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ODE-CDV

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ODE-CDV
Names

Preferred IUPAC name 2-(Octadecyloxy)ethyl ({oxy}methyl)phosphonate
Identifiers
CAS Number	444805-26-9
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL206291
ChemSpider	424002
PubChem CID	483476
CompTox Dashboard (EPA)	DTXSID701028092
InChI InChI=1S/C28H54N3O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-36-21-22-38-39(34,35)25-37-26(24-32)23-31-19-18-27(29)30-28(31)33/h18-19,26,32H,2-17,20-25H2,1H3,(H,34,35)(H2,29,30,33)/t26-/m0/s1Key: BLYNHZVAZVOTGV-SANMLTNESA-N InChI=1/C28H54N3O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-36-21-22-38-39(34,35)25-37-26(24-32)23-31-19-18-27(29)30-28(31)33/h18-19,26,32H,2-17,20-25H2,1H3,(H,34,35)(H2,29,30,33)/t26-/m0/s1Key: BLYNHZVAZVOTGV-SANMLTNEBA
SMILES CCCCCCCCCCCCCCCCCCOCCOP(=O)(CO(Cn1ccc(nc1=O)N)CO)O
Properties
Chemical formula	C₂₈H₅₄N₃O₇P
Molar mass	575.728 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

ODE-CDV (octadecyloxyethyl-cidofovir) is a cidofovir derivative with antiviral activity.

References

Kern, E. R.; Hartline, C.; Harden, E.; Keith, K.; Rodriguez, N.; Beadle, J. R.; Hostetler, K. Y. (2002). "Enhanced inhibition of orthopoxvirus replication in vitro by alkoxyalkyl esters of cidofovir and cyclic cidofovir". Antimicrobial Agents and Chemotherapy. 46 (4): 991–995. doi:10.1128/AAC.46.4.991-995.2002. PMC 127114. PMID 11897580.