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Home > Active Pharmaceutical Ingredients > Other Chemical Drugs > Letermovir for Sale > High Quality LeterMovir CAS 917389-32-3 Powder Fast Delivery Good Price
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High Quality LeterMovir CAS 917389-32-3 Powder Fast Delivery Good Price

Unit Price: Get Latest Price
CAS No.:

917389-32-3

Grade:

Pharmaceutical Grade

Content:

99.5%

Port:

Hangzhou

Brand:

HyperChem

Packaging:

1kg/Bag

Price valid (until):

2025-01-17

Company Type:
Trader
Location:
China
Qualification:
Main Products:

Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

  • Product Description

  • Seller Information

  • Description

    Name

    LeterMovir

    CAS number

    917389-32-3

    Synonym

    MK-8828; MK 8828; MK8828; AIC-246; AIC 246; AIC246; Letermovir; 

    Description

    Letermovir, also known as MK-8828 and AIC-246, is an antiviral drug that is being developed for the treatment of cytomegalovirus (CVM) infections. Letermovir has been tested in CMV infected patients with allogeneic stem cell transplants and may also be useful for other patients with a compromised immune system such as those with organ transplants or HIV infections.

    Structure

    Shop High Quality LeterMovir CAS 917389-32-3 Powder Fast Delivery Good Price-Detailed Image 1

    Molecular Formula

    C29H28F4N4O4

    Molecular Weight

    572.55 g/mol

    Appearance

    White Powder

    Quality Standard

    99%

    Shipping Condition

    Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

    Storage Condition

    Dry, dark and at 2~8 for short term (days to weeks) or -20 for long term (months to years).

    Shelf Life

    >2 years if stored properly

    Sample package

    Aluminium foil bag, Bottle

    Commercial package

    Aluminium Tin

    Origin

    China

    LeterMovir More Info


    Leterovir (also known as Leterovir) is an investigational antiviral medication primarily being studied for the treatment of human immunodeficiency virus (HIV) infections. It belongs to a class of drugs known as nucleoside reverse transcriptase inhibitors (NRTIs), which function by inhibiting the reverse transcription process critical for viral replication.

     

    Mechanism of Action

    Leterovir works by blocking the activity of reverse transcriptase, an enzyme that HIV requires to replicate its genetic material. By doing so, it interferes with the ability of the virus to reproduce within the host cells, ultimately leading to a reduction of viral load in the bloodstream. This in turn helps to prevent the progression of HIV infection and the associated immune system damage.

     

    Indications

    Leterovir is being investigated for:

     

    HIV Treatment: It is primarily intended to be used as part of a combination antiretroviral therapy (cART) regimen for individuals diagnosed with HIV. The goal of therapy is to achieve and maintain viral suppression, improve immune function, and reduce the risk of transmission.

    Dosage and Administration

    As Leterovir is still under investigation, specific dosing recommendations and administration routes depend on clinical trial protocols and ongoing studies. Typically, antiviral medications for HIV are administered orally, often in combination with other antiretroviral agents.

     

    Side Effects

    Common side effects associated with NRTIs and potentially with Leterovir may include:

     

    Gastrointestinal symptoms, such as nausea, diarrhea, or abdominal pain.

    Fatigue or malaise.

    Changes in liver function tests.

    Lactic acidosis, a rare but serious condition that can occur with NRTIs, characterized by the buildup of lactic acid in the body.

    More serious side effects may involve immune reconstitution inflammatory syndrome (IRIS) in patients with advanced HIV when they start therapy, where the immune system begins to recover and can cause inflammatory responses to previously acquired infections.

     

    Contraindications and Cautions

    Due to its mechanism of action, Leterovir may be contraindicated in individuals with known hypersensitivity to the drug or any of its components. Additionally, caution should be exercised in:

     

    Patients with pre-existing liver disease or those who consume alcohol heavily, as liver metabolism can be affected.

    Patients with a history of lactic acidosis or pancreatitis.

    Pregnant or breastfeeding individuals should discuss treatment options with their healthcare provider, as the safety of Leterovir in these populations is still being evaluated.

     

    Clinical Considerations

    When prescribing Leterovir, healthcare providers should:

     

    Monitor patients for effectiveness and side effects regularly.

    Counsel patients on the importance of adherence to the antiretroviral regimen to prevent viral resistance and ensure optimal therapy outcomes.

    Discuss potential drug interactions with other medications the patient may be taking, as HIV treatments often require careful management of polypharmacy.

    In summary, Leterovir is an investigational NRTI aimed at treating HIV infections by inhibiting reverse transcriptase and reducing viral replication. While it shows promise, ongoing clinical trials will determine its efficacy, safety profile, and place in therapy within the broader context of HIV treatments. As new data emerges, it is crucial for healthcare providers to stay updated on the latest findings regarding this medication.

     

     


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    FAQ


    Q1. Can I get a free sample?

    We can send you a samll free sample, and you only need to pay for the shipping cost.

     

    Q2. What is the HyperChem payment term?

    T/T in advance
    LC at sight
    DP at sight

    Bank transfer

    PayPal

    Bitcoin...

     

    Q3. What is HyperChem shipment policy?

    Our policy is to strive for the quickest shipment time possible.

    For ready stock samples, they are usually shipped within 3 working days after payment received.
    For non-ready stock, please contact HyperChem sales team to negotiate.

     

    Q4. What is HyperChem shipment term?

    By Express  
    FedEx  UPS  DHL  EMS                               
    Fast: 3-7 days around, high cost, door to door service

    By Air                                        
    Suitable for more than 50kg 
    Fast: 3-7 days, hight cost, port to port, professional broker needed 

    By Sea
    Suitable for more than 500kg      
    Fast: 7-45 days, low cost, port to port, professional broker needed 

     

    We will always attempt to utilize the quickest and most affordable way for customers to receive orders. And follow -up with customers via email for all shipment details as well as updated track information until it arrives without damage.

     

    Q5. What HyperChem will provide after shipment?

    For sample orders: 
    After shipment is done, an timely email including:

    1. Track details (Fedex /TNT/DHL/EMS Track number)
    2. Packaging photo
    3. COA, MSDS, etc
    4. Dispatch date & Estimated arriving time
    5. Shipping invoice

    For commercial orders:
    A full set of shipment documents as well as package photos can be provided in scan-copy and original, to help customers complete the customs clearance process.

    Basic Info
    Product Name:

    Letermovir

    CAS No.:

    917389-32-3

    Molecular Formula:

    C29H28F4N4O4

    InChIKeys:

    InChIKey=FWYSMLBETOMXAG-QHCPKHFHSA-N

    Molecular Weight:

    572.551

    Exact Mass:

    572.55

    Categories:

    Other Chemical Drugs

    Characteristics
    PSA:

    77.84

    XLogP3:

    5.2109

  • Seller Information
    Business Type:

    Trader

    Main Products:

    Pharmaceuticals,Peptide,Cosmetics,Nutritional Supplements

    Location:

    Rm. 803, Tower 4, LOFT49 Creative City Pioneer Zone, No.88 Jiru Rd. Gongshu Dist., Hangzhou, 310015 ZJ, China

    Payment Terms:

    TT against copy of documents,D/P,L/C,D/A,O/A,TT against B/L draft before shipment,100% TT in advance

    Average lead Time:

    10

    Total Annual Revenue:

    $5 million-$10 million

    Total Employees:

    11-50

    Year of Establishment:

    2013

    Certifications:

    Certification Report by Bureau Veritas

    About HyperChem

    Established in 2013, Hyper Chem has exclusive tie-ups with leading manufacturers, supplying raw materials produced in GMP and ISO 9002 certified facilities, and provides high-quality ingredients and raw materials to meet the needs of a diverse range of pharmaceutical cosmetics ingredients and nootropic supplements companies worldwide.

    Our Competitiveness

    One-stop supply

    Wide Range Of products including pharmaceutical, Cosmetic Ingredients and nootropic supplements

    Among all the pharmaceuticals,

    90% of them with GMP certificates,

    85% of them with DMF files and

    50% of them passed FDA approval,

    30% get CEP certificate

    20% are new R&D products.

    Custom Repackaging Service


    We can efficiently repackage your material into sample sizes, custom batch-specific sizes, or semi-bulk package sizes according to your specifications. And ensures the product is packaged in a quality-controlled environment and will maintain its integrity throughout every stage of the process.

    Quality Control/Quality Assurance


    HyperChem is committed to delivering on its promises of top-quality products with verified quality data.

    All materials are vigorously inspected by the factory and/or outsourced analytical laboratories to ensure each and every lot meets or exceeds our reference standards.

    Trade assurance service with 100% payment protection, It is best achieved by delivering products and services 100% right the first time, on time, every time.

    Professional

    Transparent Communication

    Fast Reaction,

    Professional Suggestion

    Beyond Expectation.

    We have exclusive partnerships with research and production facilities across the country and we offer varied pharmaceutical services in the most cost-efficient way. The production facilities are GMP, WHO-GMP, EU GMP and US FDA approved and are backed by strong regulatory support such as Dossier, DMF, Tech Pack and relevant Stability studies for regulatory filings.

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