Amdoxovir

Amdoxovir
Clinical data
ATC code	none;
Identifiers
	IUPAC name [(2R,4R)-4-(2,6-diaminopurin-9-yl)-1,3-dioxolan-2-yl]methanol;
CAS Number	145514-04-1 ;
PubChem CID	124088;
ChemSpider	110576 ;
UNII	54I81H0M9C;
KEGG	D02890 ;
ChEMBL	ChEMBL458876 ;
NIAID ChemDB	005431;
CompTox Dashboard (EPA)	DTXSID801027435 ;
Chemical and physical data
Formula	C9H12N6O3
Molar mass	252.234 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES n2c1c(nc(nc1n(c2)[C@@H]3O[C@@H](OC3)CO)N)N;
	InChI InChI=1S/C9H12N6O3/c10-7-6-8(14-9(11)13-7)15(3-12-6)4-2-17-5(1-16)18-4/h3-5,16H,1-2H2,(H4,10,11,13,14)/t4-,5-/m1/s1 ; Key:RLAHNGKRJJEIJL-RFZPGFLSSA-N ;
	(verify)

Amdoxovir is a pharmaceutical drug that has undergone research for the treatment of HIV/AIDS. It acts as a nucleoside reverse transcriptase inhibitor (NRTI). The drug was discovered by Raymond F. Schinazi (Emory University) and C.K. Chu (University of Georgia) and developed by RFS Pharma.^[1]

Amdoxovir was in advanced Phase II clinical trials around 2010.^[2] In 2013, a Phase II trial was terminated^[3] and another was withdrawn before it started.^[4] No further studies appear to have been done.

References

^ "Amdoxovir". AIDSmeds.com. January 13, 2009. Archived from the original on 2008-03-21. Retrieved March 21, 2008.
^ Murphy RL, Kivel NM, Zala C, Ochoa C, Tharnish P, Mathew J, Pascual ML, Schinazi RF (2010). "Antiviral activity and tolerability of amdoxovir with zidovudine in a randomized double-blind placebo-controlled study in HIV-1-infected individuals". Antivir Ther. 15 (2): 185–192. doi:10.3851/IMP1514. PMC 7733239. PMID 20386073.
^ Clinical trial number NCT01737359 for "A Safety and Efficacy Study of Amdoxovir in HIV-1 Treatment-experienced Subjects" at ClinicalTrials.gov
^ Clinical trial number NCT01738555 for "A Safety and Efficacy Study of Amdoxovir in HIV-1 Treatment-experienced Subjects" at ClinicalTrials.gov

This antiinfective drug article is a stub. You can help Wikipedia by expanding it.

[1] "Amdoxovir". AIDSmeds.com. January 13, 2009. Archived from the original on 2008-03-21. Retrieved March 21, 2008.

[2] Murphy RL, Kivel NM, Zala C, Ochoa C, Tharnish P, Mathew J, Pascual ML, Schinazi RF (2010). "Antiviral activity and tolerability of amdoxovir with zidovudine in a randomized double-blind placebo-controlled study in HIV-1-infected individuals". Antivir Ther. 15 (2): 185–192. doi:10.3851/IMP1514. PMC 7733239. PMID 20386073.

[3] Clinical trial number NCT01737359 for "A Safety and Efficacy Study of Amdoxovir in HIV-1 Treatment-experienced Subjects" at ClinicalTrials.gov

[4] Clinical trial number NCT01738555 for "A Safety and Efficacy Study of Amdoxovir in HIV-1 Treatment-experienced Subjects" at ClinicalTrials.gov

[1]

[2]

[3]

[4]

Clinical data

ATC code	none
Identifiers
IUPAC name [(2R,4R)-4-(2,6-diaminopurin-9-yl)-1,3-dioxolan-2-yl]methanol
CAS Number	145514-04-1^Y
PubChem CID	124088
ChemSpider	110576^Y
UNII	54I81H0M9C
KEGG	D02890^Y
ChEMBL	ChEMBL458876^Y
NIAID ChemDB	005431
CompTox Dashboard (EPA)	DTXSID801027435
Chemical and physical data
Formula	C₉H₁₂N₆O₃
Molar mass	252.234 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES n2c1c(nc(nc1n(c2)[C@@H]3O[C@@H](OC3)CO)N)N
InChI InChI=1S/C9H12N6O3/c10-7-6-8(14-9(11)13-7)15(3-12-6)4-2-17-5(1-16)18-4/h3-5,16H,1-2H2,(H4,10,11,13,14)/t4-,5-/m1/s1^Y Key:RLAHNGKRJJEIJL-RFZPGFLSSA-N^Y
(verify)