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Paromomycin

Catalog No. DB01421 Name DrugBank
CAS Number 1263-89-4 Website http://www.ualberta.ca/
M. F. C23H45N5O14 Telephone (780) 492-3111
M. W. 615.6285 Fax (780) 492-1071
Purity Email david.wishart@ualberta.ca
Storage Chembase ID: 1229

SYNONYMS

IUPAC name
(2R,3S,4R,5R,6S)-5-amino-6-{[(1R,2R,3S,4R,6S)-4,6-diamino-2-{[(2S,3R,4S,5R)-4-{[(2R,3R,4R,5S,6S)-3-amino-6-(aminomethyl)-4,5-dihydroxyoxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3-hydroxycyclohexyl]oxy}-2-(hydroxymethyl)oxane-3,4-diol
IUPAC Traditional name
(2R,3S,4R,5R,6S)-5-amino-6-{[(1R,2R,3S,4R,6S)-4,6-diamino-2-{[(2S,3R,4S,5R)-4-{[(2R,3R,4R,5S,6S)-3-amino-6-(aminomethyl)-4,5-dihydroxyoxan-2-yl]oxy}-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-3-hydroxycyclohexyl]oxy}-2-(hydroxymethyl)oxane-3,4-diol
Brand Name
Humatin
Synonyms
Paramomycin sulfate
Aminosidine
paromomycin
Aminosidin

DATABASE IDS

PubChem CID 165580
CAS Number 1263-89-4
PubChem SID 46505391

PROPERTIES

DETAILS

Description (English)
Item Information
Drug Groups approved; investigational
Description An oligosaccharide antibiotic produced by various streptomyces. [PubChem]
Indication For the treatment of acute and chronic intestinal amebiasis (it is not effective in extraintestinal amebiasis). Also for the management of hepatic coma as adjunctive therapy.
Pharmacology Paromomycin is a broad spectrum aminoglycoside antibiotic produced by Streptomyces rimosus var. paromomycinus. The in vitro and in vivo antibacterial action of paromomycin closely parallels that of neomycin.
Affected Organisms
Enteric bacteria and other eubacteria
Absorption Poorly absorbed after oral administration, with almost 100% of the drug recoverable in the stool.
References
Vicens Q, Westhof E: Crystal structure of paromomycin docked into the eubacterial ribosomal decoding A site. Structure. 2001 Aug;9(8):647-58. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com

REFERENCES

  • Vicens Q, Westhof E: Crystal structure of paromomycin docked into the eubacterial ribosomal decoding A site. Structure. 2001 Aug;9(8):647-58. Pubmed