Pramlintide

Pramlintide

Pramlintide

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1 Gram

Negotiable

  • Min.Order :1 Gram
  • Purity: 98%
  • Payment Terms : T/T

Keywords

Pramlintide 196078-30-5 98

Quick Details

  • Appearance:White power
  • Application:INTERMEDITD
  • PackAge:According to your needs
  • ProductionCapacity:1000|Metric Ton|Day
  • Storage:room temp
  • Transportation:by air/sea/courier

Superiority:

Pramlintide acetate Basic information
Product Name:    Pramlintide acetate
Synonyms:    AMYLIN (HUMAN), 25-L-PROLINE-28-L-PROLINE-29-L-PROLINE-, ACETATE (SALT), HYDRATE;pramlintide acetate;pramlintide acetate hydrate;25-L-Proline-28-L-proline-29-L-proline-aMylin (huMan) Acetate Hydrate;AC-137 Acetate Hydrate, SyMlin Acetate Hydrate;Tripo-aMylin Acetate Hydrate;Pramlintide Acetate, Amylin Rat;Pramlintide Acetate impurity
CAS:    196078-30-5
MF:    C173H273N51O56S2
MW:    4027.46
EINECS:    251-228-4
Product Categories:    Amino Acids & Derivatives;Bases & Related Reagents;Drug Analogues;Heterocycles;Intermediates & Fine Chemicals;Nucleotides;Peptide;Pharmaceuticals
Mol File:    196078-30-5.mol
Pramlintide acetate Structure
Pramlintide acetate Chemical Properties
Melting point     >175°C (dec.)
storage temp.     Refrigerator
solubility     Acetic Acid (Slightly), DMSO (Slightly)
form     Solid
color     White to Off-White
CAS DataBase Reference    196078-30-5(CAS DataBase Reference)

Details:

Pramlintide acetate Usage And Synthesis
Description    Pramlintide acetate is an injectable human amylin analog that has been launched for the treatment of both type 1 and type 2 diabetes, in conjunction with insulin. While it is also a 37-amino acid peptide, it differs from its parent predecessor by the substitution of Ala-25, Ser-28, and Ser-29 with prolines. Not only do these modifications improve the solubility of the peptide, they also eliminate the aggregation observed with amylin, resulting in a stable synthetic analog with retention of biological activity that is suitable for pharmaceutical use. As an indication of potency, Pramlintide acetate inhibits the binding of radioiodinated rat amylin to rat nucleus accumbens membranes with a Ki value of 23 pM. Its mechanism of action mimics amylin; as a neurohormone that is cosecreted with insulin from the pancreatic β cells in response to meals, it is involved in glucose homeostasis. Both peptides lower postprandial glucose levels by inhibiting glucagon and by restraining the vagus-mediated rate of gastric emptying, thereby, slowing intestinal carbohydrate absorption. Furthermore, amylin, orPramlintide acetate, has the added benefit of inducing postprandial satiety resulting in weight loss in the patients with type 2 diabetes. Since Pramlintide acetate slows gastric emptying, it is contraindicated in patients with gastroparesis and in patients taking drugs that alter gastrointestinal motility (anticholinergic agents, such as, atropine) or slow down the intestinal absorption of nutrients (such as α-glucosidase inhibitors). Pramlintide acetate is also contraindicated in patients with hypoglycemic tendencies; due to co-administration with insulin, severe insulin-induced hypoglycemia is a risk. The most commonly reported adverse events include nausea, vomiting, anorexia, headache, abdominal pain, fatigue, dizziness, coughing, and pharyngitis.
Chemical Properties    Pramlintide acetate is White Solid
Originator    Amylin (US)
Uses    Pramlintide acetate is an analogue of human amylin used in the treatment of insulin dependent diabetes.
Brand name    Symlin (Amylin).
Clinical Use    Pramlintide acetate is a synthetic analogue of amylin (a 37-peptide) with proline substitutions at residues 25, 28, and 29. These substitutions change its physical properties such that it is commercially available for SC injection. When pramlintide is used in combination with insulin, it slows gastric emptying, lowers blood glucose levels after meals, and affords a feeling of fullness that leads to decreased caloric intake and the potential for weight loss. Pramlintide has been approved for use in adults with type I or type II diabetes as an adjunct along with insulin. The dose is quite different for type I (15–60 μg SC before meals) and type II diabetes (60–120 μg). The drug should be refrigerated before opening and may be kept at room temperature for up to 28 days after opening.

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