Inhibitors of phenylalanine ammonia-lyase: 1-aminobenzylphosphonic acids substituted in the benzene ring
-
Add time:07/16/2019 Source:sciencedirect.com
Dextrorotatory 1-amino-3′,4′-dichlorobenzylphosphonic acid was found to be a potent inhibitor of the plant enzyme phenylalanine ammonia-lyase both in vitro and in vivo from among the ring-substituted 1-aminobenzylphosphonic acids and other analogues of phenylglycine. A structure activity relationship analysis of the results obtained permits predictions on the geometry of the pocket of the enzyme and is a basis in the strategy of better inhibitor synthesis.
We also recommend Trading Suppliers and Manufacturers of 2-AMINOINDAN-2-CARBOXYLIC ACID HYDROCHLORIDE (cas 33584-60-0). Pls Click Website Link as below: cas 33584-60-0 suppliers
Prev:Asymmetric synthesis of unusual α-amino acids
Next:On the stereoselectivity of the Paternò–Büchi reaction between carbonyl compounds and 2-furylmethanol (cas 93793-62-5) derivatives. The case of aliphatic aldehydes and ketones) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Asymmetric synthesis of unusual α-amino acids07/15/2019
- Asymmetric synthesis of (S)-1-aminoindan-1,5-dicarboxylic acid and related analogues via intramolecular acylation of enantiopure α,α-disubstituted amino acids07/14/2019
- Organic crystal engineering with piperazine-2,5-diones. 1. Crystal packing of piperazinediones derived from substituted 2-aminoindan-2-carboxylic acids07/12/2019
-
Health and Chemical more >


