Josamycin

Josamycin Struktur
16846-24-5
CAS-Nr.
16846-24-5
Englisch Name:
Josamycin
Synonyma:
C12662;EN 141;Jomybel;YL-704A3;Iosalide;Josacine;Josamina;Wilprafen;Vilprafen;JOSAMYCIN
CBNumber:
CB5444692
Summenformel:
C42H69NO15
Molgewicht:
827.99
MOL-Datei:
16846-24-5.mol

Josamycin Eigenschaften

Schmelzpunkt:
131.5℃
alpha 
D25 -70° (c = 1 in ethanol)
Siedepunkt:
763.27°C (rough estimate)
Dichte
1.1547 (rough estimate)
Brechungsindex
1.6220 (estimate)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
Löslichkeit
Soluble in ethanol
pka
7.1 (40% aq methanol)
Aggregatzustand
powder
Farbe
white to slightly yellow
Merck 
13,5286
Stabilität:
Hygroscopic
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
WGK Germany  2
RTECS-Nr. OH4725810
10
Toxizität LD50 oral in rat: > 7gm/kg
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitsschädlich bei Verschlucken. Akute Toxizität oral Kategorie 4 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P270, P301+P312, P330, P501
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P270 Bei Gebrauch nicht essen, trinken oder rauchen.
P301+P312 BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P330 Mund ausspülen.
P501 Inhalt/Behälter ... (Entsorgungsvorschriften vom Hersteller anzugeben) zuführen.

Josamycin Chemische Eigenschaften,Einsatz,Produktion Methoden

Chemische Eigenschaften

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.

Verwenden

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.

Pharmazeutische Anwendungen

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.

Biologische Aktivität

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.

Josamycin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Josamycin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 219)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hubei Ipure Biology Co., Ltd
+8613367258412
ada@ipurechemical.com China 10326 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5993 58
Firsky International Trade (Wuhan) Co., Ltd
+8615387054039
admin@firsky-cn.com China 436 58
airuikechemical co., ltd.
+undefined86-15315557071
sales02@airuikechemical.com China 994 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714
fandachem@gmail.com China 9348 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795
ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Zhejiang ZETian Fine Chemicals Co. LTD
18957127338
stella@zetchem.com China 2141 58
Shandong chuangyingchemical Co., Ltd.
18853181302
sale@chuangyingchem.com CHINA 5909 58

16846-24-5()Verwandte Suche:


  • 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
  • 3-acetate4(supb)-(3-methylbutanoate)
  • C12662
  • Josamycin solution solution,1000ppm
  • Josamycin solution
  • JOSAMYCIN
  • LEUCOMYCIN V,3-AC-ETA 4B-(3-METHYLBUTANOATE)
  • LEUCOMYCIN V,3-ACETA 4BETA-(3-METHYL BUTANOATE)
  • LEUCOMYCIN A3
  • antibioticyl-704a3
  • kitasamycina3
  • leucomycinv,3-acetate4(supb)-(3-methylbutanoate)
  • turimycina5
  • EN 141
  • Iosalide
  • Jomybel
  • Josacine
  • Josamina
  • Leucomycin A3 (8CI)
  • Leucomycin V, 3-acetate 4B-(3-methylbutanoate) (9CI)
  • LEUCOMYCIN V,3-ACETA 4β-(3-METHYL BUTANOATE)
  • Josamycin Standard
  • Josamycin for peak identification CRS
  • Josamycin CRS
  • JOSAMYCIN USP/EP/BP
  • (2S,3S,4R,6S)-6-(((2R,3S,4R,5R,6S)-6-(((4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-Acetoxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-6-yl)oxy)-4-(dimethylamino)-5-hydroxy-2-methyltetrahydro-2H-pyran-3-yl)oxy)-4-hydroxy-2,4-
  • [(2S,3S,4R,6S)-6-[(2R,3S,4R,5R,6S)-6-[[(4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-acetyloxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-5-hydroxy-2-methyloxan-3-yl]oxy-4-hydroxy-2,4-dimethyloxa
  • Pre-validation
  • JOSAMYCIN(16846-24-5)
  • (4R,5S,6S,7R,9R,10R,11E,13E,16R)-4-(acetyloxy)-6-[[3,6-dideoxy-4-O-[2,6-dideoxy-3-C-methyl-4-O-(3-methylbutanoyl)-α-L-ribo-hexopyranosyl]-3-(dimethylamino)-β-D-glucopyranosyl]oxy]-10-hydroxy-5-methoxy-9,16-dimethyl-7-(2-oxoethyl)oxacyclohexadeca-11,13-dien-2-one (josamycin)
  • Sparsentan Impurity 65
  • Leucomycin A3 (>90%)
  • lucamycin
  • 16846-24-5
  • C42H69NO15
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