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22189-32-8 | Spectinomycin (dihydrochloride pentahydrate)

Spectinomycin (dihydrochloride pentahydrate) NLT 98%

Product Number : MC541895

CAS Number : 22189-32-8

Molecular Formula : C14H36Cl2N2O12 | Molecular Weight : 495.35

Synonyms : Spectinomycin (hydrochloride hydrate)

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Purity NLT 98%
Storage at 20ºC 2 years
MolCore specializes in manufacturing high-purity CAS No.22189-32-8, Spectinomycin (dihydrochloride pentahydrate) with the molecular formula C14H36Cl2N2O12 and molecular weight 495.35 delivering critical API intermediates for global pharmaceutical and research industries, certified under ISO quality systems.

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Chemical Name Spectinomycin (dihydrochloride pentahydrate)
CAS Number 22189-32-8
MDL Number MFCD00070403
Molecular Formula C14H36Cl2N2O12
Molecular Weight 495.35
Synonyms Spectinomycin (hydrochloride hydrate)
Introduction of 22189-32-8 :

Spectinomycin dihydrochloride pentahydrate is a broad-spectrum aminocyclitol antibiotic that inhibits the growth of a variety of gram-positive and gram-negative organisms. In Vitro: Spectinomycin selectively inhibits protein synthesis in cells and in extracts of Escherichia coli. When added to an exponentially growing culture, spectinomycin (50 μg/mL) rapidly and reversibly inhibits growth of Escherichia coli. Amino acid incorporation is slowed immediately but RNA synthesis continued. In extracts of Escherichia coli B, spectinomycin inhibits polypeptide synthesis directed either by endogenous messenger RNA or by MS-2 bacteriophage RNA. Maximum inhibition (70 to 80%) is achieved at 1 μg/mL (3 μM). [1]. Spectinomycin blocks the translocation of peptidyl-tRNAs from the A-site to the P-site by inhibiting the binding of elongation factor G to the ribosome. Spectinomycin interacts specifically with the residues G1064 and 01192 in 16S rRNA and potentially change this molecule into an inactive conformation[2]. Spectinomycin acts as a mixed noncompetitive inhibitor for the td intron RNA with a Ki of 7.2 mM. The splicing inhibition by spectinomycin is dependent on pH changes and Mg2+ concentration, indicating electrostatic interactions with the intron RNA[3]. In Vivo: Renal excretion is a major elimination pathway for spectinomycin. Following IV administration, approximately 55% of the drug is excreted into the urine in unchanged form. After IV administration of 10 mg/kg spectinomycin shows a peak plasma concentration of 37.8 μg/mL and a systemic exposure (area-under the curve AUC0-∞) of 15.7 μg/mL. Following single dose intramuscular administration, the overall elimination half-life of spectinomycin is 1.2 h in cattle, 1.0 h in sheep, 1.0 h in pigs, 1.65 h in chicken and 1.85 h in humans[4].