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Avexitide

Base Information Edit
  • Chemical Name:Avexitide
  • CAS No.:133514-43-9
  • Molecular Formula:C149H234N40O47S
  • Molecular Weight:3369.76
  • Hs Code.:
  • ChEMBL ID:CHEMBL4070972
  • DSSTox Substance ID:DTXSID00158156
  • Metabolomics Workbench ID:155107
  • NCI Thesaurus Code:C133230
  • Mol file:133514-43-9.mol
Avexitide

Synonyms:exendin (9-39);exendin (9-39) amide;exendin(9-39)amide;exendin-(9-39)

Suppliers and Price of Avexitide
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
  • Tocris
  • Exendin-3(9-39)amide
  • 1
  • $ 441.00
  • Sigma-Aldrich
  • Exendin Fragment 9-39 ≥95% (HPLC)
  • .1mg
  • $ 315.00
  • Sigma-Aldrich
  • Exendin Fragment 9-39 ≥95% (HPLC)
  • 0.1 mg
  • $ 327.00
  • ChemScene
  • Avexitide 99.70%
  • 5mg
  • $ 972.00
  • ChemScene
  • Avexitide 99.70%
  • 1mg
  • $ 324.00
  • ChemScene
  • Avexitide 99.70%
  • 500ug
  • $ 204.00
  • Cayman Chemical
  • Exendin-3 (9-39) amide ≥95%
  • 1mg
  • $ 209.00
  • Cayman Chemical
  • Exendin-3 (9-39) amide ≥95%
  • 500μg
  • $ 355.00
  • Biorbyt Ltd
  • Exendin (9-39) peptide > 95%
  • 1 mg
  • $ 397.80
  • American Custom Chemicals Corporation
  • EXENDIN (9-39) 95.00%
  • 0.5MG
  • $ 762.30
Total 27 raw suppliers
Chemical Property of Avexitide Edit
Chemical Property:
  • PSA:1415.58000 
  • Density:1.51g/cm3 
  • LogP:0.73500 
  • Storage Temp.:−20°C 
  • Water Solubility.:Soluble in water at 1mg/ml 
  • XLogP3:-16.7
  • Hydrogen Bond Donor Count:45
  • Hydrogen Bond Acceptor Count:52
  • Rotatable Bond Count:109
  • Exact Mass:3368.6904307
  • Heavy Atom Count:237
  • Complexity:8000
Purity/Quality:

98%,99%, *data from raw suppliers

Exendin-3(9-39)amide *data from reagent suppliers

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

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • 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)N
  • Isomeric SMILES:CC[C@H](C)[C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(=O)N)C(=O)NCC(=O)NCC(=O)N3CCC[C@H]3C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](C)C(=O)N4CCC[C@H]4C(=O)N5CCC[C@H]5C(=O)N6CCC[C@H]6C(=O)N[C@@H](CO)C(=O)N)NC(=O)[C@H](CC7=CC=CC=C7)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](C(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(=O)O)N
  • Recent ClinicalTrials:Avexitide Safety and Efficacy to Treat Acquired Hyperinsulinemic Hypoglycemia
  • Description Exendin-3 (9-39) amide is a truncated form of the exendin-4 peptide that acts as a potent competitive antagonist for the glucagon-like peptide 1 receptor (GLP-1R; Kd = 1.7 nM in CHL cells transfected with cloned human GLP-1). It inhibits exendin-3-induced increases in cAMP levels in guinea pig pancreas cells (IC50 = 20 nM). Exendin-3 (9-39) amide administration in the hypothalamus (10 and 100 μg, i.c.v.) reverses GLP-1 inhibition of feeding behavior in rats.
  • Uses Biological probe. Exendin-3 (9-39) is a potent and selective GLP-1 receptor antagonist.
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