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Actinorhodin

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Actinorhodin
Names
IUPAC name isochromen)-3-yl]acetic acid
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C32H26O14/c1-9-21-15(3-11(45-9)5-19(35)36)29(41)23-17(33)7-13(27(39)25(23)31(21)43)14-8-18(34)24-26(28(14)40)32(44)22-10(2)46-12(6-20(37)38)4-16(22)30(24)42/h7-12,33-34,39-40H,3-6H2,1-2H3,(H,35,36)(H,37,38)/t9-,10-,11+,12+/m1/s1Key: VTIKDEXOEJDMJP-WYUUTHIRSA-N
  • InChI=1/C32H26O14/c1-9-21-15(3-11(45-9)5-19(35)36)29(41)23-17(33)7-13(27(39)25(23)31(21)43)14-8-18(34)24-26(28(14)40)32(44)22-10(2)46-12(6-20(37)38)4-16(22)30(24)42/h7-12,33-34,39-40H,3-6H2,1-2H3,(H,35,36)(H,37,38)/t9-,10-,11+,12+/m1/s1Key: VTIKDEXOEJDMJP-WYUUTHIRBL
SMILES
  • OC(=O)C5CC=6C(=O)c4c(O)cc(c3cc(O)c2C(=O)C=1C(CC(O)=O)O(C)C=1C(=O)c2c3O)c(O)c4C(=O)C=6(C)O5
Properties
Molar mass 634.54 g mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

Actinorhodin is a benzoisochromanequinone antibiotic produced by Streptomyces coelicolor.

References

  1. "Actinorhodin (CHEBI:2448)". EBI Small Molecule Database. 18 February 2008. Retrieved 9 February 2010.
  2. Magnolo SK, Leenutaphong DL, DeModena JA; et al. (1991). "Actinorhodin production by Streptomyces coelicolor and growth of Streptomyces lividans are improved by the expression of a bacterial hemoglobin". Biotechnology (N.Y.). 9 (5): 473–6. PMID 1367312. {{cite journal}}: Explicit use of et al. in: |author= (help); Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  3. Brian P, Riggle PJ, Santos RA, Champness WC (1996). "Global negative regulation of Streptomyces coelicolor antibiotic synthesis mediated by an absA-encoded putative signal transduction system". J. Bacteriol. 178 (11): 3221–31. PMC 178074. PMID 8655502. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
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