Belinostat

Belinostat

2500-30000 USD ($)

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Product Details:

Molecular Formula C15H14N2O4S
Molecular Weight 318.347 g/mol Grams (g)
Medicine Name Belinostat
Chemical Name PXD-101, Beleodaq
CAS No 414864-00-9
Type Other
Grade Medicine Grade
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Belinostat Price And Quantity

Minimum Order Quantity 1 Kilograms
Price 2500-30000 USD ($)

Belinostat Product Specifications

Purity(%) 98.00%
Molecular Formula C15H14N2O4S
Grade Medicine Grade
Medicine Name Belinostat
CAS No 414864-00-9
Type Other
Chemical Name PXD-101, Beleodaq
Molecular Weight 318.347 g/mol Grams (g)

Belinostat Trade Information

FOB Port Nhava Sheva Port, Hajira Port, Mundra Port.
Payment Terms Letter of Credit (L/C), Paypal, Western Union, Letter of Credit at Sight (Sight L/C), Telegraphic Transfer (T/T), Cash in Advance (CID), Cash Advance (CA)
Supply Ability 2000 Kilograms Per Year
Delivery Time 6 Days
Sample Available Yes
Sample Policy If order is confirmed we will reimburse the sample cost
Packaging Details Double Liner Bag/ HDPE Drum Packing.
Main Export Market(s) Australia, Eastern Europe, Middle East, Central America, Africa, South America, Western Europe, Asia, North America
Main Domestic Market All India
Certifications EUGMP/WHOGMP/GMP.

Product Description

BelinostatA is a Histone Deacetylase Inhibitor. The mechanism of action ofA belinostatA is as a Histone Deacetylase Inhibitor.

BelinostatA is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity.A BelinostatA targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptosis, promoting cellular differentiation, and inhibiting angiogenesis.A

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Innovative Oncology Solution

Belinostat is a potent histone deacetylase inhibitor widely utilized in the treatment of various cancers, offering a new avenue for targeted therapy. Its high purity and medicine-grade quality make it suitable for advanced pharmaceutical research and clinical practices.

Strict Quality Assurance

Every batch of Belinostat supplied from India undergoes rigorous testing to ensure 98% purity, consistent molecular weight, and compliance with international pharmaceutical standards. Our product caters to researchers, hospitals, and pharmaceutical companies seeking reliable active pharmaceutical ingredients.

FAQ's of Belinostat:

Q: How is Belinostat typically administered in clinical practice?

A: Belinostat is generally administered intravenously under medical supervision, commonly for patients with relapsed or refractory peripheral T-cell lymphoma. Dosage and administration schedules are determined by healthcare professionals based on patient-specific factors.

Q: What is the primary usage of Belinostat in medicine?

A: Belinostat is primarily used as an anticancer agent, functioning as a histone deacetylase inhibitor to interrupt cancer cell growth and proliferation, particularly in certain forms of lymphoma.

Q: When does Belinostat show beneficial effects during treatment?

A: Patients may begin to observe the therapeutic effects of Belinostat after completing several cycles, as advised by their oncologist. The exact timeline depends on cancer type, disease stage, and individual response.

Q: Where can Belinostat be sourced in India?

A: Belinostat is available throughout India via reputable dealers, wholesalers, distributors, manufacturers, suppliers, and exporters specializing in pharmaceutical-grade compounds.

Q: What is the manufacturing process for Belinostat?

A: Belinostat is synthesized through advanced organic chemical processes that ensure high purity and consistent molecular structure. Each batch is tested to guarantee the specified 98% purity and compliance with pharmaceutical regulations.

Q: How does Belinostat benefit cancer patients?

A: Belinostat provides therapeutic benefit by inhibiting key enzymes responsible for cancer cell survival, thereby promoting the death of malignant cells and enhancing the effectiveness of combination cancer therapies.

Q: What precautions should be considered when using Belinostat?

A: Belinostat should only be used under strict medical supervision. Patients are advised to follow dosage instructions, report side effects, and undergo regular monitoring to ensure safety and efficacy during treatment.

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