lodenosine

{{chembox

| Verifiedfields = changed

| verifiedrevid = 462093127

| ImageFile = Lodenosine.svg

| ImageSize = 175px

| IUPACName = [(2S,4S,5R)-5-(6-Amino-9H-purin-9-yl)-4-fluorooxolan-2-yl]methanol

| OtherNames =

| Section1 = {{Chembox Identifiers

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 3WB2LGT4R1

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 65151

| 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

| InChIKey = KBEMFSMODRNJHE-JFWOZONXBK

| ChEMBL_Ref = {{ebicite|correct|EBI}}

| ChEMBL = 501916

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 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

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = KBEMFSMODRNJHE-JFWOZONXSA-N

| CASNo_Ref = {{cascite|changed|??}}

| CASNo = 110143-10-7

| PubChem = 72180

| KEGG_Ref = {{keggcite|correct|kegg}}

| KEGG = D04759

| SMILES = F[C@H]3C[C@H](O[C@H]3n2cnc1c(ncnc12)N)CO

}}

| Section2 = {{Chembox Properties

| Formula = C₁₀H₁₂FN₅O₂

| MolarMass = 253.23 g/mol

| Appearance =

| Density =

| MeltingPt =

| BoilingPt =

| Solubility =

}}

| Section3 = {{Chembox Hazards

| MainHazards =

| FlashPt =

| AutoignitionPt =

}}

}}

Lodenosine is a failed experimental agent for the treatment of HIV. Its development was discontinued on January 11, 2001.{{cite web|title=Drug Profile: Lodenosine|url=http://adisinsight.springer.com/drugs/800005453|website=AdisInsight|publisher=Adis International Ltd, part of Springer Science+Business Media|accessdate=4 December 2015}}

{{Antiretroviral drug}}