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Safety Information

912425

Sigma-Aldrich

Enantioprobe (R)-6

≥95%

Synonym(s):

(R)-N-Benzyl-3-(3-(but-3-yn-1-yl)-3H-diazirin-3-yl)-N-(1-phenylethyl)propanamide, Fully functionalized enantioprobe, Ligandability probe

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About This Item

Empirical Formula (Hill Notation):
C23H25N3O
CAS Number:
Molecular Weight:
359.46
UNSPSC Code:
12161600

Assay

≥95%

form

liquid

storage temp.

−20°C

Application

Enantioprobe (R)-6 is one of 16 fully functionalized, enantiomeric fragment probes developed in the Cravatt lab. Combining fragment-based ligand discovery (FBLD) with chemical proteomics, the enantioprobe library assesses ligandability across proteomes. Each enantioprobe contains a structurally variable fragment for interaction with proteins, photoactivatable diazirine for UV-induced covalent protein labeling, and bioorthogonal alkyne handle for detection, enrichment, and identification. Of the eight enantiomeric pairs, each differs by one stereocenter, and comparing stereoselective fragment-protein interactions between the pairs simplifies validation of authentic protein-binding events. Enantioprobe (R)-6′s paired fragment is available as Enantioprobe (S)-6 (cat# 912174).

Together, the 16 enantioprobes support ligandability studies in living cells, a significant method for development of chemical probes and lead discovery efforts to find binders for traditionally ″undruggable″ protein targets. This strategy is also compatible with multiplexing for higher throughput.
Supporting reagents:

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

912425-VAR:
912425-BULK:
912425-50MG:
912425-5MG:


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Articles

Ligandability describes the propensity of a protein target to bind a small molecule with high affinity. It is a precursor to evaluating druggability, which requires more advanced translational pharmacological effects and drug-like properties in vivo.

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