GB1351437A - N-substituted amino acids having antiviral anti-inflammatory or anti-tumour activity - Google Patents
N-substituted amino acids having antiviral anti-inflammatory or anti-tumour activityInfo
- Publication number
- GB1351437A GB1351437A GB3874872A GB3874872A GB1351437A GB 1351437 A GB1351437 A GB 1351437A GB 3874872 A GB3874872 A GB 3874872A GB 3874872 A GB3874872 A GB 3874872A GB 1351437 A GB1351437 A GB 1351437A
- Authority
- GB
- United Kingdom
- Prior art keywords
- inflammatory
- amino acids
- naphthylaminomethyl
- isoleucine
- phenylalanine
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/20—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/19—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane
-
- 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
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
Abstract
1351437 Medicines comprising amino acid derivatives AJINOMOTO CO INC 18 Aug 1972 [19 Aug 1971 (3)] 38748/72 Heading A5B [Also in Division C2] A therapeutic composition suitable for oral or parenteral administration comprises a pharmaceutical carrier and as the active ingredient novel N-#-naphthylaminomethyl-leucine, N-#- naphthylaminomethyl urethane, N-furfurylaminomethyl-phenylalanine, . N-furfuryl-4-nitrophenylalanine, N- 2 -fluorenesulphonylmethionine, N-2-fluorenesulphonyl-phenylalanine, N- ethylcarbanunomethyl-isoleucine, N-#-naphthylaminiomethyl-threonine; N-9-fluorenylacetylphenylalanine, N-myristoyl-isoleucine or N-#- naphthalenesulphpnyl-tryptophan. or a pharmaceutically acceptable salt thereof. The above composition may be in a unit dosage form and in this form the invention also includes a therapeutic composition comprising a pharmaceutical carrier and as the active ingredient N-benzylvaline, N-lauroyl-leucine' or N-propionylvaline or. a pharmaceutically acceptable salt thereof. The compositions are useful for combatting infection with influenza virus, as anti-inflammatory agents or as anti-tumour agents.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6325171A JPS5313626B2 (en) | 1971-08-19 | 1971-08-19 | |
JP6325071A JPS5218176B2 (en) | 1971-08-19 | 1971-08-19 | |
JP6325271A JPS4828612A (en) | 1971-08-19 | 1971-08-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1351437A true GB1351437A (en) | 1974-05-01 |
Family
ID=27298102
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3874872A Expired GB1351437A (en) | 1971-08-19 | 1972-08-10 | N-substituted amino acids having antiviral anti-inflammatory or anti-tumour activity |
Country Status (4)
Country | Link |
---|---|
DE (1) | DE2236876C3 (en) |
FR (1) | FR2150803B1 (en) |
GB (1) | GB1351437A (en) |
NL (1) | NL7211361A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4416820A (en) | 1981-01-14 | 1983-11-22 | Takeda Chemical Industries, Ltd. | Indole derivatives and a method for production of peptides |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2508444A1 (en) * | 1981-06-29 | 1982-12-31 | Irceba | Analgesic and anti:inflammatory sulphonyl-tryptophan(s) - prepd. from tryptophan and aryl-sulphonyl-halide |
AU736347B2 (en) * | 1996-09-04 | 2001-07-26 | Warner-Lambert Company | Compounds for and a method of inhibiting matrix metalloproteinases |
WO1999059574A1 (en) * | 1998-05-21 | 1999-11-25 | Magainin Pharmaceuticals, Inc. | A method for stimulation of defensin production by exposure to isoleucin |
DE10112882A1 (en) * | 2001-03-15 | 2002-09-19 | Max Delbrueck Centrum | Selective cytostatic treatment of serotonin-producing tumors, using non-toxic tryptophan derivatives, e.g. 7-hydroxytryptophan, which are enzymatically converted into specific toxins in the tumor cells |
DE10321759B4 (en) * | 2003-05-15 | 2006-04-27 | Henkel Kgaa | Process for spray-drying free-flowing recyclables |
-
1972
- 1972-07-27 DE DE2236876A patent/DE2236876C3/en not_active Expired
- 1972-08-10 GB GB3874872A patent/GB1351437A/en not_active Expired
- 1972-08-18 FR FR7229667A patent/FR2150803B1/fr not_active Expired
- 1972-08-18 NL NL7211361A patent/NL7211361A/xx not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4416820A (en) | 1981-01-14 | 1983-11-22 | Takeda Chemical Industries, Ltd. | Indole derivatives and a method for production of peptides |
Also Published As
Publication number | Publication date |
---|---|
DE2236876B2 (en) | 1980-06-04 |
DE2236876A1 (en) | 1973-03-01 |
NL7211361A (en) | 1973-02-21 |
FR2150803B1 (en) | 1975-10-17 |
FR2150803A1 (en) | 1973-04-13 |
DE2236876C3 (en) | 1981-02-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2039197A1 (en) | Pharmaceutic Formulation for the Treatment of Alcoholism | |
ES485065A1 (en) | Amino or acylamino-substituted pyrimidinyl cephalosporanic acid derivatives and pharmaceutical compositions thereof | |
GB1388358A (en) | Taste-improving formulations of oral penicillins | |
UA42733C2 (en) | Bis-naphthalimide derivatives and pharmaceutically acceptable acid addition salts thereof, pharmaceutical composition containing them showing cytotoxic activity | |
ZA881053B (en) | Prostaglandin e1 derivatives as pharmacologically active agents,and pharmaceutical compositions containing these compounds,especially for transcutaneous administration | |
GB1351437A (en) | N-substituted amino acids having antiviral anti-inflammatory or anti-tumour activity | |
GB1487334A (en) | Pharmaceutical preparations comprising lisuride and/or physiologically tolerable salts thereof | |
ES2037095T3 (en) | A PROCEDURE FOR PREPARING A PHARMACEUTICAL COMPOSITION. | |
OA07029A (en) | Gallium chloride, a new anti-cancer drug. | |
GB1530074A (en) | Rho-acetamidophenol derivatives the preparation thereof and the use of such derivatives as therapeutic agents | |
GB1420976A (en) | Pharmaceutical compositions for use in the treatment of certain respiratory diseases or conditions in prematurely born children | |
IE35711B1 (en) | Pharmaceutical composition for inhibiting indoleamine-n-methyl transferase | |
GB1352392A (en) | Phenylisopropylamine derivatives | |
GB1424611A (en) | Pharmaceutical compositions | |
GB1397675A (en) | Proline compounds | |
GB1375806A (en) | ||
GB1246727A (en) | Therapeutic hypotensive compositions comprising 5-alkylpicolinic acids | |
GB1464082A (en) | Pharmaceutical 'ompositions containing benzylamines | |
GB1491074A (en) | Pharmaceutical compositions for reducing cardiac frequenc | |
GB1159272A (en) | 1,5-Disubstituted Barbituric Acid Derivatives and process for the manufacture thereof | |
GB1454390A (en) | Nasal decongestants | |
GB1463260A (en) | Pharmacologically active acetic acid derivative | |
GB1392004A (en) | Propoxyphene salts | |
GB1173985A (en) | Indole Derivatives | |
IE34397B1 (en) | Therapeutic anti-depressant compositions |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |