| Weight | 713.713 g/mol |
|---|---|
| Formula | C23H47N5O18S |
| Hydrogen Acceptors | 21 |
| Hydrogen Donors | 15 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 9 |
Paromomycin sulfate (1263-89-4)
Paromomycin · Humatin · Paramomycin
Score:
#599 in Microbiology
,
#2467 in Biochemistry
,
#4829 in Biology
,
#6165 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. - Paromomycin
- Humatin
- 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
-
SMILESC1C(C(C(C(C1N)OC2C(C(C(C(O2)CO)O)O)N)OC3C(C(C(O3)CO)OC4C(C(C(C(O4)CN)O)O)N)O)O)N.OS(=O)(=O)O
-
InChIKeyLJRDOKAZOAKLDU-UHFFFAOYSA-N
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