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Vedolizumab

Product Name
Vedolizumab
CAS No.
943609-66-3
Chemical Name
Vedolizumab
Synonyms
Vedolizumab;Vedolizumab USP/EP/BP;Vedolizumab 62.6mg/ml;Research Grade Vedolizumab;Vedolizumab (anti-α4β7-integrin);Research Grade Vedolizumab(DHC98802)
CBNumber
CB54187577
Formula Weight
0
MOL File
Mol file
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Vedolizumab Property

storage temp. 
Store at -80°C
solubility 
Soluble in DMSO
form 
Solid
color 
White to off-white
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-7825
Product name
Vedolizumab
Purity
99.64%
Packaging
1mg
Price
$400
Updated
2021/12/16
Biosynth Carbosynth
Product number
BV165597
Product name
Vedolizumab
Packaging
1mg
Price
$600
Updated
2021/12/16
ChemScene
Product number
CS-7825
Product name
Vedolizumab
Purity
99.64%
Packaging
5mg
Price
$740
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
ATB0023426
Product name
VEDOLIZUMAB
Purity
95.00%
Packaging
5MG
Price
$996.68
Updated
2021/12/16
ChemScene
Product number
CS-7825
Product name
Vedolizumab
Purity
99.64%
Packaging
25mg
Price
$2800
Updated
2021/12/16
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Vedolizumab Chemical Properties,Usage,Production

Uses

Vedolizumab is a humanized IgG1 monoclonal antibody that targets the α4β7 integrin for the treatment of ulcerative colitis and Crohn's disease.

Clinical Use

Monoclonal antibody:
Treatment of ulcerative colitis and Crohn’s disease

in vivo

Blockade of α4β7 receptors on T-lymphocytes has been shown to occur for several weeks after a single dose of vedolizumab. The drug concentration following the infusion has been shown to be dose related with a mean maximum concentration of 12.5 μg/mL in those receiving 0.5 mg/kg of vedolizumab and 52.0 μg/mL in those receiving 2 mg/kg. The serum half-life of these two doses is 9-12 days respectively and saturation of α4β7 receptors on T-lymphocytes is >90% at both 4-6 weeks following infusion. In a dose ranging study, the serum drug concentrations increase with increasing dose and when regular induction infusions are used (on day 1, 15, 29 and 85), the serum half-life is between 15 and 22 days across all groups[1].

Drug interactions

Potentially hazardous interactions with other drugs
Live vaccines: risk of generalised infections - avoid.

Metabolism

The expected consequence of metabolism is proteolytic degradation to small peptides and individual amino acids, and receptor-mediated clearance. The exact elimination route of vedolizumab is unknown although renal clearance is expected to be negligible.

References

[1] Soler D, et al. The binding specificity and selective antagonism of vedolizumab, an anti-alpha4beta7 integrintherapeutic antibody in development for inflammatory bowel diseases. J Pharmacol Exp Ther. 2009 Sep;330(3):864-75. DOI:10.1124/jpet.109.153973
[2] Singh H, et al. Vedolizumab: A novel anti-integrin drug for treatment of inflammatory bowel disease. J Nat Sci Biol Med. 2016 Jan-Jun;7(1):4-9. DOI:10.4103/0976-9668.175016

Vedolizumab Preparation Products And Raw materials

Raw materials

Preparation Products

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Vedolizumab Suppliers

Wuhan Sunrise Technology Development Co., Ltd.
Tel
27-027-83314682 13554138826
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+86 (27) 8331-4682
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China
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QQ3130921841
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China
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025-57798810
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Sichuan Wei Keqi Biological Technology Co., Ltd.
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China
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Shanghai Macklin Biochemical Co.,Ltd.
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15221275939
Fax
021-50706099
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China
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Taizhou KEDE Chemical Co., Ltd
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China
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Shanghai Lollane Biological Technology Co.,Ltd.
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Shanghai Hanjing Chemicals Co., Ltd.
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021-54285032 13641685631
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+86 (21) 5443 7651
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China
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Shanghai EFE Biological Technology Co., Ltd.
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021-65675885 18964387627
Fax
021-65675885
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China
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Shanghai YuanYe Biotechnology Co., Ltd.
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021-61312847; 18021002903
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QQ:3008007432
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