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Guisinol

Guisinol
Names
IUPAC name
[5-[(E)-but-2-en-2-yl]-3-hydroxy-2-methylphenyl] 2-[(E)-but-2-en-2-yl]-3-chloro-4,6-dihydroxy-5-methylbenzoate[1]
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C23H25ClO5/c1-7-11(3)15-9-16(25)13(5)17(10-15)29-23(28)19-18(12(4)8-2)20(24)22(27)14(6)21(19)26/h7-10,25-27H,1-6H3/b11-7+,12-8+
    Key: AEQBAXLIEJZXPN-MKICQXMISA-N
  • C/C=C(\C)/C1=CC(=C(C(=C1)OC(=O)C2=C(C(=C(C(=C2O)C)O)Cl)/C(=C/C)/C)C)O
Properties
C23H25ClO5
Molar mass 416.90 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Guisinol is an antibacterial depside with the molecular formula C23H25ClO5 that has been isolated from the fungus Aspergillus unguis.[1][3][4][5]

References

  1. ^ a b "Guisinol". Pubchem.ncbi.NLM.nih.gov.
  2. ^ "KNApSAcK Metabolite Information - C00040990". www.knapsackfamily.com.
  3. ^ Nielsen, J.; Nielsen, P. H.; Frisvad, J. C. (1999). "Fungal depside, guisinol, from a marine derived strain of Emericella unguis". Phytochemistry. 50 (2): 263. Bibcode:1999PChem..50..263N. doi:10.1016/S0031-9422(98)00517-2. ISSN 0031-9422.
  4. ^ Rahman, Atta-ur- (30 August 2011). Studies in Natural Products Chemistry: Bioactive Natural Products (Part L). Elsevier. p. 502. ISBN 978-0-08-045847-2.
  5. ^ Blunt, John W.; Munro, Murray H. G. (19 September 2007). Dictionary of Marine Natural Products with CD-ROM. CRC Press. p. 989. ISBN 978-0-8493-8217-8.

Further reading

  • Stapleton, R. D. Jr.; Singh, V. P. (13 March 2002). Biotransformations: Bioremediation Technology for Health and Environmental Protection. Elsevier. p. 352. ISBN 978-0-08-052820-5.


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