N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase.

Niels Heise; Sander Friedrich; Veronika Temml; Daniela Brigitte Schuster; Bianka Siewert; René Csuk

doi:10.1016/j.ejmech.2021.113947

N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase.

Niels Heise
, Sander Friedrich
, Veronika Temml (Co-author)
, Daniela Brigitte Schuster (Co-author)
, Bianka Siewert
, René Csuk

Insitute of Pharmacy

Research output: Contribution to journal › Original Article › peer-review

10 Citations (Web of Science)

Original language	English
Pages (from-to)	113947
Journal	EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume	227
DOIs	https://doi.org/10.1016/j.ejmech.2021.113947
Publication status	Published - 2022

Keywords

POTENT INHIBITORS
DERIVATIVES

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10.1016/j.ejmech.2021.113947

Cite this

Heise, N., Friedrich, S., Temml, V., Schuster, D. B., Siewert, B., & Csuk, R. (2022). N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY , 227, 113947. https://doi.org/10.1016/j.ejmech.2021.113947

Heise, Niels ; Friedrich, Sander ; Temml, Veronika et al. / N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase. In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 2022 ; Vol. 227. pp. 113947.

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title = "N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase.",

keywords = "POTENT INHIBITORS, DERIVATIVES",

author = "Niels Heise and Sander Friedrich and Veronika Temml and Schuster, \{Daniela Brigitte\} and Bianka Siewert and Ren{\'e} Csuk",

note = "Schuster; Temml: Pharmacy/ Pharmaceutical and Medicinal Chemistry Institute, Paracelsus Medical University Salzburg, Stubergasse 21, A-5020, Salzburg, Austria",

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doi = "10.1016/j.ejmech.2021.113947",

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Heise, N, Friedrich, S, Temml, V , Schuster, DB, Siewert, B & Csuk, R 2022, 'N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase.', EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY , vol. 227, pp. 113947. https://doi.org/10.1016/j.ejmech.2021.113947

N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase. / Heise, Niels; Friedrich, Sander; Temml, Veronika (Co-author) et al.
In: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY , Vol. 227, 2022, p. 113947.

Research output: Contribution to journal › Original Article › peer-review

TY - JOUR

T1 - N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase.

AU - Heise, Niels

AU - Friedrich, Sander

AU - Temml, Veronika

AU - Schuster, Daniela Brigitte

AU - Siewert, Bianka

AU - Csuk, René

N1 - Schuster; Temml: Pharmacy/ Pharmaceutical and Medicinal Chemistry Institute, Paracelsus Medical University Salzburg, Stubergasse 21, A-5020, Salzburg, Austria

PY - 2022

Y1 - 2022

KW - POTENT INHIBITORS

KW - DERIVATIVES

U2 - 10.1016/j.ejmech.2021.113947

DO - 10.1016/j.ejmech.2021.113947

M3 - Original Article

C2 - 34731766

SN - 0223-5234

VL - 227

SP - 113947

JO - EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

JF - EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

ER -

Heise N, Friedrich S, Temml V , Schuster DB, Siewert B, Csuk R. N-methylated diazabicyclo[3.2.2]nonane substituted triterpenoic acids are excellent, hyperbolic and selective inhibitors for butyrylcholinesterase. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY . 2022;227:113947. doi: 10.1016/j.ejmech.2021.113947