| Weight | 615.634 g/mol |
|---|---|
| Formula | C23H45N5O14 |
| Hydrogen Acceptors | 19 |
| Hydrogen Donors | 13 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
paromomycin (1263-89-4, 7542-37-2)
Humatin · Paromomycin Sulfate · Paramomycin
Score:
#387 in Microbiology
,
#1198 in Biochemistry
,
#3022 in Biology
,
#3775 in Chemistry
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- Crystal structure of paromomycin docked into the eubacterial ribosomal decoding A site. (Structure, 2001)
- Injectable Paromomycin for Visceral Leishmaniasis in India (The New England Journal of Medicine, 2007)
- Paromomycin binding induces a local conformational change in the A-site of 16 S rRNA. (Journal of Molecular Biology, 1998)
- Early Bactericidal Activity of Paromomycin (Aminosidine) in Patients with Smear-Positive Pulmonary Tuberculosis (Antimicrobial Agents and Chemotherapy, 2000)
- The nucleotide sequence of the 17S ribosomal RNA gene of Tetrahymena thermophila and the identification of point mutations resulting in resistance to the antibiotics paromomycin and hygromycin. (Journal of Biological Chemistry, 1985)
- PAROMOMYCIN. I. PAROMAMINE, A GLYCOSIDE OF D-GLUCOSAMINE1 (Journal of the American Chemical Society, 1959)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Humatin
- Paromomycin Sulfate
- Paramomycin
- Aminosidine
- Paromomycin I
- Catenulin
- Gabbromycin
- Paromomycin Phosphate
- beta-D-Glucopyranosyl-Isomer Paromomycin
- Neomycin E
- Hydroxymycin
- Paromomycin Sulfate (1:1)
- Paromomycin, beta D Glucopyranosyl Isomer
- Paromomycin Sulfate (2:5)
- Estomycin
-
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-
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- Pubchem - paromomycin
- Wikipedia - paromomycin
Paromomycin is an antibiotic used to treat a number of infections including amebiasis, giardiasis, leishmaniasis, and tapeworm infection. It is a first line treatment for amebiasis or giardiasis during pregnancy. Otherwise it is generally a second line treatment option.
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