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Chemical Structure| 1051375-19-9 Chemical Structure| 1051375-19-9

Structure of Dolutegravir sodium
CAS No.: 1051375-19-9

Chemical Structure| 1051375-19-9

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Dolutegravir sodium (S/GSK1349572 sodium) is a highly potent and orally bioavailable HIV integrase strand transfer inhibitor with an IC50 of 2.7 nM for HIV-1 integrase-catalyzed strand transfer. It inhibits HIV-1 viral replication with an IC50 of 0.51 nM in peripheral blood mononuclear cells and retains high potency against the HIV-1 Y143R, N155H, and G140S/Q148H mutants (EC50 = 3.6-5.8 nM).

Synonyms: S/GSK1349572 sodium; GSK-1349572A

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Product Details of Dolutegravir sodium

CAS No. :1051375-19-9
Formula : C20H18F2N3NaO5
M.W : 441.36
SMILES Code : [O-]C(C(C(C(NCC1=CC=C(F)C=C1F)=O)=C2)=O)=C3N2C[C@]4([H])OCC[C@@H](C)N4C3=O.[Na+]
Synonyms :
S/GSK1349572 sodium; GSK-1349572A
MDL No. :MFCD28405599
InChI Key :UGWJRRXTMKRYNK-VSLILLSYSA-M
Pubchem ID :46216142

Safety of Dolutegravir sodium

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

Description
Dolutegravir sodium (S/GSK1349572 sodium) is a potent, orally available inhibitor of HIV integrase strand transfer, exhibiting an IC50 of 2.7 nM against HIV-1 integrase-mediated strand transfer. It effectively suppresses HIV-1 viral replication with an IC50 of 0.51 nM in peripheral blood mononuclear cells. Dolutegravir sodium also maintains high efficacy against HIV-1 mutants Y143R, N155H, and G140S/Q148H, with EC50 values ranging from 3.6 to 5.8 nM[1][2].

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Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.27mL

0.45mL

0.23mL

11.33mL

2.27mL

1.13mL

22.66mL

4.53mL

2.27mL

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