FR2193587A1 - Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste - Google Patents

Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste

Info

Publication number
FR2193587A1
FR2193587A1 FR7227515A FR7227515A FR2193587A1 FR 2193587 A1 FR2193587 A1 FR 2193587A1 FR 7227515 A FR7227515 A FR 7227515A FR 7227515 A FR7227515 A FR 7227515A FR 2193587 A1 FR2193587 A1 FR 2193587A1
Authority
FR
France
Prior art keywords
lauryl sulphate
vincamine
compsns
cerebral
humans
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
FR7227515A
Other languages
French (fr)
Other versions
FR2193587B1 (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CENTRE ETD IND PHARMA
Original Assignee
CENTRE ETD IND PHARMA
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 CENTRE ETD IND PHARMA filed Critical CENTRE ETD IND PHARMA
Priority to FR7227515A priority Critical patent/FR2193587A1/en
Publication of FR2193587A1 publication Critical patent/FR2193587A1/en
Application granted granted Critical
Publication of FR2193587B1 publication Critical patent/FR2193587B1/fr
Granted legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C305/00—Esters of sulfuric acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D461/00—Heterocyclic compounds containing indolo [3,2,1-d,e] pyrido [3,2,1,j] [1,5]-naphthyridine ring systems, e.g. vincamine

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Vincamine lauryl sulphate, is suitable for formulation in drops or potable solns. and for dosage 10-100 mg/day depending on age and condition of the patient. The LD50 in mice is 30 mg/kg i.v. and 1500 mg/kg s.c. It is prepd. by reaction of vineamine base with an alkali metal lauryl sulphate.
FR7227515A 1972-07-31 1972-07-31 Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste Granted FR2193587A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FR7227515A FR2193587A1 (en) 1972-07-31 1972-07-31 Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7227515A FR2193587A1 (en) 1972-07-31 1972-07-31 Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste

Publications (2)

Publication Number Publication Date
FR2193587A1 true FR2193587A1 (en) 1974-02-22
FR2193587B1 FR2193587B1 (en) 1975-08-08

Family

ID=9102594

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7227515A Granted FR2193587A1 (en) 1972-07-31 1972-07-31 Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste

Country Status (1)

Country Link
FR (1) FR2193587A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0046506A1 (en) * 1980-08-25 1982-03-03 Heinrich Mack Nachf. Vincamine saccharinate and drug containing it
WO1996032113A1 (en) * 1995-04-12 1996-10-17 Decox, S.L. Novel composition stimulating the cerebral activity and based on alcaloids having an eburnamenine nucleus, and preparation methods

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0046506A1 (en) * 1980-08-25 1982-03-03 Heinrich Mack Nachf. Vincamine saccharinate and drug containing it
WO1996032113A1 (en) * 1995-04-12 1996-10-17 Decox, S.L. Novel composition stimulating the cerebral activity and based on alcaloids having an eburnamenine nucleus, and preparation methods
ES2097703A1 (en) * 1995-04-12 1997-04-01 Decox S A Composition for stimulating the cerebral activity comprising vinpocetine citrate and a plant extract comprising xanthines
EA000189B1 (en) * 1995-04-12 1998-12-24 Декокс, С.Л. Composition based on alcaloids having an eburnamenine nucleus for stimulation of cerebral activity
US6290994B1 (en) 1995-04-12 2001-09-18 Decox, S.L. Beverage containing caffeine or theobromine and vinpocetine citrate for stimulating cerebral activity

Also Published As

Publication number Publication date
FR2193587B1 (en) 1975-08-08

Similar Documents

Publication Publication Date Title
NL7607338A (en) PROCESS FOR THE PREPARATION OF 1,4-DIHYDROPYRINE DERIVATIVES WITH VASOLICULATING AND BLOOD PRESSURE-REDUCING ACTIVITY.
ZA738488B (en) Tetrahydro-1,3,5-triazine-2,6-diones,processes for their production and their use as herbicides
RO63259A (en) PROCESS FOR THE PREPARATION OF TETRAHYDROPYROLO- (1,2-A) PYRAZINE-1- (2H), 4 (3H) -DIONES
FR2193587A1 (en) Vincamine lauryl sulphate compsns - for humans and animals, as a cerebral and coronary vasodilator, without bitter taste
NL171175B (en) PROCESS FOR THE PREPARATION OF A CORROSION-RESISTANT, FERRITIC IRON-CHROME-MOLYBENE ALLOY.
FR2193586A1 (en) Vincamine dioctyl sulphosuccinate for medical use - for humans and animals as a cerebral and coronary vasodilator, with no bitter taste
FR2187312A1 (en) Rapidly-soluble paracetamol - prepd by recrystallization from aqueous dioxan
GB1402689A (en) Resolution of 6-substituted amino phenyl-2,3,5,6-tetrahydroimidazo 2,1-b- thiazoles
NL170738C (en) PROCESS FOR THE PREPARATION OF 2'-ACETYL DERIVATIVES OF HEART GLYCOSIDES
ZA718532B (en) A process for rearrangement or reduction of 1-derivatives of 1-hydroxybenzimidazoles and 1-hydroxyimidazo(4,5-b)pyriines
ZA704089B (en) Bicyclo 2.2.2-octane-1-acetic acid derivatives
USD223911S (en) Vitamin tablet or similar article
GB1237972A (en)
FR2170974A1 (en) Amino acid salts of caffeine - with psychotonic activity
NL182640C (en) PROCESS FOR THE PREPARATION OF BICYCLO (2.2.1) HEPT-2-AN-SYN-7-CARBOXALDEHYDE DERIVATIVES.
BEHLER BRASS--A DIE CASTING ALLOY OF THE 70@ S
ZA738890B (en) 2,3-lower alkylenepenam-3-carboxylic acid derivatives and processes for the preparation thereof
ZA711332B (en) Novel 1,2-methylene-17-acyloxy(or improved hydroxy)-9beta,10alpha-steroid compounds of the pregnane series,pharmaceutical preparations on the basis of the novel compounds and methods of producing said compounds and preparations
Hoyano The total synthesis of ajmaline
McCormack The influence of emotional cues on the subsequent aggression of prejudiced persons
CA841627A (en) Procede de preparation des nouveaux derives du diazabicyclo (4,4,0) decane
Biswanger Optimal process operation in the face of uncertainty
ZA726070B (en) New process for the preparation of s.triazolo(4,3-a)pyridine derivatives
IE38265B1 (en) 5-endo hydroxy-n-substituted bicyclo 2.2.1-heptane-2,3-di-endocarboxylic acid imides
GB1194912A (en) Pharmaceutical Compositions Suitable for Cicatrization Processes and for the Treatment of Physiological Disorders of the Skin

Legal Events

Date Code Title Description
ST Notification of lapse