[CAS NO. 1051375-13-3]  Cabotegravirsodium

Ships within Stock Price Qty Total
$0.00
$0.00
Please click "REQUEST A QUOTE" button if you need other sizes or custom synthesis
request a quote
If there is no stock, or you need other sizes or custom synthesis, please:

PRODUCTS SPECIFICATIONS [1051375-13-3]

Catalog
HY-15592A
Brand
MCE
CAS
1051375-13-3

DESCRIPTION [1051375-13-3]

Overview

MDLMFCD25976749
Molecular Weight427.33
Molecular FormulaC19H16F2N3NaO5
SMILESFC1=C(CNC(C2=CN3C(C(N([C@@H](C)CO4)[C@@]4([H])C3)=O)=C(O[Na])C2=O)=O)C=CC(F)=C1

For research use only. We do not sell to patients.


Summary

Cabotegravir (GSK-1265744) sodium is a orally active and long-acting HIV integrase strand transfer inhibitor and organic anion transporter 1/3 ( OAT1 / OAT3 ) inhibitor with IC 50 values of 2.5 nM, 0.41 μM and 0.81 μM for HIV ADA , OAT3 and OAT1, respectively. Cabotegravir sodium is primarily metabolized by uridine diphosphate glucuronosyltransferase (UGT) 1A1, with low potential to interact with other antiretroviral drugs (ARVs). Cabotegravir sodium can be used to research AIDS [1] [2] .


IC50 & Target

IC 50 : 2.5 nM (HIV ADA ) [1]
IC 50 : 0.41 μM (OAT3), 0.81 μM (OAT1) [2]


In Vitro

Cabotegravir (GSK-1265744) inhibits the HIV-1 integrase catalyzed strand transfer reaction with an IC 50 of 3.0 nM in vitro. The antiviral EC 50 against HIV-1 Ba-L is 0.22 nM and that against NL432 is 0.34 nM in PBMCs, 0.57 nM using CellTiter-Glo and 1.3 nM using MTT in MT-4, and 0.5 nM in the PHIV assay, which uses a pseudotyped self-inactivating virus [3] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay [3]

Cell Line: MT-4 cells
Concentration: 0-32 nM
Incubation Time: 4 or 5 days
Result: Showed antiviral activity with an EC 50 of 1.3 nM.

In Vivo

The half-life of Cabotegravir is up to 54 days in mice [1] .
Cabotegravir (25 or 50 mg/kg; i.v.; single dose or twice) protects Macaques against intravenous challenge with SIVmac251 [4] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT01756131 ViiV Healthcare|GlaxoSmithKline
Infections, Human Immunodeficiency Virus and Herpesviridae
September 2010 Phase 1
NCT00659191 GlaxoSmithKline
HIV Infection
February 2008 Phase 1
NCT02462772 Centre for the AIDS Programme of Research in South Africa|ViiV Healthcare
Human Immunodeficiency Virus
October 2015 Phase 2

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, sealed storage, away from moisture

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)


Solvent & Solubility

In Vitro:

DMSO : 6.9 mg/mL ( 16.15 mM ; ultrasonic and warming and heat to 60°C)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.3401 mL 11.7006 mL 23.4011 mL
5 mM 0.4680 mL 2.3401 mL 4.6802 mL
10 mM 0.2340 mL 1.1701 mL 2.3401 mL
* Please refer to the solubility information to select the appropriate solvent.