Page last updated: 2024-10-15

promysalin

Description

promysalin: isolated from Pseudomonas putida; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

promysalin : A carboxylic ester resulting from the formal condensation of the carboxy group of (2S)-1-(2-hydroxybenzoyl)-2,3-dihydro-1H-pyrrole-2-carboxylic acid with the hydroxy group of (2R,8R)-2,8-dihydroxytetradecanamide. It is a metabolite isolated from Pseudomonas putida, , which resides in the rhizosphere of rice plants. The compound selectively inhibits the growth of Pseudomonas aeruginosa at low-micromolar concentrations. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID122380159
CHEBI ID171658
MeSH IDM0572363

Synonyms (3)

Synonym
CHEBI:171658
(14-amino-13-hydroxy-14-oxotetradecan-7-yl) (2s)-1-(2-hydroxybenzoyl)pyrrolidine-2-carboxylate
promysalin

Research Excerpts

Overview

Promysalin is an amphipathic antibiotic isolated from Pseudomonas promysalinigenes. It shows potent antibacterial activities against Gram-negative pathogens by inactivating succinate dehydrogenase.

ExcerptReference
"Promysalin is an amphipathic antibiotic isolated from Pseudomonas promysalinigenes (previously Pseudomonas putida RW10S1) which shows potent antibacterial activities against Gram-negative pathogens by inactivating succinate dehydrogenase. "( Enzymatic reconstitution of salicylate formation in promysalin biosynthesis.
Das, S; Mahanta, N; Pattanayakanahalli Henjarappa, K, 2023
)
"Promysalin is a small-molecule natural product that specifically inhibits growth of the Gram-negative pathogen "( Target-Based Design of Promysalin Analogues Identifies a New Putative Binding Cleft in Succinate Dehydrogenase.
Kaplan, AR; Karanicolas, J; Keohane, CE; Khowsathit, J; Matuska, K; Post, SJ; Rossiter, LM; Wuest, WM, 2020
)
"Promysalin is a species-specific Pseudomonad metabolite with unique bioactivity. "( Diverted Total Synthesis of Promysalin Analogs Demonstrates That an Iron-Binding Motif Is Responsible for Its Narrow-Spectrum Antibacterial Activity.
Keohane, CE; Knouse, KW; Rossiter, SE; Steele, AD; Williams, SJ; Wuest, WM, 2016
)
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (9)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's7 (77.78)24.3611
2020's2 (22.22)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other9 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]