Bisindolylmaleimide

Bisindolylmaleimide
Names
	Preferred IUPAC name 3,4-Di(1H-indol-2-yl)-1H-pyrrole-2,5-dione
Identifiers
CAS Number	119139-23-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	8862983;
PubChem CID	10687637;
UNII	MBK3OO5K8T ;
CompTox Dashboard (EPA)	DTXSID30152324 ;
	InChI InChI=1S/C20H13N3O2/c24-19-17(15-9-11-5-1-3-7-13(11)21-15)18(20(25)23-19)16-10-12-6-2-4-8-14(12)22-16/h1-10,21-22H,(H,23,24,25) Key: LRBHDUWDZCAYDA-UHFFFAOYSA-N; InChI=1/C20H13N3O2/c24-19-17(15-9-11-5-1-3-7-13(11)21-15)18(20(25)23-19)16-10-12-6-2-4-8-14(12)22-16/h1-10,21-22H,(H,23,24,25) Key: LRBHDUWDZCAYDA-UHFFFAOYAH;
	SMILES O=C5C(\c2cc1ccccc1[nH]2)=C(\c4cc3ccccc3[nH]4)C(=O)N5;
Properties
Chemical formula	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). Infobox references

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:

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

[1] 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.

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