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Name |
Dolutegravir |
Synonyms |
GSK1349572; (4R,12aS)-N-(2,4-difluorobenzyl)-7-hydroxy-4-methyl-6,8-dioxo-3,4,6,8,12,12a-hexahydro-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxamide;(4R,12aS)-N-[(2,4-Difluorophenyl)methyl]-3,4,6,8,12,12a-hexahydro-7-hydroxy-4-methyl-6,8-dioxo-2H-pyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazine-9-carboxamide;(4R,12aS)-N-[(2,4-difluorophenyl)methyl]-7-hydroxy-4-methyl-6,8-dioxo-3,4,12,12a-tetrahydro-2H-pyrido[5,6]pyrazino[2,6-b][1,3]oxazine-9-carboxamide;S/GSK1349572;GSK 1349572;Tivicay;DTG |
Molecular Formula |
C20H19F2N3O5 |
Molecular Weight |
419.37900 |
CAS Number |
1051375-16-6 |
purity |
≥97% |
Application:Dolutegravir (DTG) (CAS No.: 1051375-16-6) is an FDA-approved drug for the treatment of HIV infection.
Dolutegravir is an integrase inhibitor. Known as S/GSK1349572 or just
"572" the drug is marketed as Tivicay by GlaxoSmithKline (GSK). In
February, 2013 the Food and Drug Administration announced that it would fast
track dolutegravir's approval process. On August 13, 2013, dolutegravir was
approved by the FDA. On November 4, 2013, dolutegravir was approved by Health
Canada. On January 16, 2014, Tivicay was approved by the European Commission
for use throughout the European Union.