Spectinomycin dihydrochloride pentahydrate

Spectinomycin dihydrochloride pentahydrate Chemical Properties
Melting point 205-207° (dec)
alpha D +14.8° (c = 0.42 in water)
storage temp. 2-8°C
solubility H2O: 50 mg/mL, clear, faintly yellow
form powder
color white to off-white
Water Solubility Soluble in water.Soluble in water, methanol, dimethyl sulfoxide, ethanol and dimethyl formamide.
Merck 14,8739
BRN 5684150
InChIKeyDCHJOVNPPSBWHK-UXXUFHFZSA-N
CAS DataBase Reference22189-32-8
Safety Information
Safety Statements 24/25
WGK Germany 2
RTECS WG7400000
10
HS Code 29419090
Toxicitymouse,LD50,intramuscular,> 5gm/kg (5000mg/kg),BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY),Japanese Journal of Antibiotics. Vol. 29, Pg. 43, 1976.
MSDS Information
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SigmaAldrich English
Spectinomycin dihydrochloride pentahydrate Usage And Synthesis
Chemical PropertiesWhite or almost white, slightly hygroscopic powder.
OriginatorTrobicin,Upjohn,US,1971
UsesSpectinomycin Dihydrochloride Pentahydrate is a new animal drug application (ANADA) administered in the drinking water of chickens as an aid in the control of airsacculitis; Also, it is an aminocylcitol antibiotic.
UsesSpectinomycin is an aminocyclitol antibiotic produced by S. spectabilis that is active against Gram-negative and Gram-positive bacteria. Spectinomycin inhibits protein synthesis by binding to the 30S ribosomal subunit and interfering with peptidyl tRNA translocation. Mutations in the gene for ribosomal protein S5 prevents binding of spectinomycin and contributes to bacterial resistance.
UsesAminocyclotol antibacterial.
DefinitionChEBI: A hydrate that is the pentahydrate form of spectinomycin hydrochloride. An antibiotic that is active against gram-negative bacteria and used to treat gonorrhea.
Manufacturing ProcessA lyophilized culture of Streptomyces spectabilis, NRRL 2792, was used to seed the following sterile agar medium on tubed slants:Tryptone 5 K2HPO4 0.5 NaCl 0.5 FeSO4 0.1 Agar 20
Deionized water to make 1 liter
The slants were incubated for 7 days at 30°C, after which time sporulation was complete. The spores from the agar slants were used, in an aqueous suspension, to inoculate 100 ml of preseed medium in a 500 ml Erlenmeyer flask. The sterile preseed medium consisted of:
Grams Dried whole yeast 10 Glucose 10 Pancreatic digest of 5 casein (N-Z-Amine B)
Tap water to make 1 liter adjusted to pH 7.2 before sterilizing
The seed flash was incubated for 24 hours at 32°C on a reciprocating shaker after which it was used as an inoculum for a 20 liter seed fermenter in the amount of approximately 5%. the 20 liter seed fermenter contained a sterile medium consisting of:
Grams Glucose 15 Cornstarch 25 Distiller's solubles 15 Brewer's yeast 10 Corn steep liquor 20
Tap water to make 1 liter adjusted to pH 7.2 before sterilizing
The 20 liter seed fermenter was incubated for 24 hours at 32°C and aerated at the rate of 6 standard liters or about 0.2 standard cubic feet of air per minute and agitated with a sweep stirrer. The 20 liter seed fermenter was used to inoculate 250 liters of the same medium in a 100 gallon fermentation tank. 1,200 ml of lard oil were added during the fermentation to control foaming. The tank was agitated with a propeller and aerated at the rate of 75 standard liters of air per minute. After 96 hours of fermentation the beer assayed 500 mcg/ml (18.3 mcg/mg on a dry basis) of actinospectacin. Actinospectacin is assayed by its activity against Klebsiella pneumoniae by standard agar diffusion procedure and based on crystalline actinospectacin sulfate according to US Patent 3,234,092.







Therapeutic FunctionAntibacterial
General DescriptionA broad spectrum aminoglycoside antibiotic that contains two glucose moieties. Footprint studies indicate that spectinomycin exerts regional effects on ribosomal structure. A resistance gene (aph) which encodes a spectinomycin has been cloned from Legionella pneumophila (disease agent for Legionnaire’s disease) kinase and expressed in E. coli. Potency: ≥500 μg/mg.
Biological Activityspectinomycin is an aminocyclitol antibiotic produced by s. spectabilis with activity against gram-negative bacterial species. spectinomycin has been used for the treatment of gonorrhea, where it inhibits microbial protein synthesis by binding to the 30s ribosomal subunit, protects the n‐7 position of e. coli 16s rrna residue g1064 from methylation by dimethyl sulfate. binding of spectinomycin at this location is thought to stabilize helix 34, inhibiting the binding of elongation factor g, thereby blocking translocation of peptidyl‐trnas from the ribosomal a site to the p site [1].spectinomycin selectively inhibited protein synthesis in cells and in extracts of e. coli. mutations to high-level resistance to this antibiotic map close to the streptomycin locus, and the site of action of spectinomycin, like that of streptomycin, is the 30s ribosomal subunit, as shown by experiments with reconstituted 70s ribosomes containing subunits from sensitive and from resistant ribosomes [2].
Biochem/physiol ActionsMode of Action: Spectinomycin acts by inhibiting protein synthesis and elongation by binding to the bacterial 30S ribosomal subunit and interfering with peptidyl tRNA translocation.Mode of Resistance: A mutation in rpsE, the gene for ribosomal protein S5, prevents the binding of spectinomycin. Resistance is also conferred by the aminoglycoside-3′-adenyltransferase gene (aadA). Antimicrobial spectrum: Spectinomycin acts against gram-negative and gram-positive bacteria.
references[1] zimmerman j m, maher l j. in vivo selection of spectinomycin‐binding rnas[j]. nucleic acids research, 2002, 30(24): 5425-5435.
[2] davies j, anderson p, davis b d. inhibition of protein synthesis by spectinomycin[j]. science, 1965, 149(3688): 1096-1098.
Spectinomycin dihydrochloride pentahydrate Preparation Products And Raw materials
Spectinomycin, Dihydrochloride, Pentahydrate Streptomyces sp,Spectinomycin, Dihydrochloride, Pentahydrate Streptomyces sp CIS-2-AMINOCYCLOHEXANOL HYDROCHLORIDE Spectinomycin dihydrochloride pentahydrate [1,4]DIOXAN-2-YLMETHYL-METHYL-AMINE SPECTINOMYCIN DIHYDROCHLORIDE,SPECTINOMYCIN DIHYDROCHLORIDE HYDRATE,SPECTINOMYCIN DIHYDROCHLORIDE N-HYDRATE TRANS-2-METHYLAMINO-CYCLOHEXANOL HYDROCHLORIDE SPECTINOMYCIN DIHYDROCHLORIDE lincospectin C-[1,4]DIOXAN-2-YL-METHYLAMINE TRANS-2-AMINOCYCLOHEXANOL HYDROCHLORIDE 3-methoxy-tetrahydropyran-4-one Dihydrochloride Spectinomycin sulfate tetrahydrate trans-2-Aminocyclo hexanol hydrochloride [1S,2R]-trans-2-Aminocyclohexanol hydrochloride Spectinomycin CIS-2-METHYLAMINO-CYCLOHEXANOL HYDROCHLORIDE 1,4-DIOXANE-2-CARBOXALDEHYDE

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