2-n-Heptyl-4-quinolinol
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
| Category | Bioactive by-products |
| Catalog number | BBF-01341 |
| CAS | |
| Molecular Weight | 245.36 |
| Molecular Formula | C16H21NO |
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Description
It is produced by the strain of Pseudomonas. It has activity against Candida albicans, Staphylococcus aureus, Vibrio anguillarum and V. Harveyi.
Specification
| IUPAC Name | 2-heptyl-1,4-dihydroquinolin-4-ol |
| Canonical SMILES | CCCCCCCC1=CC(C2=CC=CC=C2N1)O |
| InChI | InChI=1S/C16H23NO/c1-2-3-4-5-6-9-13-12-16(18)14-10-7-8-11-15(14)17-13/h7-8,10-12,16-18H,2-6,9H2,1H3 |
| InChI Key | POWHEIUYDWIFET-UHFFFAOYSA-N |
Properties
| Antibiotic Activity Spectrum | Gram-positive bacteria; Gram-negative bacteria; Yeast |
Reference Reading
1. Antibiotic metabolites from a marine pseudomonad
S J Wratten, M S Wolfe, R J Andersen, D J Faulkner Antimicrob Agents Chemother. 1977 Mar;11(3):411-4. doi: 10.1128/AAC.11.3.411.
An antibiotic-producing pseudomonad was isolated from a seawater sample from a La Jolla, Calif., tidepool. The pseudomonad produces two novel antibacterial compounds, 2-n-pentyl-4-quinolinol and 2-n-heptyl-4-quinolinol. It also synthesizes indole-3-carboxaldehyde, 6-bromoindole-3-carboxaldehyde, and the known antibiotic p-hydroxybenzaldehyde. Each of these compounds was identified by analysis of spectral data, and the structures were confirmed by synthesis or comparison with authentic samples.
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Bio Calculators
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
