Bisindolylmaleimide
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Preferred IUPAC name
3,4-Di(1H-indol-2-yl)-1H-pyrrole-2,5-dione | |
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Properties | |
C20H13N3O2 | |
Molar mass | 327.343 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Bisindolylmaleimide is an organic compound that forms the core chemical structure of a variety of biologically active compounds.[1] This core structure includes a central maleimide group with two indole groups attached.
Examples of bisindolylmaleimide derivatives include:
- Bisindolylmaleimide I
- Enzastaurin
- Ruboxistaurin
- Tivantinib
References[]
- ^ Faul, Margaret M.; Winneroski, Leonard L.; Krumrich, Christine A. (1998). "A New, Efficient Method for the Synthesis of Bisindolylmaleimides". The Journal of Organic Chemistry. 63 (17): 6053. doi:10.1021/jo980513c. PMID 11672217.
External links[]
Media related to Bisindolylmaleimides at Wikimedia Commons
Categories:
- Heterocyclic compound stubs
- Bisindolylmaleimides