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Merck
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913405

Sigma-Aldrich

Enantioprobe (S)-3

≥95%

同義詞:

(S)-3-(3-(But-3-yn-1-yl)-3H-diazirin-3-yl)-N-(1,2,3,4-tetrahydronaphthalen-1-yl)propanamide, Fully functionalized enantioprobe, Ligandability probe

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About This Item

經驗公式(希爾表示法):
C18H21N3O
分子量::
295.38
分類程式碼代碼:
12161600

化驗

≥95%

形狀

powder

儲存溫度

−20°C

應用

Enantioprobe (S)-3 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 (S)-3′s paired fragment is available as Enantioprobe (R)-3 (cat# 912166).
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:

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Yujia Wang et al.
Nature chemistry, 11(12), 1113-1123 (2019-10-30)
A fundamental challenge in chemical biology and medicine is to understand and expand the fraction of the human proteome that can be targeted by small molecules. We recently described a strategy that integrates fragment-based ligand discovery with chemical proteomics to

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