Lodenosine

Lodenosine
	200px
Names
	IUPAC name [(2S,4S,5R)-5-(6-Aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol
Identifiers
CAS Number	110143-10-7
ChEMBL	ChEMBL501916
ChemSpider	65151
Jmol 3D model	Interactive image
KEGG	D04759
PubChem	72180
UNII	3WB2LGT4R1
	InChI InChI=1S/C10H12FN5O2/c11-6-1-5(2-17)18-10(6)16-4-15-7-8(12)13-3-14-9(7)16/h3-6,10,17H,1-2H2,(H2,12,13,14)/t5-,6-,10+/m0/s1 Key: KBEMFSMODRNJHE-JFWOZONXSA-N ; InChI=1/C10H12FN5O2/c11-6-1-5(2-17)18-10(6)16-4-15-7-8(12)13-3-14-9(7)16/h3-6,10,17H,1-2H2,(H2,12,13,14)/t5-,6-,10+/m0/s1 Key: KBEMFSMODRNJHE-JFWOZONXBK ;
	SMILES F[C@H]3C[C@H](O[C@H]3n2cnc1c(ncnc12)N)CO ;
Properties
Chemical formula	C10H12FN5O2
Molar mass	253.23 g/mol
Vapor pressure	{{{value}}}
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Lodenosine is a failed experimental agent for the treatment of HIV. Its development was discontinued on January 11, 2001.^[1]

References

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