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Josamycin

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Josamycin Basic information

Product Name:
Josamycin
Synonyms:
  • Vilprafen
  • Wilprafen
  • Josamycin Solution, 100ppm
  • Josamycin for peak identification
  • 3-Acetate 4B-(3-Methylbutanoate)leucoMycin V
  • LeucoMycin V, 3-acetate4B-(3-Methylbutanoate)
  • Leucomycin V 3-acetate 4''-(3-methylbutanoate)
  • YL-704A3
CAS:
16846-24-5
MF:
C42H69NO15
MW:
827.99
EINECS:
240-871-6
Product Categories:
  • Amines
  • Chiral Reagents
  • Antibiotic Explorer
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • A - KAntibiotics
  • Antibacterial
  • Antibiotics A to
  • Antibiotics G-MAntibiotics
  • Chemical Structure Class
  • Interferes with Protein SynthesisAntibiotics
  • Macrolides
  • Mechanism of Action
  • Spectrum of Activity
Mol File:
16846-24-5.mol
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Josamycin Chemical Properties

Melting point:
131.5℃
alpha 
D25 -70° (c = 1 in ethanol)
Boiling point:
763.27°C (rough estimate)
Density 
1.1547 (rough estimate)
refractive index 
1.6220 (estimate)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Soluble in ethanol
form 
powder
pka
7.1 (40% aq methanol)
color 
white to slightly yellow
Merck 
13,5286
Stability:
Hygroscopic
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Safety Information

WGK Germany 
2
RTECS 
OH4725810
10
Toxicity
LD50 oral in rat: > 7gm/kg

MSDS

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Josamycin Usage And Synthesis

Chemical Properties

Josamycin is a macrolide substance having antibacterial activity produced by the growth of Streptomyces narboensis var. josamyceticus.
Josamycin appears as white to yellowish white powder, slightly hygroscopic. Josamycin is very soluble in methanol or in ethanol, and very slightly soluble in water.

Originator

Josalid,Biochemie

Uses

Josamycin, is used as a macrolide antibiotic effective against a variety of pathogens.

Uses

As a 16-membered ring macrolide antibiotic with antimicrobial activity against a wide range of pathogens. Josamycin can be particularly used in the treatment of Mycoplasma infection.
Josamycin is used to study the modification of phagocytosis and cytokine production by macrolide antibiotics, immunomodulatory effects, the suppression of matrix metalloproteinase production as well as study bacteria protein synthesis at the level of the the 23S rRNA, 50S ribosomal subunit.

Definition

ChEBI: A macrolide antibiotic produced by certain strains of Streptomyces narbonensis var. josamyceticus.

Manufacturing Process

100 ml of a culture medium consisting of water containing 1.5% soybean meal, 1% starch, 1% glucose, 0.3% sodium chloride, 0.1% dipotassium hydrogen phosphate, and 0.05% magnesium sulfate was placed in a 500 ml flask and sterilized for 20 min at 120°C. After cooling, the culture medium was inoculated with strain A 205-P2 Streptomyces narbonensis var. josatny ceticus, and the strain was subjected to shaking culture at 27°-29°C and at 130 strokes per min and 8 cm amplitude. After 3 days of culture, the culture fluids in such 100 flasks were combined together and filtered to give 8700 ml of culture filtrate. The pH of the filtrate was 6.4 and showed an inhibition zone of 25 mm. to Bacillus subtilis (PCI 219 strain). The filtrate was extracted with 8700 ml of ethyl acetate. The extract (7300 ml) thus obtained was concentrated to 730 ml under vacuum at temperatures lower than 50°C, 360 ml of water added, and then concentrated hydrochloric acid added to ad just the pH to 2.0, whereby josamycin was transferred to the aqueous layer. After adjusting the pH of the aqueous layer to 7.5 by the addition of 0.1 N sodium hydroxide, josamycin was extracted with 180 ml of ethyl acetate.
Josamycin was then transferred to 90 ml of an aqueous solution at pH 2.0 and extracted again with 45 ml of ethyl acetate as above process. Ethyl acetate solution thus obtained was evaporated under reduced pressure to give a solidified product, which was dissolved in 5 ml of benzene to remove impurities and the product, solidified from the benzene solution by evaporating under reduced pressure, was dissolved in a small amount of ethyl acetate and subjected to an alumina chromatography. That is, Brockman alumina (Merck) was treated with hydrochloric acid, sufficiently rinsed with water, and activated by heating for 5 h at 150°C.
50.0 g of thus treated alumina was filled in a glass tube of 1.6 cm in diameter by using ethyl acetate. The above prepared ethyl acetate solution was added to the alumina column and the product was eluted with 200 ml of ethyl acetate. The eluate thus obtained was concentrated under reduced pressure and the solid product thus obtained was dissolved in 5 ml of benzene and 50 ml of n-hexane added to give 0.18 g of amorphous josamycin having a purity of above 90%.

Therapeutic Function

Antibiotic

Pharmaceutical Applications

A naturally occurring antibiotic produced by Streptomyces narbonensis var. josamyceticus and belonging to the leucomycin group of macrolides. It is formulated for oral administration.
Many Gram-positive and Gram-negative anaerobes are susceptible, including Peptostreptococcus spp., Propionibacterium spp., Eubacterium spp. and Bacteroides spp.
After a single 1 g oral dose, a peak serum concentration of 2.74 mg/L was achieved 0.75 h after dosing. The AUC was 4.2 mg.h/L, and the apparent elimination half-life 1.5 h. Several inactive metabolites could be detected. It penetrates into saliva, tears and sweat, and achieves high levels in bile and lungs. It is mostly metabolized and excreted in the bile in an inactive form. Less than 20% of the dose appears in the urine, producing levels of around 50 mg/L.
The drug is generally well tolerated, producing only mild gastrointestinal disturbance. Its uses are similar to those of erythromycin. It is of limited availability.

Biological Activity

Josamycin inhibits bacterial protein biosynthesis by inhibiting peptidyltransferase and ribosomal translocation, and depleting the intracellular pools of aminoacyl-tRNAs available for protein synthesis by drop-off and incomplete peptidyl-tRNA hydrolase activity. It slows down formation of the first peptide bond of a nascent peptide in an amino acid-dependent way and inhibits formation of the second or third peptide bond.

JosamycinSupplier

Wellman Pharmaceutical Group Limited Gold
Tel
027-83778875 15807197853
Email
15807197853@163.com
Hubei wei shi reagent group ltd., company Gold
Tel
027-59105166 13125137732
Email
2853863890@qq.com
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Email
waley188@sohu.com