Process for producing a-hydroxy acid or a-hydroxyamide by microorganism |
| OF THE INVENTION In the present invention, the aldehyde, prussic acid, .alpha.-hydroxynitrile and ... |
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Process for preparing .alpha.-hydroxy acids using microorganism and novel microorganism |
| What is claimed is: 1. A method for producing compounds represented by a general formula [II], RCH(O... |
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Modification of pigment charge characteristics |
| What is claimed is: 1. A positively charged dry electrophotographic developer composition comprised ... |
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Fluorescent toners surface coated with polymeric quaternary ammonium compound and slip agent |
| I claim: 1. A dry nonelectroscopic fluorescent toner comprising fluorescent pigmented organic resin ... |
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New electrostatographic toners and developers containing new charge-control agents |
| What is claimed is: 1. A dry, particulate, electrostatographic toner composition comprising a ... |
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Process for producing toner for electrophotography |
| What is claimed is: 1. A process for producing a toner for electrophotography which comprises ... |
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Liquid developer, method for manufacture thereof, image forming device, and image forming method |
| What is claimed is: 1. A liquid developer comprising: an insulating carrier liquid; toner particles ... |
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Electrophotographic toner made by polymerizing monomers in solution in presence of colorant |
| OF THE PREFERRED EMBODIMENTS Process of Embodiment (i) In the process of the embodiment (i), a ... |
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Resins for electrohotographic toners |
| OF THE INVENTION The term "amorphous poly-(.alpha.-hydroxycarboxylic acid)" herein used means "... |
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Dip coating method having intermediate bead drying step |
| The present invention is accomplished in embodiments by providing a coating method comprising: (a) ... |
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Dihydroxyphenylethylaminoalkyl theophyllines
| Details |
Inventors: Kleemann, Axel; Klingler, Karl H.; VON Schlichtegroll, Ansgar; Stroman, Fritz; Thiemer, Klaus; Westermann, Erik;
Assignee: Deutsche Gold- und Silber-Scheideanstalt vormals Roessler (Frankfurt, DE)
Primary Examiner: Rizzo; Nicholas S.
Assistant Examiner:
Attorney, Agent or Firm: Cushman, Darby & Cushman
There are prepared compounds of the formula ##STR1## in which T is the theophyllin-7-yl group and alk is a straight or branched alkylene chain with 2 to 4 carbon atoms and salts thereof. The compounds promote circulation and produce a marked and persistent increase in renal circulation. |
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DETAILED DESCRIPTION What is claimed is: 1. A compound corresponding to the general formula ##STR6## in which T is the theophyllin-7-yl radical and alk is an alkylene chain with 3 carbon atoms, or a pharmaceutically acceptable salt thereof. 2. A compound according to claim 1 in the form of the free base. 3. A compound according to claim 1 in the form of a pharmaceutically acceptable salt. 4. A method of increasing renal circulation in a mammal comprising administering to the mammal an effective amount to increase renal circulation of a compound corresponding to the general formula ##STR7## in which T is the theophyllin-7-yl radical and alk is an alkylene chain with 2 to 4 carbon atoms, or a pharmaceutically acceptable salt thereof. 5. A method according to claim 4 wherein the compound is 7-{3-[3,4,-dihydroxyphenyl)-ethylamino]-propyl}-theophylline. 6. A method according to claim 4 wherein alk is ##STR8## 7. A method according to claim 6 wherein the compound is 7-{2-[2-(3,4-dihydroxyphenyl)-ethylamino]-ethyl}-theophylline. 8. A compound according to claim 6 which is 7-{3-[2-(3,4-dihydroxyphenyl)-ethylamino]-propyl}-theophylline. 9. A method according to claim 6 wherein the compound is 7-{3-[2-(3,4-dihydroxyphenyl)-ethylamino]-butyl}-theophylline. 10. A method according to claim 4 wherein there is administered orally at least 0. 1 mg/kg body weight of the mammal. 11. A method according to claim 4 wherein there is administered intravenously at least 0. 001 mg/kg body weight of the mammal.
Description:
BACKGROUND OF THE INVENTION This invention relates to new basically substituted theophylline derivatives. Klingler German Patent Specification No. 1,221,641 described the production of theophylline derivatives corresponding to the general formula ##STR2## in which T represents theophylline radical, Alk represents a straight or branched alkylene chain with 2 to 6 carbon atoms, R represents a hydrogen atom or a lower alkyl group and A represents a phenyl radical which is substituted once, twice or three times by hydroxyl, methoxy, alkyl, aralkyl or alkoxy alkyl groups with 1 to 3 carbon atoms in the alkyl radical or by chlorine or bromine atoms or once by a methylene dioxy group in the 3,4-position
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