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Carperitide

Carperitide

Quick Details P roduct name: 98% purity Carperitide Acetate peptides, China Carperitide CAS No.: 89213-87-6 Other Names: ATRIAL NATRIURETIC PEPTIDE HUMAN MF: C127H203N45O39S3 Place of Origin: wuhan, China (Mainland) Type: Auxiliaries and Other Medicinal Chemicals Grade Standard: Medicine Grade...

Products Specifications:

Quick Details
Product name: 98% purity Carperitide Acetate peptides, China Carperitide
CAS No.: 89213-87-6

Other Names: ATRIAL NATRIURETIC PEPTIDE HUMAN

MF: C127H203N45O39S3

Place of Origin: wuhan, China (Mainland)

Type: Auxiliaries and Other Medicinal Chemicals

Grade Standard: Medicine Grade

Usage: Animal Pharmaceuticals

Brand Name: Dahua

Purity: 99.0%, 99%, 98%

Name: Carperitide Acetate

Packing: 1g/Plastic bottles

apperance: White powder


SupplyAbility
3000 Kilogram/Kilograms per Month 89213-87-6


Packaging & Delivery
Packaging Details
Carperitide Acetate, 1g plastic vial(dedicated for peptide packing) or glass via
Port
Shanghai
Lead Time: 2-3days
   
Specification example:

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


Product:

Carperitide

Cas No.:

89213-87-6

Molecular Formula:

C127H203N45O39S3

Structure:

图片5_副本.jpg


Related products

图片6_副本.jpg 


Pharmacological action of capecitabine

This product is synthesized by stimulating myocardial stretching, by intraventricular particles, and then through the coronary vein to distribute the whole body, acting on vascular smooth muscle and kidney and other tissues, regulating blood pressure and electrolyte balance in the body. It is a cyclic regulating hormone composed of 28 amino acids. Experiments have shown that particles in the ventricle of the rat can also synthesize this substance. Genetic recombination technology has been developed. Clinical trials have shown that this drug binds to GC-A receptor in vascular smooth muscle and kidney, activates guanylate cyclase, increases cyclic guanosine phosphate, and induces vasodilation and diuresis. Healthy male volunteers were intravenously injected with this drug at 50 and 100 ug/kg. The disappearance half-life of phases alpha, beta and alpha was 2.13 [0.38], 9.22 [1.24], 2.31 [0.56], and 10.9 [2.37] minutes respectively. The patients with heart failure were given 0.1 UG / (kg.min) for 60 minutes. The disappearance half-life of alpha phase was 2.83 (0.63) minutes, and that of beta phase was 25.3 (5.12) minutes.

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