monensin B Produced byStreptomyces cinnamonensis
12. MeaA, a putative coenzyme B12-dependent mutase, provides methylmalonyl coenzyme A for monensin biosynthesis in Streptomyces cinnamonensis.
13. Analysis of the biosynthetic gene cluster for the polyether antibiotic monensin in Streptomyces cinnamonensis and evidence for the role of monB and monC genes in oxidative cyclization
14. Characterisation of actI-homologous DNA encoding polyketide synthase genes from the monensin producer Streptomyces cinnamonensis
15. Resistance of Streptomyces cinnamonensis to butyrate and isobutyrate: production and properties of a new anti-isobutyrate (AIB) factor
16. Insights into polyether biosynthesis from analysis of the nigericin biosynthetic gene cluster in Streptomyces sp. DSM4137.
17. High titer production of tetracenomycins by heterologous expression of the pathway in a Streptomyces cinnamonensis industrial monensin producer strain.
18. Enhancing macrolide production in Streptomyces by coexpressing three heterologous genes
19. Vitamins as effectors of monensin production by Streptomyces cinnamonensis
20. Characterization of three pathway-specific regulators for high production of monensin in Streptomyces cinnamonensis.
21. Terrosamycins A and B, Bioactive Polyether Ionophores from Streptomyces sp. RKND004 from Prince Edward Island Sediment
22. 2-Demethylmonensins A and B. Novel minor congeners of monensins from Streptomyces cinnamonensis
23. Propionate and the production of monensins in Streptomyces cinnamonensis
24. Biosynthesis of monensins A and B
25. Polyether biosynthesis. 2. Origin of the oxygen atoms of monensin A
26. Determination of monensins A and B in the fermentation broth ofStreptomyces cinnamonensis by high performance liquid chromatography
27. Biosynthesis of the polyether antibiotic monensin A: incorporation of a polyketide chain elongation intermediate
28. The incorporation of thymine and β-aminoisobutyrate into the polyether antibiotic, monensin-A
29. The biosynthesis of monensin-A: thymine, beta-aminoisobutyrate and methacrylate metabolism in Streptomyces cinnamonensis
30. Biosynthesis of the polyether antibiotic monensin-a: stereochemical aspects of the incorporation and metabolism of isobutyrate
31. Effect of precursors on biosynthesis of monensins A and B
32. Biosynthesis of monensins A and B: the role of isoleucine
33. Biosynthesis of the polyether ionophore antibiotic monensin A: assignment of the carbon-13 and proton n.m.r. spectra of monensin A by two-dimensional spectroscopy. Incorporation of oxygen-18 labelled molecular oxygen
34. Biosynthesis of monensin. The intramolecular rearrangement of isobutyryl-CoA to n-butyryl-CoA
35. Biosynthesis of monensins and 3-O-demethylmonensins in Streptomyces cinnamonensis in the presence of methylation inhibitors
36. Biosynthesis of the polyether antibiotic monensin-A. Results from the incorporations of labelled acetate and propionate as a probe of the carbon chain assembly processes
37. MONENSIN. Hazardous Substances Data Bank. 2019
38. Monensin. ECHA Substance Infocard database
39. Medical Subject Headings
40. ChEBI
41. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
42. [OpenAlex](https://docs.openalex.org/download-snapshot/snapshot-data-format)
43. UniChem