© 2019 A p-tert-butylthiacalix[4]arene derivative containing tryptophan moieties on the lower rim was synthesized and proposed as a chymotrypsin inhibitor. Its ability to competitively inhibit the enzyme was revealed by kinetic methods. A mechanism of the inhibitory action has been established, which consists in the binding of macrocycle tryptophan moieties to the enzyme active site, resulting in its blocking
Available from British Library Document Supply Centre-DSC:DXN009646 / BLDSC - British Library Docume...
O-Acetylserine sulfhydrylase (isoform A, OASS-A) is a pyridoxal-5’-phosphate-dependent enzyme respon...
Disclosed herein is the use of HLM-008182, as well as its analogues formed via in-house synthesis, a...
© 2019 A p-tert-butylthiacalix[4]arene derivative containing tryptophan moieties on the lower rim wa...
This paper deals with the design, synthesis, and evaluation of a new series of receptors for protein...
This paper deals with the design, synthesis, and evaluation of a new series of receptors for protei...
© 2019 Elsevier Inc. Novel ammonium and betaine derivatives of p-tert-butylthiacalix[4]arene in cone...
Silanediol peptidomimetics are demonstrated to inhibit a serine protease. Asymmetric synthesis of th...
The binding of the three competitive inhibitors benzyl alcohol, tryptophol, and N-acetyl-D-tryptopha...
Serine proteases are involved in a number of physiological processes and have proved to be a valuabl...
The enzyme tryptophan dioxygenase (E.C.1.13.11.11), found in mammalian liver, catalyzes the initial,...
Proteinases play key roles in various physiological processes. However, excessive activity of protei...
Light regulation of drug molecules has gained growing interest in biochemical and pharmacological re...
Novel enediyne-amino acid conjugates 1-4 have been synthesized. All of these effectively target the ...
A family of macrodilactam natural products, the syrbactins, are known proteasome inhibitors. A small...
Available from British Library Document Supply Centre-DSC:DXN009646 / BLDSC - British Library Docume...
O-Acetylserine sulfhydrylase (isoform A, OASS-A) is a pyridoxal-5’-phosphate-dependent enzyme respon...
Disclosed herein is the use of HLM-008182, as well as its analogues formed via in-house synthesis, a...
© 2019 A p-tert-butylthiacalix[4]arene derivative containing tryptophan moieties on the lower rim wa...
This paper deals with the design, synthesis, and evaluation of a new series of receptors for protein...
This paper deals with the design, synthesis, and evaluation of a new series of receptors for protei...
© 2019 Elsevier Inc. Novel ammonium and betaine derivatives of p-tert-butylthiacalix[4]arene in cone...
Silanediol peptidomimetics are demonstrated to inhibit a serine protease. Asymmetric synthesis of th...
The binding of the three competitive inhibitors benzyl alcohol, tryptophol, and N-acetyl-D-tryptopha...
Serine proteases are involved in a number of physiological processes and have proved to be a valuabl...
The enzyme tryptophan dioxygenase (E.C.1.13.11.11), found in mammalian liver, catalyzes the initial,...
Proteinases play key roles in various physiological processes. However, excessive activity of protei...
Light regulation of drug molecules has gained growing interest in biochemical and pharmacological re...
Novel enediyne-amino acid conjugates 1-4 have been synthesized. All of these effectively target the ...
A family of macrodilactam natural products, the syrbactins, are known proteasome inhibitors. A small...
Available from British Library Document Supply Centre-DSC:DXN009646 / BLDSC - British Library Docume...
O-Acetylserine sulfhydrylase (isoform A, OASS-A) is a pyridoxal-5’-phosphate-dependent enzyme respon...
Disclosed herein is the use of HLM-008182, as well as its analogues formed via in-house synthesis, a...