ES2000842A6 - Un procedimiento para la preparacion de analogos semisinteticos de compactina y mevinolina - Google Patents
Un procedimiento para la preparacion de analogos semisinteticos de compactina y mevinolinaInfo
- Publication number
- ES2000842A6 ES2000842A6 ES8600874A ES8600874A ES2000842A6 ES 2000842 A6 ES2000842 A6 ES 2000842A6 ES 8600874 A ES8600874 A ES 8600874A ES 8600874 A ES8600874 A ES 8600874A ES 2000842 A6 ES2000842 A6 ES 2000842A6
- Authority
- ES
- Spain
- Prior art keywords
- hydrogen
- reductase inhibitors
- image
- coa reductase
- hmg
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H9/00—Compounds containing a hetero ring sharing at least two hetero atoms with a saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/16—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D309/28—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D309/30—Oxygen atoms, e.g. delta-lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
Abstract
SE DESCRIBE UN PROCEDIMIENTO PARA LA PREPARACION DE ANALOGOS SEMISINTETICOS DE COMPACTINA Y MEVINOLINA, QUE SON NUEVOS INHIBIDORES DE 3-HIDROXI-3-METILGLUTARILCOENZIMA A (HMG-GA) REDUCTASA, UTILES COMO AGENTES ANTIHIPERCOLESTEROLEMICOS Y ESTAN REPRESENTADOS POR LAS FORMULAS ESTRUCTURALES GENERALES (I) O (II) DESCRITAS EN LA MEMORIA DONDE: N ES 1 A 5; R ES HIDROGENO O (ALQUILO C1-5)C-; R1 ES HIDROGENO O METILO; R2 ES HIDROGENO O METILO; Y R3 ES HIDROGENO, ALQUILO C1-5 O ALQUILO C1-5 SUSTITUIDO CON UN MIEMBRO DEL GRUPO FORMADO POR FENILO, DIMETILAMINO O ACETILAMINO Y LAS LINEAS DE PUNTOS EN A, B Y C REPRESENTAN DOBLES ENLACES OPCIONALES Y LAS SALES FARMACEUTICAMENTE ACEPTABLES DE LOS COMPUESTOS (II) DONDE R3 ES HIDROGENO, MEDIANTE EL TRATAMIENTO DE UN COMPUESTO DE FORMULA (4), DESCRITO EN LA MEMORIA, CON UN HALURO DE TETRA(ALQUIL C1-5)AMONIO Y UN ACIDO ORGANICO, SEGUIDO DE POSTERIOR CONVERSION PARA OBTENER LOS PRODUCTOS FINALES DESEADOS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/762,736 US4668699A (en) | 1985-08-05 | 1985-08-05 | Novel HMG-CoA reductase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2000842A6 true ES2000842A6 (es) | 1988-03-16 |
Family
ID=25065902
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES8600874A Expired ES2000842A6 (es) | 1985-08-05 | 1986-08-05 | Un procedimiento para la preparacion de analogos semisinteticos de compactina y mevinolina |
Country Status (13)
Country | Link |
---|---|
US (2) | US4668699A (es) |
EP (1) | EP0211416B1 (es) |
JP (1) | JPS6233133A (es) |
KR (1) | KR870002158A (es) |
AU (1) | AU6084686A (es) |
CA (1) | CA1291143C (es) |
DE (1) | DE3681991D1 (es) |
DK (1) | DK370486A (es) |
ES (1) | ES2000842A6 (es) |
GR (1) | GR862006B (es) |
IL (1) | IL79530A0 (es) |
PT (1) | PT83077B (es) |
ZA (1) | ZA865779B (es) |
Families Citing this family (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3682557D1 (de) * | 1985-09-13 | 1992-01-02 | Sankyo Co | Hydroxy-ml-236b-derivate, deren herstellung und anwendung. |
US4916162A (en) * | 1986-05-05 | 1990-04-10 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
USRE36481E (en) * | 1986-06-23 | 2000-01-04 | Merck & Co., Inc. | HMG-CoA reductase inhibitors |
US4940727A (en) * | 1986-06-23 | 1990-07-10 | Merck & Co., Inc. | Novel HMG-CoA reductase inhibitors |
US5116870A (en) * | 1986-06-23 | 1992-05-26 | Merck & Co., Inc. | HMG-CoA reductase inhibitors |
US4789682A (en) * | 1987-03-17 | 1988-12-06 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
US4845237A (en) * | 1987-04-15 | 1989-07-04 | Merck & Co., Inc. | Acylation process for the synthesis of HMG-CoA reductase inhibitors |
PT88364A (pt) * | 1987-09-02 | 1989-07-31 | Merck & Co Inc | Process for preparing novel hmg-coa reductase inhibitors |
US4939143A (en) * | 1987-12-21 | 1990-07-03 | Rorer Pharmaceutical Corporation | Substituted cyclohexene derivatives as HMG-CoA reductase inhibitors |
US4900754A (en) * | 1987-12-21 | 1990-02-13 | Rorer Pharmaceutical Corp. | HMG-COA reductase inhibitors |
US4904692A (en) * | 1987-12-21 | 1990-02-27 | Rorer Pharmaceutical Corporation | Novel HMG-CoA reductase inhibitors |
US4994494A (en) * | 1987-12-21 | 1991-02-19 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | HMG-COA reductase inhibitors |
US5001128A (en) * | 1987-12-21 | 1991-03-19 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | HMG-COA reductase inhibitors |
US4892884A (en) * | 1987-12-21 | 1990-01-09 | Rorer Pharmaceutical Corporation | Novel hmg-coa reductase inhibitors |
US4904691A (en) * | 1987-12-21 | 1990-02-27 | Rorer Pharmaceutical Corporation | Novel HMG-CoA reductase inhibitors |
US5001144A (en) * | 1987-12-21 | 1991-03-19 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Substituted cyclohexene derivatives as HMG-CoA reductase inhibitors |
US4857546A (en) * | 1988-01-07 | 1989-08-15 | Merck & Co., Inc. | Novel HMG-CoA reductase inhibitors |
US4857547A (en) * | 1988-01-07 | 1989-08-15 | Merck & Co., Inc. | Novel HMG-CoA reductase inhibitors |
US4866068A (en) * | 1988-02-01 | 1989-09-12 | Merck & Co., Inc. | Novel HMG-CoA reductase inhibitors |
US5049696A (en) * | 1988-04-11 | 1991-09-17 | Merck & Co., Inc. | Antihypercholesterolemic compounds |
FI893004A (fi) * | 1988-06-29 | 1989-12-30 | Merck & Co Inc | 5-oxygenerade hmg-coa-reduktas -inhibitorer. |
US5075327A (en) * | 1988-08-10 | 1991-12-24 | Hoffmann-La Roche Inc. | Antipsoriatic agents |
US5073568A (en) * | 1988-11-14 | 1991-12-17 | Hoffmann-La Roche Inc. | Antipsoriatic agents |
US5021451A (en) * | 1988-11-14 | 1991-06-04 | Hoffman-La Roche Inc. | Method for inhibiting hyperproliferative diseases |
US5200549A (en) * | 1988-11-14 | 1993-04-06 | Hoffman-La Roche Inc. | Antipsoriatic agents |
US5130306A (en) * | 1989-03-13 | 1992-07-14 | Merck & Co., Inc. | 5-Oxygenated HMG-COA reductase inhibitors |
US5132312A (en) * | 1989-03-27 | 1992-07-21 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Substituted cyclohexene derivatives as HMG-CoA reductase inhibitors |
IL90847A0 (en) * | 1989-06-09 | 1990-02-09 | Merck & Co Inc | 3-keto hmg-coa reductase inhibitors and pharmaceutical compositions containing them |
GB8915280D0 (en) * | 1989-07-04 | 1989-08-23 | British Bio Technology | Compounds |
FI94339C (fi) | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
US4992429A (en) * | 1989-08-24 | 1991-02-12 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Novel HMG-COA reductase inhibitors |
EP0415188B1 (en) * | 1989-08-28 | 1996-03-20 | F. Hoffmann-La Roche Ag | Enzymatic method for determining analyte concentrations |
US4946860A (en) * | 1989-11-03 | 1990-08-07 | Rorer Pharmaceutical Corporation | Benzothiopyranyl derivatives as HMG-CoA reductase inhibitors |
US6630502B2 (en) | 1990-05-15 | 2003-10-07 | E.R. Squibb & Sons, Inc. | Method for preventing, stabilizing or causing regression of atherosclerosis employing a combination of a cholesterol lowering drug and an ace inhibitor |
GB9100174D0 (en) * | 1991-01-04 | 1991-02-20 | British Bio Technology | Compounds |
IL108432A (en) * | 1993-01-29 | 1997-09-30 | Sankyo Co | DERIVATIVES OF 3, 5-DIHYDROXY-7- £1, 2, 6, 7, 8, 8a-HEXAHYDRO-2- METHYL-8- (SUBSTITUTED ALKANOYLOXY)-1-NAPHTHYL| HEPTANOIC ACID AND THEIR LACTONES, THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
GB0003305D0 (en) | 2000-02-15 | 2000-04-05 | Zeneca Ltd | Pyrimidine derivatives |
JP2003012607A (ja) * | 2001-06-26 | 2003-01-15 | Mercian Corp | 新規なメバスタチン誘導体 |
AU2002366444A1 (en) * | 2001-11-08 | 2003-09-09 | Merck & Co., Inc. | Compounds useful in the treatment of anthrax |
JP4615309B2 (ja) | 2002-05-17 | 2011-01-19 | オセラ・ホールディング・インコーポレイテッド | 白内障および他の眼球疾患の進行の改善 |
US20040119052A1 (en) * | 2002-12-20 | 2004-06-24 | Beavers William Anthony | Process for preparing alpha- and beta- methyl-gamma-butyrolactone and 3-methyltetrahydrofuran |
US7825134B2 (en) * | 2003-05-19 | 2010-11-02 | Othera Holding, Inc. | Amelioration of cataracts, macular degeneration and other ophthalmic diseases |
WO2007020079A2 (en) * | 2005-08-17 | 2007-02-22 | Synthon B.V. | Orally disintegratable simvastatin tablets |
WO2012100835A1 (en) | 2011-01-28 | 2012-08-02 | Laboratorios Del Dr. Esteve, S.A. | Methods and compositions for the treatment of aids |
EA026148B1 (ru) * | 2012-06-05 | 2017-03-31 | ДСМ АйПи АССЕТС Б.В. | Способ получения 4-алканоилокси-2-метилбутановой кислоты |
EP3638044B1 (en) * | 2017-06-15 | 2024-03-13 | DSM IP Assets B.V. | Frozen enzyme pellets |
CN111225672B (zh) | 2017-10-16 | 2023-09-29 | 清华大学 | 甲羟戊酸通路抑制剂及其药物组合物 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2748825C2 (de) * | 1976-11-02 | 1986-11-27 | Sankyo Co., Ltd., Tokio/Tokyo | Substituierte 3,5-Dihydroxyheptansäurederivate und diese enthaltende Arzneimittel gegen Hyperlipämie |
AU548996B2 (en) * | 1980-02-04 | 1986-01-09 | Merck & Co., Inc. | Tetrahydro-2h-pyran-2-one derivatives |
MX7065E (es) * | 1980-06-06 | 1987-04-10 | Sankyo Co | Un procedimiento microbiologico para preparar derivados de ml-236b |
US4376863A (en) * | 1981-08-21 | 1983-03-15 | Merck & Co., Inc. | Hypocholesterolemic fermentation products |
JPS5835144A (ja) * | 1981-08-27 | 1983-03-01 | Sankyo Co Ltd | Mb−530b誘導体およびその製造法 |
EP0094443A1 (en) * | 1982-05-17 | 1983-11-23 | Merck & Co. Inc. | 6(R)-(2-(8(S) (2,2-dimethylbutyryloxy)-2(S),6(S)-dimethyl-1,2,3,4,4a(S),5,6,7,8,8a(S)-decahydronaphthyl-1(S))ethyl)-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one, process for preparing and pharmaceutical composition containing the same |
JPS59122483A (ja) * | 1982-12-28 | 1984-07-14 | Nippon Chemiphar Co Ltd | 新規なモナコリン誘導体 |
DE3480923D1 (de) * | 1983-10-11 | 1990-02-08 | Merck & Co Inc | Verfahren zur c-methylierung von 2-methylbutyraten. |
JPH09122483A (ja) * | 1995-10-31 | 1997-05-13 | Matsushita Electric Ind Co Ltd | 窒素酸化物・硫黄酸化物吸収剤 |
-
1985
- 1985-08-05 US US06/762,736 patent/US4668699A/en not_active Expired - Fee Related
-
1986
- 1986-07-28 IL IL79530A patent/IL79530A0/xx unknown
- 1986-07-28 PT PT83077A patent/PT83077B/pt unknown
- 1986-07-29 GR GR862006A patent/GR862006B/el unknown
- 1986-07-31 CA CA000515138A patent/CA1291143C/en not_active Expired - Fee Related
- 1986-08-01 DE DE8686110655T patent/DE3681991D1/de not_active Expired - Fee Related
- 1986-08-01 EP EP86110655A patent/EP0211416B1/en not_active Expired - Lifetime
- 1986-08-01 ZA ZA865779A patent/ZA865779B/xx unknown
- 1986-08-04 KR KR1019860006430A patent/KR870002158A/ko not_active Application Discontinuation
- 1986-08-04 DK DK370486A patent/DK370486A/da not_active Application Discontinuation
- 1986-08-04 AU AU60846/86A patent/AU6084686A/en not_active Abandoned
- 1986-08-05 JP JP61182847A patent/JPS6233133A/ja active Pending
- 1986-08-05 ES ES8600874A patent/ES2000842A6/es not_active Expired
-
1987
- 1987-03-11 US US07/024,439 patent/US4851436A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
IL79530A0 (en) | 1986-11-30 |
ZA865779B (en) | 1987-03-25 |
EP0211416A3 (en) | 1987-09-23 |
PT83077B (en) | 1988-07-13 |
US4851436A (en) | 1989-07-25 |
JPS6233133A (ja) | 1987-02-13 |
EP0211416B1 (en) | 1991-10-16 |
CA1291143C (en) | 1991-10-22 |
GR862006B (en) | 1986-12-23 |
EP0211416A2 (en) | 1987-02-25 |
DE3681991D1 (de) | 1991-11-21 |
DK370486D0 (da) | 1986-08-04 |
AU6084686A (en) | 1987-02-12 |
KR870002158A (ko) | 1987-03-30 |
PT83077A (en) | 1986-08-01 |
US4668699A (en) | 1987-05-26 |
DK370486A (da) | 1987-02-06 |
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