The fate of certain organic acids and amides in the rabbit; further observations on the hydrolysis of amides by tissue extracts.

نویسندگان

  • H G BRAY
  • S P JAMES
  • J W V THORPE
  • M R WASDELL
چکیده

Studies of the amidase activity ofextracts of various animal tissues have been reported in earlier papers (Bray, James, Ryman & Thorpe, 1948; Bray, James, Raffan, Ryman & Thorpe, 1949a; Bray, Thorpe & Wood, 1949c; Bray, James, Thorpe, Wasdell & Wood, 1949 b). The present paper records further observations, including the behaviour of the enzyme towards some saturated long-chain and w-phenylsubstituted aliphatic amides andthe effect ofincrease in chain length on the degree of hydrolysis. The action of the enzyme upon amides previously examined has been reinvestigated in the absence of chloroform, which was used as a preservative in earlier experiments, since it was found that this substance had some retarding effect on amidase activity (Bray et al. 1949b). Some other amides have also been examined. The amides studied can be divided into three

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

The fate of certain organic acids and amides in the rabbit; nitrobenzoic acids and amides.

Studies in vitro (Bray, James, Ryman & Thorpe, 1948a) have shown that rabbit-liver extracts are able to hydrolyze all three nitrobenzamides. The para isomer is most readily attacked, the average hydrolysis being 82 %; under the same conditions the meta and ortho isomers are hydrolyzed to the extent of 31 and 23 %, respectively. It was, therefore, of interest to study the metabolism of these com...

متن کامل

Theoretical study of the effect of internal strain on the bond length and rate of hydrolysis in cyclic amides

The internal strain in cyclic amides are explained as a factor of resonance that are effected on the bond length C-N  and are a major factor of rates of hydrolysis. The cyclic amides in this study are optimized by Gaussian program and the bond length of C-N in the rings are studied by HF/6-31G*.

متن کامل

Internal strain on the bond length and rate of hydrolysis in cyclic amides

The internal strain in cyclic amides are explained as a factor of resonance that are effected on the bond length C-N and are a major factor of rates of hydrolysis. The cyclic amides in this study are optimized by Gaussian program and the bond length of C-N in the rings are studied by HF/6-31G*.

متن کامل

Ultrasound-Promoted Synthesis of Aryl Amides from Isocyanides and Carboxylic Acids under Ambient Conditions

The synthesis of aryl amides via the reactions of carboxylic acids and isocyanides in methanol was carried out in 78-95% yields under ultrasound irradiation. The method has wide applicability, and the protocol is mild, fast and efficient compared to the existing methods based on silent conditions.

متن کامل

Theoretical study of the effect of internal strain on the bond length and rate of hydrolysis in cyclic amides

The internal strain in cyclic amides are explained as a factor of resonance that are effected on the bond length C-N  and are a major factor of rates of hydrolysis. The cyclic amides in this study are optimized by Gaussian program and the bond length of C-N in the rings are studied by HF/6-31G*.  

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 Biochemical journal

دوره 47 3  شماره 

صفحات  -

تاریخ انتشار 1950