GB916242A - Aryloxy aliphatic derivatives and therapeutic compositions containing them - Google Patents
Aryloxy aliphatic derivatives and therapeutic compositions containing themInfo
- Publication number
- GB916242A GB916242A GB666/59A GB66659A GB916242A GB 916242 A GB916242 A GB 916242A GB 666/59 A GB666/59 A GB 666/59A GB 66659 A GB66659 A GB 66659A GB 916242 A GB916242 A GB 916242A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- hydrogen
- oxy
- alkyl
- phenyl
- 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
- 239000000203 mixture Substances 0.000 title abstract 2
- 230000001225 therapeutic effect Effects 0.000 title 1
- -1 methyl- Chemical group 0.000 abstract 13
- 150000001875 compounds Chemical class 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- 150000002148 esters Chemical class 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 2
- 239000008187 granular material Substances 0.000 abstract 2
- 150000002576 ketones Chemical class 0.000 abstract 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 2
- 150000002825 nitriles Chemical class 0.000 abstract 2
- 231100000252 nontoxic Toxicity 0.000 abstract 2
- 230000003000 nontoxic effect Effects 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- LGLHQRIDKDVEGC-UHFFFAOYSA-N 2-(4-phenylphenoxy)propanedioic acid Chemical compound C1(=CC=C(C=C1)OC(C(=O)O)C(=O)O)C1=CC=CC=C1 LGLHQRIDKDVEGC-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- WIYQCLDTSROCTN-UHFFFAOYSA-N 2-phenoxypropanal Chemical class O=CC(C)OC1=CC=CC=C1 WIYQCLDTSROCTN-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 229920002261 Corn starch Polymers 0.000 abstract 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 235000019759 Maize starch Nutrition 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 abstract 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical group 0.000 abstract 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- UOCJDOLVGGIYIQ-PBFPGSCMSA-N cefatrizine Chemical group S([C@@H]1[C@@H](C(N1C=1C(O)=O)=O)NC(=O)[C@H](N)C=2C=CC(O)=CC=2)CC=1CSC=1C=NNN=1 UOCJDOLVGGIYIQ-PBFPGSCMSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- WLWCQKMQYZFTDR-UHFFFAOYSA-N diethyl 2-chloropropanedioate Chemical compound CCOC(=O)C(Cl)C(=O)OCC WLWCQKMQYZFTDR-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 abstract 1
- 125000001207 fluorophenyl group Chemical group 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000007937 lozenge Substances 0.000 abstract 1
- 150000001457 metallic cations Chemical class 0.000 abstract 1
- 150000007530 organic bases Chemical class 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 abstract 1
- 235000019260 propionic acid Nutrition 0.000 abstract 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract 1
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract 1
- NKAAEMMYHLFEFN-ZVGUSBNCSA-M sodium;(2r,3r)-2,3,4-trihydroxy-4-oxobutanoate Chemical compound [Na+].OC(=O)[C@H](O)[C@@H](O)C([O-])=O NKAAEMMYHLFEFN-ZVGUSBNCSA-M 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 235000020357 syrup Nutrition 0.000 abstract 1
- 239000006188 syrup Substances 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
- 235000002906 tartaric acid Nutrition 0.000 abstract 1
- 239000011975 tartaric acid Substances 0.000 abstract 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 230000000699 topical effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/28—Preparation of azo dyes from other azo compounds by etherification of hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/26—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C243/28—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/06—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/08—Preparation of carboxylic acids or their salts, halides or anhydrides from nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/29—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with halogen-containing compounds which may be formed in situ
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/36—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by hydrogenation of carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/367—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/377—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
- C07C51/38—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups by decarboxylation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
- C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE586247D BE586247A (enrdf_load_html_response) | 1959-01-07 | ||
LU38115D LU38115A1 (enrdf_load_html_response) | 1959-01-07 | ||
GB666/59A GB916242A (en) | 1959-01-07 | 1959-01-07 | Aryloxy aliphatic derivatives and therapeutic compositions containing them |
ES0254777A ES254777A1 (es) | 1959-01-07 | 1960-01-05 | Procedimiento para producir una composiciën terapeutica |
FR837266A FR504M (enrdf_load_html_response) | 1959-01-07 | 1960-08-30 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB666/59A GB916242A (en) | 1959-01-07 | 1959-01-07 | Aryloxy aliphatic derivatives and therapeutic compositions containing them |
Publications (1)
Publication Number | Publication Date |
---|---|
GB916242A true GB916242A (en) | 1963-01-23 |
Family
ID=9708394
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB666/59A Expired GB916242A (en) | 1959-01-07 | 1959-01-07 | Aryloxy aliphatic derivatives and therapeutic compositions containing them |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE586247A (enrdf_load_html_response) |
ES (1) | ES254777A1 (enrdf_load_html_response) |
FR (1) | FR504M (enrdf_load_html_response) |
GB (1) | GB916242A (enrdf_load_html_response) |
LU (1) | LU38115A1 (enrdf_load_html_response) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2015729A1 (enrdf_load_html_response) * | 1968-08-15 | 1970-04-30 | Lilly Co Eli | |
US4031134A (en) | 1969-04-16 | 1977-06-21 | Sumitomo Chemical Company, Limited | Phenoxy carboxylic acid derivative |
US4128573A (en) * | 1970-03-16 | 1978-12-05 | Boots Pure Drug Company Limited | 2-(Substituted phenyl)propionic acids |
EP0013144A1 (en) * | 1978-12-22 | 1980-07-09 | Ici Australia Limited | Substituted diphenylamine derivatives, compositions and herbicidal uses thereof, and processes for their preparation |
EP0039857A1 (de) * | 1980-05-12 | 1981-11-18 | Henkel Kommanditgesellschaft auf Aktien | Hautpflegemittel |
AT380166B (de) * | 1981-02-16 | 1986-04-25 | Ciba Geigy Ag | Verfahren zur herstellung topisch applizierbarer pharmazeutischer praeparate, enthaltend salze von alkancarbonsaeuren |
US4883901A (en) * | 1988-03-21 | 1989-11-28 | Hoechst Celanese Corporation | Synthesis of 2-(4-aminophenoxy)alkanoic acids and esters and their derivatives |
EP3013796A4 (en) * | 2013-06-27 | 2016-11-23 | Lg Life Sciences Ltd | BIARYL DERIVATIVES AS GPR120 AGONISTS |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1121722A (en) * | 1966-03-31 | 1968-07-31 | Ici Ltd | New carboxylic acid derivatives |
US4259105A (en) * | 1978-05-10 | 1981-03-31 | Nippon Soda Company, Ltd. | Diphenylamine derivatives |
FR2460286A1 (fr) * | 1979-06-29 | 1981-01-23 | Rhone Poulenc Agrochimie | Procede de preparation d'acide phenoxy-2 propioniques optiquement actifs |
FR2486071A2 (fr) * | 1979-06-29 | 1982-01-08 | Rhone Poulenc Agrochimie | Procede de preparation de composes aryloxyalcanoiques optiquement actifs |
US4451474A (en) * | 1980-01-22 | 1984-05-29 | Frank M. Berger | T-Butyl-phenoxy-alkylene esters of benzoic and nicotinic acids, compositions containing same and their antihistaminic method of use |
-
0
- BE BE586247D patent/BE586247A/xx unknown
- LU LU38115D patent/LU38115A1/xx unknown
-
1959
- 1959-01-07 GB GB666/59A patent/GB916242A/en not_active Expired
-
1960
- 1960-01-05 ES ES0254777A patent/ES254777A1/es not_active Expired
- 1960-08-30 FR FR837266A patent/FR504M/fr active Active
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2015729A1 (enrdf_load_html_response) * | 1968-08-15 | 1970-04-30 | Lilly Co Eli | |
US4031134A (en) | 1969-04-16 | 1977-06-21 | Sumitomo Chemical Company, Limited | Phenoxy carboxylic acid derivative |
US4128573A (en) * | 1970-03-16 | 1978-12-05 | Boots Pure Drug Company Limited | 2-(Substituted phenyl)propionic acids |
EP0013144A1 (en) * | 1978-12-22 | 1980-07-09 | Ici Australia Limited | Substituted diphenylamine derivatives, compositions and herbicidal uses thereof, and processes for their preparation |
EP0039857A1 (de) * | 1980-05-12 | 1981-11-18 | Henkel Kommanditgesellschaft auf Aktien | Hautpflegemittel |
AT380166B (de) * | 1981-02-16 | 1986-04-25 | Ciba Geigy Ag | Verfahren zur herstellung topisch applizierbarer pharmazeutischer praeparate, enthaltend salze von alkancarbonsaeuren |
US4883901A (en) * | 1988-03-21 | 1989-11-28 | Hoechst Celanese Corporation | Synthesis of 2-(4-aminophenoxy)alkanoic acids and esters and their derivatives |
EP3013796A4 (en) * | 2013-06-27 | 2016-11-23 | Lg Life Sciences Ltd | BIARYL DERIVATIVES AS GPR120 AGONISTS |
AU2017203392B2 (en) * | 2013-06-27 | 2018-05-10 | Lg Chem, Ltd. | Biaryl derivatives as GPR120 agonists |
US10221138B2 (en) | 2013-06-27 | 2019-03-05 | Lg Chem, Ltd. | Biaryl derivatives as GPR120 agonists |
EP3628661A1 (en) * | 2013-06-27 | 2020-04-01 | Lg Chem, Ltd. | Biaryl derivatives as gpr120 agonists |
Also Published As
Publication number | Publication date |
---|---|
BE586247A (enrdf_load_html_response) | |
FR504M (enrdf_load_html_response) | 1961-05-15 |
LU38115A1 (enrdf_load_html_response) | |
ES254777A1 (es) | 1960-08-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB916242A (en) | Aryloxy aliphatic derivatives and therapeutic compositions containing them | |
GB1038725A (en) | Substituted indanes and indenes | |
JPS6442476A (en) | Benzothiazole derivative and antirheumatic agent containing said derivative as active ingredient | |
RU95110766A (ru) | Способ получения сложных эфиров баккатина-iii и 10-дезацетил-баккатина-iii, активированные кислоты и их производные | |
FR2453133A1 (fr) | Nouveaux acides acetohydroxamiques, leur procede de preparation et leur application en therapeutique | |
GB1121027A (en) | New carboxylic acid derivatives, processes for the preparation thereof and compositions containing the same | |
FR2429019A1 (fr) | Medicaments contenant des esters de 1-b-d-arabinofuranosylcytosine-5'-phosphate | |
ES263127A1 (es) | Un procedimiento para la fabricaciën de derivados de 1,4-benzodiazepinas | |
GB1314830A (en) | Pharmaceutically useful benzomorphanes and their production | |
GB859546A (en) | Composition for treatment of the skin | |
GB1388834A (en) | Cyclic acetal derivatives and their use as herbicides | |
JPS5716898A (en) | Prostaglandin controller containing aminobenzoic derivative | |
GB843752A (en) | Novel morphinane derivatives and a process for the manufacture thereof | |
GB978088A (en) | N-acyl-ª-amino acid amides | |
GB999583A (en) | Pharmaceutical preparations containing trihydroxamic acids | |
GB1041787A (en) | Novel medicament having as a base thiazolidine carboxylic acid for treatment of illnesses caused by disturbances of the liver | |
GB1098835A (en) | Spiro-oxazolidinones, spiro-oxazines, their process of preparation and therapeutic compositions containing said derivatives | |
ES389252A1 (es) | Procedimiento para la preparacion de acidos propionicos sustituidos por fenilo en la posicion 2. | |
GB880278A (en) | Novel hydrazine derivatives and a process for the manufacture thereof | |
SE8603792D0 (sv) | Nya bicykliska katekolderivat, forfarande for framstellning derav och terapeutiska kompositioner innehallande dem | |
ES436198A1 (es) | Un procedimiento para la preparacion de compuestos de cefa- losporina sustituidas. | |
GB1420759A (en) | Piperidine derivatives | |
GB1105151A (en) | New imidazole derivatives, their production and use | |
SU1573813A1 (ru) | 1-фенил-3-окси-4-этоксикарбонил-5-п-бромфенил-2,5-дигидропиррол-2-он, проявляющий противовирусную активность | |
GB960894A (en) | Preparation of carboxylic acids and derivatives thereof |