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| BML-2840-0100 |
1 Library |
100 µl/well |
INQUIRE |
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The ICCB Known Bioactives Library is an important product for use in chemical genetics and drug discovery. The library is a collection of 480 diverse biologically active compounds with defined biological activity and was developed in collaboration with the Harvard Institute of Chemistry and Cell Biology. It includes the following classes of compounds: GPCR ligands, Second messenger modulators, Nuclear receptor ligands, Actin & tubulin modulators, Kinase inhibitors, Protease inhibitors, Ion channel blockers, Gene regulation agents, Lipid biosynthesis inhibitors, many other classes.
Each compound is supplied dissolved in DMSO at 100µL and is ready for assaying. The library can be used for assay development and validation, mechanism profiling, lead screening or as a reference library.Contact
compoundlibraries@enzolifesciences.com for a complete list of compounds in the library.
For details on the terms of use of this product, click here.
Product Specification
| Concentration: | DMSO solutions (concentration vary by compound and are provided in the documentation) |
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| Quantity: | 100µl per well |
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| Kit/Set Contains: | 480 compounds. Includes compounds that affect most cellular processes and drug targer classes, including: GPCR ligands, Second messenger modulators, Nuclear receptor ligands, Actin and tubulin modulators, Kinase inhibitors, Protease inhibitors, Ion channel blockers, Gene regulation agents, Lipid biosynthesis inhibitors, Phosphodiesterase inhibitors, and many other classes. |
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| Long Term Storage: | -80°C |
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| Background / Technical Information: | Please click here for the comprehensive product data sheet. |
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Product Literature References
Disease allele-dependent small-molecule sensitivities in blood cells from monogenic diabetes: S.Y. Shaw et al.; Proc. Natl. Acad. Sci. USA
108, 492 (2011), Application,
Abstract;
High-content chemical and RNAi screens for suppressors of neurotoxicity in a Huntington's disease model: J. Schulte et al.; PLoS One
6, e23841 (2011), Application,
Abstract;
Chemical genetics reveals bacterial and host cell functions critical for type IV effector translocation by Legionella pneumophila: X. Charpentier et al.; PLoS Pathog.
5, e1000501 (2009), Application,
Abstract;
Identification of AML1-ETO modulators by chemical genomics: S.M. Corsello; Blood
113, 6193 (2009), Application,
Abstract;
General Literature References
Human ATAC Is a GCN5/PCAF-containing acetylase complex with a novel NC2-like histone fold module that interacts with the TATA-binding protein: H. Pan et al.; J. Biol. Chem.
283, 33808 (2008),
Abstract;
Scaffold composition and biological relevance of screening libraries: A. Shelat et al.; Nat. Chem. Biol.
3, 442 (2007),
Abstract;
Small molecule regulators of autophagy identified by an image-based high-throughput screen: L. Zhang et al.; Proc. Natl. Acad. Sci. USA
104, 19023 (2007),
Abstract;