No determination is made of the product's enantiomeric composition.
Quality Segment
assay
≥98% (TLC)
form
powder
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria, parasites
mode of action
protein synthesis | interferes
SMILES string
O[C@H]1[C@H](O)[C@@H](CO)O[C@H](O[C@@]2([H])[C@H](O[C@@]3([H])[C@H](O)[C@H](O[C@]4([H])[C@H](N)[C@@H](O)[C@H](O)[C@H](CN)O4)[C@@H](CO)O3)[C@@H](O)[C@H](N)C[C@@H]2N)[C@@H]1N.C
InChI
1S/C23H45N5O14.CH4/c24-2-7-13(32)15(34)10(27)21(37-7)41-19-9(4-30)39-23(17(19)36)42-20-12(31)5(25)1-6(26)18(20)40-22-11(28)16(35)14(33)8(3-29)38-22;/h5-23,29-36H,1-4,24-28H2;1H4/t5-,6+,7+,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+;/m1./s1
InChI key
OYJABWUHUYVDMJ-UDXJMMFXSA-N
General description
Application
It is used to study bacterial protein synthesis at the level of 16S ribosomal RNA and 30S ribosome assembly. Paromomycin is used to study cytosine-cytosine (CC) mismatch-containing RNA molecules[1] and is used to inhibit Cryptosporidium infection of a human enterocyte cell line[2].
Biochem/physiol Actions
Mode of Action: Inhibits initiation and elongation during protein synthesis.
Packaging
Other Notes
1 of 1
This Item | |||
|---|---|---|---|
| antibiotic activity spectrum Gram-negative bacteria, parasites, Gram-positive bacteria | antibiotic activity spectrum Gram-negative bacteria, Gram-positive bacteria | antibiotic activity spectrum Gram-negative bacteria, Gram-positive bacteria | antibiotic activity spectrum - |
| Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level - |
| form powder | form powder | form powder | form solid |
| assay ≥98% (TLC) | assay - | assay - | assay - |
| mode of action protein synthesis | interferes | mode of action protein synthesis | interferes | mode of action protein synthesis | interferes | mode of action - |
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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I have found that Paranomycin has 2 forms, cys and trans. What form is this compound?
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