- Product Details
Keywords
- Exenatide acetate
- 141732-76-5
- C186H284N50O62S
Quick Details
- ProName: lower price Exenatide acetate(141732-...
- CasNo: 141732-76-5
- Molecular Formula: C186H284N50O62S
- Appearance: white powder
- Application: used for research
- DeliveryTime: 3 days
- PackAge: aluminum foil bag
- Port: shenzhen
- ProductionCapacity: 1 Metric Ton/Day
- Purity: 99%min
- Storage: Store in cool, dry, ventilated place
- Transportation: by sea or by air
- LimitNum: 1 Gram
- Related Substances: N/A
- Residue on Ignition: N/A
- Heavy Metal: N/A
- Valid Period: one year
- N/A: N/A
Superiority
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Details
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Exenatide Acetate
product Name Exenatide acetate
Synonyms enfuvirtide acetate; His-Gly-Gly-Gly-Thr-Phe-Thr-Ser-Asp-Leu-Ser-Lys-Gln-Met-Glu-Glu-Glu-Ala-Val-Arg-Leu-Phe-Ile-Glu-Trp-Leu-Lys-Asn-Gly-Gly-Pro-Ser-Gly-Ala-Pro-Pro-Pro-Ser-NH{2}; ExenatideAcetate
Molecular Formula C184H282N50O60S C2H4O2
Molecular Weight 4262.67
CAS Registry Number 141732-76-5
Exenatide, an incretin mimic peptide comprised of 39 amino acid residue, is a new antidiabetic drug approved by FDA in 2005 for the treatment of diabetes mellitus type 2.The main physiological functions are followings: Promote insulin excretion in glucose-dependence manner, restoration of glucose sensitivity to the islets, inhibition of apoptosis of existing cells and increase the number of β Cells, inhibition of gastric emptying leads to decreased food intake and reduced body weight. The exenatide therapy has the following advantages to compare with insulin therapy: No hypoglycemia effect, reducing body weight, improving insulin resistance, promoting islets cell function of patients.
Exenatide is developed and marketed (brand name Byetta) by Amylin Pharmaceuticals and Eli Lilly and Company. Due to some historical reasons, there is no compound patent for the drug in many countries. The API of the drug and generics have been developed and currently under clinical trial in China. Beyel Pharmaceutical is capable of manufacturing Exenatide Acetate by solid phase synthesis under GMP compliance