• Je něco špatně v tomto záznamu ?

Utilization of 1,3-Dioxolanes in the Synthesis of α-branched Alkyl and Aryl 9-[2-(Phosphonomethoxy)Ethyl]Purines and Study of the Influence of α-branched Substitution for Potential Biological Activity

K. Pomeisl, R. Pohl, R. Snoeck, G. Andrei, M. Krečmerová,

. 2019 ; 38 (2) : 119-156. [pub] 20181207

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc19028009

Syntheses of α-branched alkyl and aryl substituted 9-[2-(phosphonomethoxy)ethyl]purines from substituted 1,3-dioxolanes have been developed. Key synthetic precursors, α-substituted dialkyl [(2-hydroxyethoxy)methyl]phosphonates were prepared via Lewis acid mediated cleavage of 1,3-dioxolanes followed by reaction with dialkyl or trialkyl phosphites. The best preparative yields were achieved under conditions utilizing tin tetrachloride as Lewis acid and triisopropyl phosphite. Attachment of purine bases to dialkyl [(2-hydroxyethoxy)methyl]phosphonates was performed by Mitsunobu reaction. Final α-branched 9-[2-(phosphonomethoxy)ethyl]purines were tested for antiviral, cytostatic and antiparasitic activity, the latter one determined as inhibitory activity towards Plasmodium falciparum enzyme hypoxanthine-guanine-xanthine phosphoribosyltransfesase. In most cases biological activity was only marginal.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc19028009
003      
CZ-PrNML
005      
20190823103158.0
007      
ta
008      
190813s2019 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1080/15257770.2018.1506884 $2 doi
035    __
$a (PubMed)30526265
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Pomeisl, Karel $u a Institute of Organic Chemistry and Biochemistry , Czech Academy of Sciences , Prague , Czech Republic. b Institute of Physics , Czech Academy of Sciences , Prague , Czech Republic.
245    10
$a Utilization of 1,3-Dioxolanes in the Synthesis of α-branched Alkyl and Aryl 9-[2-(Phosphonomethoxy)Ethyl]Purines and Study of the Influence of α-branched Substitution for Potential Biological Activity / $c K. Pomeisl, R. Pohl, R. Snoeck, G. Andrei, M. Krečmerová,
520    9_
$a Syntheses of α-branched alkyl and aryl substituted 9-[2-(phosphonomethoxy)ethyl]purines from substituted 1,3-dioxolanes have been developed. Key synthetic precursors, α-substituted dialkyl [(2-hydroxyethoxy)methyl]phosphonates were prepared via Lewis acid mediated cleavage of 1,3-dioxolanes followed by reaction with dialkyl or trialkyl phosphites. The best preparative yields were achieved under conditions utilizing tin tetrachloride as Lewis acid and triisopropyl phosphite. Attachment of purine bases to dialkyl [(2-hydroxyethoxy)methyl]phosphonates was performed by Mitsunobu reaction. Final α-branched 9-[2-(phosphonomethoxy)ethyl]purines were tested for antiviral, cytostatic and antiparasitic activity, the latter one determined as inhibitory activity towards Plasmodium falciparum enzyme hypoxanthine-guanine-xanthine phosphoribosyltransfesase. In most cases biological activity was only marginal.
650    _2
$a zvířata $7 D000818
650    _2
$a antiparazitární látky $x chemická syntéza $x chemie $x farmakologie $7 D000977
650    _2
$a antivirové látky $x chemická syntéza $x chemie $x farmakologie $7 D000998
650    _2
$a nádorové buněčné linie $7 D045744
650    _2
$a DNA viry $x účinky léků $7 D004267
650    _2
$a dioxolany $x chemie $7 D004148
650    _2
$a inhibitory enzymů $x chemická syntéza $x chemie $x farmakologie $7 D004791
650    _2
$a lidé $7 D006801
650    _2
$a myši $7 D051379
650    _2
$a mikrobiální testy citlivosti $7 D008826
650    _2
$a molekulární struktura $7 D015394
650    _2
$a pentosyltransferasy $x antagonisté a inhibitory $x metabolismus $7 D010430
650    _2
$a Plasmodium falciparum $x účinky léků $x enzymologie $7 D010963
650    _2
$a puriny $x chemická syntéza $x chemie $x farmakologie $7 D011687
655    _2
$a časopisecké články $7 D016428
700    1_
$a Pohl, Radek $u a Institute of Organic Chemistry and Biochemistry , Czech Academy of Sciences , Prague , Czech Republic.
700    1_
$a Snoeck, Robert $u c Rega Institute for Medical Research , Katholieke Universiteit Leuven , Belgium.
700    1_
$a Andrei, Graciela $u c Rega Institute for Medical Research , Katholieke Universiteit Leuven , Belgium.
700    1_
$a Krečmerová, Marcela $u a Institute of Organic Chemistry and Biochemistry , Czech Academy of Sciences , Prague , Czech Republic.
773    0_
$w MED00008893 $t Nucleosides, nucleotides & nucleic acids $x 1532-2335 $g Roč. 38, č. 2 (2019), s. 119-156
856    41
$u https://pubmed.ncbi.nlm.nih.gov/30526265 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20190813 $b ABA008
991    __
$a 20190823103412 $b ABA008
999    __
$a ok $b bmc $g 1433158 $s 1066469
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2019 $b 38 $c 2 $d 119-156 $e 20181207 $i 1532-2335 $m Nucleosides, nucleotides & nucleic acids $n Nucleosides Nucleotides Nucleic Acids $x MED00008893
LZP    __
$a Pubmed-20190813

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...