Structure via PubChem · Public domain (PubChem)
lodenosine
Sign in to saveLodenosine is a failed experimental agent for the treatment of HIV. Its development was discontinued on January 11, 2001.
In the Vinony graph
Vinony's link graph records 126 inbound references to lodenosine, and connects out to tenofovir alafenamide, nucleoside analogue and medication.
It is catalogued under topics including Abandoned drugs, Chembox image size set and Hydroxymethyl compounds.
Vinony links it to 6 Wikipedia language editions.
Chemical data
- Formula
- C10H12FN5O2
- Molecular weight
- 253.23 g/mol
- IUPAC name
- [(2S,4S,5R)-5-(6-aminopurin-9-yl)-4-fluorooxolan-2-yl]methanol
- SMILES
- C1[C@H](O[C@H]([C@H]1F)N2C=NC3=C(N=CN=C32)N)CO
- InChIKey
- KBEMFSMODRNJHE-JFWOZONXSA-N
- XLogP
- -0.2
- Polar surface area
- 99.1 Ų
- H-bond donors
- 2
- H-bond acceptors
- 7
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 253.098
Show 4 more facts
- canonical SMILES
- C1C(OC(C1F)N2C=NC3=C2N=CN=C3N)CO
- chemical formula
- C₁₀H₁₂FN₅O₂
- isomeric SMILES
- C1[C@H](O[C@H]([C@H]1F)N2C=NC3=C2N=CN=C3N)CO
- Commons category
- Lodenosine
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Lodenosine is a failed experimental agent for the treatment of HIV. Its development was discontinued on January 11, 2001.
==References==
Excerpted from Wikipedia’s “lodenosine” article, available under the CC BY-SA 4.0 licence.