Modification of α-Chymotrypsin by Bromomethyl Naphthyl Ketones and Behavior of Reporter Groups in the Active Site
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/65/11/65_11_2948/_pdf
Reference14 articles.
1. Structure and mechanism of chymotrypsin
2. Modification of a Methionine Residue Near the Active Site of Chymotrypsin
3. Modification of a Methionine Residue near the Active Site of Chymotrypsin by p-Nitrophenyl Bromoacetyl-α-aminoisobutyrate*
4. Über das aktive Zentrum von Chymotrypsin, II. Modifizierung eines Methioninrestes in Chymotrypsin durch einfache Benzolderivate
5. Alkylation of Chymotrypsin by α-Bromo-4-nitroacetophenone, a Charge-Transfer Acceptor
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1. Regioselective α-Bromination of Aralkyl Ketones Using N-Bromosuccinimide in the Presence of Montmorillonite K-10 Clay: A Simple and Efficient Method;Synthetic Communications;2013-06-26
2. Proton-Dissociation Behavior of Sulfonium-Salt Pendants Having a Coumarin Skeleton Introduced into the .ALPHA.-Chymotrypsin Active Site.;NIPPON KAGAKU KAISHI;2000
3. Association Behavior of 1-Pyrenyl Pendants Introduced into the Papain Active Site;Bulletin of the Chemical Society of Japan;1999-04
4. Novel Behaviour of Naphthoylmethyl Pendants Introduced into the Papain Active Site;Journal of Chemical Research;1998
5. The Role ofα-Chymotrypsin Active Site in the Proton Dissociation of Aromatic Sulfonium-Salt Pendants Attached to the Methionine-192 Residue;Chemistry Letters;1997-08
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