GB1278790A - Aminoalkane carboxylic acids, process for their manufacture and compositions containing such compounds - Google Patents
Aminoalkane carboxylic acids, process for their manufacture and compositions containing such compoundsInfo
- Publication number
- GB1278790A GB1278790A GB31508/69A GB3150869A GB1278790A GB 1278790 A GB1278790 A GB 1278790A GB 31508/69 A GB31508/69 A GB 31508/69A GB 3150869 A GB3150869 A GB 3150869A GB 1278790 A GB1278790 A GB 1278790A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compounds
- hypotensive
- june
- alkyl
- formula
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 239000000203 mixture Substances 0.000 title abstract 2
- 150000001735 carboxylic acids Chemical class 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- JZUFKLXOESDKRF-UHFFFAOYSA-N Chlorothiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC2=C1NCNS2(=O)=O JZUFKLXOESDKRF-UHFFFAOYSA-N 0.000 abstract 2
- RPTUSVTUFVMDQK-UHFFFAOYSA-N Hidralazin Chemical compound C1=CC=C2C(NN)=NN=CC2=C1 RPTUSVTUFVMDQK-UHFFFAOYSA-N 0.000 abstract 2
- 208000001953 Hypotension Diseases 0.000 abstract 2
- -1 alkane carboxylic acid Chemical class 0.000 abstract 2
- 239000002220 antihypertensive agent Substances 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 208000021822 hypotensive Diseases 0.000 abstract 2
- 230000001077 hypotensive effect Effects 0.000 abstract 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 abstract 1
- SZLZWPPUNLXJEA-UHFFFAOYSA-N 11,17-dimethoxy-18-[3-(3,4,5-trimethoxy-phenyl)-acryloyloxy]-yohimbane-16-carboxylic acid methyl ester Natural products C1C2CN3CCC(C4=CC=C(OC)C=C4N4)=C4C3CC2C(C(=O)OC)C(OC)C1OC(=O)C=CC1=CC(OC)=C(OC)C(OC)=C1 SZLZWPPUNLXJEA-UHFFFAOYSA-N 0.000 abstract 1
- BKYKPTRYDKTTJY-UHFFFAOYSA-N 6-chloro-3-(cyclopentylmethyl)-1,1-dioxo-3,4-dihydro-2H-1$l^{6},2,4-benzothiadiazine-7-sulfonamide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(S(N2)(=O)=O)=C1NC2CC1CCCC1 BKYKPTRYDKTTJY-UHFFFAOYSA-N 0.000 abstract 1
- CVBMAZKKCSYWQR-BPJCFPRXSA-N Deserpidine 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)cccc3 CVBMAZKKCSYWQR-BPJCFPRXSA-N 0.000 abstract 1
- RNPABQVCNAUEIY-GUQYYFCISA-N Germine Chemical compound O1[C@@]([C@H](CC[C@]23C)O)(O)[C@H]3C[C@@H](O)[C@@H]([C@]3(O)[C@@H](O)[C@H](O)[C@@H]4[C@]5(C)O)[C@@]12C[C@H]3[C@@H]4CN1[C@H]5CC[C@H](C)C1 RNPABQVCNAUEIY-GUQYYFCISA-N 0.000 abstract 1
- 229930189630 Protoveratrine Natural products 0.000 abstract 1
- HYTGGNIMZXFORS-MGYKWWNKSA-N Protoveratrine A Chemical compound O1[C@@]([C@H](CC[C@]23C)OC(=O)[C@@](C)(O)CC)(O)[C@H]3[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]3[C@@]12C[C@H]1[C@H](CN2[C@@H](CC[C@H](C)C2)[C@@]2(C)O)[C@@H]2[C@@H](O)[C@H](OC(=O)[C@H](C)CC)[C@@]31O HYTGGNIMZXFORS-MGYKWWNKSA-N 0.000 abstract 1
- SZLZWPPUNLXJEA-FMCDHCOASA-N Rescinnamine Natural products O=C(O[C@H]1[C@@H](OC)[C@@H](C(=O)OC)[C@@H]2[C@H](C1)CN1[C@@H](c3[nH]c4c(c3CC1)ccc(OC)c4)C2)/C=C/c1cc(OC)c(OC)c(OC)c1 SZLZWPPUNLXJEA-FMCDHCOASA-N 0.000 abstract 1
- LCQMZZCPPSWADO-UHFFFAOYSA-N Reserpilin Natural products COC(=O)C1COCC2CN3CCc4c([nH]c5cc(OC)c(OC)cc45)C3CC12 LCQMZZCPPSWADO-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- ZCDNRPPFBQDQHR-SSYATKPKSA-N Syrosingopine Chemical compound C1=C(OC)C(OC(=O)OCC)=C(OC)C=C1C(=O)O[C@H]1[C@H](OC)[C@@H](C(=O)OC)[C@H]2C[C@@H]3C(NC=4C5=CC=C(OC)C=4)=C5CCN3C[C@H]2C1 ZCDNRPPFBQDQHR-SSYATKPKSA-N 0.000 abstract 1
- 241000489523 Veratrum Species 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 229930013930 alkaloid Natural products 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229940030600 antihypertensive agent Drugs 0.000 abstract 1
- 229960002155 chlorothiazide Drugs 0.000 abstract 1
- JIVPVXMEBJLZRO-UHFFFAOYSA-N chlorthalidone Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C2(O)C3=CC=CC=C3C(=O)N2)=C1 JIVPVXMEBJLZRO-UHFFFAOYSA-N 0.000 abstract 1
- 229960003206 cyclopenthiazide Drugs 0.000 abstract 1
- 229960001993 deserpidine Drugs 0.000 abstract 1
- ISMCNVNDWFIXLM-WCGOZPBSSA-N deserpidine Chemical compound O([C@H]1[C@@H]([C@H]([C@H]2C[C@@H]3C4=C([C]5C=CC=CC5=N4)CCN3C[C@H]2C1)C(=O)OC)OC)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 ISMCNVNDWFIXLM-WCGOZPBSSA-N 0.000 abstract 1
- VQKLRVZQQYVIJW-UHFFFAOYSA-N dihydralazine Chemical compound C1=CC=C2C(NN)=NN=C(NN)C2=C1 VQKLRVZQQYVIJW-UHFFFAOYSA-N 0.000 abstract 1
- 229960002877 dihydralazine Drugs 0.000 abstract 1
- 239000002934 diuretic Substances 0.000 abstract 1
- 229940030606 diuretics Drugs 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 239000003457 ganglion blocking agent Substances 0.000 abstract 1
- RNPABQVCNAUEIY-UHFFFAOYSA-N germine Natural products O1C(C(CCC23C)O)(O)C3CC(O)C(C3(O)C(O)C(O)C4C5(C)O)C12CC3C4CN1C5CCC(C)C1 RNPABQVCNAUEIY-UHFFFAOYSA-N 0.000 abstract 1
- ACGDKVXYNVEAGU-UHFFFAOYSA-N guanethidine Chemical compound NC(N)=NCCN1CCCCCCC1 ACGDKVXYNVEAGU-UHFFFAOYSA-N 0.000 abstract 1
- 229960003602 guanethidine Drugs 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229960002474 hydralazine Drugs 0.000 abstract 1
- 229960002003 hydrochlorothiazide Drugs 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229940080360 rauwolfia alkaloid Drugs 0.000 abstract 1
- 229960001965 rescinnamine Drugs 0.000 abstract 1
- SMSAPZICLFYVJS-QEGASFHISA-N rescinnamine 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)\C=C\C1=CC(OC)=C(OC)C(OC)=C1 SMSAPZICLFYVJS-QEGASFHISA-N 0.000 abstract 1
- 229960003147 reserpine Drugs 0.000 abstract 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 abstract 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 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000001624 sedative effect Effects 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000008223 sterile water Substances 0.000 abstract 1
- 229950006534 syrosingopine Drugs 0.000 abstract 1
- 229940057613 veratrum Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- H—ELECTRICITY
- H02—GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
- H02K—DYNAMO-ELECTRIC MACHINES
- H02K3/00—Details of windings
- H02K3/32—Windings characterised by the shape, form or construction of the insulation
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH934068 | 1968-06-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1278790A true GB1278790A (en) | 1972-06-21 |
Family
ID=4350938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB31508/69A Expired GB1278790A (en) | 1968-06-24 | 1969-06-23 | Aminoalkane carboxylic acids, process for their manufacture and compositions containing such compounds |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3740439A (enExample) |
| AT (6) | AT301528B (enExample) |
| BE (1) | BE735032A (enExample) |
| BR (1) | BR6910097D0 (enExample) |
| DE (1) | DE1931240A1 (enExample) |
| FR (1) | FR2011551A1 (enExample) |
| GB (1) | GB1278790A (enExample) |
| IE (1) | IE33170B1 (enExample) |
| NL (1) | NL6909590A (enExample) |
| SU (1) | SU383280A3 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA964672A (en) * | 1970-04-09 | 1975-03-18 | Ciba-Geigy Ag | Propionic acid and processes for its manufacture |
| DE2115763A1 (de) * | 1970-04-09 | 1971-10-28 | Ciba Geigy Ag | Neue Amine und Verfahren zu ihrer Herstellung |
| US3904681A (en) * | 1971-03-30 | 1975-09-09 | Ciba Geigy Corp | Propionic acid |
| US4154851A (en) * | 1975-09-08 | 1979-05-15 | Science Union Et Cie, Societe Francaise De Recherche Medicale | Benzylamino alkanoic acid derivatives, using compositions containing the same, and methods for utilizing said derivatives and compositions |
| CH656560A5 (de) * | 1982-03-19 | 1986-07-15 | Castolin Sa | Verfahren zum auftragen einer schutzschicht durch thermisches spritzen. |
| AU5659796A (en) * | 1995-05-19 | 1996-11-29 | Kissei Pharmaceutical Co. Ltd. | 2-hydroxyphenylalkylamine derivatives and maillard reaction inhibitors |
| ZA991105B (en) * | 1998-03-04 | 2000-02-11 | Searle & Co | Synthesis of chiral beta-amino acids. |
| DE19948145C1 (de) * | 1999-09-28 | 2001-06-21 | Mannesmann Ag | Vermeidung von umrichterbedingten Lagerschäden bei Drehstrommotoren |
| JP6280033B2 (ja) * | 2011-07-12 | 2018-02-14 | ヴァンダービルト ユニバーシティーＶａｎｄｅｒｂｉｌｔ Ｕｎｉｖｅｒｓｉｔｙ | ガンマ−ケトアルデヒド捕捉剤による炎症および高血圧の治療方法 |
| FR3116130B1 (fr) | 2020-11-10 | 2025-03-21 | Psa Automobiles Sa | Procédé d’affichage pour un dispositif d’affichage tête haute d’un véhicule |
-
1969
- 1969-06-18 US US00834535A patent/US3740439A/en not_active Expired - Lifetime
- 1969-06-19 FR FR6920505A patent/FR2011551A1/fr not_active Withdrawn
- 1969-06-20 DE DE19691931240 patent/DE1931240A1/de active Pending
- 1969-06-23 IE IE855/69A patent/IE33170B1/xx unknown
- 1969-06-23 BE BE735032D patent/BE735032A/xx unknown
- 1969-06-23 AT AT365671A patent/AT301528B/de not_active IP Right Cessation
- 1969-06-23 GB GB31508/69A patent/GB1278790A/en not_active Expired
- 1969-06-23 AT AT774470A patent/AT301526B/de not_active IP Right Cessation
- 1969-06-23 AT AT774170A patent/AT301524B/de not_active IP Right Cessation
- 1969-06-23 AT AT774270A patent/AT301525B/de not_active IP Right Cessation
- 1969-06-23 AT AT365571A patent/AT301527B/de not_active IP Right Cessation
- 1969-06-23 AT AT593469A patent/AT301523B/de not_active IP Right Cessation
- 1969-06-23 NL NL6909590A patent/NL6909590A/xx unknown
- 1969-06-24 SU SU1341440A patent/SU383280A3/ru active
- 1969-06-24 BR BR210097/69A patent/BR6910097D0/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AT301523B (de) | 1972-09-11 |
| AT301524B (de) | 1972-09-11 |
| FR2011551A1 (enExample) | 1970-03-06 |
| IE33170L (en) | 1969-12-24 |
| SU383280A3 (enExample) | 1973-05-25 |
| BR6910097D0 (pt) | 1973-01-09 |
| AT301526B (de) | 1972-09-11 |
| BE735032A (enExample) | 1969-12-23 |
| AT301525B (de) | 1972-09-11 |
| IE33170B1 (en) | 1974-04-03 |
| US3740439A (en) | 1973-06-19 |
| AT301528B (de) | 1972-09-11 |
| DE1931240A1 (de) | 1970-01-02 |
| NL6909590A (enExample) | 1969-12-30 |
| AT301527B (de) | 1972-09-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |