Abstract: A communications device is presented that allows dynamic bandwidth allocation of an unswitched data path based upon the current utilization of one or more switched data channels. The device operates over the local loop of a digital communications carrier, such as a T1 line, that has a variety of time division multiplexed channels. Each data channel can be configured to operate as a channel dedicated to carrying unswitched data on the unswitched data path, or as a switched channel. Switched channels maintain status information about their current status, allowing switched data communication when the channel's status is active, and permitting the unswitched data path to utilize the channel when the channel's status is idle. In one embodiment, channel status information is passed to a remote unit by altering a redundant robbed-bit signaling bit in a multiframe. In a second embodiment, channel status is determined by monitoring switching information that is already transmitted about the channel.

Abstract: A communications device is presented that allows dynamic bandwidth allocation of an unswitched data path based upon the current utilization of one or more switched data channels. The device operates over the local loop of a digital communications carrier, such as a T1 line, that has a variety of time division multiplexed channels. Each data channel can be configured to operate as a channel dedicated to carrying unswitched data on the unswitched data path, or as a switched channel. Switched channels maintain status information about their current status, allowing switched data communication when the channel's status is active, and permitting the unswitched data path to utilize the channel when the channel's status is idle. In one embodiment, channel status information is passed to a remote unit by altering a redundant robbed-bit signaling bit in a multiframe. In a second embodiment, channel status is determined by monitoring switching information that is already transmitted about the channel.

Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted in the 4 position by a carbamyl or acylamino group, which carbamyl or acylamino group is substituted by a group which includes an acidic substituent are useful as inhibitors of leukotriene biosynthesis and as antiallergic agents. Pharmacological methods for using such compounds and synthetic intermediates for preparing such compounds are also disclosed.

Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted in the 4 position by an alkoxy or benzyloxy group or a benzylthio group, which alkoxy or benzyloxy group is directly substituted by a tetrazole ring, and which benzylthio group is directly substituted by carboxy or tetrazolyl are useful as inhibitors of leukotriene biosynthesis and as antiallergic agents. Synthetic intermediates for preparing such compounds are also described.

Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted in the 4 position by a carbamyl or acylamino group, which carbamyl or acylamino group is substituted by a group which includes an acidic substituent are useful as inhibitors of leukotriene biosynthesis and as antiallergic agents. Pharmacological methods for using such compounds and synthetic intermediates for preparing such compounds are also disclosed.

Abstract: Novel compounds which are di-t-butylphenyl alkyl or benzyl ethers which alkyl or benzyl group is substituted by an acidic group are useful an antiallergic agents. Synthetic intermediates for making such compounds are also disclosed.

Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted in the 4 position by an alkoxy or benzyloxy group or a benzylthio group, which alkoxy or benzyloxy group is directly substituted by a tetrazole ring, and which benzylthio group is directly substituted by carboxy or tetrazolyl are useful as inhibitors of leukotriene biosynthesis and as antiallergic agents. Synthetic intermediates for preparing such compounds are also described.

Abstract: Novel compounds which are 2,6-di-t-butylphenols substituted on the 4 position by an anilino group, which anilino group is substituted by a group which includes carboxyl, tetrazolyl or N-methyltetrazolyl are useful as inhibitors of leukotriene synthesis and as antiallergic agents. Pharmaceutical compositions containing such compounds and pharmacological methods for use of such compounds are also disclosed.

Abstract: Compounds wherein 2-nitrobenzofuran is substituted by one or two phenyl groups and certain other substituents which are active as antimicrobial agents, processes for their use and intermediates therefor.

Abstract: Compounds wherein 2-nitrobenzofuran is substituted by one or two phenyl groups and certain other substituents which are active as antimicrobial agents, processes for their use and intermediates therefor.

Abstract: Compounds wherein 2-nitrobenzofuran is substituted by one or two phenyl groups and certain other substituents which are active as antimicrobial agents, a processes for their use and intermediates therefor.

Abstract: Compounds wherein 2-nitrobenzofuran is substituted by one or two phenyl groups and certain other substituents which are active as antimicrobial agents, processes for their use and intermediates therefor.

Abstract: Compounds wherein 2-nitrobenzofuran is substituted by one or two phenyl groups and certain other substituents which are active as antimicrobial agents, processes for their use and intermediates therefor.

Abstract: Compounds wherein a phenylalkanoic acid is substituted by a 2-nitro-3-phenylbenzofuran group which are active as antimicrobial agents, processes for their use and intermediates therefor are described.

Abstract: Compounds wherein 2-nitrobenzofuran is substituted by one or two phenyl groups and certain other substituents which are active as antimicrobial agents, processes for their use and intermediates therefor.

Abstract: Compounds wherein a phenylalkanoic acid is substituted by a 2-nitro-3-phenylbenzofuran group which are active as antimicrobial agents, processes for their use and intermediates therefor are described.