Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1994-7-11
pubmed:abstractText
Some derivatives of 2-hydroxy-N-(3,4-dimethyl-5-isoxazolyl)- 1,4-naphthoquinone 4-imine (3), a poorly soluble drug, were synthesized in an attempt to improve their physicochemical properties. The new compounds were characterized by spectroscopic methods including an iterative NMR method (the LAOCOON III program). The physicochemical properties such as solubility, relative lipophilicity (RM), and partition coefficients (Leo-Hansch fragmental system) were determined. Some derivatives were more lipophilic than 3 and one was water soluble. In vitro antibacterial activity was also reported for some derivatives.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-3549
pubmed:author
pubmed:issnType
Print
pubmed:volume
83
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
332-5
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:8207676-Animals, pubmed-meshheading:8207676-Anti-Bacterial Agents, pubmed-meshheading:8207676-Bacteria, pubmed-meshheading:8207676-Bacterial Infections, pubmed-meshheading:8207676-Chemistry, Physical, pubmed-meshheading:8207676-Isoxazoles, pubmed-meshheading:8207676-Lipids, pubmed-meshheading:8207676-Magnetic Resonance Spectroscopy, pubmed-meshheading:8207676-Mass Spectrometry, pubmed-meshheading:8207676-Mice, pubmed-meshheading:8207676-Mice, Inbred BALB C, pubmed-meshheading:8207676-Microbial Sensitivity Tests, pubmed-meshheading:8207676-Naphthols, pubmed-meshheading:8207676-Physicochemical Phenomena, pubmed-meshheading:8207676-Solubility, pubmed-meshheading:8207676-Spectrophotometry, Infrared, pubmed-meshheading:8207676-Spectrophotometry, Ultraviolet, pubmed-meshheading:8207676-Trypanocidal Agents
pubmed:year
1994
pubmed:articleTitle
Synthesis and some physiochemical properties of 2-hydroxy-N-(3,4-dimethyl-5-isoxazolyl)-1,4-naphthoquinone 4-imine derivatives.
pubmed:affiliation
Departamento de Farmacia, Facultad de Ciencias Quimicas, Córdoba, Argentina.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't