Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Org Biomol Chem ; 10(32): 6491-7, 2012 Aug 28.
Article in English | MEDLINE | ID: mdl-22766576

ABSTRACT

Here we describe the synthesis of new 7-substituted 8-aza-7-deazaadenosine ribonucleoside phosphoramidites and their use in generating major groove-modified duplex RNAs. A 7-ethynyl analog leads to further structural diversification of the RNA via post-automated RNA synthesis azide-alkyne cycloaddition reactions. In addition, we report preliminary studies on the effects of eight different purine 7-position modifications on RNA duplex stability and pairing specificity. Finally, the effect on RNAi activity of this type of modification at eight different positions in an siRNA guide strand has been explored. Analogs were identified with large 7-position substituents that maintain adenosine pairing specificity and are well-tolerated at specific positions in an siRNA guide strand.


Subject(s)
Adenosine/chemistry , Aza Compounds/chemistry , Organophosphorus Compounds/chemistry , RNA, Small Interfering/chemistry , Ribonucleosides/chemistry , Adenosine/pharmacology , Aza Compounds/pharmacology , Drug Stability , HeLa Cells , Humans , Models, Molecular , Molecular Structure , Organophosphorus Compounds/pharmacology , Protein Denaturation , RNA, Small Interfering/drug effects , Ribonucleosides/pharmacology , Temperature
2.
J Nat Prod ; 73(3): 365-72, 2010 Mar 26.
Article in English | MEDLINE | ID: mdl-20102170

ABSTRACT

The focus of this study is on the bastadin class of bromotyrosine derivatives, commonly isolated from Ianthella marine sponges, and is the first report on the secondary metabolites from Ianthella cf. reticulata. Two new bastadins were isolated, (E,Z)-bastadin 19 (1a), a diastereoisomer of the known (E,E)-bastadin 19 (1b), and dioxepine bastadin 3 (2), an unusual dibenzo-1,3-dioxepine. A bastadin NMR database was created and assisted in the structure determination of 1b and 2 and the rapid dereplication of 10 other known compounds including bastadins 2-9 (3-10), 13 (11), and 19 (1a). The geometry of the 2-(hydroxyimino)-N-alkylamide chains, a chemical feature present in all bastadins, was further probed, and new insights regarding the natural oxime configuration are discussed. Bastadins possessing (E,Z)-, (Z,E)-, or (E,E)-dioxime configurations could be artifacts of isolation or storage in solution. Therefore, this point was explored by photochemical and thermal isomerization studies, as well as molecular mechanics calculations. Bastadins 13 (11) and 19 (1a) exhibited moderate inhibition against Trypanosoma brucei, and bastadin 4 (5) was cytotoxic to HCT-116 colon cancer cells.


Subject(s)
Halogenated Diphenyl Ethers/isolation & purification , Porifera/chemistry , Trypanosoma brucei brucei/drug effects , Animals , Drug Screening Assays, Antitumor , HCT116 Cells , Halogenated Diphenyl Ethers/chemistry , Halogenated Diphenyl Ethers/pharmacology , Humans , Molecular Structure , Nuclear Magnetic Resonance, Biomolecular , Oximes/chemistry , Parasitic Sensitivity Tests , Stereoisomerism
SELECTION OF CITATIONS
SEARCH DETAIL
...