Compound ID | 3126

Update compound information

Ribosylparomamine

Synonym(s): LL-BM408  |  5-Ribosylparomamine

Class: Aminoglycoside

Spectrum of activity: Gram-positive  &  Gram-negative
Details of activity: Active against Staphylococcus aureus, Shigella flexneri, and Proteus mirabilis
Description: Natural product from Streptomyces sp.; protects mice from Proteus mirabilis infection when administered parenterally
Institute where first reported: Process and Analytical Research Section Lederle Laboratories, A Division of American Cyanamid Company
Year first mentioned: 1977
Development status: Experimental
Chemical structure(s):
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Molecular weight: 455.46
Iso. SMILES: C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)N)O[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)O)N
InChI Key: QTUJBJINYXOXOU-VVPCINPTSA-N
Can. SMILES: C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@@H](CO)O2)O)O)N)O[C@H]3[C@@H]([C@@H]([C@@H](CO)O3)O)O)O)N
InChI: InChI=1S/C17H33N3O11/c18-4-1-5(19)14(30-16-8(20)12(26)10(24)6(2-21)28-16)15(9(4)23)31-17-13(27)11(25)7(3-22)29-17/h4-17,21-27H,1-3,18-20H2/t4-,5+,6-,7-,8-,9+,10-,11-,12-,13-,14-,15-,16-,17+/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/191385
Citation: https://www.jstage.jst.go.jp/article/antibiotics1968/30/2/30_2_175/_article/-char/en

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