Cart summary

You have no items in your shopping cart.

Dolutegravir

SKU: orb1300988

Description

Dolutegravir is a potent two-metal-binding HIV-1 integrase inhibitor with an IC50 of 2.7 nM. It demonstrates intermediate antiviral activity against key raltegravir-resistant mutants, including Y143R, Q148K, N155H, and G140S/Q148H. This small molecule is widely used in antiretroviral research for both in vitro mechanistic studies and in vivo efficacy models.

Research Area

Infectious Disease & Virology, Protein Biochemistry

Images & Validation

Key Properties

CAS Number1051375-16-6
MW419.38
Purity99.08%
FormulaC20H19F2N3O5
SMILESC[C@@H]1CCO[C@H]2Cn3cc(C(=O)NCc4ccc(F)cc4F)c(=O)c(O)c3C(=O)N12
TargetHIV Protease
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:3.3 mg/mL (7.87 mM);Ethanol:< 1 mg/mL (insoluble or slightly soluble);DMSO:84 mg/mL (200.3 mM);H2O:< 1 mg/mL (insoluble or slightly soluble)

Bioactivity

Target IC50
HIV integrase:2.7 nM
In Vivo
Following a single intravenous (IV) administration, Dolutegravir demonstrates low plasma clearance in rats (0.23 mL/min/kg) and monkeys (2.12 mL/min/kg), with a half-life of approximately 6 hours and a low steady-state volume of distribution (VSS). When orally administered as a solution to fasted male rats and a single monkey, Dolutegravir is rapidly absorbed, showing high oral bioavailability (75.6% and 87.0%, respectively). Dolutegravir exposure, assessed by peak concentration (Cmax) and area under the curve (AUC), increases with dose escalation in oral suspension forms up to 250 mg/kg in non-fasted rats and 50 mg/kg in non-fasted monkeys, albeit with a less than proportional increase.
In Vitro
S/GSK1349572 shows the potent inhibitory effect on nine clinical isolates from integrase inhibitor-naive HIV-2-infected patients with EC50 ranging from 0.2 nM -1.4 nM. In vitro, S/GSK1349572 inhibits recombinant HIV-1 integrase-catalyzed strand transfer with IC50 of 2.7 nM. Furthermore, S/GSK1349572 potently inhibits HIV replication in cells such as peripheral blood mononuclear cells (PBMCs), MT-4 cells and CIP4 cells infected with a self-inactivating PHIV lentiviral vector with EC50 of 0,51 nM, 0.71 nM and 2.2 nM, respectively. In vitro, S/GSK1349572 exhibits potent activity against five different nonnucleoside reverse transcription inhibitor--resistant or nucleoside reverse transcription inhibitor--resistant viruses with EC50 ranging from 1.3 nM -2.1 nM. Similarly to that against wild-type virus, S/GSK1349572 shows equivalent activity against two protease inhibitor-resistant viruses with EC50 of 0.36 nM and 0.37 nM, respectively.
Cell Research
MT-4 cells growing exponentially at a density of 500000 or 600000 /mL are infected with HIV-1 strain IIIB at a viral multiplicity of infection of 0.001 or a 50% tissue culture infective dose of 4 to 10. The cells are then aliquoted to 96-well plates in the presence of varying concentrations of S/GSK1349572. After incubation for 4 or 5 days, antiviral activity is determined by a cell viability assay that either measured bioluminescence with a CellTiter-Glo luminescent reagent or measured absorbance at 560 and 690 nm using the yellow tetrazolium MTT reagent [3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyltetrazolium bromide]. (Only for Reference)

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Dolutegravir, inhibit, Inhibitor, Human immunodeficiency virus, HIVProtease, HIV, HIV integrase, HIV Integrase, HIV Protease, GSK 1349572, GSK1349572, GSK-1349572, S/GSK 1349572, S/GSK1349572, S/GSK-1349572

Similar Products

  • Dolutegravir sodium [orb1305676]

    99.74% (May vary between batches)

    1051375-19-9

    441.36

    C20H18F2N3NaO5

    2 mg, 5 mg, 10 mg, 25 mg, 50 mg, 1 mg, 1 ml x 10 mM (in DMSO), 100 mg
  • Dolutegravir SR Isomer [orb1738471]

    1309560-49-3

    419.38

    C20H19F2N3O5

    50 mg, 100 mg, 25 mg
  • Dolutegravir RR Isomer [orb1738599]

    1357289-29-2

    419.38

    C20H19F2N3O5

    50 mg, 100 mg, 25 mg
  • Dolutegravir intermediate-1 [orb1309751]

    99.52%

    1335210-23-5

    315.28

    C13H17NO8

    1 ml x 10 mM (in DMSO), 5 g
  • Baloxavir [orb1308587]

    99.46%

    1985605-59-1

    483.49

    C24H19F2N3O4S

    1 mg, 5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 200 mg, 1 ml x 10 mM (in DMSO)
Quality Guarantee

Quality Guarantee

Explore bioreagents carefree to elevate your research. All our products are rigorously tested for performance. If a product does not perform as described on its datasheet, our scientific support team will provide expert troubleshooting, a prompt replacement, or a refund. For full details, please see our Terms & Conditions and Buying Guide. Contact us at support@biorbyt.com.

Key Properties

No computed properties available.

Documents Download

Datasheet
Product Information
Download

Request a Document

Protocol Information

Dolutegravir (orb1300988)

  • Star
  • Star
  • Star
  • Star
  • Star
  • 0.0
Based on 0 reviews

Participating in our Biorbyt product reviews program enables you to support fellow scientists by sharing your firsthand experience with our products.

Login to Submit a Review

No reviews yet

Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

Step 2: Enter the in vivo formulation

(This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 70.00
1 ml x 10 mM (in DMSO)
$ 110.00
5 mg
$ 110.00
10 mg
$ 160.00
25 mg
$ 220.00
50 mg
$ 290.00
100 mg
$ 370.00
200 mg
$ 520.00
DispatchUsually dispatched within 3-5 working days
Bulk Enquiry