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Design, synthesis a...
Design, synthesis and evaluation of novel polypharmacological antichlamydial agents
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- Sunduru, Naresh (author)
- Umeå universitet,Kemiska institutionen,Umeå Centre for Microbial Research (UCMR)
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- Salin, Olli (author)
- Umeå universitet,Kemiska institutionen,Institutionen för klinisk mikrobiologi,Umeå Centre for Microbial Research (UCMR)
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- Gylfe, Åsa (author)
- Umeå universitet,Kemiska institutionen,Umeå Centre for Microbial Research (UCMR),Molekylär Infektionsmedicin, Sverige (MIMS)
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- Elofsson, Mikael (author)
- Umeå universitet,Kemiska institutionen,Umeå Centre for Microbial Research (UCMR)
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(creator_code:org_t)
- Elsevier BV, 2015
- 2015
- English.
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In: European Journal of Medicinal Chemistry. - : Elsevier BV. - 0223-5234 .- 1768-3254. ; 101, s. 595-603
- Related links:
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Subject headings
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- Discovery of new polypharmacological antibacterial agents with multiple modes of actions can be an alternative to combination therapy and also a possibility to slow development of antibiotic resistance. In support to this hypothesis, we synthesized 16 compounds by combining the pharmacophores of Chlamydia trachomatis inhibitors and inhibitors of type III secretion (T3S) in gram-negative bacteria. In this study we have developed salicylidene acylhydrazide sulfonamides (11c & 11d) as new antichlamydial agents that also inhibit T3S in Yersinia pseudotuberculosis.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)
Keyword
- Sulfonamides
- Acylhydrazones
- Heck coupling
- Cyanation
- Urea derivatives
- Thiourea derivatives
- lamydia trachomatis
- Chlamydia pneumoniae
- Type III secretion system
- Antibiotic development
Publication and Content Type
- ref (subject category)
- art (subject category)
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