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Supplying the newest API's & rarest Molecules for your R&D needsSupplying the newest API's & rarest Molecules for your R&D needs
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Featured Products

LGM Pharma is proud to present to you our new line of Immunosuppressive Ingredients.

Immunosuppressive drugs inhibit or prevent activity of the immune system.

Currently LGM Pharma supplies the following products, available for your R&D purposes:

Product Name: CAS#:
Abetimus 169147-32-4
Anakinra 143090-92-0
Azathioprine 446-86-6
Cyclosporine 59865-13-3, 79217-60-0
Deforolimus 572924-54-0
Everolimus 159351-69-6
Fingolimod HCL 162359-56-0
Gusperimus 84937-45-1
Leflunomide 75706-12-6
Lenalidomide 191732-72-6
Methotrexate 59-05-2, 7413-34-5
Mycophenolic Acid 24280-93-1
Pimecrolimus 137071-32-0
Sirolimus 53123-88-9
Tacrolimus 104987-11-3, 109581-93-3
Temsirolimus 162635-04-3
Teriflunomide 108605-62-5
Thalidomide 50-35-1
Umirolimus 851536-75-9
Zotarolimus 221877-54-9


Disclaimer: Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271(e)+A13(1). Any patent infringement and resulting liability is solely at buyer risk.

   

Recent Blog Posts

Immunosuppressive Drugs & Organ Transplantation - Treatments, Side Effects, and Future Research & Development
Posted on: 3/17/11

For organ transplant patients, the normally protective immune response can threaten the longevity and function of the transplanted organ. Currently, organ transplant patients must take immunosuppressive or anti-rejection medication to prevent....
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Monoclonal Antibodies (mAb's) – Growth, Supply, and Uses for Cancer Treatment
Posted on: 2/11/11

What is a monoclonal antibody? A monoclonal antibody is a laboratory-produced molecule that's carefully engineered to attach to specific defects in your cancer cells. Monoclonal antibodies mimic the antibodies...
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Dutasteride – FDA Denies Specific Use, But Does Not Affect Existing Approval
Posted on: 1/27/11

On Wednesday January 26, 2011, GlaxoSmithKline (GSK) announced that the Company has received a Complete Response letter from the U.S. Food and Drug Administration (FDA) for the supplemental New Drug Application (sNDA)....
More >


 
 

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