Claims
- 1. A process for preventing the release of pharmocological mediators from an immediate hypersensitivity reaction between reaginic type antibodies and an antigen, thereby preventing the symptoms manifest in bronchial asthma, seasonal pollinosis, allergic rhinitis, urticaria, allergic conjunctivitis, food allergy and anaphylactoid reactions of a sensitized animal, which comprises prophylactically administering to said animal an effective amount of a compound of the formula: ##STR9## in which A is a member selected from the group consisting of .alpha.-naphthyl, .beta.-naphthyl, phenyl, 2,6-dichlorophenyl, and substituted phenyl moieties containing from one to three substituents in any of the 2,3,4 and 5 positions of the phenyl ring, independently selected from the group consisting of lower alkyl, lower alkylsulfinyl, lower alkoxy, hydroxy(lower) alkoxy, 2-(lower alkoxy oxalyloxy)ethoxy, N-mono- and di-lower alkylamino(lower)alkoxy, halo, sulfamyl, polyhalo(lower)alkyl, carbamoyl, N-lower alkylcarbamoyl, mono- and di-lower alkylamino, carboxy, lower alkylcarbonyl, cyano, carb(lower)alkoxy, phenoxy(lower)alkoxy, lower alkoxy-oxalamido and lower alkoxyoxalamidophenoxy radicals;
- of a pharmaceutically acceptable salt thereof.
- 2. The process of claim 1 which comprises administering to said sensitive animal a compound of the formula ##STR10## in which R.sup.1 is --CN or CONH.sub.2 ;
- R.sup.2 is lower alkoxy, hydroxy(lower)alkoxy, lower alkylamino or di(lower)alkyl amino;
- R.sup.3 is hydrogen, lower alkyl, lower alkoxy, halo, poly-halo(lower)alkyl, lower alkyl carbonyl or carb(lower) alkoxy;
- or pharmaceutically acceptable salt thereof.
- 3. The process of claim 1 in which said compound is of the formula: ##STR11## in which R.sup.2 is lower alkylamino or di(lower)alkyl amino;
- R.sup.3 is hydrogen, lower alkyl, lower alkoxy, halo, polyhalo(lower)alkyl, lower alkyl carbonyl or carb(lower) alkoxy;
- or pharmaceutically acceptable salt thereof.
- 4. The process of claim 1 in which said compound is of the formula: ##STR12## in which R.sup.2 is lower alkoxy or hydroxy(lower)alkoxy;
- R.sup.3 is hydrogen, lower alkyl, lower alkoxy, halo, polyhalo(lower)alkyl, lower alkyl carbonyl or carb(lower)alkoxy;
- or pharmaceutically acceptable salt thereof.
- 5. The process of claim 1 which comprises orally administering to said sensitized animal an effective amount of 1H-tetrazole-5-carboxanilide or a pharmaceutically acceptable salt thereof.
- 6. The process of claim 1 which comprises orally administering to said sensitized animal an effective amount of N-[2-carbamyl-3-methoxyphenyl]-1H-tetrazole-5-carboxamide.
- 7. A compound of the formula: ##STR13## in which A is .alpha.-naphthyl, .beta.-naphthyl, 2,6-dichlorophenyl or a substituted phenyl moiety having from one to three substituents selected from the group consisting of lower alkyl, lower alkylsulfinyl, lower alkoxy, hydroxy(lower)alkoxy, 2-(lower alkoxyoxalyloxy)-ethoxy, N-mono- and di-(lower) alkylamino(lower) alkoxy, sulfamyl, polyhalo(lower) alkyl, carbamoyl, N-(lower)alkycarbamyl, mono- and di-(lower) alkylamino, carboxy, lower alkyl carbonyl, cyano, carb(lower)alkoxy, phenoxy(lower)alkoxy, lower alkoxyoxalamido and lower alkoxyoxalamidophenoxy;
- or a pharmaceutically acceptable salt thereof.
- 8. A compound of the formula: ##STR14## in which R.sup.1 is --CN or CONH.sub.2 ;
- R.sup.2 is lower alkoxy, hydroxy lower alkoxy, lower alkylamino or di(lower)alkyl amino;
- R.sup.3 is hydrogen, lower alkyl, lower alkoxy, halo, polyhalo(lower)alkyl, lower alkyl carbonyl or carb(lower)alkoxy;
- or a pharmaceutically acceptable salt thereof.
- 9. The compound of claim 8 in which is N-[2-carbamoyl-3-methoxyphenyl]-1H-tetrazole-5-carboxamide or a pharmaceutically acceptable salt thereof.
RELATED APPLICATIONS
This application is a continuation-in-part of Ser. No. 542,465, filed Jan. 20, 1975 now U.S. Pat. No. 3,966,965; which in turn is a continuation-in-part of Ser. No. 344,466, filed Mar. 23, 1973, now abandoned.
US Referenced Citations (3)
Number |
Name |
Date |
Kind |
3578674 |
Buckler |
May 1971 |
|
3824249 |
Regnier et al. |
Jul 1974 |
|
3887574 |
Ellis et al. |
Jun 1975 |
|
Non-Patent Literature Citations (1)
Entry |
Fisher et al., J. Organic Chem., vol. 24, 1650-1654. (1959) |
Continuation in Parts (2)
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Number |
Date |
Country |
Parent |
542465 |
Jan 1975 |
|
Parent |
344466 |
Mar 1973 |
|