| Company Name: |
Shanghai HongTide Biotechnology Co.,Ltd. Gold
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| Tel: |
19961912513 |
| Email: |
sales@hongtide.com |
| Products Intro: |
Product Name:Pramlintide
Purity:99% HPLC MS Package:1mg；5mg；10mg；100mg；500mg；1kg；5kg；25kg
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| Company Name: |
Chengdu Youngshe Chemical Co., Ltd.
|
| Tel: |
028-62328193 17380623303 |
| Email: |
Caroline@youngshechem.com |
| Products Intro: |
Product Name:Pramlintide
Purity:>95% Package:1g; 10g; 100g
|
| Company Name: |
Hangzhou Go Top Peptide Biotech
|
| Tel: |
0571-88211921 13355716090 |
| Email: |
Sales@gotopbio.com |
| Products Intro: |
Product Name:Pramlintide
Purity:98% HPLC Package:1mg;10mg;100mg;1g;100g
|
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| | Pramlintide Basic information |
| | Pramlintide Chemical Properties |
| | Pramlintide Usage And Synthesis |
| Description | Pramlintide is an analogue of amylin in which proline has replaced the normal amino acids at positions 25, 28, and 29, as
indicated above. The result of these substitutions is an increase in water solubility and a reduced tendency for
self-aggregation. | | Uses | Antidiabetic. | | General Description | Pramlintide is the 25-L-proline-28-L-proline-29-L-prolinetrisubstitution product of human amylin. The marketedformulation (Symlin) is an acetate salt, the exactcomposition of which may not be public-domain knowledge,although salts containing up to four acetic acidmolecules per pramlintide molecule would be possible byvirtue of the free amino terminus andLys1, Arg11, andHis18 residues. The carboxyl terminus of pramlintide, as inamylin, is amidated, and there are no appreciably acidicmoities in the structure; thus, in solution at the pH of bloodand tissues pramlintide would be present almost entirely asone or the other of two significant molecular species, onehaving a +3 charge (histidine imidazole deprotonated anduncharged) predominating modestly over the quadruplyprotonated (+4) species. | | Mechanism of action | Amylin receptors have been identified in distinct areas of the brain, including the nucleus accumbens and the dorsal vagal
complex. Stimulation of these receptors reduces food intake and depresses GI motility. It is assumed that pranlintide
stimulates these receptors, leading to the reported benefits of the drug in patients with diabetes, although the exact
mechanism is still poorly understood. Pranlintide causes a moderate reduction in HbA1c and postprandial glucose levels
when used in combination with insulin, which has benefits in normalizing fluctuations of circulating glucose levels. | | Pharmacokinetics | Pramlintide is administered via subcutaneous injection immediately before meals, reaches maximum circulating
concentrations within 20 minutes, and has a half-life of 29 minutes. The drug is eliminated from the body primarily through
the kidney. The plasma concentrations are similar to those seen with postprandial amylin. Because the drug is formulated
at pH 4.0, it is potentially incompatible with insulin (pH 7.8) if administered within the same syringe, although one study of
pramlintide combined with Novolin or Humulin did not show changes in the pharmacokinetics of either drugs. | | Clinical Use | Pramlintide’s effects upon administration to patients almostcertainly arise in significant measure from directAMY-mediated actions within the brainstem. Amylin receptorsare abundant in the circumventricular organs, includingthe subfornical organ (where AMY1(a) receptors areknown to be expressed in relative abundance), the organumvasculosum lateralis terminalis, and the area postrema(AMY3(a)), where the action of pramlintide (or of -cell–secretedamylin) is not precluded by a diffusional BBB.Amylin receptors are also expressed in various other brainareas, in particular the nucleus accumbens, but neitheramylin or pramlintide circulating in the bloodstream arelikely to exert any action at these BBB-shielded locations.Direct amylin receptor–mediated actions of pramlintide in the periphery, if any, remain poorly characterized.Unsurprisingly, though, the appetite-suppressing actions,and benefits of pramlintide and amylin agonists in general,are receiving significant clinical and scientific attention. | | Side effects | The major side effects reported for pramlintide consist of mild to moderate nausea, with severe nausea appearing in
patients using large doses of the drug. The nausea may decrease on continued use of the drug. The rate of hypoglycemia
appears to be quite low. |
| | Pramlintide Preparation Products And Raw materials |
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