Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors. / Nørager, Niels G; Poulsen, Mette H; Jensen, Anna G; Jeppesen, Nanna S; Kristensen, Anders S; Strømgaard, Kristian.

In: Journal of Medicinal Chemistry, Vol. 57, No. 11, 12.06.2014, p. 4940-9.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Nørager, NG, Poulsen, MH, Jensen, AG, Jeppesen, NS, Kristensen, AS & Strømgaard, K 2014, 'Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors', Journal of Medicinal Chemistry, vol. 57, no. 11, pp. 4940-9. https://doi.org/10.1021/jm5004705

APA

Nørager, N. G., Poulsen, M. H., Jensen, A. G., Jeppesen, N. S., Kristensen, A. S., & Strømgaard, K. (2014). Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors. Journal of Medicinal Chemistry, 57(11), 4940-9. https://doi.org/10.1021/jm5004705

Vancouver

Nørager NG, Poulsen MH, Jensen AG, Jeppesen NS, Kristensen AS, Strømgaard K. Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors. Journal of Medicinal Chemistry. 2014 Jun 12;57(11):4940-9. https://doi.org/10.1021/jm5004705

Author

Nørager, Niels G ; Poulsen, Mette H ; Jensen, Anna G ; Jeppesen, Nanna S ; Kristensen, Anders S ; Strømgaard, Kristian. / Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors. In: Journal of Medicinal Chemistry. 2014 ; Vol. 57, No. 11. pp. 4940-9.

Bibtex

@article{7f8e3b91d519492296b0d477bf459aa9,
title = "Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors",
abstract = "Polyamine toxins from spiders and wasps are potent open-channel blockers of ionotropic glutamate (iGlu) receptors. It is well-established that secondary amino groups in the polyamine moiety of these toxins are key to both selectivity and potency at iGlu receptors, still some native spider polyamine toxins comprise both N-methyl and N-hydroxy functionalities. Here, we investigate the effect of both N-methylation and N-hydroxylation of spider polyamine toxins by the synthesis and biological evaluation of the naturally occurring N-methylated argiopinines and pseudoargiopinines I and II, N-hydroxylated Agel-489 and Agel-505, as well as N-methylated analogues of the NMDA and AMPA iGlu receptor subtype selective antagonists ArgTX-93 and ArgTX-48. Efficient synthetic strategies for the synthesis of target compounds were developed, and evaluation of biological activity at AMPA and NMDA receptors identified highly potent and in some cases very selective ligands.",
author = "N{\o}rager, {Niels G} and Poulsen, {Mette H} and Jensen, {Anna G} and Jeppesen, {Nanna S} and Kristensen, {Anders S} and Kristian Str{\o}mgaard",
year = "2014",
month = jun,
day = "12",
doi = "10.1021/jm5004705",
language = "English",
volume = "57",
pages = "4940--9",
journal = "Journal of Medicinal Chemistry",
issn = "0022-2623",
publisher = "American Chemical Society",
number = "11",

}

RIS

TY - JOUR

T1 - Structure-activity relationship studies of N-methylated and N-hydroxylated spider polyamine toxins as inhibitors of ionotropic glutamate receptors

AU - Nørager, Niels G

AU - Poulsen, Mette H

AU - Jensen, Anna G

AU - Jeppesen, Nanna S

AU - Kristensen, Anders S

AU - Strømgaard, Kristian

PY - 2014/6/12

Y1 - 2014/6/12

N2 - Polyamine toxins from spiders and wasps are potent open-channel blockers of ionotropic glutamate (iGlu) receptors. It is well-established that secondary amino groups in the polyamine moiety of these toxins are key to both selectivity and potency at iGlu receptors, still some native spider polyamine toxins comprise both N-methyl and N-hydroxy functionalities. Here, we investigate the effect of both N-methylation and N-hydroxylation of spider polyamine toxins by the synthesis and biological evaluation of the naturally occurring N-methylated argiopinines and pseudoargiopinines I and II, N-hydroxylated Agel-489 and Agel-505, as well as N-methylated analogues of the NMDA and AMPA iGlu receptor subtype selective antagonists ArgTX-93 and ArgTX-48. Efficient synthetic strategies for the synthesis of target compounds were developed, and evaluation of biological activity at AMPA and NMDA receptors identified highly potent and in some cases very selective ligands.

AB - Polyamine toxins from spiders and wasps are potent open-channel blockers of ionotropic glutamate (iGlu) receptors. It is well-established that secondary amino groups in the polyamine moiety of these toxins are key to both selectivity and potency at iGlu receptors, still some native spider polyamine toxins comprise both N-methyl and N-hydroxy functionalities. Here, we investigate the effect of both N-methylation and N-hydroxylation of spider polyamine toxins by the synthesis and biological evaluation of the naturally occurring N-methylated argiopinines and pseudoargiopinines I and II, N-hydroxylated Agel-489 and Agel-505, as well as N-methylated analogues of the NMDA and AMPA iGlu receptor subtype selective antagonists ArgTX-93 and ArgTX-48. Efficient synthetic strategies for the synthesis of target compounds were developed, and evaluation of biological activity at AMPA and NMDA receptors identified highly potent and in some cases very selective ligands.

U2 - 10.1021/jm5004705

DO - 10.1021/jm5004705

M3 - Journal article

C2 - 24824658

VL - 57

SP - 4940

EP - 4949

JO - Journal of Medicinal Chemistry

JF - Journal of Medicinal Chemistry

SN - 0022-2623

IS - 11

ER -

ID: 120136792