
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
RongCheng K&S Chemical Co.,Ltd
Contact:0631-7336369
Address:rongcheng ,shandong province china
shijiazhuang shuanglian chemical industry co.,ltd
Contact:0311-82190302
Address:Luquan Intersection , Shijiazhuang--Taiyuan Expressway,Shijiazhuang City
Henan zhongda Biological Engineering Co., Ltd
Contact:86-28-18109029985
Address:shenzhou road,xuedian industrial estate,zhengzhou city,henan province CHN
ZiBO KuoDing Trade company Ltd
website:http://www.sdzbkd.com
Contact:86-13361591822
Address:GongQingTuan road
SuZhou Bichal Biological Technology CO.,LTD
Contact:+86-512-68051130
Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou 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)