CH416600A - Verfahren zur Herstellung von Farnesylessigsäureestern - Google Patents
Verfahren zur Herstellung von FarnesylessigsäureesternInfo
- Publication number
- CH416600A CH416600A CH301066A CH301066A CH416600A CH 416600 A CH416600 A CH 416600A CH 301066 A CH301066 A CH 301066A CH 301066 A CH301066 A CH 301066A CH 416600 A CH416600 A CH 416600A
- Authority
- CH
- Switzerland
- Prior art keywords
- farnesyl
- formula
- preparation
- acetic acid
- acid esters
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 5
- VOKDWPMRYSKGTB-NCZFFCEISA-N (4e,8e)-5,9,13-trimethyltetradeca-4,8,12-trienoic acid Chemical class CC(C)=CCC\C(C)=C\CC\C(C)=C\CCC(O)=O VOKDWPMRYSKGTB-NCZFFCEISA-N 0.000 title claims description 3
- -1 n -Butyl Chemical group 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 3
- 125000004030 farnesyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000000490 cinnamyl group Chemical group C(C=CC1=CC=CC=C1)* 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000002350 geranyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 230000007062 hydrolysis Effects 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000001189 phytyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])([H])[C@@](C([H])([H])[H])([H])C([H])([H])C([H])([H])C([H])([H])[C@@](C([H])([H])[H])([H])C([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 15
- 230000000694 effects Effects 0.000 description 8
- 208000025865 Ulcer Diseases 0.000 description 7
- 231100000397 ulcer Toxicity 0.000 description 7
- 241000700159 Rattus Species 0.000 description 5
- 229940007703 farnesyl acetate Drugs 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- ZGIGZINMAOQWLX-UHFFFAOYSA-N Farnesyl acetate Natural products CC(C)=CCCC(C)=CCCC(C)=CCOC(C)=O ZGIGZINMAOQWLX-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 230000001387 anti-histamine Effects 0.000 description 2
- 230000000767 anti-ulcer Effects 0.000 description 2
- 239000000739 antihistaminic agent Substances 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- DNXIKVLOVZVMQF-UHFFFAOYSA-N (3beta,16beta,17alpha,18beta,20alpha)-17-hydroxy-11-methoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]-yohimban-16-carboxylic acid, methyl ester Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(C(=O)OC)C(O)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 DNXIKVLOVZVMQF-UHFFFAOYSA-N 0.000 description 1
- 229930008281 A03AD01 - Papaverine Natural products 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 235000003911 Arachis Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 229930003347 Atropine Natural products 0.000 description 1
- 241000700198 Cavia Species 0.000 description 1
- 208000007882 Gastritis Diseases 0.000 description 1
- ZPACYDRSPFRDHO-ROBAGEODSA-N Gefarnate Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CCC(=O)OC\C=C(/C)CCC=C(C)C ZPACYDRSPFRDHO-ROBAGEODSA-N 0.000 description 1
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 208000008469 Peptic Ulcer Diseases 0.000 description 1
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 description 1
- QEVHRUUCFGRFIF-SFWBKIHZSA-N Reserpine Natural products O=C(OC)[C@@H]1[C@H](OC)[C@H](OC(=O)c2cc(OC)c(OC)c(OC)c2)C[C@H]2[C@@H]1C[C@H]1N(C2)CCc2c3c([nH]c12)cc(OC)cc3 QEVHRUUCFGRFIF-SFWBKIHZSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 description 1
- 229960000396 atropine Drugs 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 206010009887 colitis Diseases 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 210000000981 epithelium Anatomy 0.000 description 1
- MCLZSZQLOAXPSX-UHFFFAOYSA-N ethyl 5,9,13-trimethyltetradeca-4,8,12-trienoate Chemical compound CCOC(=O)CCC=C(C)CCC=C(C)CCC=C(C)C MCLZSZQLOAXPSX-UHFFFAOYSA-N 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 201000005917 gastric ulcer Diseases 0.000 description 1
- 231100000029 gastro-duodenal ulcer Toxicity 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 229960003779 gefarnate Drugs 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- 239000012052 hydrophilic carrier Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229960001789 papaverine Drugs 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000007971 pharmaceutical suspension Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- BJOIZNZVOZKDIG-MDEJGZGSSA-N reserpine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C([C]5C=CC(OC)=CC5=N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 BJOIZNZVOZKDIG-MDEJGZGSSA-N 0.000 description 1
- 229960003147 reserpine Drugs 0.000 description 1
- MDMGHDFNKNZPAU-UHFFFAOYSA-N roserpine Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(OC(C)=O)C(OC)C1OC(=O)C1=CC(OC)=C(OC)C(OC)=C1 MDMGHDFNKNZPAU-UHFFFAOYSA-N 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000002511 suppository base Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/40—Radicals substituted by oxygen atoms
- C07D307/42—Singly bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/03—Monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
- C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
- C07C69/587—Monocarboxylic acid esters having at least two carbon-to-carbon double bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB18812/61A GB938712A (en) | 1961-05-24 | 1961-05-24 | Farnesyl acetic esters |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH416600A true CH416600A (de) | 1966-07-15 |
Family
ID=10118834
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH590862A CH420117A (de) | 1961-05-24 | 1962-05-16 | Verfahren zur Herstellung von Farnesylessigsäureestern |
| CH301066A CH416600A (de) | 1961-05-24 | 1962-05-16 | Verfahren zur Herstellung von Farnesylessigsäureestern |
| CH300966A CH416599A (de) | 1961-05-24 | 1962-05-16 | Verfahren zur Herstellung von Farnesylessigsäureestern |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH590862A CH420117A (de) | 1961-05-24 | 1962-05-16 | Verfahren zur Herstellung von Farnesylessigsäureestern |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH300966A CH416599A (de) | 1961-05-24 | 1962-05-16 | Verfahren zur Herstellung von Farnesylessigsäureestern |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US3154570A (en, 2012) |
| AT (3) | AT244317B (en, 2012) |
| BE (1) | BE617994A (en, 2012) |
| CH (3) | CH420117A (en, 2012) |
| DE (2) | DE1793591B2 (en, 2012) |
| DK (3) | DK114825B (en, 2012) |
| FI (3) | FI40163C (en, 2012) |
| FR (1) | FR1981M (en, 2012) |
| GB (1) | GB938712A (en, 2012) |
| IN (1) | IN138556B (en, 2012) |
| SE (3) | SE305864B (en, 2012) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2245607B1 (en, 2012) * | 1973-04-18 | 1979-04-20 | Kuraray Co | |
| JPS5623415B2 (en, 2012) * | 1973-07-13 | 1981-05-30 | ||
| US3928403A (en) * | 1974-07-10 | 1975-12-23 | Kuraray Co | Process for preparing farnesyl acetic acid esters and 2-substituted-products thereof |
| US4028385A (en) * | 1974-09-02 | 1977-06-07 | Kuraray Co., Ltd. | Process for preparing stereospecific farnesylacetic acid and ester thereof |
| JPS5855129B2 (ja) * | 1974-11-21 | 1983-12-08 | 株式会社クラレ | ２−置換または無置換のゲラニル酢酸エステル類の製造方法 |
| JPS53145922A (en) * | 1977-05-26 | 1978-12-19 | Eisai Co Ltd | Remedy for peptic ulcer containing prenyl ketone compound |
| FR2420523A1 (fr) * | 1978-03-23 | 1979-10-19 | Nisshin Flour Milling Co | Nouveaux derives acides et esters et leur application comme agents antiulcere |
| US4738801A (en) * | 1978-03-23 | 1988-04-19 | Nisshin Flour Milling Co., Ltd. | Antiulcer compounds |
| US4483871A (en) * | 1978-03-23 | 1984-11-20 | Nisshin Flour Milling Co., Ltd. | Antiulcer compounds |
| US4642314A (en) * | 1978-03-23 | 1987-02-10 | Nisshin Flour Milling Co., Ltd. | Antiulcer compounds |
| JPS5573642A (en) * | 1978-11-28 | 1980-06-03 | Kuraray Co Ltd | Farnesyl-acetic ester derivative |
| JPS57106644A (en) * | 1980-12-20 | 1982-07-02 | Kotobuki Seiyaku Kk | Farnesence derivative, mucosa stabilizer comprising it as active ingredient, and its preparation |
| CA1280414C (en) * | 1985-03-15 | 1991-02-19 | Saichi Matsumoto | Isoprenoidamine derivatives and antiulcer agents |
| US5298655A (en) * | 1991-09-27 | 1994-03-29 | Merck & Co., Inc. | Farnesyl pyrophosphate analogs |
| US5574025A (en) * | 1994-10-26 | 1996-11-12 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferases |
| AU757104B2 (en) * | 1998-06-24 | 2003-01-30 | Merck & Co., Inc. | Compositions and methods for inhibiting bone resorption |
| WO2014207235A1 (en) * | 2013-06-28 | 2014-12-31 | Castrol Limited | Lubricating compositions containing isoprene based components |
| CN105753696B (zh) * | 2016-03-04 | 2019-03-08 | 湖南晶天科技实业有限公司 | 一种香芹酚酯、饲料添加剂和饲料 |
-
1961
- 1961-05-24 GB GB18812/61A patent/GB938712A/en not_active Expired
-
1962
- 1962-05-04 FI FI90662A patent/FI40163C/fi active
- 1962-05-10 US US193876A patent/US3154570A/en not_active Expired - Lifetime
- 1962-05-11 DE DE19621793591 patent/DE1793591B2/de active Granted
- 1962-05-11 DE DE19621468055 patent/DE1468055A1/de active Pending
- 1962-05-15 AT AT1003363A patent/AT244317B/de active
- 1962-05-15 AT AT398262A patent/AT240341B/de active
- 1962-05-15 AT AT1003263A patent/AT243773B/de active
- 1962-05-16 CH CH590862A patent/CH420117A/de unknown
- 1962-05-16 DK DK221362AA patent/DK114825B/da unknown
- 1962-05-16 CH CH301066A patent/CH416600A/de unknown
- 1962-05-16 CH CH300966A patent/CH416599A/de unknown
- 1962-05-22 FR FR898375A patent/FR1981M/fr active Active
- 1962-05-23 SE SE5796/62A patent/SE305864B/xx unknown
- 1962-05-23 BE BE617994A patent/BE617994A/fr unknown
-
1964
- 1964-06-05 SE SE6864/64A patent/SE301475B/xx unknown
- 1964-06-05 SE SE6865/64A patent/SE301313B/xx unknown
- 1964-11-13 DK DK561664AA patent/DK115469B/da unknown
- 1964-11-13 DK DK561764AA patent/DK115254B/da unknown
-
1966
- 1966-08-25 FI FI2229/66A patent/FI40284B/fi active
- 1966-08-25 FI FI2230/66A patent/FI40285B/fi active
-
1973
- 1973-12-20 IN IN2772/CAL/1973A patent/IN138556B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FI40285B (en, 2012) | 1968-09-02 |
| FI40163B (en, 2012) | 1968-07-31 |
| DE1793591B2 (de) | 1973-08-23 |
| DE1793591A1 (de) | 1971-03-18 |
| DK114825B (da) | 1969-08-11 |
| AT240341B (de) | 1965-05-25 |
| AT243773B (de) | 1965-11-25 |
| FI40284B (en, 2012) | 1968-09-02 |
| US3154570A (en) | 1964-10-27 |
| SE301475B (sv) | 1968-06-10 |
| DE1793591C3 (en, 2012) | 1974-03-28 |
| CH420117A (de) | 1966-09-15 |
| IN138556B (en, 2012) | 1976-02-21 |
| AT244317B (de) | 1965-12-27 |
| FR1981M (fr) | 1963-08-26 |
| DK115469B (da) | 1969-10-13 |
| SE301313B (sv) | 1968-06-04 |
| BE617994A (fr) | 1962-09-17 |
| DK115254B (da) | 1969-09-22 |
| DE1468055A1 (de) | 1969-04-03 |
| SE305864B (en, 2012) | 1968-11-11 |
| GB938712A (en) | 1963-10-02 |
| FI40163C (fi) | 1968-11-11 |
| CH416599A (de) | 1966-07-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH416600A (de) | Verfahren zur Herstellung von Farnesylessigsäureestern | |
| CH644370A5 (de) | 4-substituierte thiazoloxamsaeuren sowie ihre salze und ester. | |
| DE2830079A1 (de) | Neue prostaglandinderivate der delta 2,4-11-desoxy-pge-reihe | |
| DE2745598A1 (de) | Arylschwefelverbindungen, verfahren zu ihrer herstellung und sie enthaltendes pharmazeutisches mittel | |
| DE3113149A1 (de) | 3,7,11,15-tetramethyl-2,4,6,10,14-hexadecapentaensaeure, verfahren zu ihrer herstellung, sie enthaltende arzneimittel und ihre verwendung als antikrebsmittel und therapeutisches mittel fuer die behandlung von hauterkrankungen | |
| EP0068250A1 (de) | Dioxybenzoletherderivate, diese enthaltende Arzneimittel, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE1793462C3 (de) | N-Aryl-anthranilsäureester monosubstituierter gem-Diole, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende pharmazeutische Präparate | |
| DE871896C (de) | Verfahren zur Herstellung des Nicotinsaeure-[ª-(N-morpholino)-aethyl]-esters | |
| DE2438884A1 (de) | Neue derivate des 5-hydroxymethylthiazols, verfahren zu ihrer herstellung und pharmazeutische zusammensetzungen | |
| DE3718946A1 (de) | Neue derivate der 4-phenyl-4-oxo-2-butensaeure, verfahren zu deren herstellung, deren verwendung als arzneimittel und diese enthaltende zusammensetzungen | |
| AT330754B (de) | Verfahren zur herstellung von neuen 4- (4-biphenylyl)-butandiolen | |
| AT293361B (de) | Verfahren zur Herstellung von neuen β-Aminoacrylophenonen und deren Salzen | |
| DE1620690C3 (de) | Verfahren zur Herstellung von 1-Tricyclo- eckige Klammer auf 2,2,1,0 eckige Klammer zu -heptyl-(2')-1-phenyl-3-piperidino-propanol-(1) | |
| DE959277C (de) | Verfahren zur Herstellung von Benzilsaeure-[1-alkyl-piperidyl-(4)]-estern | |
| DE1468055C (de) | Verfahren zur Herstellung von Farnesylessigsäureestern | |
| DE728360C (de) | Verfahren zur Darstellung einer trisubstituierten Barbitursaeure | |
| DE1936695C3 (de) | 2-n-PropyI-5-thiazolcarbonsäure, ihre Salze und Ester, Verfahren zu deren Herstellung sowie therapeutische Zusammensetzungen | |
| AT371814B (de) | Verfahren zur herstellung von neuen lactonderivaten des cyclopentanols | |
| DE814001C (de) | Verfahren zur Herstellung von 5, 8-Dialkoxy-2-tetralonen | |
| AT232977B (de) | Verfahren zur Herstellung von neuen, ungesättigten primär-tertiären Glykolen | |
| DE2217044A1 (de) | Neue Prostaglandin Analoga | |
| AT257601B (de) | Verfahren zur Herstellung von neuen 1,3-Dioxan-2-carbonsäuren und deren Alkalisalzen | |
| AT261109B (de) | Verfahren zur Gewinnung von therapeutisch wirksamen Verbindungen aus Valerianaceae | |
| AT217994B (de) | Verfahren zur Herstellung von neuen Derivaten von Polyhydroxyalkoholen | |
| AT221502B (de) | Verfahren zur Herstellung neuer basischer Phenoläther und ihrer Salze |