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Home > Products >  linaclotide 98% high quality low price in stock

linaclotide 98% high quality low price in stock CAS NO.851199-59-2

  • Min.Order: 20 Milligram
  • Payment Terms: L/C,D/A,D/P,T/T,MoneyGram,Other
  • Product Details

Keywords

  • Linaelotide
  • Linaelotide Acetate
  • Peptide high quality low price in stock

Quick Details

  • ProName: linaclotide 98% high quality low price...
  • CasNo: 851199-59-2
  • Molecular Formula: C59H79N15O21S6
  • Appearance: White powder
  • Application: Research USE
  • DeliveryTime: In stock or 2-3day
  • PackAge: Foil bag
  • Port: HongKong or other
  • ProductionCapacity: 10 Kilogram/Month
  • Purity: 98(%)
  • Storage: Closed, - 2 ~ - 8℃ preservation.
  • Transportation: Fedex,EMS,UPS,TNT,DHL
  • LimitNum: 20 Milligram

Superiority

Item

Specification 

Specific rotation

+39.5 to +41.5° 

State of solution(transmittance)

Clear 98.0% min.

Chloride[cl]

0.020% max. 

Ammonium [NH4]

0.02% max. 

Sulfate[SO4]

0.020% max

Iron[Fe]

10ppm max.

Heavy metals [Pb]

10ppm max

Arsenic[As2O3]

1ppm max

Other amino acids

Chromatographically not detectable

Loss on drying

0.20% max. 

Residue on ignition[sulfated]

0.10% max.

Assay

99.0% min

Shipping

 

Details

Description

In August 2012, the US FDA approved linaclotide (also referred to as MD-1100), a first-in-class, orally administered 14-amino acid peptide as a therapy for patients suffering from chronic idiopathic constipation (CIC) and irritable bowel syndrome with constipation (IBS-C). Linaclotide and its active metabolite MM-419447, which results from the cleavage of the C-terminal tyrosine residue by carboxypeptidase A, mimic the actions of the endogenous intestinal peptides guanylin (15 amino acids) and uroguanylin (16 amino acids) by activating guanylyl cyclase C (GC-C) on the intestinal epithelium. Activation of GC-C leads to increased intra- and extracellular levels of cGMP and activation of the CFTR ion channel, resulting in increased levels of HCO3-, Cl-, and water in the intestinal lumen and accelerated gastrointestinal transit. Based on an in vitro assaymeasuring the accumulation of cGMP in T84 cell exposed to an agonist, the EC50 of linaclotide at pH 7.0 was 99±17.5 nM. In preclinical studies in mice using the transit of activated charcoal as ameasure of efficacy, linaclotide at 100 μg/kg significantly accelerated transit compared to wild-type mice treated with charcoal only or GC-Cnullmice treatedwith and without linaclotide.118 Efficacy was also seen in rats treatedwith linaclotide atdoses of 5, 10, and 20 μg/kg. Linaclotide has been synthesized using conventional solid-phase peptide technology.

 

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