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S-benzylisothiourea derivatives as small-molecule inhibitors of indoleamine-2,3-dioxygenase.

Bioorganic & medicinal chemistry letters (2010-08-07)
Kenji Matsuno, Kazushige Takai, Yoshinobu Isaka, Yuka Unno, Masayuki Sato, Osamu Takikawa, Akira Asai
ZUSAMMENFASSUNG

S-benzylisothiourea 3a was discovered by its ability to inhibit indoleamine-2,3-dioxygenase (IDO) in our screening program. Subsequent optimization of the initial hit 3a lead to the identification of sub-muM inhibitors 3r and 10h, both of which suppressed kynurenine production in A431 cells. Synthesis and structure-activity relationship of S-benzylisothiourea analogues as small-molecule inhibitors of IDO are described.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Benzylmercaptan, 99%
Sigma-Aldrich
4-Chlorbenzylalkohol, 99%
Sigma-Aldrich
4-Chlorbenzylamin, 98%
Sigma-Aldrich
Benzylmercaptan, 99%, FG
Sigma-Aldrich
S-Benzylisothioharnstoff -hydrochlorid, 98%