Biaryl sulfonamides as cisoid azosteres for photopharmacology

Piermichele Kobauri; Wiktor Szymanski; Fangyuan Cao; Sebastian Thallmair; Siewert J. Marrink; Martin D. Witte; Frank J. Dekker; Ben L. Feringa

doi:10.1039/d1cc00950h

Biaryl sulfonamides as cisoid azosteres for photopharmacology

Piermichele Kobauri, Wiktor Szymanski^*, Fangyuan Cao, Sebastian Thallmair, Siewert J. Marrink, Martin D. Witte, Frank J. Dekker^*, Ben L. Feringa^*

^*Bijbehorende auteur voor dit werk

Onderzoeksoutput › Academic › peer review

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Biaryl sulfonamides are excellent candidates for the azologization approach that yields photoswitchable drugs more active in their metastable cis state, compared to the stable trans state. Here we present the scope and limitations of this strategy for rational design in photopharmacology.

Originele taal-2	English
Pagina's (van-tot)	4126-4129
Aantal pagina's	4
Tijdschrift	Chemical Communications
Volume	57
Nummer van het tijdschrift	34
Vroegere onlinedatum	18-mrt.-2021
DOI's	https://doi.org/10.1039/d1cc00950h
Status	Published - 27-apr.-2021

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10.1039/d1cc00950hLicentie: CC BY-NC

Biaryl sulfonamides as cisoid azosteres for photopharmacologyFinal publisher's version, 2,51 MBLicentie: CC BY-NC

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title = "Biaryl sulfonamides as cisoid azosteres for photopharmacology",

abstract = "Biaryl sulfonamides are excellent candidates for the azologization approach that yields photoswitchable drugs more active in their metastable cis state, compared to the stable trans state. Here we present the scope and limitations of this strategy for rational design in photopharmacology.",

author = "Piermichele Kobauri and Wiktor Szymanski and Fangyuan Cao and Sebastian Thallmair and Marrink, {Siewert J.} and Witte, {Martin D.} and Dekker, {Frank J.} and Feringa, {Ben L.}",

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T1 - Biaryl sulfonamides as cisoid azosteres for photopharmacology

AU - Kobauri, Piermichele

AU - Szymanski, Wiktor

AU - Cao, Fangyuan

AU - Thallmair, Sebastian

AU - Marrink, Siewert J.

AU - Witte, Martin D.

AU - Dekker, Frank J.

AU - Feringa, Ben L.

PY - 2021/4/27

Y1 - 2021/4/27

N2 - Biaryl sulfonamides are excellent candidates for the azologization approach that yields photoswitchable drugs more active in their metastable cis state, compared to the stable trans state. Here we present the scope and limitations of this strategy for rational design in photopharmacology.

AB - Biaryl sulfonamides are excellent candidates for the azologization approach that yields photoswitchable drugs more active in their metastable cis state, compared to the stable trans state. Here we present the scope and limitations of this strategy for rational design in photopharmacology.

U2 - 10.1039/d1cc00950h

DO - 10.1039/d1cc00950h

M3 - Article

C2 - 33908493

SN - 1359-7345

VL - 57

SP - 4126

EP - 4129

JO - Chemical Communications

JF - Chemical Communications

IS - 34

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