Oxaline

Oxaline
Identifiers
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:70400;
ChemSpider	10225680;
PubChem CID	6438440;
CompTox Dashboard (EPA)	DTXSID60893990 ;
	InChI InChI=1S/C24H25N5O4/c1-6-22(2,3)23-12-19(32-4)21(31)28-18(11-15-13-25-14-26-15)20(30)27-24(23,28)29(33-5)17-10-8-7-9-16(17)23/h6-14H,1H2,2-5H3,(H,25,26)(H,27,30)/b18-11+/t23-,24-/m1/s1 Key: SOHAVULMGIITDH-SSDCDQDPSA-N; InChI=1/C24H25N5O4/c1-6-22(2,3)23-12-19(32-4)21(31)28-18(11-15-13-25-14-26-15)20(30)27-24(23,28)29(33-5)17-10-8-7-9-16(17)23/h6-14H,1H2,2-5H3,(H,25,26)(H,27,30)/b18-11+/t23-,24-/m1/s1 Key: SOHAVULMGIITDH-SSDCDQDPBU;
	SMILES CC(C)(C=C)[C@]12C=C(C(=O)N\3[C@@]1(NC(=O)/C3=C\c4c[nH]cn4)N(c5c2cccc5)OC)OC;
Properties
Chemical formula	C24H25N5O4
Molar mass	447.495 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

Oxaline is a fungal isolate with anticancer activity in vitro.[1] It is an O-methylated derivative of meleagrin.

References

Koizumi, Y; Arai, M; Tomoda, H; Omura, S (2004). "Oxaline, a fungal alkaloid, arrests the cell cycle in M phase by inhibition of tubulin polymerization". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1693 (1): 47–55. doi:10.1016/j.bbamcr.2004.04.013. PMID 15276324.

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