Xantocillin
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| Names | |
|---|---|
| IUPAC name
4,4′-[(1Z,3Z)-2,3-Diisocyanobuta-1,3-diene-1,4-diyl]diphenol | |
| Other names
Xanthocillin X, Ophthocillin | |
| Identifiers | |
| 580-74-5 | |
| 3D model (Jmol) | Interactive image |
| ChEMBL | ChEMBL1977264 |
| ChemSpider | 21106491 |
| PubChem | 5378293 |
| UNII | EX637I77PC  |
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| Properties | |
| C18H12N2O2 | |
| Molar mass | 288.31 g·mol−1 |
| Appearance | Yellow crystals |
| Melting point | 200 °C (392 °F; 473 K) (decomposes) |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Xantocillin (INN), also known as xanthocillin X or ophthocillin, was the first reported natural product found to contain the isocyanide functional group. It was first isolated from Penicillium notatum by Rothe in 1950[1] and subsequently from several other sources.[2][3]
See also
References
- ↑ W. ROTHE (1950). "Vorläufige Mitteilung über eine neues Antibiotikum". Pharmazie. 5: 190.
- ↑ Paul J. Scheuer (1992). "Isocyanides and cyanides as natural products". Accounts of Chemical Research. 25 (10): 433–439. doi:10.1021/ar00022a001.
- ↑ Kozlovskiĭ AG, Zhelifonova VP, Antipova TV, Adanin VM, Novikova ND, Deshevaia EA, et al. (2004). "[Penicillium expansum, a resident fungal strain of the orbital complex Mir, producing xanthocillin X and questiomycin A].". Prikl Biokhim Mikrobiol. 40 (3): 344–9. PMID 15283339.
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