Narciclasine

Narciclasine
Names
	Preferred IUPAC name (2S,3R,4S,4aR)-2,3,4,7-Tetrahydroxy-3,4,4a,5-tetrahydro-9H-[1,3]dioxolo[4,5-j]phenanthridin-6(2H)-one
	Other names BRN 1087400, Lycoricidin-A, Lycoricidinol, NSC 266535
Identifiers
CAS Number	29477-83-6 ;
3D model (JSmol)	Interactive image;
ChemSpider	65310 ;
ECHA InfoCard	100.214.093
KEGG	C08533;
PubChem CID	72376;
CompTox Dashboard (EPA)	DTXSID70183677 ;
	InChI InChI=1S/C14H13NO7/c16-6-1-5-4-2-7-13(22-3-21-7)11(18)8(4)14(20)15-9(5)12(19)10(6)17/h1-2,6,9-10,12,16-19H,3H2,(H,15,20)/t6-,9 ,10 ,12-/m0/s1 Key: LZAZURSABQIKGB-AEKGRLRDSA-N; InChI=1/C14H13NO7/c16-6-1-5-4-2-7-13(22-3-21-7)11(18)8(4)14(20)15-9(5)12(19)10(6)17/h1-2,6,9-10,12,16-19H,3H2,(H,15,20)/t6-,9 ,10 ,12-/m0/s1 Key: LZAZURSABQIKGB-AEKGRLRDBO;
	SMILES C1OC2=C(O1)C(=C3C(=C2)C4=C[C@@H]([C@H]([C@H]([C@@H]4NC3=O)O)O)O)O;
Properties
Chemical formula	C14H13NO7
Molar mass	307.258 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). (what is ?) Infobox references

Narciclasine is a toxic alkaloid found in various Amaryllidaceae species.^[1]

References

Gwendoline Van Goietsenoven; Véronique Mathieu; Florence Lefranc; Alexander Kornienko; Antonio Evidente; Robert Kiss (March 2013). "Narciclasine as well as other Amaryllidaceae Isocarbostyrils are Promising GTP-ase Targeting Agents against Brain Cancers". Medicinal Research Reviews. 33 (2): 439–455. doi:10.1002/med.21253.

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