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ComInnex IAP Ligand Library

产品编号:4117489
包装规格:1 EACH
产品类别:进口试剂
品牌:Sigma-Aldrich
优惠价:立即咨询
产品价格
产品编号包装单位单价(元)国内现货国外库存询价单
41174891 EACH31320
产品性质
Quality Level【质量水平】
200
form【形式】
solid (powder or film on well wall)
concentration【浓度】
125 μg/well
suitability【适用性】
suitable for H-NMR
suitable for LC-MS
storage temp.【储存温度】
2-8℃
基本信息
Application【应用】
The ComInnex IAP Ligand Library is an 80-member collection of in-silico-derived ligands targeting cellular inhibitor of apoptosis protein 1 (cIAP1). cIAP1 is an E3 ligase of interest for the development of protein degraders, specifically called specific and non-genetic IAP-dependent protein erasers (SNIPERs).

Based on the SAR rules outlined in IAP antagonist research, the binding tetrapeptide anchor of the natural SMAC inhibitor protein of IAPs (AVPI and AVPF) was used in identification of novel derivatives designed by 3D similarity.

The initial library was filtered via in silico IFD methods by docking to the BIR3 domain of the IAP crystal structures. The highest binding derivatives were selected and collected in a screening library, including the natural binding tetrapeptides and known MV1 reference compounds. IAP in silico leads are an optimal collection to begin IAP lead discovery at the bench for eventual development into bifunctional protein degraders. With the proper assay setup to measure protein degradation or protein-protein interactions (PPIs), the ComInnex IAP Ligand Library can also be a platform for molecular glue discovery.

Learn more about this library: Accelerating IAP Lead Discovery for Targeted Protein Degradation

To view a complete list of compounds in the library, including sdf, visit the CIX001 Plate Map.

To streamline the assessment of these in silico leads for target-specific bifunctional degraders, three IAP ligands with the highest docking scores were also prepared as degrader building blocks for simple attachment of a target warhead. Read more here: Degrader Building Blocks with IAP in silico-Derived Ligands.
Screening, targeted protein degradation, IAP ligands, development of protein degraders (SNIPERs) and molecular glues.
Biochem/physiol Actions【生化/生理作用】
80 compounds are arranged in 96-microtube format with two open rows for screening controls if using liquid handling setups. One compound per tube (125 μg in solid form). Compound concentration in assays will vary depending on assay type, but common screening library stock solutions are 2 mM or 10 mM in DMSO. Product IDs, names, FW, MW, and SMILES can be found in plate map link and attached technical bulletin and SDF.
Other Notes【其他说明】
Inhibitor of Apoptosis Protein (IAP) Antagonists in Anticancer Agent Discovery: Current Status and Perspectives

Web Portal: Building PROTAC® Degraders for Targeted Protein Degradation

Degrader Building Blocks (including CRBN- and VHL-targeting ligands)
Legal Information【法律信息】
PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license
安全信息
Storage Class Code【储存分类代码】
11 - Combustible Solids
WGK
WGK 3
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