Product
Supplier
Encyclopedia
Inquiry
Home > Organic Chemistry > Nitrile Compound > Etravirine for Sale > Manufacturer of Etravirine CAS NO (269055-15-4) White Powder at best price
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - large image1
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - image1
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - image2
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - image3
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - image4
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - image5
Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder at best price buy - image6

Manufacturer of Etravirine CAS NO (269055-15-4) White Powder at best price

Unit Price: Get Latest Price
CAS No.:

269055-15-4

Grade:

Industrial Grade

Content:

99%

Port:

Durban

Brand:

Custom

Packaging:

As per customer requirement

Sample Available:

Yes

Price valid (until):

2024-06-01

Company Type:
Distributor
Location:
South Africa
Payment Terms:
TT against copy of documents,TT against B/L draft before shipment
Average Lead Time:
60 days
Qualification:
Main Products:

Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

  • Product Details

  • Seller Information

  • Description


      Product Detail  


          1. Comprehensive Overview of Etravirine (CAS number 269055-15-4): Etravirine, a potent non-nucleoside reverse transcriptase inhibitor (NNRTI), represents a pivotal advancement in the therapeutic landscape of HIV/AIDS management. This organic compound, identified by the CAS number 269055-15-4, embodies a complex molecular architecture that underscores its multifaceted pharmacological activity and clinical utility in combating the human immunodeficiency virus type 1 (HIV-1) infection.

          2. Chemical Structure Elucidation and Pharmacodynamic Insights: At its molecular essence, etravirine encapsulates a structurally intricate diarylpyrimidine nucleus ornamented with characteristic molecular appendages, conferring upon it a nuanced repertoire of pharmacodynamic interactions pivotal for its mechanism of action as an NNRTI.

          3. Mechanistic Profundity and Molecular Interactions: The mechanistic underpinnings of etravirine's pharmacological efficacy are rooted in its ability to selectively antagonize the enzymatic activity of HIV-1 reverse transcriptase, thereby impeding the conversion of viral RNA into proviral DNA, an indispensable step in the viral replication cycle.

          4. Clinical Efficacy and Therapeutic Imperatives: Etravirine's clinical efficacy is underscored by its inclusion as a cornerstone agent in combination antiretroviral therapy (cART) regimens, where its distinctive pharmacological profile augments treatment outcomes, particularly in individuals harboring multidrug-resistant strains of HIV-1.

          5. Pharmacokinetic Proficiency and Dose Optimization: The pharmacokinetic properties of etravirine, characterized by favorable oral bioavailability, extensive tissue distribution, and prolonged half-life, facilitate its seamless integration into once-daily dosing paradigms, ensuring therapeutic continuity and patient adherence.

          6. Adverse Event Spectrum and Risk Stratification: Navigating the adverse event spectrum of etravirine necessitates a nuanced appreciation of its tolerability profile, characterized by a mosaic of mild-to-moderate adverse reactions such as rash, gastrointestinal disturbances, and central nervous system manifestations, necessitating vigilant monitoring and preemptive management strategies.

          7. Interactions and Contraindications: Etravirine's metabolic trajectory intersects with an intricate web of drug interactions, notably mediated by cytochrome P450 enzymes, mandating judicious consideration of coadministered medications and vigilance against potential contraindications to ensure therapeutic harmony and efficacy.

          8. Stratified Therapeutic Paradigms and Special Populations: The therapeutic landscape of etravirine extends to diverse patient cohorts, including pregnant individuals living with HIV-1, where its safe utilization underscores its pivotal role in maternal-fetal health optimization and vertical transmission prevention strategies.

          9. Global Epidemiological Context and Health Economics: Etravirine's global epidemiological footprint is indelibly etched in the annals of HIV/AIDS management, contributing substantively to global health equity and socioeconomic resilience through its pivotal role in mitigating morbidity, mortality, and economic burden associated with HIV-1 infection.

          10. Scientific Inquiry and Translational Research Horizons: Pioneering scientific inquiry into etravirine's molecular architecture and pharmacological dynamics underscores a vibrant landscape of translational research, where elucidating novel drug targets, optimizing treatment paradigms, and unraveling mechanisms of drug resistance represent cardinal imperatives in advancing HIV/AIDS therapeutics.

          11. Patient-Centered Care and Adherence Optimization: The ethos of patient-centered care permeates etravirine therapy, necessitating a holistic approach to patient education, empowerment, and engagement aimed at fostering treatment adherence, mitigating treatment-related stigma, and enhancing health-related quality of life.

          12. Therapeutic Continuum and Longitudinal Management: Etravirine's therapeutic continuum unfolds within the crucible of longitudinal management paradigms, characterized by meticulous monitoring of virological and immunological indices, dynamic treatment adjustments, and individualized care pathways tailored to the evolving needs of patients living with HIV-1.

          13. Ethical Imperatives and Social Justice Mandates: Navigating the ethical complexities of etravirine therapy entails a profound commitment to social justice imperatives, ensuring equitable access to life-saving medications, advocating for marginalized populations, and dismantling structural barriers to healthcare delivery.

          14. Interdisciplinary Collaboration and Healthcare Ecosystem Integration: Etravirine's transformative potential in HIV/AIDS management underscores the imperative of interdisciplinary collaboration and healthcare ecosystem integration, fostering synergistic partnerships among clinicians, researchers, policymakers, and community stakeholders to optimize treatment outcomes and catalyze scientific innovation.

          15. Future Trajectories and Therapeutic Frontiers: Embarking upon the vista of future trajectories and therapeutic frontiers, etravirine stands poised at the vanguard of HIV/AIDS therapeutics, charting a course towards enhanced treatment efficacy, improved safety profiles, and equitable access to life-saving medications, thereby affirming its indomitable legacy in the annals of medical history.







      Specifications  


    Items Specifications
    Chemical Formula C20H15BrN6O
    Molecular Weight 435.27 g/mol
    Appearance White to off-white solid
    Melting Point 216-218°C
    Boiling Point Not applicable
    Density Not applicable
    Solubility Soluble in DMSO, slightly soluble in water
    pH Not applicable
    Purity ≥ 98%
    Moisture Content ≤ 0.5%
    Stability Stable under recommended storage conditions
    Hazard Class Not applicable
    Flash Point Not applicable
    Storage Store in a cool, dry place away from heat, sparks, and flames






      Product Pictures


    Shop Best Manufacturer of Etravirine  CAS NO (269055-15-4) White Powder-Detailed Image 5

    ECHEMI Editorial Reference
    Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used for the treatment of HIV.
    Etravirine is an aminopyrimidine that consists of 2,6-diaminopyrimidine bearing a bromo substituent at position 5, a 4-cyano-2,6-dimethylphenoxy substituent at position 4 and having a 4-cyanophenyl substituent attached to the 2-amino group. NNRTI of HIV-1, binds directly to RT and blocks RNA-dependent and DNA-dependent DNA polymerase activities It has a role as a HIV-1 reverse transcriptase inhibitor and an antiviral agent. It is a dinitrile, an organobromine compound, an aminopyrimidine and an aromatic ether.|Etravirine is an antiretroviral agent more specifically classified as a Non-Nucleoside Reverse Transcriptase Inhibitor(NNRTI). Etraverine is used clinically for the treatment of human immunodeficiency virus type 1 (HIV-1) infection. On January 18, 2007, the FDA granted accelerated approved for the use of etravirine 100mg tablets in the treatment of adult HIV-1 infection documented to be resistant to therapy with other NNRTIs and antiretroviral agents. On March 26, 2012, approval was extended for use in treatment-experienced pediatric patients 6 to 18 years of age, weighing at least 16 kg. Etravarine must always be used in combination with other antiretroviral drugs. Etravirine exerts its effects via direct inhibition of the reverse transcriptase enzyme of human immunodeficiency virus type 1 (HIV-1), and consequently blocks DNA-dependent and RNA-dependent polymerase activity. Etravirine does not inhibit human DNA polymerase alpha, beta or gamma. Common side effects of use include mild to moderate rash within the first 6 weeks of therapy, nausea, diarrhea and peripheral neuropathy. Patients are advised to immediately contact their healthcare provider if a rash develops. In 2009, postmarketing case reports of Stevens-Johnson Syndrome, toxic epidermal necrolysis, erythema multiforme, and other hypersensitivity reactions lead to a revision of etravirine's "Warnings and Precautions," as well as notification of health care providers. In 2013, reports of Autoimmune disorders (such as Graves’ disease, polymyositis, and Guillain-Barré syndrome) in the setting of immune reconstitution, as well as more in depth information about the development of rashes in patients taking etravirine, lead to a modification of etravirine's monograph.|Etravirine is a Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor. The mechanism of action of etravirine is as a Non-Nucleoside Reverse Transcriptase Inhibitor, and Cytochrome P450 3A Inducer, and Cytochrome P450 2C9 Inhibitor, and Cytochrome P450 2C19 Inhibitor, and P-Glycoprotein Inhibitor.|Etravirine is a nonnucleoside reverse transcriptase inhibitor used in combination with other agents in the therapy of human immunodeficiency virus (HIV) infection and the acquired immunodeficiency syndrome (AIDS). Etravirine has been associated with transient serum aminotransferase elevations and with hypersensitivity reactions that can be associated with liver injury including acute liver failure.|Etravirine is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor. Etravirine is designed to be active against HIV isolates with mutations that confer resistance to the two most commonly prescribed first-generation NNRTIs. It can bind the enzyme reverse transcriptase (RT) in multiple conformations, both for native and mutant RT, thereby blocking the enzymatic activity of RT.

    Basic Info
    Product Name:

    Etravirine

    Other Name:

    Benzonitrile,4-[[6-amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethyl-;4-[[6-Amino-5-bromo-2-[(4-cyanophenyl)amino]-4-pyrimidinyl]oxy]-3,5-dimethylbenzonitrile;TMC 125;Etravirine;R 165335;Intelence;394729-17-0

    CAS No.:

    269055-15-4

    Molecular Formula:

    C20H15BrN6O

    InChIKeys:

    InChIKey=PYGWGZALEOIKDF-UHFFFAOYSA-N

    Molecular Weight:

    435.284

    Exact Mass:

    435.28

    EC Number:

    1592732-453-0

    UNII:

    0C50HW4FO1

    DSSTox ID:

    DTXSID30181412

    NCI Thesaurus Code:

    C73195

    ATC Code:

    J05AG04|J - Antiinfectives for systemic use

    Categories:

    Nitrile Compound

    Characteristics
    PSA:

    121

    XLogP3:

    4.5

    Density:

    1.439 g/cm3

    Melting Point:

    255-257 °C

    Flash Point:

    339.3±34.3 °C

    Refractive Index:

    1.703

    Storage Conditions:

    -20°C Freezer

    Hazard Identification

    Classification of the substance or mixture

    Acute toxicity - Category 4, Oral

    Hazardous to the aquatic environment, long-term (Chronic) - Category Chronic 4

    GHS label elements, including precautionary statements

    Pictogram(s)
    Signal word

    Warning

    Hazard statement(s)

    H302 Harmful if swallowed

    H413 May cause long lasting harmful effects to aquatic life

    Precautionary statement(s)
    Prevention

    P264 Wash ... thoroughly after handling.

    P270 Do not eat, drink or smoke when using this product.

    P273 Avoid release to the environment.

    Response

    P301+P317 IF SWALLOWED: Get medical help.

    P330 Rinse mouth.

    Storage

    none

    Disposal

    P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Distributor

    Main Products:

    Sodium Lauryl Ether Sulfate,Caustic Soda,Soda Ash,Citric Acid,Calcium Hypochlorite,Oxalic Acid

    Location:

    13 PROTEA PARK MILKWOOD STREET RANGEVIEW GAUTENG 1739

    Payment Terms:

    TT against copy of documents,TT against B/L draft before shipment

    Average lead Time:

    60 days

    Total Annual Revenue:

    $1 million-$2.5 million

    Total Employees:

    11-50

    Year of Establishment:

    2012

  • Country Product Purchase Quantity Date Posted
    Post an enquiry for this product
pic ×

Scan the QR Code to Share

All products displayed on this website are only for non-medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.

According to relevant laws and regulations and the regulations of this website, units or individuals who purchase hazardous materials should obtain valid qualifications and qualification conditions.

The information shown above is provided by the enterprise itself, and the authenticity, accuracy and legitimacy of the content are the responsibility of the publishing company. ECHEMI does not bear any guarantee responsibility for this. Please be aware that risks in internet transactions objectively exist.

Feedback & Suggestions
Send Message

Thank you for your feedback. If you require further assistance, please contact us by email at info@echemi.com or call us at +86-532-55729510.