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Galtamycin B

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Galtamycin B
Names

IUPAC name 1,6,10-Trihydroxy-8-methyl-2-tetracene-5,12-dione
Systematic IUPAC name (2R,2R,2S,2R,4S,4S,4S,4S,6S,6S,6S,8R,8S)-1,1,1,2,4-Pentahydroxy-1,2,4,6,8-pentamethyl-8H-3,5,7-trioxa-8(2)-pyrana-2,4,6(2,5)-tris(oxana)-1(2)-tetracenaoctaphane-1,1,8(8H)-trione
Identifiers
CAS Number	855779-79-2
3D model (JSmol)	Interactive image
ChemSpider	9938973
PubChem CID	72823501
UNII	NP8M36JU4W
InChI InChI=1S/C43H48O15/c1-17-12-25-24(28(45)13-17)14-26-37(40(25)50)39(49)23-7-6-22(38(48)36(23)41(26)51)32-15-29(46)42(20(4)52-32)58-35-16-30(47)43(21(5)55-35)57-34-11-9-31(19(3)54-34)56-33-10-8-27(44)18(2)53-33/h6-8,10,12-14,18-21,29-35,42-43,45-48,50H,9,11,15-16H2,1-5H3Key: NWYUSUAHSWSTCK-UHFFFAOYSA-N
SMILES O=C1\C=C/(O1C)O2CC(O2C)O8(O(O3(O)C(O3C)c7ccc6C(=O)c5c(O)c4cc(cc(O)c4cc5C(=O)c6c7O)C)C8O)C
Properties
Chemical formula	C₄₃H₄₈O₁₅
Molar mass	804.842 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Galtamycin B is a chemical compound that has been isolated from Micromonospora.

References

Ströch, K.; Zeeck, A.; Antal, N.; Fiedler, H. P. (2005). "Retymicin, galtamycin B, saquayamycin Z and ribofuranosyllumichrome, novel secondary metabolites from Micromonospora sp. Tü 6368. II. Structure elucidation". The Journal of Antibiotics. 58 (2): 103–10. doi:10.1038/ja.2005.13. PMID 15835722.

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