Peptide ligation assisted by an auxiliary attached to amidyl nitrogen
摘要:
New thiol-containing auxiliaries were developed for peptide ligation. They were placed at the amidyl N-atom in the second amino acid residue of a peptide fragment. With the new auxiliaries, peptide ligation could be conducted at non-Cys and non-Gly sites. Compared to other recently developed auxiliaries, an important feature of the present design was that the new auxiliaries were generally applicable and readily removable. (C) 2010 Elsevier Ltd. All rights reserved.
Peptide ligation assisted by an auxiliary attached to amidyl nitrogen
摘要:
New thiol-containing auxiliaries were developed for peptide ligation. They were placed at the amidyl N-atom in the second amino acid residue of a peptide fragment. With the new auxiliaries, peptide ligation could be conducted at non-Cys and non-Gly sites. Compared to other recently developed auxiliaries, an important feature of the present design was that the new auxiliaries were generally applicable and readily removable. (C) 2010 Elsevier Ltd. All rights reserved.
[EN] PYRIMIDOPYRIDAZINE DERIVATIVES USEFUL AS P38 MAPK INHIBITORS<br/>[FR] DÉRIVÉS DE PYRIMIDOPYRIDAZINE UTILES COMME INHIBITEURS DE LA P38 MAP KINASE
申请人:PULMAGEN THERAPEUTICS INFLAMMA
公开号:WO2010094955A1
公开(公告)日:2010-08-26
A compound formula (IA) or (IB), or a pharmaceutically acceptable thereof; wherein the substituents are defined as in the claims, and their use as P38 MAP kinase.
PYRIMIDOPYRIDAZINE DERIVATIVES USEFUL AS P38 MAPK INHIBITORS
申请人:Beswick Amanda
公开号:US20120077809A1
公开(公告)日:2012-03-29
A compound formula (IA) or (IB), or a pharmaceutically acceptable thereof; wherein the substituents are defined as in the claims, and their use as P38 MAP kinase.
Pyrimidopyridazine derivatives useful as P38 MAPK inhibitors
申请人:Beswick Amanda
公开号:US08450314B2
公开(公告)日:2013-05-28
A compound formula (IA) or (IB), or a pharmaceutically acceptable thereof; wherein the substituents are defined as in the claims, and their use as P38 MAP kinase.
Peptide ligation assisted by an auxiliary attached to amidyl nitrogen
作者:Juan Li、Hong-Kui Cui、Lei Liu
DOI:10.1016/j.tetlet.2010.01.108
日期:2010.3
New thiol-containing auxiliaries were developed for peptide ligation. They were placed at the amidyl N-atom in the second amino acid residue of a peptide fragment. With the new auxiliaries, peptide ligation could be conducted at non-Cys and non-Gly sites. Compared to other recently developed auxiliaries, an important feature of the present design was that the new auxiliaries were generally applicable and readily removable. (C) 2010 Elsevier Ltd. All rights reserved.