All Photos(2)
Synonym(s):
(R)-1-(3-(1-(4-(N-(4-Bromophenyl)acrylamido)phenyl)-1-oxo-5,8,11-trioxa-2-azatetradecan-14-amido)phenyl)-3-(3,4-dimethoxyphenyl)propyl (S)-1-(3,3-dimethyl-2-oxopentanoyl)piperidine-2-carboxylate, Electrophilic PROTAC®, Heterobifunctional conjugate for E3 ubiquitin ligase discovery
Empirical Formula (Hill Notation):
C55H67BrN4O12
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ligand
electrophilic fragment
Quality Level
form
powder
storage temp.
−20°C
SMILES string
O=C(C=C)N(C1=CC=C(C(NCCOCCOCCOCCC(NC2=CC=CC([C@H](OC([C@@H]3CCCCN3C(C(C(C)(C)CC)=O)=O)=O)CCC4=CC(OC)=C(OC)C=C4)=C2)=O)=O)C=C1)C5=CC=C(Br)C=C5
Related Categories
Application
KB05-SLF is an electrophilic PROTAC developed in the Cravatt lab and is useful for the discovery of ligandable E3 ligases, an area of interest for the targeted protein degradation (TPD) field seeking to map out and utilize a larger repertoire of the available human E3 ligases. This bifunctional tool compound comprises a synthetic ligand for FKBP12 (SLF) on one end and scout fragment 913715 on the other end. Scout fragments are electrophiles that covalently modify targetable cysteine residues on proteins, an approach that has been scaled to globally quantitate Cys reactivity across human proteomes and cells. When SLF and the electrophilic fragment are fused together, monitoring the levels of FKBP12 in cells may indicate scout-mediated FKBP12 degradation, for which follow-up studies would validate the mechanism of FKPB12 depletion and any targets to which the scout fragment is covalently bound. Scout-bound proteins leading to FKBP12 (or other targets) depletion discovered by this strategy will further expand the communal TPD toolbox. Due to the reactive nature of the scout fragment, other proteins will also be modified, so careful controls and validation should be considered.
This proteomic approach to E3 discovery was demonstrated by Zhang et al in the discovery that DCAF16 mediated nuclear FKBP12 degradation via KB02-SLF.
Additional electrophilic PROTACs were developed incorporating scout fragments with broad cysteine reactivity:
Related tools:
This proteomic approach to E3 discovery was demonstrated by Zhang et al in the discovery that DCAF16 mediated nuclear FKBP12 degradation via KB02-SLF.
Additional electrophilic PROTACs were developed incorporating scout fragments with broad cysteine reactivity:
- KB02-SLF (914738) containing chloroacetamide scout fragment 912131
- KB03-SLF (914975) containing chloroacetamide scout fragment 912654
Related tools:
- Additional bifunctional tools for FKPB12 variants: dTAG-13 (SML2601 for FKBP12F36V) and Biotin-SLF (914223 for FKBP12)
- Inhibitors useful in validation of proteasomal-mediated degradation: MG123 (SML1135) and MLN4924 (5.05477 for Cullin-RING ubiquitin ligases that regulate neddylation of Cullin proteins)
- Cereblon (CRBN) affinity probe: Biotin-Thalidomide (913979)
Other Notes
Electrophilic PROTACs that degrade nuclear proteins by engaging DCAF16
Technology Spotlight: Proteomic Ligandability Assessment
Technology Spotlight: Building PROTAC® Degraders for Targeted Protein Degradation
Technology Spotlight: Proteomic Ligandability Assessment
Technology Spotlight: Building PROTAC® Degraders for Targeted Protein Degradation
Legal Information
PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license
related product
Product No.
Description
Pricing
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
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Certificates of Analysis (COA)
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Xiaoyu Zhang et al.
Nature chemical biology, 15(7), 737-746 (2019-06-19)
Ligand-dependent protein degradation has emerged as a compelling strategy to pharmacologically control the protein content of cells. So far, however, only a limited number of E3 ligases have been found to support this process. Here, we use a chemical proteomic
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