Carbanions. XI. Reactions of 4-chloro-1,1,1-triphenylbutane, 5-chloro-1,1,1-triphenylpentane, and 1,1,1-triphenylethane with alkali metals. 1,4 and 1,5 Migration of phenyl
Carbanions. XI. Reactions of 4-chloro-1,1,1-triphenylbutane, 5-chloro-1,1,1-triphenylpentane, and 1,1,1-triphenylethane with alkali metals. 1,4 and 1,5 Migration of phenyl
Reagents And Methods for Detecting Protein Lysine 3-Hydroxybutyrylation
申请人:PTM Biolabs, Inc.
公开号:US20150051093A1
公开(公告)日:2015-02-19
The invention provides an isolated peptide comprising a lysine 3-hydroxybutyrylation site, a lysine 3-hydroxybutyrylation specific affinity reagent that specifically binds to the peptide, and a method for detecting protein lysine 3-hydroxybutyrylation in a sample using the reagent.
Reagents and methods for detecting protein lysine 3-hydroxybutyrylation
申请人:PTM BIO LLC
公开号:US11385240B2
公开(公告)日:2022-07-12
The invention provides an isolated peptide comprising a lysine 3-hydroxybutyrylation site, a lysine 3-hydroxybutyrylation specific affinity reagent that specifically binds to the peptide, and a method for detecting protein lysine 3-hydroxybutyrylation in a sample using the reagent.
Triphenylmethylamides (TPMAs): Structure–activity relationship of compounds that induce apoptosis in melanoma cells
作者:Rahul Palchaudhuri、Paul J. Hergenrother
DOI:10.1016/j.bmcl.2008.07.128
日期:2008.11
Triphenylmethylamides (TPMAs) have been previously identified as compounds that arrest cells in the G1-phase of the cell cycle and induce apoptotic death in melanoma cell lines in culture. Here we report the synthesis of a series of TPMA derivatives, allowing the structure-activity relationship of this class of molecules to be established. Several new compounds have been identified that induce death in UACC-62 and SK-MEL-5 human melanoma cell lines, including a compound with enhanced aqueous solubility. (C) 2008 Elsevier Ltd. All rights reserved.
REAGENTS AND METHODS FOR DETECTING PROTEIN LYSINE 3-HYDROXYBUTYRYLATION
申请人:PTM BIO LLC
公开号:US20190331695A1
公开(公告)日:2019-10-31
The invention provides an isolated peptide comprising a lysine 3-hydroxybutyrylation site, a lysine 3-hydroxybutyrylation specific affinity reagent that specifically binds to the peptide, and a method for detecting protein lysine 3-hydroxybutyrylation in a sample using the reagent.