Pharmaceutical Intermediate Weight Loss 99% Purity API Powder Peptide CAS 204656-20-2 Saxenda Liraglutide with Bulk Price

China Pharmaceutical Intermediate Weight Loss 99% Purity API Powder Peptide CAS 204656-20-2 Saxenda Liraglutide with Bulk Price, Find details about China Liraglutide, Liraglutid from Pharmaceutical Intermediate Weight Loss 99% Purity API Powder Peptide CAS 204656-20-2 Saxenda Liraglutide with Bulk Price

Model NO.
A-161
Sample
Available
MOQ
1kg
Appearance
White Powder
Assay
99%
Test Method
HPLC
Packing
1kg/Bag; 25kg/Drum
Storage
Cool&Dry Places
CAS No.
204656-20-2
Molecular Formula
C172h265n43o51
Molecular Weight
3751.202
Coa
Available
MSDS
Available
Grade
Pharmaceutical Grade
Application
Pharmaceutical
Brand
Greenway
Trademark
Greenway
Transport Package
1kg/Bag; 25kg/Drum
Specification
1kg/Bag; 25kg/Drum
Origin
Jiangsu
HS Code
2942000000
Model NO.
A-161
Sample
Available
MOQ
1kg
Appearance
White Powder
Assay
99%
Test Method
HPLC
Packing
1kg/Bag; 25kg/Drum
Storage
Cool&Dry Places
CAS No.
204656-20-2
Molecular Formula
C172h265n43o51
Molecular Weight
3751.202
Coa
Available
MSDS
Available
Grade
Pharmaceutical Grade
Application
Pharmaceutical
Brand
Greenway
Trademark
Greenway
Transport Package
1kg/Bag; 25kg/Drum
Specification
1kg/Bag; 25kg/Drum
Origin
Jiangsu
HS Code
2942000000
Pharmaceutical Intermediate Weight Loss 99% Purity API Powder Peptide CAS 204656-20-2 Saxenda Liraglutide with Bulk Price
Product NameLiraglutide
CAS No.204656-20-2
Molecular FormulaC172H265N43O51
Molecular Weight3751.202
AppearanceWhite Powder
Assay99%
GradePharmaceutical Grade
BrandGreenway

Product Introduction:

Liraglutide (NN2211) is a long-acting glucagon-like peptide-1 receptor agonist, binding to the same receptors as does the endogenous metabolic hormone GLP-1 that stimulates insulin secretion. Marketed under the brand name Victoza, it is an injectable drug developed by Novo Nordisk for the treatment of type 2 diabetes. In 2015, Novo Nordisk began marketing it in the U.S. under the brand name Saxenda as a treatment for obesity in adults with at least one weight-related comorbid condition.
Liraglutide was approved for treatment of type 2 diabetes by the European Medicines Agency (EMA) on July 3, 2009, and by the U.S. Food and Drug Administration (FDA) on January 25, 2010. More recently, Liraglutide was approved by the FDA on December 23, 2014 for treatment for obesity in adults with some related comorbidity.

Pharmaceutical Intermediate Weight Loss 99% Purity API Powder Peptide CAS 204656-20-2 Saxenda Liraglutide with Bulk PriceProduct Functions&Applications:
Medical Uses
Liraglutide is a once-daily injectable derivative of the human incretin (metabolic hormone) glucagon-like peptide-1 (GLP-1), for the treatment of type 2 diabetes or obesity.

Type 2 Diabetes
Liraglutide improves control of blood glucose. It reduces meal-related hyperglycemia (for 24 hours after administration) by increasing insulin secretion (only) when required by increasing glucose levels, delaying gastric emptying, and suppressing prandial glucagon secretion.
In common to various degrees with other GLP-1 receptor agonists, liraglutide has advantages over more traditional therapies for type 2 diabetes:
It acts in a glucose-dependent manner, meaning it will stimulate insulin secretion only when blood glucose levels are higher than normal, preventing "overshoot". Consequently, it shows negligible risk of hypoglycemia.
It has the potential for inhibiting apoptosis and stimulating regeneration of beta cells (seen in animal studies).
It decreases appetite and inhibits body weight gain, as shown in a head-to-head study versus glimepiride.
It lowers blood triglyceride levels.
Obesity
Liraglutide has been approved as an injectable adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adult patients. The specified criteria are an initial body mass index (BMI) of 30 kg/m2 or greater (obese), or 27 kg/m2 or greater (overweight), in the presence of at least one weight-related comorbid condition (e.g. hypertension, type 2 diabetes mellitus, or dyslipidemia). In late 2014, data were reported from the SCALE™ Obesity and Prediabetes trial, which is a randomised, double-blind, placebo-controlled, multinational trial in non-diabetic people with obesity and non-diabetic people who are overweight with comorbidities. In this phase 3a trial, there were 3,731 participants randomised to treatment with liraglutide 3 mg or placebo, both in combination with diet and exercise. Those who completed the 56-week trial achieved an average weight loss of 9.2%, to be compared with a 3.5% reduction in the placebo group.

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