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Byetta

Base Information Edit
  • Chemical Name:Byetta
  • CAS No.:141758-74-9
  • Molecular Formula:C184H282N50O60S
  • Molecular Weight:4186.57
  • Hs Code.:2933290000
  • European Community (EC) Number:686-356-3
  • Wikipedia:Exenatide
  • NCI Thesaurus Code:C65611
  • RXCUI:60548
  • Mol file:141758-74-9.mol
Byetta

Synonyms:AC 2993;AC 2993 LAR;bydureon;Byetta;Ex4 peptide;exenatide;exendin 4;exendin-4;ITCA 650;Peptide, Ex4

Suppliers and Price of Byetta
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Exendin 4
  • 1mg
  • $ 672.00
  • Usbiological
  • Exendin 4
  • 1mg
  • $ 742.00
  • Tocris
  • Exendin 4
  • 1
  • $ 393.00
  • Sigma-Aldrich
  • Exendin 4 ≥97%
  • 500 μg
  • $ 727.00
  • Sigma-Aldrich
  • Exendin 4 ≥97%
  • 0.5mg
  • $ 700.00
  • Sigma-Aldrich
  • Exendin 4 ≥97%
  • 0.1 mg
  • $ 245.00
  • Sigma-Aldrich
  • Exendin 4 ≥97%
  • .1mg
  • $ 236.00
  • DC Chemicals
  • Exenatide >98%
  • 5 mg
  • $ 128.00
  • DC Chemicals
  • Exenatide >98%
  • 25 mg
  • $ 348.00
  • ChemScene
  • Exendin 4 99.98%
  • 25mg
  • $ 360.00
Total 121 raw suppliers
Chemical Property of Byetta Edit
Chemical Property:
  • PSA:1775.05000 
  • LogP:-2.16940 
  • Storage Temp.:−20°C 
  • Solubility.:≥145 mg/mL in DMSO; insoluble in EtOH; ≥52 mg/mL in H2O with gentle warming 
  • XLogP3:-21
  • Hydrogen Bond Donor Count:58
  • Hydrogen Bond Acceptor Count:66
  • Rotatable Bond Count:135
  • Exact Mass:4185.0306624
  • Heavy Atom Count:295
  • Complexity:10300
Purity/Quality:

99% *data from raw suppliers

Exendin 4 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Drug Classes:Antidiabetic Agents
  • Canonical SMILES:CCC(C)C(C(=O)NC(CCC(=O)O)C(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)NC(CC(C)C)C(=O)NC(CCCCN)C(=O)NC(CC(=O)N)C(=O)NCC(=O)NCC(=O)N3CCCC3C(=O)NC(CO)C(=O)NC(CO)C(=O)NCC(=O)NC(C)C(=O)N4CCCC4C(=O)N5CCCC5C(=O)N6CCCC6C(=O)NC(CO)C(=O)N)NC(=O)C(CC7=CC=CC=C7)NC(=O)C(CC(C)C)NC(=O)C(CCCNC(=N)N)NC(=O)C(C(C)C)NC(=O)C(C)NC(=O)C(CCC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CCC(=O)O)NC(=O)C(CCSC)NC(=O)C(CCC(=O)N)NC(=O)C(CCCCN)NC(=O)C(CO)NC(=O)C(CC(C)C)NC(=O)C(CC(=O)O)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C(CC8=CC=CC=C8)NC(=O)C(C(C)O)NC(=O)CNC(=O)C(CCC(=O)O)NC(=O)CNC(=O)C(CC9=CNC=N9)N
  • Recent ClinicalTrials:Diabetes Islet Preservation Immune Treatment
  • Recent EU Clinical Trials:A Phase III randomised, placebo-controlled, double-blind, multi-centre, clinical trial to determine the efficacy and safety of Presendin in idiopathic intracranial hypertension
  • Recent NIPH Clinical Trials:Effects of exenatide on gastric emptying in Japanese patients with type 2 diabetes
  • Uses Exendin-4 can activate the GLP-1 receptor, the receptor can increase cAMP levels of pancreatic acinar cells in intracellular , but it has no effect on VIP receptor. Exendin-4 has been used as incretin mimetics for the treatment in HepG2 cells to exclude the influence of auxiliary material. It has also been used as an r (GLP-1R) agonist to exclude interference from auxiliary material. Antidiabetic.
  • Description Exenatide is the first drug in a new class of anti-diabetics known as the incretin mimetics, and it is indicated as adjunctive therapy to improve glycemic control in patients with type 2 diabetes who are taking metformin, a sulfonylurea, or both, but have not achieved adequate glycemic control. Exenatide is a functional analog of the human incretin Glucagon-Like Peptide-1 (GLP-1). GLP-1 is naturally released from cells in the GI tract in response to food intake and acts on its receptor on b-cells to potentiate glucose-stimulated insulin secretion. Exenatide is a long-acting agonist at the GLP-1 receptor. It is a synthetic version of a 39-amino acid peptide found in the salivary secretions of the Gila monster lizard.also moderates peak serum glucagon levels during hyperglycemic periods following meals, but does not interfere with glucagon release in response to hypoglycemia. The dosing regimen for exenatide is 5 or 10 mg twice daily, administered as a subcutaneous injection within an hour before morning and evening meals. Following subcutaneous administration, peak plasma concentrations of exenatide are reached in 2.1 h, and the plasma pharmacokinetic profile is dose proportional. The most common adverse events reported with exenatide include nausea, vomiting, diarrhea, feeling jittery, dizziness, headache, and dyspepsia.
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