DK142364B - Analogifremgangsmåde til fremstilling af vincamin-pyridoxal-5-phosphat. - Google Patents
Analogifremgangsmåde til fremstilling af vincamin-pyridoxal-5-phosphat. Download PDFInfo
- Publication number
- DK142364B DK142364B DK204877AA DK204877A DK142364B DK 142364 B DK142364 B DK 142364B DK 204877A A DK204877A A DK 204877AA DK 204877 A DK204877 A DK 204877A DK 142364 B DK142364 B DK 142364B
- Authority
- DK
- Denmark
- Prior art keywords
- vincamine
- pyridoxal
- phosphate
- analogous process
- preparing
- Prior art date
Links
- RXPRRQLKFXBCSJ-GIVPXCGWSA-N vincamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@](O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-GIVPXCGWSA-N 0.000 title description 39
- RXPRRQLKFXBCSJ-UHFFFAOYSA-N dl-Vincamin Natural products C1=CC=C2C(CCN3CCC4)=C5C3C4(CC)CC(O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-UHFFFAOYSA-N 0.000 title description 19
- 229960002726 vincamine Drugs 0.000 title description 19
- 235000007682 pyridoxal 5'-phosphate Nutrition 0.000 title description 6
- 239000011589 pyridoxal 5'-phosphate Substances 0.000 title description 6
- NGVDGCNFYWLIFO-UHFFFAOYSA-N pyridoxal 5'-phosphate Chemical compound CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O NGVDGCNFYWLIFO-UHFFFAOYSA-N 0.000 title description 6
- 229960001327 pyridoxal phosphate Drugs 0.000 title description 6
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000282472 Canis lupus familiaris Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000283973 Oryctolagus cuniculus Species 0.000 description 2
- RADKZDMFGJYCBB-UHFFFAOYSA-N Pyridoxal Chemical compound CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 description 2
- 238000007912 intraperitoneal administration Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 201000006474 Brain Ischemia Diseases 0.000 description 1
- 206010048962 Brain oedema Diseases 0.000 description 1
- 206010008120 Cerebral ischaemia Diseases 0.000 description 1
- 206010052895 Coronary artery insufficiency Diseases 0.000 description 1
- 208000020401 Depressive disease Diseases 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- CEEQUQSGVRRXQI-UHFFFAOYSA-N Pyridoxal 5-phosphate monohydrate Chemical compound O.CC1=NC=C(COP(O)(O)=O)C(C=O)=C1O CEEQUQSGVRRXQI-UHFFFAOYSA-N 0.000 description 1
- 102000002852 Vasopressins Human genes 0.000 description 1
- 108010004977 Vasopressins Proteins 0.000 description 1
- LUTSRLYCMSCGCS-BWOMAWGNSA-N [(3s,8r,9s,10r,13s)-10,13-dimethyl-17-oxo-1,2,3,4,7,8,9,11,12,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate Chemical compound C([C@@H]12)C[C@]3(C)C(=O)CC=C3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)C)C1 LUTSRLYCMSCGCS-BWOMAWGNSA-N 0.000 description 1
- 208000007502 anemia Diseases 0.000 description 1
- 230000001430 anti-depressive effect Effects 0.000 description 1
- KBZOIRJILGZLEJ-LGYYRGKSSA-N argipressin Chemical compound C([C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CSSC[C@@H](C(N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N1)=O)N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(N)=O)C1=CC=CC=C1 KBZOIRJILGZLEJ-LGYYRGKSSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 208000006752 brain edema Diseases 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 206010008118 cerebral infarction Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000000004 hemodynamic effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 208000030159 metabolic disease Diseases 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229940072644 pitressin Drugs 0.000 description 1
- 229960003581 pyridoxal Drugs 0.000 description 1
- 235000008164 pyridoxal Nutrition 0.000 description 1
- 239000011674 pyridoxal Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
(li) FREMLÆG 6 EIS ESSKRIFT 1 42354 DANMARK «Ήη..α> c 07 D 461/00 §(21) Ansøgning nr. 2048/77 (22) Indleveret den 10· maj 1977 (24) Lebedag 10. maj 1977 (44) Ansøgningen fremlagt og .
fremlæggelsesskriftet offentliggjort den 20. Okt. 1980
DIREKTORATET FOR
PATENT-OG VAREMÆRKEVÆSENET (30) Prioritet begæret fra den 11. maj 1976, 19290/76, gb (71) SOCIETE D'ETUDES DE PRODUITS CHIMIQUES SOCIETE ANONYME, 4, rue Theo= dule Ribot, 75017 Paris, PR.
(72) Opfinder: Andre ESanu, 119> rue de la Croix-Nivert, 75015 Paris, PR.
(74) Fuldmægtig under sagens behandling:
Ingeniørfirmaet Hofman-Bang & Boutard.
(54) Analogifremgangsmåde til fremstilling af vincamin-pyridoxal-5-phosphat.
Den foreliggende opfindelse angår en analogifremgangsmåde til fremstilling af et hidtil ukendt terapeutisk virksomt vincaminsalt, nærmere bestemt vincamin-pyridoxal-5-phosphat med den i kravets indledning anførte formel.
Dette salt er et gult pulver, der er temmelig opløseligt i vand under dannelse af en farveløs opløsning. Forbindelsen er tungt opløselig i ethanol, uopløselig i chloroform, og opløselig i dimethylsul-phoxid ved stuetemperatur. Det har en molekylvægt på 601,58 og et vincaminindhold på 58,92 vægtprocent.
U2364 2
Det omhandlede salt er interessant derved, at det generelt har en bedre opløselighed end vincamin og ligeledes har en stærkere terapeutisk virkning. Forsøg har således vist, at det er 4 - 10 gange aktivere end vincamin. Endvidere udviser den omhandlede forbindelse visse antidepressive virkninger, der er særligt interessante for patienter, der modtager vincaminbehandling samtidigt med at de lider af depressive syndromer.
Fremgangsmåden ifølge opfindelsen er ejendommelig ved, at man omsætter vincamin med pyridoxal-5-phosphat, og omsætningen sker fortrinsvis ved 105° C under anvendelse af støkiometriske mængder af en suspension af vincamin i en blanding af lige dele vand og lavere al-kanol og pyridoxal-5-phosphat. Den således opnåede opløsning kan lyofiliseres til dannelse af det omhandlede salt i højt udbytte.
Fremgangsmåden ifølge opfindelsen illustreres nærmere ved nedenstående eksempel.
EKSEMPEL
1 en reaktor forsynet med omrører og opvarmningsorganer anbragtes 2 liter af en 50 volumenpct. opløsning af methanol i vand og 141,75 g (0,4 mol) vincamin. Blandingen omrørtes og opvarmedes til 40° C tander dannelse af en suspension, hvortil der sattes 106,5 g (0,4 mol) pyridoxal-5-phosphat, monohydrat. Blandingen opvarmedes til 105° C under omrøring under dannelse af en klar opløsning, hvorfra metha-nolen extraheredes ved 35° C under reduceret tryk. Efter filtrering af den tilbageværende opløsning for at fjerne nogle urenheder lyo-filiseredes opløsningen tander dannelse af 233 g af et gult pulver med smp: ca. 150° C (pastaagtig smeltning). Udbytte: 93 %. Elementæranalyse viste en god overensstemmelse med formlen C29H36N3°9P·
Toxicitet
O
Toxiciteten af den omhandlede forbindelse er bestemt på mus. LD^q var 1,4 g/kg ved oral indgivelse, og 0,380 g/kg ved intraperitoneal indgivelse. I sammenligning med vincamin er den omhandlede forbind- 142364 3 else en smule mere toxisk ved oral indgivelse, men væsentligt mindre toxisk ved intraperitoneal indgivelse.
Pharmakologl
Den omhandlede forbindelse er underkastet forskellige pharmakolo-giske undersøgelser.
A Indvirkning på per-hypocapno-anæmisk cerebralt syndrom hos hunde.
Ved denne prøve observeredes det, at man kunne opnå de samme resultater ved venøs perfusion af 0,42 mg/kg af den omhandlede forbindelse (teoretisk svarende til 0,25 mg/kg vincamin) som ved tilsvarende indgivelse af 1 mg/kg vincamin. Dette indicerer således, at vincamin-pyridoxal-5-phosphat er fire gange mere aktivt end den ækvivalente mængde fri vincamin.
B Virkning på funktionel coronarinsufficiens fremkaldt af pitressin _(hunde)._
Ved denne prøve udviste det omhandlede salt en meget favorabel virkning ved korrektion af hæmodynamiske og metaboliske forstyrrelser i doser på 1 mg/kg, mens frit vincamin ikke udviste nogen virkning på de nævnte indikationer i samme dosis.
C Virkning på forstyrrelser af elektrogenese fremkaldt ved cerebral ischemia (kaniner).
Ved denne prøve havde den omhandlede forbindelse en særdeles god virkning i doser på 50 - 100/ug/kg. Med frit vincamin opnåedes nogen virkning med 1000y.ug/kg intravenøst. Denne prøve indicerede således, at vincamin-pyridoxal-5-phosphat er mindst ti gange mere aktivt end frit vincamin.
D Virkning på EEG-forstyrrelser fremkaldt af unilateral cerebralt ødem (kaniner)._
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB19290/76A GB1525885A (en) | 1976-05-11 | 1976-05-11 | Vincamine salt of pyridoxal phosphate |
| GB1929076 | 1976-05-11 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DK204877A DK204877A (da) | 1977-11-12 |
| DK142364B true DK142364B (da) | 1980-10-20 |
| DK142364C DK142364C (da) | 1981-03-02 |
Family
ID=10126939
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK204877AA DK142364B (da) | 1976-05-11 | 1977-05-10 | Analogifremgangsmåde til fremstilling af vincamin-pyridoxal-5-phosphat. |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4137316A (da) |
| JP (1) | JPS5312413A (da) |
| AR (1) | AR210802A1 (da) |
| AT (1) | AT352913B (da) |
| AU (1) | AU504254B2 (da) |
| BE (1) | BE854437A (da) |
| CA (1) | CA1064496A (da) |
| CH (1) | CH602629A5 (da) |
| DE (1) | DE2721171C3 (da) |
| DK (1) | DK142364B (da) |
| EG (1) | EG12663A (da) |
| ES (1) | ES458643A1 (da) |
| FR (2) | FR2351117A1 (da) |
| GB (1) | GB1525885A (da) |
| HK (1) | HK58979A (da) |
| IN (1) | IN145671B (da) |
| MY (1) | MY8000068A (da) |
| NL (1) | NL170096C (da) |
| NZ (1) | NZ183912A (da) |
| OA (1) | OA06089A (da) |
| PT (1) | PT66495B (da) |
| ZA (1) | ZA772489B (da) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56117080A (en) * | 1980-02-16 | 1981-09-14 | Kobe Steel Ltd | Method of measuring location of surface layer of charge in vertical eurnace |
| DE3113132A1 (de) * | 1981-04-01 | 1982-10-21 | Heinrich Mack Nachf., 7918 Illertissen | Vincamin-cyclamat, verfahren zu seiner herstellung und dieses enthaltende arzneimittel |
| US4931002A (en) * | 1987-05-29 | 1990-06-05 | The University Of Vermont | Pyridoxal-5'-phosphate as an in vitro anticoagulant for whole blood |
| JPH0624581U (ja) * | 1992-07-13 | 1994-04-05 | 山水工業有限会社 | 衣服掛け |
| US6043259A (en) * | 1998-07-09 | 2000-03-28 | Medicure Inc. | Treatment of cardiovascular and related pathologies |
| CA2366602A1 (en) | 1999-03-08 | 2000-09-14 | Medicure Inc. | Pyridoxal analogues for vitamin b-6 disorders |
| CA2376029A1 (en) | 1999-07-13 | 2001-01-18 | Medicure Inc. | Use of pyridoxin derivatives for the treatment of diabetes and related complications |
| US6677356B1 (en) * | 1999-08-24 | 2004-01-13 | Medicure International Inc. | Treatment of cardiovascular and related pathologies |
| US7442689B2 (en) * | 2000-02-29 | 2008-10-28 | Medicure International Inc. | Cardioprotective phosphonates and malonates |
| WO2001064692A1 (en) | 2000-02-29 | 2001-09-07 | Medicure International Inc. | Cardioprotective phosphonates and malonates |
| CA2404329A1 (en) | 2000-03-28 | 2001-10-04 | Medicure International Inc. | Treatment of cerebrovascular disease |
| NZ523815A (en) | 2000-07-07 | 2004-07-30 | Medicure Int Inc | Pyridoxine and pyridoxal analogues: cardiovascular therapeutics |
| US6548519B1 (en) | 2001-07-06 | 2003-04-15 | Medicure International Inc. | Pyridoxine and pyridoxal analogues: novel uses |
| US6897228B2 (en) * | 2000-07-07 | 2005-05-24 | Medicure International Inc. | Pyridoxine and pyridoxal analogues: new uses |
| US20040121988A1 (en) * | 2001-03-28 | 2004-06-24 | Medicure International Inc. | Treatment of cerebrovascular disease |
| US20040186077A1 (en) * | 2003-03-17 | 2004-09-23 | Medicure International Inc. | Novel heteroaryl phosphonates as cardioprotective agents |
| JP2008505126A (ja) * | 2004-07-07 | 2008-02-21 | メディキュア インターナショナル インコーポレイテッド | 血小板凝集薬を用いる併用療法 |
| US20070060549A1 (en) * | 2004-08-10 | 2007-03-15 | Friesen Albert D | Combination therapies employing ace inhibitors and uses thereof for the treatment of diabetic disorders |
| US7459468B2 (en) * | 2004-10-28 | 2008-12-02 | Medicure International, Inc. | Aryl sulfonic pyridoxines as antiplatelet agents |
| US20060094749A1 (en) * | 2004-10-28 | 2006-05-04 | Medicure International Inc. | Substituted pyridoxines as anti-platelet agents |
| EP1817288A4 (en) * | 2004-10-28 | 2009-08-26 | Medicure Int Inc | DUAL ANTIPLÄTTCHEN / ANTIKOAGULANS PYRIDOXINANALOGE |
| JP2009517411A (ja) * | 2005-11-28 | 2009-04-30 | メディキュア インターナショナル インコーポレーテッド | 心血管及び関連病状の処置のための調剤 |
| CA2590605A1 (en) * | 2007-05-28 | 2008-11-28 | Medicure International Inc. | Improvement of mood, memory and cognitive function with pyridoxal 5'-phosphate |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2828315A (en) * | 1957-01-16 | 1958-03-25 | Merck & Co Inc | Procaine salt of pyridoxal phosphate and process |
| FR2176516B1 (da) * | 1972-03-22 | 1975-03-14 | Synthelabo | |
| FR2191891B1 (da) * | 1972-07-13 | 1975-08-08 | Roussel Uclaf | |
| CH585226A5 (en) * | 1974-03-08 | 1977-02-28 | Vifor Sa | Slightly soluble vincamine pamoates - with long duration of action as cerebral vasodilators |
| FR2275211A2 (fr) * | 1974-06-19 | 1976-01-16 | Synthelabo | Nouveaux amides de l'acide dihydroapovincaminique, leurs sels, leur preparation et les medicaments qui en contiennent |
| FR2283669A1 (fr) * | 1974-09-06 | 1976-04-02 | Elmu Sa | 2-cetoglutarate de vincamine et son procede de preparation |
-
1976
- 1976-05-11 GB GB19290/76A patent/GB1525885A/en not_active Expired
-
1977
- 1977-04-25 ZA ZA00772489A patent/ZA772489B/xx unknown
- 1977-04-27 IN IN628/CAL/77A patent/IN145671B/en unknown
- 1977-04-29 PT PT66495A patent/PT66495B/pt unknown
- 1977-05-03 CH CH549177A patent/CH602629A5/xx not_active IP Right Cessation
- 1977-05-05 NZ NZ183912A patent/NZ183912A/xx unknown
- 1977-05-05 AU AU24894/77A patent/AU504254B2/en not_active Expired
- 1977-05-05 AT AT320277A patent/AT352913B/de not_active IP Right Cessation
- 1977-05-06 CA CA277,920A patent/CA1064496A/en not_active Expired
- 1977-05-09 OA OA56163A patent/OA06089A/xx unknown
- 1977-05-09 US US05/794,938 patent/US4137316A/en not_active Expired - Lifetime
- 1977-05-09 EG EG277/77A patent/EG12663A/xx active
- 1977-05-09 BE BE177422A patent/BE854437A/xx unknown
- 1977-05-10 JP JP5270177A patent/JPS5312413A/ja active Granted
- 1977-05-10 NL NLAANVRAGE7705129,A patent/NL170096C/xx not_active IP Right Cessation
- 1977-05-10 ES ES458643A patent/ES458643A1/es not_active Expired
- 1977-05-10 DK DK204877AA patent/DK142364B/da not_active IP Right Cessation
- 1977-05-11 AR AR267580A patent/AR210802A1/es active
- 1977-05-11 FR FR7714334A patent/FR2351117A1/fr active Granted
- 1977-05-11 DE DE2721171A patent/DE2721171C3/de not_active Expired
- 1977-05-11 FR FR7714333A patent/FR2350842A1/fr active Granted
-
1979
- 1979-08-23 HK HK589/79A patent/HK58979A/xx unknown
-
1980
- 1980-12-31 MY MY198068A patent/MY8000068A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL170096B (nl) | 1982-05-03 |
| NZ183912A (en) | 1978-09-25 |
| CA1064496A (en) | 1979-10-16 |
| AR210802A1 (es) | 1977-09-15 |
| AT352913B (de) | 1979-10-10 |
| FR2350842B1 (da) | 1980-05-09 |
| OA06089A (fr) | 1981-06-30 |
| NL7705129A (nl) | 1977-11-15 |
| DK142364C (da) | 1981-03-02 |
| CH602629A5 (da) | 1978-07-31 |
| DK204877A (da) | 1977-11-12 |
| FR2351117A1 (fr) | 1977-12-09 |
| MY8000068A (en) | 1980-12-31 |
| GB1525885A (en) | 1978-09-20 |
| PT66495A (en) | 1977-05-01 |
| ES458643A1 (es) | 1978-03-16 |
| EG12663A (en) | 1979-12-31 |
| US4137316A (en) | 1979-01-30 |
| FR2350842A1 (fr) | 1977-12-09 |
| AU504254B2 (en) | 1979-10-04 |
| JPS5312413A (en) | 1978-02-03 |
| AU2489477A (en) | 1978-11-09 |
| FR2351117B1 (da) | 1980-06-27 |
| ATA320277A (de) | 1979-03-15 |
| JPS5618598B2 (da) | 1981-04-30 |
| IN145671B (da) | 1985-01-05 |
| DE2721171C3 (de) | 1980-07-10 |
| DE2721171B2 (de) | 1979-10-31 |
| ZA772489B (en) | 1978-05-30 |
| HK58979A (en) | 1979-08-31 |
| BE854437A (fr) | 1977-09-01 |
| DE2721171A1 (de) | 1977-11-24 |
| PT66495B (en) | 1978-09-29 |
| NL170096C (nl) | 1982-10-01 |
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