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FI870695A - HETEROCYCLISKA FOERENINGAR OCH DERAS FRAMSTAELLNING OCH PHARMACEUTISKT PREPARAT. - Google Patents

HETEROCYCLISKA FOERENINGAR OCH DERAS FRAMSTAELLNING OCH PHARMACEUTISKT PREPARAT. Download PDF

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Publication number
FI870695A
FI870695A FI870695A FI870695A FI870695A FI 870695 A FI870695 A FI 870695A FI 870695 A FI870695 A FI 870695A FI 870695 A FI870695 A FI 870695A FI 870695 A FI870695 A FI 870695A
Authority
FI
Finland
Prior art keywords
alkyl
och
pharmaceutiskt
preparat
deras framstaellning
Prior art date
Application number
FI870695A
Other languages
Finnish (fi)
Other versions
FI870695A0 (en
FI87200C (en
FI87200B (en
Inventor
Claudio Semeraro
Dino Micheli
Daniele Pieraccioli
Giovanni Gaviraghi
Alan David Borthwick
Original Assignee
Glaxo Spa
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Glaxo Spa filed Critical Glaxo Spa
Priority to FI870695A priority Critical patent/FI87200C/en
Publication of FI870695A0 publication Critical patent/FI870695A0/en
Publication of FI870695A publication Critical patent/FI870695A/en
Application granted granted Critical
Publication of FI87200B publication Critical patent/FI87200B/en
Publication of FI87200C publication Critical patent/FI87200C/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

The invention relates to a method for production of compounds with formula (I), <IMAGE> and the physiologically acceptable salts thereof, where R1 is hydrogen or C1-4 alkyl, R2 is hydrogen or C1-4 alkyl, Alk is a methylene or ethylene group, R3 and R4 denote a C1-6 alkyl or alkoxyalkyl group, R5 is C1-4 alkyl, R6 is C1-13 alkyl or C5-8 cycloalkyl which can be substituted with C1-3 alkyl, and R7 is a halogen or hydrogen atom or C1-3 alkyl. The compounds with formula (I) reduce the intracellular calcium ion concentration by limiting the transmembranal calcium ion influx and they can be used in the treatment of cardiovascular disorders, such as hypertension.
FI870695A 1987-02-19 1987-02-19 FORM OF THERAPEUTIC FREQUENCY ACTIVATION 6-ALKYL-2-AMINOALKYL-4-PHENYL-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLATHER FI87200C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FI870695A FI87200C (en) 1987-02-19 1987-02-19 FORM OF THERAPEUTIC FREQUENCY ACTIVATION 6-ALKYL-2-AMINOALKYL-4-PHENYL-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLATHER

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FI870695A FI87200C (en) 1987-02-19 1987-02-19 FORM OF THERAPEUTIC FREQUENCY ACTIVATION 6-ALKYL-2-AMINOALKYL-4-PHENYL-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLATHER
FI870695 1987-02-19

Publications (4)

Publication Number Publication Date
FI870695A0 FI870695A0 (en) 1987-02-19
FI870695A true FI870695A (en) 1988-08-20
FI87200B FI87200B (en) 1992-08-31
FI87200C FI87200C (en) 1992-12-10

Family

ID=8523966

Family Applications (1)

Application Number Title Priority Date Filing Date
FI870695A FI87200C (en) 1987-02-19 1987-02-19 FORM OF THERAPEUTIC FREQUENCY ACTIVATION 6-ALKYL-2-AMINOALKYL-4-PHENYL-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLATHER

Country Status (1)

Country Link
FI (1) FI87200C (en)

Also Published As

Publication number Publication date
FI870695A0 (en) 1987-02-19
FI87200C (en) 1992-12-10
FI87200B (en) 1992-08-31

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