摘要:
In a photosensitive material processing apparatus, a photosensitive material taking on the form of a long strip is fed into a conveyance mechanism and conveyed in this form along a predetermined conveyance path. An exposure device, a reservoir section, a development processing section, and a cutter are located in the conveyance path. The exposure device carries out scanning exposing operations on the long strip of the photosensitive material and thereby forms latent images on the long strip of the photosensitive material. In the reservoir section, a looped portion for serving as a buffer for conveyance is formed in the long strip of the photosensitive material, on which the latent images have been formed. In the development processing section, development processing is carried out on the long strip of the photosensitive material, which is fed via the reservoir section. The cutter cuts the long strip of the photosensitive material, which has been subjected to the development processing, into sheets having a predetermined length.
摘要:
A compound of formula I, having antibacterial activity and a pharmaceutical composition containing the compound of formula I: ##STR1## wherein Q represents a partial structure of formula II: ##STR2## wherein all substituents are defined in the specification.
摘要:
A digital copier is provided with mechanism for reading images of both sides of an original, and mechanism for storing image data read by the reading mechanism in an area of an image memory in order, and when a predetermined signal is applied thereto, for storing image data in the next area by one area. The predetermined signal may be generated when a skip key is depressed. Therefore, since it is not necessary to read images which needs not to be recorded, the appearance of the recorded images on a record sheet is improved and the processing time is shortened. The digital copier may be also provided with mechanism for storing blank data in remaining areas in the image memory when a predetermined signal is applied thereto. The predetermined signal may be generated when an end key is depressed.
摘要:
The present invention relates to spiro compounds of general formula I: ##STR1## wherein the substituents are herein below defined. The present invention relates to antibacterial spiro compounds which are of value as drugs for humans, veterinary drugs or drugs for use in fish culture or as preservatives, and to antibacterial compositions containing one or more of the same compounds as active ingredients.
摘要:
There is disclosed a communication method of a communication system having a base station for transmitting a beacon and a terminal for receiving the beacon transmitted from the base station and performing communication with the base station, the communication method including the steps of: transmitting the beacon by the base station, the beacon being made of a plurality of sub-beacons including an ID for identifying the terminal; and stopping processing for communication with the base station by the terminal when at least one of the plural sub-beacons has a portion that does not match an ID of the terminal.
摘要:
The present invention provides an antibacterial compound useful as medicines, animal drugs, fisheries drugs or antibacterial preservatives and to an antibacterial agent or preparation which contains the same, more particularly a compound which possesses high safety and excellent activity against a broad range of bacterial species including quinolone-resistant strains. A quinolone derivative of the following formula (I) which has a group derived from the heterocyclic spiro-compound at the 7-positioned R2 and the halogenocyclopropyl group at the N1-position, prefereably a compound of pure isomer, and an antibacterial agent containing the derivative compound.
摘要:
A quinolone derivative represented by formula (I): wherein R1 represents a cycloalkyl group; R2 represents a hydrogen atom, an amino group, a hydroxyl group, a thiol group, a halogenomethyl group, an alkyl group, an alkenyl group, an alkynyl group, or an alkoxyl group; R3 represents an amino group, a halogenomethyl group, a halogenomethoxyl group, an alkyl group, an alkenyl group, an alkynyl group, or an alkoxyl group; R4 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms; R5 represents a cycloalkyl group having 3 to 6 carbon atoms; the above R1 to R5 may be substituted; X represents a halogen atom or a hydrogen atom; and Y represents a hydrogen atom, a phenyl group, an acetoxymethyl group, a pivaloyloxymethyl group, an ethoxycarbonyl group, a choline group, a dimethylaminoethyl group, a 5-indanyl group, a phthalidinyl group, a 5-alkyl-2-oxo-1,3-dioxol-4-ylmethyl group, a 3-acetoxy-2-oxobutyl group, an alkyl group having 1 to 6 carbon atoms, an alkoxymethyl group having 2 to 7 carbon atoms, or a phenylalkyl group having 1 to 6 carbon atoms in the alkyl moiety thereof, or a salt thereof. The compound exhibits high and broad antimicrobial activity against various bacteria including bacteria resistant to drugs and high safety.
摘要:
A box nailing machine includes a piston within a cylinder to drive a nail. A main selector valve introduces compressed air into the cylinder and discharges the compressed air from the cylinder. A start operation valve operates the main selector valve. A trigger device for the box nailing machine comprises: a trigger switch operated by a trigger lever; a contact switch operated by the contact arm; an electromagnetic valve serving as the start operation valve; a logical circuit for applying a drive current to the electromagnetic valve when both the trigger switch and the contact switch are turned on; and a controller which includes a timer with a predetermined time limit. The timer is started in accordance with a trigger signal of the trigger switch and prohibits the drive current from the electromagnetic valve when the timer counts the predetermined time period. The timer is reset upon release of the trigger.
摘要:
N.sub.1 -(1,2-cis-2-halogenocydopropyl)-substituted pyridonecarboxylic acid derivatives represented by formula (I) and the salts thereof are disclosed. These compounds have patent antibacterial activities against a wide variety of infectious bacteria, and are useful as antibacterial agents by oral or parenteral administration.
摘要:
Quinolone derivatives are known as synthetic antimicrobial agents having a condensed pyridonecarboxylic acid skeleton, and those having substituents on various replaceable positions of said skeleton are known. In particular, if diastereomers exist, there are 4 or more kinds of stereoisomers. A mixture of diastereomers is a mixture of isomers having different physical properties and is difficult to apply as a drug as such. The present invention provides an antimicrobial 1-(1,2-cis-2-fluorocyclopropyl)-substituted quinolone derivative represented by formula I shown below which, although involving diastereomers, consists of a single stereoisomer. ##STR1## wherein R.sup.1 represents a methyl group, a difluoromethyl group, etc.; R.sup.2 represents a saturated nitrogen-containing heterocyclic group; A represents C--X.sup.3 or a nitrogen atom; X.sup.1 and X.sup.2 each represents a halogen atom; and X.sup.3 and Z represent a hydrogen atom, etc.