Eleutherobin

Eleutherobin
Identifiers
3D model (JSmol)	Interactive image;
ChemSpider	5293539;
PubChem CID	6918335;
CompTox Dashboard (EPA)	DTXSID20893496 ;
	InChI InChI=1S/C35H48N2O10/c1-20(2)25-10-8-21(3)26-15-29(46-30(40)11-9-24-16-37(6)19-36-24)34(5)12-13-35(42-7,47-34)23(14-27(25)26)17-43-33-32(45-22(4)38)31(41)28(39)18-44-33/h8-9,11-14,16,19-20,25-29,31-33,39,41H,10,15,17-18H2,1-7H3/b11-9+,23-14-/t25-,26+,27-,28-,29+,31-,32+,33-,34+,35-/m1/s1 Key: XOPYFXBZMVTEJF-PDACKIITSA-N; InChI=1/C35H48N2O10/c1-20(2)25-10-8-21(3)26-15-29(46-30(40)11-9-24-16-37(6)19-36-24)34(5)12-13-35(42-7,47-34)23(14-27(25)26)17-43-33-32(45-22(4)38)31(41)28(39)18-44-33/h8-9,11-14,16,19-20,25-29,31-33,39,41H,10,15,17-18H2,1-7H3/b11-9+,23-14-/t25-,26+,27-,28-,29+,31-,32+,33-,34+,35-/m1/s1 Key: XOPYFXBZMVTEJF-PDACKIITBR;
	SMILES CC1=CC[C@@H]([C@@H]/2[C@H]1C[C@@H]([C@@]3(C=C[C@@](O3)(/C(=C2)/CO[C@H]4[C@H]([C@@H]([C@@H](CO4)O)O)OC(=O)C)OC)C)OC(=O)/C=C/C5=CN(C=N5)C)C(C)C;
Properties
Chemical formula	C35H48N2O10
Molar mass	656.773 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Eleutherobin is a marine diterpene glycoside with in vitro anticancer activity.[1]

References

Singh R, Sharma M, Joshi P, Rawat DS (2008). "Clinical status of anti-cancer agents derived from marine sources". Anticancer Agents Med Chem. 8 (6): 603–617. doi:10.2174/187152008785133074. PMID 18690825.

Berrué, F; McCulloch, M. W; Kerr, R. G (2011). "Marine diterpene glycosides". Bioorganic & Medicinal Chemistry. 19 (22): 6702–19. doi:10.1016/j.bmc.2011.06.083. PMID 21783368.

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