Skip to search formSkip to main contentSkip to account menu

indolmycin

Known as: 5-(1-(1H-indol-3-yl)ethyl)-2-(methylamino)- 4(5H)-oxazolone 
National Institutes of Health

Related topics

Related topics

1 relation

Broader (1)

Indoles

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2001
2001
Development of a stereoselective practical synthetic route to indolmycin, a candidate anti-H. pylori agent.
A stereoselective practical synthetic route to indolmycin is described. The route is composed of the regioselective coupling of… 
1981
1981
Directed biosynthesis of new indolmycins.
Tryptophan in a concentration of 0.4 microgram/ml increased the production of indolmycin by 37%. The lipophilic character of… 
1980
1980
Uptake of indolmycin in gram-positive bacteria
The antimicrobial activity of indolmycin correlates with the generation time of the investigated strains. Thus, in Staphylococcus… 
1979
1979
Interaction of indolmycin in the metabolism of tryptophan in rat liver.
When compared with other tryptophan analogues, indolmycin is a potent inhibitor of tryptophan pyrrolase and tryptophan… 
1978
1978
Thiazolinone analogues of indolmycin with antiviral and antibacterial activity.
Total synthesis of a series of thiazolinone and thiazolidinone analogues of the antibacterial oxazolinone antibiotic indolmycin… 
1977
1977
Total synthesis of thiazolinone analogues of indolmycin.
The synthesis of thiazolinone analogues of the naturally occurring oxazolinone antibiotic indolmycin is described. Relative… 
1977
1977
Synthesis of methionine carrying a chiral methyl group and its use in determining the steric course of the enzymatic C-methylation of indolepyruvate during indolmycin biosynthesis.
1974
1974
Regulation of antibiotic production: catabolite inhibition and the dualistic effect of glucose on indolmycin production.
The production of the antibiotic, indolmycin, was shown to be inhibited by glucose at 0.5%. Concentrations of glucose of 0.005… 
1971
1971
The biosynthesis of indolmycin.
1970
1970
The absolute configuration of indolmycin.
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)