DE2507974C3 - Copper orotate - Google Patents

Copper orotate

Info

Publication number
DE2507974C3
DE2507974C3 DE19752507974 DE2507974A DE2507974C3 DE 2507974 C3 DE2507974 C3 DE 2507974C3 DE 19752507974 DE19752507974 DE 19752507974 DE 2507974 A DE2507974 A DE 2507974A DE 2507974 C3 DE2507974 C3 DE 2507974C3
Authority
DE
Germany
Prior art keywords
copper
orotate
copper orotate
salt
cell systems
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.)
Expired
Application number
DE19752507974
Other languages
German (de)
Other versions
DE2507974B2 (en
DE2507974A1 (en
Inventor
Hans A Dr.med 3000 Hannover Nieper
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.)
Nadrol Chemie Pharma Keizer Kg 4500 Osnabrueck
Original Assignee
Nadrol Chemie Pharma Keizer Kg 4500 Osnabrueck
Filing date
Publication date
Application filed by Nadrol Chemie Pharma Keizer Kg 4500 Osnabrueck filed Critical Nadrol Chemie Pharma Keizer Kg 4500 Osnabrueck
Priority to DE19752507974 priority Critical patent/DE2507974C3/en
Publication of DE2507974A1 publication Critical patent/DE2507974A1/en
Publication of DE2507974B2 publication Critical patent/DE2507974B2/en
Application granted granted Critical
Publication of DE2507974C3 publication Critical patent/DE2507974C3/en
Expired legal-status Critical Current

Links

Description

2. Pharmazeutische Zubereitung für die Kupfer-Therapie in oraler oder rektaler Verabreichung, gekennzeichnet durch einen Gehalt an Kupfer-orotat neben üblichen Hilfs- und Trägerstoffen.2. Pharmaceutical preparation for copper therapy in oral or rectal administration, characterized by a content of copper orotate in addition to the usual auxiliaries and carriers.

Die Erfindung betrifft das Kupfersalz der Orotsäure der StrukturformelThe invention relates to the copper salt of orotic acid of the structural formula

H
ι
H
ι
O
Y
O
Y
O
Ύ
O
Ύ
H
I
H
I.
I
N
I.
N
I
NH
I.
NH
NHNH II.
NN

COO — Cu — OOCCOO - Cu - OOC

und der Bruttoformel Cu(C5H3N204)2. Die erfindungsgemäße Verbindung eignet sich insbesondere zur therapeutischen Verwendung bei der Kupfer-Therapie in oraler oder rektaler Verabreichung.and the gross formula Cu (C 5 H 3 N204) 2. The compound according to the invention is particularly suitable for therapeutic use in copper therapy in oral or rectal administration.

Es wurde gefunden, daß sich Kupfer-orotat in besonders wirksamer Weise für die Behandlung von menschlichen Erkrankungen eignet, die mit einer krankheitstypischen Mobilisierung von Kupfer aus Zellsystemen einhergehen, insbesondere die Behandlung des chronischen Rheumatismus.It has been found that copper orotate is particularly effective for the treatment of human diseases that are characterized by a mobilization of copper that is typical of the disease Cell systems, especially the treatment of chronic rheumatism.

Es ist an sich seit langem bekannt, daß Kupfer-Verbindungen eine interessante Wirkung gegen Rheuma-Erkrankungen entfalten können, z. B. das S-Kupfersalz des N-Allyl-N'-(3-carboxyphenyI)-isothioharnstoffs und Kupfer-Caseinhydrolysat-Komplexe. Diese bekannten Präparate mußten jedoch im Laufe der Zeit aufgegeben werden, weil ihre Giftigkeit, z. B. auf die Nieren, groß war. It has long been known that copper compounds can have an interesting effect against rheumatic diseases, e.g. B. the S-copper salt of N-allyl-N '- (3-carboxyphenyI) -isothiourea and copper-casein hydrolyzate complexes. However, these known preparations had to be abandoned over time because their toxicity, e.g. B. on the kidneys, was great .

Untersuchungen mit dem Ziel einer gerichteten bzw. gezielten Kupfer-Aufladung von entzündlich veränderten Zellsystemen führten nun zum erfindungsgemäßen Kupfer-orotatInvestigations with the aim of a directed or targeted copper charge of inflammatory changes Cell systems now led to the copper orotate according to the invention

Bei am Menschen (16 Patienten) durchgeführten Versuchen mit primär chronischem Gelenkrheumatismus (PcP) ergab sich, daß Kupfer-orotat, im Vergleich zum eingangs erwähnten Kupfer-Isothioharnstoff-Salz 600- bis 800mal stärker wirksam istIn tests carried out on humans (16 patients) with primarily chronic rheumatoid arthritis (PcP) it was found that copper orotate, in comparison to the copper isothiourea salt mentioned at the beginning Is 600 to 800 times more effective

Außerdem wurde bei weiteren Tierversuchen an Impftumoren der Ratte und Spontantumoren der Maus festgestellt, daß Kupfer-orotat stark regressiv wirkt.In addition, in further animal experiments on vaccinated tumors in rats and spontaneous tumors in mice found that copper orotate has a strong regressive effect.

Aufgrund dieser Erkenntnisse stellt sich Kupfer-orotat als ein hochwirksamer, allen bisher bekannten Kupfer-Verbindungen weit überlegener Stoff von antirheumatischer, entzündungshemmender Wirkung dar, der bei hauptsächlich oraler Verabreichung für die Behandlung von menschlichen Erkrankungen, die mit einer krankheitstypischen Mobilisierung von Kupfer aus Zellsystemen einhergehen, insbesondere dem chronischen Rheumatismus, besonders geeignet erscheint.Based on these findings, copper orotate turns out to be a highly effective one known to all Copper compounds far superior substance of anti-rheumatic, anti-inflammatory effects when administered primarily orally for the treatment of human diseases associated with mobilization of copper from cell systems typical of the disease, especially the chronic one Rheumatism, seems particularly suitable.

Kupfer-orotat (bzw. di-orotat) kann synthetisch in der Weise gewonnen werden, daß man bei normaler oder etwas erhöhter Temperatur ein lösliches Kupfersalz in stöchiometrischer Menge in einer wäßrigen Lösung mit Orotsäure umsetzt Das Kupfersalz, z. B. CuCl2 oder Cu(CHsCOO)2, wird unter Rühren langsam eingegeben, wobei Kupfer-orotat ausfällt und abfiltriert wird. Die Kristalle werden mit heißem Wasser gewaschen und dann getrocknet Es entstehen eine türkisfarbene, feinkristalline Substanz, die in den üblichen Lösungsmitteln schwer löslich ist, d. h. ihre Lösungsfähigkeit liegt unter 0,25%; der Schmelzpunkt liegt über 3500C. Die Gehaltsbestimmung im Wege der komplexometrischen Kupfertitration (Fehlergrenze ± 1%) ergibt ber. 1532% Cu.Copper orotate (or di-orotate) can be obtained synthetically in such a way that a soluble copper salt is reacted in a stoichiometric amount in an aqueous solution with orotic acid at normal or slightly elevated temperature. B. CuCl 2 or Cu (CHsCOO) 2 is slowly added with stirring, whereupon copper orotate precipitates and is filtered off. The crystals are washed with hot water and then dried. The result is a turquoise, finely crystalline substance which is sparingly soluble in the usual solvents, ie its solubility is below 0.25%; the melting point is above 350 ° C. The determination of the content by means of complexometric copper titration (error limit ± 1%) results in 1532% Cu.

Claims (1)

Patentansprüche: 1. Kupfer-orotat der FormelClaims: 1. Copper orotate of the formula H HH H I II I ONOONONOON COO — Cu — OOCCOO - Cu - OOC
DE19752507974 1975-02-25 Copper orotate Expired DE2507974C3 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE19752507974 DE2507974C3 (en) 1975-02-25 Copper orotate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19752507974 DE2507974C3 (en) 1975-02-25 Copper orotate

Publications (3)

Publication Number Publication Date
DE2507974A1 DE2507974A1 (en) 1976-09-02
DE2507974B2 DE2507974B2 (en) 1977-04-14
DE2507974C3 true DE2507974C3 (en) 1977-12-01

Family

ID=

Similar Documents

Publication Publication Date Title
DE2507974C3 (en) Copper orotate
DE2507974B2 (en) COPPER OROTATE
DE1518377B1 (en) Aluminum tri- [N- (3-trifluoromethylphenyl) anthranilate] and process for its preparation
DE1229543B (en) Process for the preparation of 1, 3-dithia-2-arsacyclopentane-4, 5-dicarboxylic acids
DE2052819C3 (en) Cytosininosinate, process for its preparation and medicinal products containing it
DE2901914C2 (en) Zinc salt of 6-N-acetylamino-caproic acid, process for its preparation and pharmaceuticals containing this compound
DE2428039C3 (en) Medicines with choleretic effects, containing 2,6-dihydroxycineol
DE1793769C2 (en) Process for the preparation of bis (thiosemicarbazones). Eliminated from: 151205
DE488610C (en) Process for the preparation of N-haloalkenyl derivatives of norcodeine
DE2622977C2 (en) p-Chlorophenoxyisobutyryl-glycine amide, a process for its preparation and a lipid metabolism-promoting agent containing this compound
DE2235400C3 (en) ^ Chlor-S-sulfamoyl-anthranilic acids, their salts, processes for the preparation of these compounds and medicaments containing these compounds
DE862341C (en) Process for the preparation of aqueous solutions of derivatives of p-aminobenzene sulfonamide
CH649536A5 (en) WATER-SOLUBLE DERIVATIVES FROM 6,6'-METHYLENE-BIS (2,2,4-TRIMETHYL-1,2-DIHYDROQUINOLINE) AND METHOD FOR THE PRODUCTION THEREOF.
AT103978B (en) Process for the preparation of new arsenic compounds from china bases
DE2901629A1 (en) 4-PYRIMIDYL SULFIDES, METHOD FOR MANUFACTURING IT, MEDICINAL PRODUCTS AND USES
DE255030C (en)
DE2521905A1 (en) FUMARIC SALT OF 1-DIAETHYLAMINO-AETHYL-3-(P-METHOXYBENZYL)-1,2-DIHYDRO-QUINOXALIN-2-ONE, PROCESS FOR ITS PREPARATION AND PHARMACEUTICALS CONTAINING THIS COMPOUND
AT217022B (en) Process for the production of the new cysteamine orotate
DE1808173B2 (en) CALCIUM OROTATE
AT205670B (en)
DE604070C (en) Process for the production of neutral soluble complex salts of trivalent antimony
DE1518377C (en) Aluminum square bracket on N- (3-trifluoromethylphenyl) -anthtanilate square bracket and process for its preparation
AT77319B (en) Process for the preparation of water-soluble compounds of cystine and its derivatives with disinfectants for combating typhoid and other infectious diseases which have their origin in the liver.
DE2235400A1 (en) 4-CHLORO-5-SULPHAMOYL-ANTHRANILIC ACID DERIVATIVES
DE2007451A1 (en) Anesthetic drugs for fish