KF77-AG6, an antipain-related metabolite.

نویسندگان

  • K Fujimoto
  • K Tatsuta
  • T Tsuchiya
  • S Umezawa
  • H Umezawa
چکیده

Recently we reported') the isolation and structural elucidation of a SAKAGUCHI-positive metabolite of Streptomyces, found in the course of chemical screening of microbial metabolites. The compound proved to be identical to antipain=' discovered as a protease inhibitor. In the present paper, we wish to report the isolation of another SAKAGUCHI-positive metabolite, KF77-AG6, which corresponds to the ureylene group-containing part of antipain, i.e. [(S)-1-carboxy-2-phenylethyl]carbamoyl-Larginine". KF77-AG6 is produced by a strain of Streptomyces fllipinensis3' (the Laboratory No. KF77-AG6), from which antipain was not produced. A part of the biological effect of KF77AG6 (described as AN) has already been reported'.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Optical properties of the hydrated charged silver tetramer and silver hexamer encapsulated inside the sodalite cavity of an LTA-type zeolite.

The optical spectra in the UV-VIS region of the hydrated doubly charged tetramer Ag4(2+) and hydrated multiply charged hexamer Ag6(p+) silver clusters encapsulated inside the sodalite cavity of an LTA-type zeolite have been systematically predicted using DFT, TD-DFT and CASSCF/CASPT2 methods. The optical behaviour of the model hydrated clusters [Ag6(H2O)8(Si24H24O36)](p+) is very sensitive to t...

متن کامل

A Polyoxometalate-templated Inorganic-Organic Hybrid Compound Containing a Crown-like Metallamacrocyclic Cation [Ag6(1,2,4-triazole)6]

A new polyoxometalate(POM)-templated inorganic-organic hybrid compound, [Ag6(trz)6][PMo12O40]2 · 6H2O (1) (trz = 1,2,4-triazole) has been prepared under hydrothermal conditions and characterized by single-crystal X-ray diffraction, elemental analyses, IR spectroscopy, thermogravimetric analysis and cyclic voltammetry. In compound 1, six Ag+ ions are linked by six trz molecules to give a hexanuc...

متن کامل

Inhibition of H-ras oncogene transformation of NIH3T3 cells by protease inhibitors.

The protease inhibitors antipain, leupeptin, alpha 1-antitrypsin, and epsilon-aminocaproic acid were found to inhibit transformation of NIH3T3 cells after transfection with an activated H-ras oncogene. Inhibition of focus formation by protease inhibitors was concentration dependent and maximal at 50% of control values. Transfection of a gene for neomycin resistance was not affected by protease ...

متن کامل

Effects of protease inhibitors on radiation transformation in vitro.

We have investigated the effects of three protease inhibitors, antipain, leupeptin, and soybean trypsin inhibitor, on the induction of oncogenic transformation in mouse C3H10T 1/2 cells by X-rays. The patterns of inhibition by the three protease inhibitors were different. Antipain was the most effective, having the ability to suppress completely radiation transformation as well as radiation tra...

متن کامل

Antipain inhibits thyroxine-induced synthesis of carbamyl phosphate synthetase I in tadpole liver.

The increased activity of carbamyl phosphate synthetase I [carbamoyl-phosphate synthase (ammonia); ATP: carbamate phosphotransferase (diphosphorylating), EC 2.7.2.5] in tadpole liver observed during thyroxine-induced metamorphosis was markedly inhibited by intraperitoneal injection of the microbial protease inhibitor antipain (0.1 micrometermol/g of body weight, twice daily). A somewhat less th...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of antibiotics

دوره 27 9  شماره 

صفحات  -

تاریخ انتشار 1974