THE CARCINOGENICITY OF CERTAIN DERIVATIVES OF p-DIMETHYLAMINOAZOBENZENE IN THE RAT
نویسندگان
چکیده
1. Eighteen known or possible metabolites of the hepatic carcinogen 4- (or p-) dimethylaminoazobenzene were tested for carcinogenic activity in the rat. Of these compounds only 4-monomethylaminoazobenzene, a known metabolite, proved to be active. Eight compounds, which appear to be metabolites of the dye, were inactive; these included 4-aminoazobenzene, 4'-hydroxy-4-monomethylaminoazobenzene, 4'-hydroxy-4-aminoazobenzene, N-methyl-p-phenylenediamine, p-phenylenediamine, aniline, p-aminophenol, and o-aminophenol. Nine compounds which may possibly be metabolites also were inactive; these compounds were 4'-hydroxy-, 3'-hydroxy-, and 2'-hydroxy-4-dimethylaminoazobenzene, 4-formylaminoazobenzene, 4-hydroxyazobenzene, 2, 4'-diamino-5-dimethylaminodiphenyl, 3-dimethylaminocarbazole, N,N-dimethyl-p-phenylenediamine, and p-hydroquinone. A mixture of 9 known and possible metabolites was also found to be inactive. These data indicate that the primary carcinogen operative in tumor formation by 4-dimethylaminoazobenzene is probably an azo dye closely related to the parent carcinogen. This conclusion is supported by recent work from this laboratory which indicates that the primary carcinogen consists of either or both of the protein-bound dyes found in the liver, i.e. 4-monomethylaminoazobenzene and an unidentified polar aminoazo dye, and that the formation of bound dye constitutes one of the first steps in this carcinogenic process. 2. The carcinogenic activities of 19 other compounds related to 4-dimethyl-aminoazobenzene were tested to obtain more information on the structural features needed for a 4-aminoazo dye to possess strong activity in the rat. 3'-Methyl-4-monomethylaminoazobenzene and the corresponding dimethylamino derivative were nearly twice as active and 4-ethylmethylaminoazobenzene had the same activity as 4-dimethylaminoazobenzene. As tested 3'-nitro- and 3'-chloro-4-dimethylaminoazobenzene both had about the same activity as 4-dimethylaminoazobenzene; however, since the 3'-nitro derivative was incompletely absorbed its real activity appears to be about 1(1/2) times that of 4-dimethylaminoazobenzene. 2'-Nitro- and 2'-chloro-4-dimethylaminoazobenzene were about one-half to one-third as active and 4'-chloro-4-dimethylaminoazobenzene was approximately one-fourth as active as the parent dye. 3'-Ethoxy-4-dimethylaminoazobenzene and 3-methyl-4-monomethylaminoazobenzene exhibited only slight carcinogenic activity. The following compounds proved inactive: the benzamide of N,N-dimethyl-p-phenylenediamine; the diethyl, monoethyl, benzylmethyl, beta-hydroxyethylmethyl, and formyl derivatives of 4-aminoazobenzene on the amino group; and the 3-methyl, 3', 5'-dimethyl, 2',5'-dimethyl, and 2',4'-dimethyl derivatives of 4-dimethylaminoazobenzene. From the available data two conditions appear to be essential if a dye is to possess high activity: (1) at least one methyl group must be attached to the amino group together with the proper second substituent, and (2) the rings must bear either no substituents or carry only certain substituents, preferably in the 3' position. 3. The data on the carcinogenicity of the 2'-, 3'-, or 4'-methyl, chloro, and nitro derivatives of 4-dimethylaminoazobenzene show that the position of these groups determines the carcinogenicity of these compounds to a greater extent than does the type of group. The activity relationship was 3' > 2' > 4'. 4. Primary, secondary, and tertiary aminoazo dyes were determined in the livers and blood of rats fed aminoazo dyes which differed in the substituents on the amino group. The data show that deethylation of 4-diethyl-, 4-monoethyl-, and 4-ethylmethylaminoazobenzene occurs in vivo just as 4-dimethyl- and 4-monomethylaminoazobenzene are demethylated in vivo. However, 4-benzylmethylaminoazobenzene and 4-beta-hydroxyethylmethylaminoazobenzene were dealkylated only slightly under similar conditions. 5. The following new compounds are described: 4-ethylmethyl-, 4-monoethyl-, 4-benzylmethyl-, and 4-beta-hydroxyethylmethylaminoazobenzene; 4'-hydroxy-, 3-methyl-, and 3'-methyl-4-monomethylaminoazobenzene; 2'-hydroxy-, 3'-hydroxy, 3-methyl-, 3'-ethoxy-, 3', 5'-dimethyl-, 2', 5'-dimethyl-, and 2',4'-dimethyl-4-dimethylaminoazobenzene.
منابع مشابه
The carcinogenic activities of certain halogen derivatives of 4-dimethylaminoazobenzene in the rat.
Previous studies from this laboratory (17, 19) have demonstrated that methyl, chioro, or nitro groups in the @†̃, 3', or 4' positions of the hepatic carcinogen, 4-dimethylaminoazobenzene, pro duced parallel alterations in the carcinogenicity of this dye. In each series the 4'-isomer was the least active and the 3'-isomer was the most active. Fur thermore, except for the very high activity of t...
متن کاملThe carcinogenicity of 3-methoxy-4-aminoazobenzene and its N-methyl derivatives for extrahepatic tissues of the rat.
In contrast to all previous results with many derivatives of 4-dimethylaminoazobenzene, the ingestion by the rat of 3-methoxy-4-aminoazobenzene or its N-monomethyl or N,N-dimethyl derivatives was found to induce high incidences of squamouscell carcinomas of the ear duct. $-Methoxy-4-aminoazobenzene also induced low incidences of adenocarcinomas in the small intestine and mammary gland. In addit...
متن کاملThe carcinogenicity of certain compounds related to p-dimethylaminoazobenzene.
Many aminoazobenzene derivatives have been tested for carcinogenic activity in the rat (1-7). N,N-dimethyl-p-aminoazobenzene and N-methyl-paminoazobenzene have been found to be equally carcinogenic (4, 7). They produced cholangiomas and hepatomas in all animals tested in approximately the same period of time. N,N-dimethyl-3'methyl-4-aminoazobenzene was more carcinogenic than the parent compound...
متن کاملFurther studies on the carcinogenicity of dyes related to 4-dimethylaminoazobenzene; the requirement for an unsubstituted 2-position.
Our preceding report (24) dealt with the carcinogenicity of several polyfluoro derivatives of 4-dimethylaminoazobenzene (DAB) involving the equivalent positions of the prime ring (Chart 1). As in the case of the monofluoro derivatives (24, 26), all these compounds are more active carcino gens for the rat liver than the unsubstituted dye. These results are in great contrast to those ob tained af...
متن کاملThe inhibition of the carcinogenicity of p-dimethyl-aminoazobenzene by certain detergents and the effect of diet on the levels of azo dyes in rat tissues.
It is well established that the rate at which liver tumors occur in rats fed p-dimethylaminoazobenzene can be altered greatly by dietary means. This subject has been reviewed through 1944 (15) and extended in more recent work (3~ 16, 17). The dietary inhibitors and accelerators that have been reported include members of the vitamin B complex, certain lipids, some sulfur-containing amino acids, ...
متن کاملذخیره 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 ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of Experimental Medicine
دوره 87 شماره
صفحات -
تاریخ انتشار 1948