Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Ali souldozi"'
Publikováno v:
Medical Laboratory Journal, Vol 15, Iss 5, Pp 13-18 (2021)
Background and objectives: Antibiotic resistance is a major public health challenge. The pervasive antibiotic misuse can lead to increased antibiotic resistance. Thus, there is a need for discovery of new compounds against drug-resistant microorganis
Externí odkaz:
https://doaj.org/article/e38e43edbd0c45c68535c3453d360720
Publikováno v:
Iranian Journal of Toxicology, Vol 12, Iss 1, Pp 33-37 (2018)
Background: In this study, we evaluated antibacterial and antifungle activity of these derivatives against gram positive (Staphylococcus aureus, Bacillus subtilis, B. cereus), gram negative (Proteus vulgaris) bacteria and fungale (Candida albicans, C
Externí odkaz:
https://doaj.org/article/9ef190fcd9a440c5826b83237efe9a90
Autor:
Ali Ramazani, Ali Souldozi
Publikováno v:
ARKIVOC, Vol 2008, Iss 16, Pp 235-242 (2008)
Externí odkaz:
https://doaj.org/article/f44bd9a3ec3e4c3a8f3eb5f269912e11
Publikováno v:
Avicenna Journal of Clinical Microbiology and Infection. 8:11-16
Background: New drugs must be designed and synthesized for combating resistant pathogens. In this study, antibacterial and antifungal activities of 4 new derivatives of 1,3,4-oxadiazole were assessed against 8 bacterial and 2 fungal pathogens. Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96a83d348e24f67462a3df80e0c0e2ee
https://doi.org/10.34172/ajcmi.2021.03
https://doi.org/10.34172/ajcmi.2021.03
Publikováno v:
Avicenna Journal of Clinical Microbiology and Infection. 8:27-33
Background: Oxadiazoles are a group of anti-inflammatory compounds that have a wide range of activity due to their higher efficacy. Pseudomonas aeruginosa is an opportunistic pathogen and a major pathogen of nosocomial infections. This study aimed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::477d54f058d0e8c10e479e45dd9aaace
https://doi.org/10.34172/ajcmi.2021.06
https://doi.org/10.34172/ajcmi.2021.06
Publikováno v:
Infection Epidemiology and Microbiology. 6:177-192
AimsAntibiotic resistance is recognized as one of the most challenging public health problems in the world. The need for new antibacterial and antifungal drugs is justified because many pathogens are currently resistant to available drugs. Several co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b845a9ff32fc53de73823c786b99eb23
https://doi.org/10.29252/iem.6.3.177
https://doi.org/10.29252/iem.6.3.177
Publikováno v:
Infection Epidemiology and Microbiology. 6:37-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::692c0613c01564e7deea501e918b78df
https://doi.org/10.29252/iem.6.1.37
https://doi.org/10.29252/iem.6.1.37
Autor:
Zahra Ranjdoost, Ali Ramazani, Hamideh Aghahosseini, Nastaran Safarvand Jalayer, Katarzyna Ślepokura, Ali Souldozi, Tadeusz Lis
Publikováno v:
Organic Letters. 21:22-26
An efficient, one-pot, and convenient approach for the reaction of the same precursors, trialkyl(aryl) phosphines, acetylene diesters, and benzhydroxamic acids has been developed to produce two important classes of heterocyclic compounds: N-benzoylaz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5022824d1008ba0f2ce74bc301bcec63
https://doi.org/10.1021/acs.orglett.8b03388
https://doi.org/10.1021/acs.orglett.8b03388
Publikováno v:
Iranian Journal of Toxicology, Vol 12, Iss 1, Pp 33-37 (2018)
Background: In this study, we evaluated antibacterial and antifungle activity of these derivatives against gram positive (Staphylococcus aureus, Bacillus subtilis, B. cereus), gram negative (Proteus vulgaris) bacteria and fungale (Candida albicans, C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ee02d1af10e6367c54a3556633f7583
https://doi.org/10.29252/arakmu.12.1.33
https://doi.org/10.29252/arakmu.12.1.33
Publikováno v:
Iranian Chemical Communication, Vol 5, Iss Issue 4, pp. 364-493, Pp 449-470 (2017)
Dimethyl (z)-2-[(2-methyl-5-oxo-1-cyclopentyl)oxy]-2-butenedioate has been synthesized using one-pot three component reaction between N-isocyaniminotriphenylphosphorane (Ph3PNNC), 3-methylcyclopentene-1,2-dione and dimethyl acetylenedicarboxylate. Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::0d0d2e77096e14b11510cb14d570a796
http://icc.journals.pnu.ac.ir/article_3897_60885bf15513a25ec99660fbef404af3.pdf
http://icc.journals.pnu.ac.ir/article_3897_60885bf15513a25ec99660fbef404af3.pdf