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BML-2840 Revised 01-Feb-10 New product
ICCB known bioactives library
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PRODUCT LINE Drug Discovery
PRODUCT CATEGORY Compound Libraries
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
BML-2840-0100 100 µl/well 1 Library Inquire
Product Specification
QUANTITY: 100µl per well
CONCENTRATION: DMSO solutions (concentration vary by compound and are provided in the documentation)
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.
SHIPPING: SHIPPED ON DRY ICE
LONG TERM STORAGE: -80°C
Product Description

The ICCB Known Bioactives Library is an important new 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 100 µL 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.

General Information
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
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
Scaffold composition and biological relevance of screening libraries: A. Shelat et al.; Nat. Chem. Biol. 3, 442 (2007) Abstract
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