
European Journal of Medicinal Chemistry p. 355 - 361 (1993)
Update date:2022-08-04
Topics:
Oesapay, G
Csiba, A
A series of phosphonic analogs of amino acids, peptides, and their derivatives was synthesized in order to examine their ability to inhibit human carbonic anhydrase (HCA) isoenzymes (I and II).The aminophosphonic acids with amino protection possess much stronger inhibitory capacity (Ki = 10-6 - 10-5 M) than the free aminophosphonic acids (Ki = 10-5 - 10-3 M).The aminophosphonic acids with both N- and P-protection do not have an inhibitory effect on the esterase activity of HCA.In a comparison of the enantiomeric pairs of Cbz-AlaP(OH)2, the D-conformer has several-fold stronger inhibitory potency.All aminoalkylphosphonates investigated possess one order of magnitude stronger inhibitory activity towards isoenzyme HCA-I than towards HCA-II.A computer-directed analysis was used to study the possible interactions in an aminoalkylphosphonate
Anhui Sunsing Chemicals Co.,Ltd
website:http://www.sunsingchem.com
Contact:0086-566-2023179
Address:Jin An industry park, Chizhou economic technical development zone, Anhui
website:https://www.yacoo.com.cn/en/
Contact:86-512-87182055
Address:No.112 Xinqing Rd, Suzhou Industrial Park, China, 215125, China
Shandong Xinke Petrochemical Co., Ltd.
Contact:+86-546-7277016
Address:Gudao Industrial Park, Hekou District, Dongying, Shandong Province, China
Contact:+86-21-38228826
Address:Room 505 Building 2, No 3377 Kangxin Highway, Shanghai, Republic China
Luoyang Aoda chemical Co.,Ltd.
Contact:+86-379-67518785 67516588
Address:MiaoWan industry district,YanShi City,Henan,China
Doi:10.1016/S0040-4020(03)00438-1
(2003)Doi:10.1039/c6ra25562k
(2017)Doi:10.1021/ol035128a
(2003)Doi:10.1016/j.ejmech.2021.113325
(2021)Doi:10.1039/P19760000532
(1976)Doi:10.1080/10426509808545471
(1998)