| dc.contributor.author |
Padron, JM |
en |
| dc.contributor.author |
Martin, VS |
en |
| dc.contributor.author |
Hadjipavlou-Litina, D |
en |
| dc.contributor.author |
Noula, C |
en |
| dc.contributor.author |
Constantinou-Kokotou, V |
en |
| dc.contributor.author |
Peters, GJ |
en |
| dc.contributor.author |
Kokotos, G |
en |
| dc.date.accessioned |
2014-06-06T06:43:59Z |
|
| dc.date.available |
2014-06-06T06:43:59Z |
|
| dc.date.issued |
1999 |
en |
| dc.identifier.issn |
0960894X |
en |
| dc.identifier.uri |
http://dx.doi.org/10.1016/S0960-894X(99)00084-0 |
en |
| dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1606 |
|
| dc.subject.other |
3 amino 1,2 diol |
en |
| dc.subject.other |
antiinflammatory agent |
en |
| dc.subject.other |
gentamicin |
en |
| dc.subject.other |
indometacin |
en |
| dc.subject.other |
sphingosine derivative |
en |
| dc.subject.other |
unclassified drug |
en |
| dc.subject.other |
antiinflammatory activity |
en |
| dc.subject.other |
article |
en |
| dc.subject.other |
cytotoxicity |
en |
| dc.subject.other |
drug mechanism |
en |
| dc.subject.other |
drug structure |
en |
| dc.subject.other |
drug synthesis |
en |
| dc.subject.other |
enantiomer |
en |
| dc.subject.other |
intraperitoneal drug administration |
en |
| dc.subject.other |
paw edema |
en |
| dc.subject.other |
structure activity relation |
en |
| dc.subject.other |
Amino Alcohols |
en |
| dc.subject.other |
Animals |
en |
| dc.subject.other |
Anti-Inflammatory Agents |
en |
| dc.subject.other |
Cell Survival |
en |
| dc.subject.other |
Edema |
en |
| dc.subject.other |
Inhibitory Concentration 50 |
en |
| dc.subject.other |
Kinetics |
en |
| dc.subject.other |
Models, Chemical |
en |
| dc.subject.other |
Rats |
en |
| dc.subject.other |
Sphingosine |
en |
| dc.subject.other |
Tumor Cells, Cultured |
en |
| dc.title |
Synthesis, in vitro cytotoxicity and in vivo anti-inflammatory activity of long chain 3-amino-1,2-diols |
en |
| heal.type |
journalArticle |
en |
| heal.identifier.primary |
10.1016/S0960-894X(99)00084-0 |
en |
| heal.publicationDate |
1999 |
en |
| heal.abstract |
The synthesis of long chain 3-amino-1,2-diols was carried out based on Sharpless asymmetric epoxidation of long chain allylic alcohols and regioselective nucleophilic ring opening by azido group. The in vitro cytotoxicity of the compounds prepared was evaluated against six solid tumor cell lines (A2780, H322, LL, WiDr, C26-10, UMSCC-22B). Free 3-amino-1,2- diols exhibited IC50 values between 1.45 μM and 32 μM. These compounds also presented interesting inhibition of carrageenin-induced paw edema in rats (85.3%-79.6% at a concentration of 0.15 mmol/kg). |
en |
| heal.journalName |
Bioorganic and Medicinal Chemistry Letters |
en |
| dc.identifier.issue |
6 |
en |
| dc.identifier.volume |
9 |
en |
| dc.identifier.doi |
10.1016/S0960-894X(99)00084-0 |
en |
| dc.identifier.spage |
821 |
en |
| dc.identifier.epage |
826 |
en |