Alemtuzumab

Alemtuzumab Suppliers list
Company Name: Shaanxi Haibo Biotechnology Co., Ltd
Tel: +undefined18602966907
Email: qinhe02@xaltbio.com
Products Intro: Product Name:Alemtuzumab
CAS:216503-57-0
Purity:99% Package:25kg Remarks:White Powder
Company Name: Shanghai Minbiotech Co., Ltd.
Tel: +8617315815539
Email: sales@minbiotech.com
Products Intro: Product Name:Alemtuzumab
CAS:216503-57-0
Purity:NLT 20MG/ML Package:10g;200USD
Company Name: Baoji Guokang Healthchem co.,ltd
Tel: +8615604608665 15604608665
Email: dominicguo@gk-bio.com
Products Intro: Product Name:Alemtuzumab
CAS:216503-57-0
Purity:0.99 Package:100g,1kg,5kg
Company Name: Hefei Hirisun Pharmatech Co., Ltd
Tel: +8615056975894
Email: shawn@hirisunpharm.com
Products Intro: Product Name:Alemtuzumab
CAS:216503-57-0
Purity:0.95 Package:1G;5G;25G;Bulk for inquiry Remarks:HR150025
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354
Email: support@targetmol.com
Products Intro: Product Name:Alemtuzumab
CAS:216503-57-0
Package:5 mg Remarks:REAGENT;FOR LABORATORY USE ONLY

Alemtuzumab manufacturers

  • Alemtuzumab
  • Alemtuzumab pictures
  • $0.00 / 25kg
  • 2024-04-12
  • CAS:216503-57-0
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 2000ton
Alemtuzumab Basic information
Product Name:Alemtuzumab
Synonyms:Alemtuzumab;Alemtuzumab (usan/inn);Campath (tn);D02802;MabCampath;Research Grade Alemtuzumab(DHD95101);Research Grade Alemtuzumab
CAS:216503-57-0
MF:
MW:0
EINECS:
Product Categories:
Mol File:Mol File
Alemtuzumab Structure
Alemtuzumab Chemical Properties
form Liquid
color Colorless to light yellow
Safety Information
Hazardous Substances Data216503-57-0(Hazardous Substances Data)
MSDS Information
Alemtuzumab Usage And Synthesis
DescriptionAlemtuzumab was first introduced in the US for the treatment of B-cell chronic lymphocytic leukemia (CLL) in patients who have been treated with alkylating agents and have failed fludarabine therapy. Alemtuzumab is a humanized monoclonal antibody of the IgG1 isotype specific for the glycoprotein CD52 expressed on the cell surface of over 95% of normal and malignant B and T lymphocytes and monocytes. It was genetically engineered by adding six hypervariable regions from the heavy-chain and light-chain variable domains of an IgG2a rat monoclonal antibody onto a human IgG1 immunoglobulin molecule. The exact mechanism of action of alemtuzumab is unknown but the antibody probably causes the lysis of lymphocytes via complement fixation and antibody-dependent cytotoxicity. In a phase III clinical trial with 93 fiudarabine-resistant CLL patients, treatment with alemtuzumab gave a positive response in 31 patients with 2 complete remissions and 29 partial remissions. This study demonstrated a higher response rate in patients having malignancy confined to the blood and bone marrow. Alemtuzumab does not seem to penetrate well into solid tissues and it was found to be concentrated in the blood which seems to correlate with the fact that it appears to be inefficient against tumor cells from lymph nodes and extranodal masses. The half-life of the antibody ranged between 23 and 30 hours. Premedication with acetaminophen and diphenhydramine is effective in reducing infusion-related reactions such as fevers, rigors, rash, nausea or hypotension. The most significant adverse effect is lymphopenia resulting in increased risk of opportunistic infections. As a consequence, prophylactic treatment with antibiotics is recommended for patients under alemtuzumab therapy.
OriginatorCambridge University (UK)
UsesAntineoplastic (monoclonal antibody).
Brand nameCampath (Boehringer Ingelheim KG, Germany).
General DescriptionAlemtuzumab (Campath) is humanized MAb (Campath-1H)that is directed against the 21- to 28-kDa cell surface glycoproteinCD52. CD52 is expressed on the surface of normaland malignant B and T lymphocytes, NK cells, monocytes,macrophages, and tissues of the male reproductive system.The Campath-1H antibody is an IgG1 κ form with humanizedvariable and constant regions and CDRs from a ratMAb, Campath-1G.
Alemtuzumab is indicated for the treatment of B-cellchronic lymphocytic leukemia in patients who have beentreated with alkylating agents and who have failed on thistherapy. Alemtuzumab binds to CD52, a nonmodulating antigen that is present on the surface of essentially all B andT lymphocytes; most monocytes, macrophages, and NKcells, and a subpopulation of granulocytes. The proposedmechanism of action is antibody-dependent lysis ofleukemic cells following cell surface binding.
Clinical Use
Treatment of chronic lymphocytic leukaemia (CLL) not totally responsive to other treatment
Induction therapy in renal transplantation
Treatment of relapsing remitting multiple sclerosis (MS)
Drug interactionsPotentially hazardous interactions with other drugs
Other chemotherapy: do not give within 3 weeks of each other.
Live vaccines: avoid for at least 12 months after treatment.
MetabolismThe metabolic pathway of alemtuzumab has not been elucidated. Clearance decreases with repeated administration due to decreased receptor mediated clearance (loss of CD52 receptors in the periphery).
Alemtuzumab Preparation Products And Raw materials
Tag:Alemtuzumab(216503-57-0) Related Product Information
Rovalpituzumab Tinurilimab Zolbetuximab Eculizumab CETUXIMAB Unii-fys6T7F842 Rituximab Panitumumab Bortezomib Ibrutinib