Xantocillin

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Xantocillin
Xantocillin.svg
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Names
Preferred IUPAC name
4,4′-[(1Z,3Z)-2,3-Diisocyanobuta-1,3-diene-1,4-diyl]diphenol
Other names
Xanthocillin X, Ophthocillin
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
PubChem CID
UNII
  • [C-]#[N+]C(=CC1=CC=C(C=C1)O)C(=CC2=CC=C(C=C2)O)[N+]#[C-]
Properties
C18H12N2O2
Molar mass 288.306 g·mol−1
AppearanceYellow 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).

Xantocillin [1] (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 [2] and subsequently from several other sources. [3] [4]

See also

Related Research Articles

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<span class="mw-page-title-main">Methyl isocyanide</span> Chemical compound

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<span class="mw-page-title-main">Transition metal isocyanide complexes</span> Class of chemical compounds

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References

  1. PubChem. "Xantocillin". pubchem.ncbi.nlm.nih.gov. Retrieved 2023-11-03.
  2. W. ROTHE (1950). "Vorläufige Mitteilung über eine neues Antibiotikum". Pharmazie . 5: 190.
  3. Paul J. Scheuer (1992). "Isocyanides and cyanides as natural products". Accounts of Chemical Research . 25 (10): 433–439. doi:10.1021/ar00022a001.
  4. 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.