Elvitegravir

"目录号: HY-14740

Metabolic Enzyme/ProteaseAnti-infection-

Elvitegravir 是一种HIV integrase抑制剂,作用于 HIV-1IIIB,HIV-2EHO和 HIV-2ROD,IC50分别为 0.7 nM,2.8 nM 和 1.4 nM。

HIV IntegraseHIV

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Dolutegravir-Maraviroc-Atazanavir sulfate-Tenofovir Disoproxil Fumarate-Tipranavir-Triciribine-Emtricitabine-Efavirenz-Miltefosine-Ritonavir-Delavirdine mesylate-Lamivudine-Abacavir-BI 224436-Cabotegravir-

生物活性

Description

Elvitegravir is anHIV integraseinhibitor for HIV-1IIIB, HIV-2EHOand HIV-2RODwithIC50of 0.7 nM, 2.8 nM and 1.4 nM, respectively.

IC50& Target

IC50: 0.7 nM (HIV-1IIIB), 2.8 nM (HIV-2EHO), 1.4 nM(HIV-2ROD)[1]

In Vitro

Elvitegravir (EVG) blocks the integration of HIV-1 cDNA through the inhibition of DNA strand transfer. Elvitegravir exerts potent anti-HIV activity against not only wild-type strains but also drug-resistant clinical isolates. Interestingly, Elvitegravir also shows antiviral activity against murine leukemia virus (MLV) and simian immunodeficiency virus (SIV). Elvitegravir shows potent antiviral activity against three laboratory strains of HIV, with EC50values in the subnanomolar to nanomolar range. Next, the activity of Elvitegravir is evaluated against wild-type clinical isolates representing various subtypes of HIV-1. Elvitegravir suppresses the replication of all HIV-1 subtypes tested, with an antiviral EC50ranging from 0.1 to 1.26 nM. Moreover, Elvitegravir suppresses the replication of HIV-1 clinical isolates carrying NRTI, NNRTI, and PI resistance-associated genotypes, as did a control IN inhibitor, the compound L-870,810. The cytotoxicities of these inhibitors are also determined using an MTT colorimetric assay. Mean values for the concentration that suppresses the viability of target cells by 50% for Elvitegravir and L-870,810 in PBMC obtained from three independent donors are 4.6±0.5 μM and 2.7±0.6 μM, respectively. Thus, Elvitegravir can suppress various HIV strains, including diverse HIV-1 subtypes and clinical isolates carrying multiple mutations associated with resistance to currently approved antiretroviral drugs[1].

Clinical Trial

NCT00708162

Gilead Sciences

HIV Infection

July 2008

Phase 3

NCT01929759

Massachusetts General Hospital-Brigham and Women's Hospital-Gilead Sciences

HIV Disease

January 2014

NCT02219217

St Stephens Aids Trust-ViiV Healthcare

HIV

October 2014

Phase 1

NCT02198443

Fundacion Clinic per a la Recerca Biomédica

HIV

June 6, 2015

Phase 4

NCT02882230

Fondation Ophtalmologique Adolphe de Rothschild

HIV

September 2016

NCT02180438

University of Washington-Clinique des Maladies Infectieuses Ibrahima DIOP Mar/CRCF, Centre Hospitalier Universitaire de Fann-Gilead Sciences

HIV-2 Infection

September 2014

Phase 4

NCT02351908

St Stephens Aids Trust-Merck Sharp & Dohme Corp.

HIV

March 2015

Phase 4

NCT02859558

AIDS Clinical Trials Group-National Institute of Allergy and Infectious Diseases (NIAID)

HIV-1 Infection

January 2017

Phase 2

NCT02475135

Janssen Sciences Ireland UC

Healthy

June 2015

Phase 1

NCT02470650

Juan A. Arnaiz-Hospital Clinic of Barcelona

Patient Compliance-Antiretroviral Therapy Intolerance

June 2015

Phase 4

NCT02203461

Technische Universität München-Gilead Sciences-MUC Research GmbH

Insulin Resistance

July 2014

Phase 1

NCT02397096

Merck Sharp & Dohme Corp.

HIV-1 Infection

June 9, 2015

Phase 3

NCT00042289

National Institute of Allergy and Infectious Diseases (NIAID)-Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

HIV Infections

March 2003

Phase 4

NCT00537966

University of Zurich

HIV Infections

January 2002

NCT00445146

Gilead Sciences

HIV Infections

February 2007

Phase 2

NCT01923311

Gilead Sciences

Acquired Immune Deficiency Syndrome (AIDS)-HIV Infections

August 26, 2013

Phase 2-Phase 3

NCT01721109

Gilead Sciences

Acquired Immunodeficiency Syndrome-HIV Infections

December 6, 2012

Phase 2-Phase 3

NCT02383108

PENTA Foundation

HIV Infection

June 2016

Phase 2-Phase 3

NCT02284035

Juan A. Arnaiz-Hospital Clinic of Barcelona

AIDS

January 2015

Phase 3

NCT00298350

Gilead Sciences

HIV-HIV-1-Human Immunodeficiency Virus

February 2006

Phase 2

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References

[1].Shimura K, et al. Broad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137). J Virol. 2008 Jan;82(2):764-74.

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