Pharmaceutical Valnemulin HCl Valnemulin

Product Details
Customization: Available
Powder: Yes
Customized: Customized
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  • Pharmaceutical Valnemulin HCl Valnemulin
  • Pharmaceutical Valnemulin HCl Valnemulin
  • Pharmaceutical Valnemulin HCl Valnemulin
  • Pharmaceutical Valnemulin HCl Valnemulin
  • Pharmaceutical Valnemulin HCl Valnemulin
  • Pharmaceutical Valnemulin HCl Valnemulin
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  • Overview
  • Product Description
  • Product Details
  • Application&Function
  • Specification
Overview

Basic Info.

Model NO.
D-sung Valnemulin
Certification
GMP, HSE, ISO 9001, USP, BP
Suitable for
Elderly, Children, Adult
State
Powder
Purity
>99%
Product Name
Valnemulin
Name
Valnemulin Powder
Assay
HPLC 99%
Appearance
White Powder
Color
White
CAS No.
101312-92-9
Mf
C31h52n2o5s
MW
564.82
Melting Point
140-143°c
Boiling Point
672.7
Density
1.13
Test Method
HPLC
Grade
Veterinary Grade
Application
Antibacterial
Specific
COA
Transport Package
Negotiable
Specification
99%
Trademark
D-sung
Origin
Shaanxi Xi′an
Production Capacity
1000kg/Month

Product Description

Pharmaceutical Valnemulin HCl Valnemulin
Pharmaceutical Valnemulin HCL Valnemulin 
Product Description

Pharmaceutical Valnemulin HCl ValnemulinPharmaceutical Valnemulin HCl Valnemulin

Product Details

Pharmaceutical Valnemulin HCl Valnemulin

Product Name Valnemulin 
Appearance White Powder
CAS No. 101312-92-9
MF C31H52N2O5S
MW 564.82
Valnemulin is a new generation of pleuromutilin, a semi synthetic antibiotic belonging to the diterpenoid class. It belongs to the same class of drugs as tetracycline and is a specialized antibiotic for animals. Mainly used for preventing and treating mycoplasma disease and Gram positive bacterial infections in pigs, cattle, sheep, and poultry. In 1999, it was approved by the European Community for the prevention and treatment of swine dysentery caused by Brachyspira hyodyssenteriae infection and porcine endemic pneumonia caused by Mycoplasma pneumoniae infection. It is the first approved veterinary drug premix in Europe and is listed as a prescription drug for veterinary use. In January 2004, it was approved by the European Community for the prevention of porcine colonic spirochetes (colitis) caused by Brachyspira pilosicoli infection - a mild form of dysentery in growing pigs - and for the treatment of porcine proliferative bowel disease (ileitis) caused by intracellular Lawson bacteria infection. Porcine dysentery short spirochetes, colonic trichomonas short spirochetes, and intracellular Lawson bacteria are the main culprits of most growing pig enteritis.
Application&Function

Pharmaceutical Valnemulin HCl Valnemulin
Oral administration of vonimilin to pigs rapidly absorbs, with an absorption rate greater than 90%. The highest plasma concentration is reached 1-4 hours after administration, and the plasma half-life is 1.3-2.7 hours. Oral single dose of 10 mg/kg body weight vonidazole hydrochloride, peak time 1.85 hours, peak concentration 1.29 μ g/ml, area under the curve (AUC) 5.58 μ g/ml/hour. When the dose is 25mg/kg body weight, the peak time is 2.9 hours, the peak concentration is 2.67 μ g/ml, and the area under the curve (AUC) is 18.23 μ g/ml/hour; When the dose is 50mg/kg body weight, the peak time is 4.15 hours, the peak concentration is 6.23 μ g/ml, and the area under the curve (AUC) is 67.3 μ g/ml/hour; There is a linear relationship between plasma concentration and dosage. After repeated administration, slight accumulation occurred, but remained stable within 5 hours. Administer 5 mg/kg body weight twice a day, and maintain a stable plasma concentration for 7.5 days. Due to the obvious first pass effect, plasma concentration is affected by the administration method. But Vanillin is mainly concentrated in tissues, especially in lung and liver tissues. Five days after the last administration of 15 doses of radioactive markers of Warnimilin to pigs, the liver concentration was greater than six times the plasma concentration. 15mg/kg body weight per day, fed twice a day for 4 consecutive weeks. Two hours after discontinuation, the liver concentration was 1.58ug/g and the lung concentration was 0.23ug/g, while the plasma concentration was lower than the detection value.
Wonimaolin 200ppm mixed feeding, with a drug concentration of 5.20ug/ml in the colon contents; 75ppm mixed feeding, with a drug concentration of 1.68ug/ml in the colon contents. The concentration of colonic contents is linearly related to the concentration of mixed feeding.
Vanillin undergoes extensive metabolism and excretion in pigs, with metabolites mainly rapidly excreted through bile and feces. 87% of radioactive markers are excreted within 3 days after the last administration, and approximately 3% are excreted in urine during the same period.Pharmaceutical Valnemulin HCl Valnemulin

Specification

Pharmaceutical Valnemulin HCl ValnemulinPharmaceutical Valnemulin HCl Valnemulin
Pharmaceutical Valnemulin HCl ValnemulinPharmaceutical Valnemulin HCl ValnemulinPharmaceutical Valnemulin HCl ValnemulinPharmaceutical Valnemulin HCl ValnemulinPharmaceutical Valnemulin HCl Valnemulin

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