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Synthesis of uriedo and thiouriedo derivatives of peptide conjugated heterocycles - A new class of promising antimicrobials.
- Source :
-
European journal of medicinal chemistry [Eur J Med Chem] 2012 Feb; Vol. 48, pp. 179-91. Date of Electronic Publication: 2011 Dec 14. - Publication Year :
- 2012
-
Abstract
- Forty five new derivatives of ureas and thioureas were synthesized by the reaction of peptide conjugated heterocycles with isocyanates and isothiocyanates respectively. All the compounds have been characterized by IR, (1)H NMR, mass and elemental analysis. The compounds were evaluated for their ability to inhibit the growth of a panel of microorganisms and all the synthesized compounds displayed an excellent antimicrobial activity. From structure-activity relationship studies, it was apparent that thioureas infact is slightly more active than ureas. Also, substituents on the phenyl ring of the title compounds play a key role in the activity. Further, compound 40 is nearly twenty times more potent than the standard used. These results present a platform for the further studies in this line.<br /> (Copyright © 2011 Elsevier Masson SAS. All rights reserved.)
- Subjects :
- Amino Acid Sequence
Anti-Infective Agents chemistry
Anti-Infective Agents pharmacology
Heterocyclic Compounds chemistry
Heterocyclic Compounds pharmacology
Magnetic Resonance Spectroscopy
Microbial Sensitivity Tests
Molecular Sequence Data
Molecular Structure
Peptides chemistry
Peptides pharmacology
Spectrometry, Mass, Electrospray Ionization
Spectroscopy, Fourier Transform Infrared
Structure-Activity Relationship
Thiourea chemistry
Thiourea pharmacology
Anti-Infective Agents chemical synthesis
Heterocyclic Compounds chemical synthesis
Peptides chemical synthesis
Thiourea analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1768-3254
- Volume :
- 48
- Database :
- MEDLINE
- Journal :
- European journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 22209564
- Full Text :
- https://doi.org/10.1016/j.ejmech.2011.12.012