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1611493-60-7

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1611493-60-7 Usage

Description

Bictegravir (BIC) is a second-generation integrase strand transfer inhibitor (InSTI) used in the treatment of human immunodeficiency virus (HIV) infection. It is a potent inhibitor of HIV-1 integrase with an IC50 of 7.5 nM and has a higher genetic barrier to resistance compared to earlier integrase inhibitors like raltegravir and elvitegravir. Bictegravir is characterized by its low rate of serum aminotransferase elevations during therapy and has not been linked to instances of acute, clinically apparent liver injury.

Uses

Used in HIV Treatment:
Bictegravir is used as an antiretroviral agent for the treatment of HIV-1 infection. It is administered in combination with other antiretroviral agents, such as tenofovir and emtricitabine, to enhance the therapeutic effect and manage the infection more effectively.
Used in HIV-1 Monotherapy:
Bictegravir is approved for HIV-1 monotherapy combined with two other antiretrovirals in a single tablet. This combination therapy is particularly useful for patients who are not previously treated with antiretroviral therapy or those who are virologically suppressed (HIV-1 RNA <50 c/mL) on a regular antiretroviral regimen for a minimum of three months without a history of treatment failure and no known factors associated with resistance to the individual components of the medication.
Used in Clinical Trials:
Bictegravir has been used in trials studying the treatment of HIV-1 and HIV-2 infection. These trials aim to evaluate the safety, efficacy, and potential benefits of Bictegravir in managing and treating HIV infections, further expanding its applications in the field of HIV treatment.

Mechanism of action

This single dose medication inhibits the strand transfer of viral DNA into the human genome, preventing HIV-1 virus replication and propagation 2. In vitro, bictegravir has shown powerful antiviral activity against HIV-2 and various subtypes of HIV-1. It has shown synergistic effects when combined with other ARVs, including tenofovir alafenamide (TAF), emtricitabine (FTC), and darunavir (DRV) Label. The three components of the first USA approved medication ( trade name: Biktarvy ) are as follows: Bictegravir: integrase strand transfer inhibitor; INSTI), an HIV-1 encoded enzyme necessary for viral replication. Inhibition of the integrase enzyme prevents the integration of HIV-1 into host DNA, blocking the conversion of the HIV-1 provirus and progression of the virus. Emtricitabine: FTC, is phosphorylated by cellular enzymes to form emtricitabine 5'-triphosphate. Emtricitabine is phosphorylated to form emtricitabine 5'-triphosphate intracellularly. This metabolite inhibits the activity of human immunodeficiency virus (HIV) reverse transcriptase by competing with the substrate deoxycytidine 5'-triphosphate and by incorporating itself into viral DNA preventing DNA chain elongation. Tenofovir Alafenamide: TAF is a phosphonamidate prodrug of tenofovir (2′-deoxyadenosine monophosphate analog). Plasma exposure to TAF leads to leakage into cells and then TAF is intracellularly converted to tenofovir by hydrolysis by cathepsin. Tenofovir is subsequently phosphorylated by cellular kinases to the metabolite tenofovir diphosphate, which is the active form of the drug. Tenofovir diphosphate inhibits HIV-1 replication by incorporating into viral DNA by the HIV reverse transcriptase, resulting in DNA chain-termination. Tenofovir diphosphate also weakly inhibits mammalian DNA polymerases.

Pharmacokinetics

Bictegravir is an HIV-1 integrase strand transfer inhibitor (INSTI). Bictegravir (BIC) inhibits HIV-1 virus replication into the human genome. It can be taken once daily without additional dosing. Bictegravir (BIC) inhibits strand transfer of viral DNA into the host genome and thereby prevents HIV-1 replication.

Check Digit Verification of cas no

The CAS Registry Mumber 1611493-60-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,1,4,9 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1611493-60:
(9*1)+(8*6)+(7*1)+(6*1)+(5*4)+(4*9)+(3*3)+(2*6)+(1*0)=147
147 % 10 = 7
So 1611493-60-7 is a valid CAS Registry Number.

1611493-60-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,5S,13aR)-8-hydroxy-7,9-dioxo-N-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide

1.2 Other means of identification

Product number -
Other names 2,5-Methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide, 2,3,4,5,7,9,13,13a-octahydro-8-hydroxy-7,9-dioxo-N-[(2,4,6-trifluorophenyl)methyl]-, (2R,5S,13aR)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1611493-60-7 SDS

1611493-60-7Downstream Products

1611493-60-7Relevant articles and documents

Process for Preparation of Intermediates Used for the Synthesis of HIV Integrase Inhibitor

-

, (2021/01/25)

Provided herein is a process for the intermediates used for preparation of HIV Integrase Inhibitor such as Bictegravir, Dolutegravir, Cabotegravir or their pharmaceutically acceptable salts.

PROCESS AND POLYMORPHIC FORMS OF BICTEGRAVIR AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS OR CO-CRYSTALS THEREOF

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, (2021/01/22)

The present invention generally relates to polymorphic forms of bictegravir, its salts, co-crystals, solvates or hydrates thereof and process for the preparation of the same and also relates to pharmaceutical compositions containing the same. The present

PROCESS FOR THE PREPARATION OF BICTEGRAVIR AND INTERMEDIATE THEREOF

-

, (2019/01/07)

The present invention provides processes and intermediates for the synthesis of bictegravir and its pharmaceutical salt.

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