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Spectinomycin (hydrochloride hydrate)

Catalog No.
C5621
aminocyclitol antibiotic
Grouped product items
SizePriceStock Qty
1g
$50.00
In stock
5g
$70.00
In stock
10g
$120.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

Tel: +1-832-696-8203

Email: [email protected]

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Background

Spectinomycin (hydrochloride hydrate; CAS 22189-32-8) is an aminocyclitol antibiotic derived from Streptomyces spectabilis, targeting bacterial protein synthesis by interacting specifically with the 30S ribosomal subunit. Binding near helix 34 of the 16S rRNA, spectinomycin inhibits protein translation by preventing elongation factor G-mediated translocation of peptidyl-tRNA from the ribosomal A-site to the P-site. Resistance mutations to spectinomycin align closely with those conferring streptomycin resistance, confirming the 30S subunit as its primary target. It is applied in biomedical research to study ribosomal function, antibiotic binding dynamics, and bacterial resistance mechanisms.

Chemical Properties

StorageStore at -20°C
M.Wt495.4
Cas No.22189-32-8
FormulaC14H24N2O7·2HCl [5H2O]
Solubility≥49.5 mg/mL in H2O; ≥3.61 mg/mL in EtOH with gentle warming and ultrasonic; ≥92 mg/mL in DMSO
Chemical Name(5aR,9aR,10aS)-decahydro-4aR,7S,9S-trihydroxy-2R-methyl-6S,8R-bis(methylamino)-4H-pyrano[3-b][1,4]benzodioxin-4-one, dihydrochloride pentahydrate
SDFDownload SDF
Canonical SMILES[H][C@@]12[C@@](C(C[C@@H](C)O2)=O)(O)O[C@]3([H])[C@@H](NC)[C@@H](O)[C@@H](NC)[C@H](O)[C@@]3([H])O1.Cl.Cl.O.O.O.O.O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Protocol

Cell experiment:[1]

Cell lines

Escherichia coli B

Reaction Conditions

50 μg/mL spectinomycin

Applications

When added to an exponentially growing culture, spectinomycin (50 μg/mL) rapidly and reversibly inhibited growth of Escherichia coli B. Amino acid incorporation was slowed immediately but RNA synthesis continued.

Animal experiment:[2]

Animal models

Male Sprague-Dawley rats, 200 ~ 225 g

Dosage form

10 mg/kg

Administered intravenously (IV)

Applications

Following IV administration, approximately 55% of the drug was excreted into the urine in unchanged form. Spectinomycin at the dose of 10 mg/kg showed a peak plasma concentration of 37.8 μg/mL and a systemic exposure (area-under the curve AUC0-∞) of 15.7 μg h/mL.

Note

The technical data provided above is for reference only.

References:

1. Davies J, Anderson P, Davis BD. Inhibition of protein synthesis by spectinomycin. Science, 1965, 149(3688): 1096-1098.

2. Madhura DB, Lee R, Meibohm B. Pharmacokinetic profile of spectinomycin in rats. Pharmazie, 2013, 68(8): 675-676.

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