GB1331705A - Rauwolfia alkalois derivatives - Google Patents
Rauwolfia alkalois derivativesInfo
- Publication number
- GB1331705A GB1331705A GB1331705DA GB1331705A GB 1331705 A GB1331705 A GB 1331705A GB 1331705D A GB1331705D A GB 1331705DA GB 1331705 A GB1331705 A GB 1331705A
- Authority
- GB
- United Kingdom
- Prior art keywords
- rauwolfia
- alkalois
- derivatives
- alkaloid
- yofimbine
- 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
- 241000208332 Rauvolfia Species 0.000 title 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- GRTOGORTSDXSFK-XJTZBENFSA-N ajmalicine Chemical compound C1=CC=C2C(CCN3C[C@@H]4[C@H](C)OC=C([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 GRTOGORTSDXSFK-XJTZBENFSA-N 0.000 abstract 2
- 229940080360 rauwolfia alkaloid Drugs 0.000 abstract 2
- CZJDUZOWQVAEEV-XIEZEKGWSA-N (+)-19-epi-Ajmalicine Natural products O=C(OC)C=1[C@@H]2[C@@H]([C@@H](C)OC=1)C[N+]1[C@H](c3[nH]c4c(c3CC1)cccc4)C2 CZJDUZOWQVAEEV-XIEZEKGWSA-N 0.000 abstract 1
- 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
- CJDRUOGAGYHKKD-RQBLFBSQSA-N 1pon08459r Chemical compound CN([C@H]1[C@@]2(C[C@@]3([H])[C@@H]([C@@H](O)N42)CC)[H])C2=CC=CC=C2[C@]11C[C@@]4([H])[C@H]3[C@H]1O CJDRUOGAGYHKKD-RQBLFBSQSA-N 0.000 abstract 1
- CJDRUOGAGYHKKD-UHFFFAOYSA-N Iso-ajmalin Natural products CN1C2=CC=CC=C2C2(C(C34)O)C1C1CC3C(CC)C(O)N1C4C2 CJDRUOGAGYHKKD-UHFFFAOYSA-N 0.000 abstract 1
- 244000061121 Rauvolfia serpentina Species 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
- 229940007897 ajmalicine Drugs 0.000 abstract 1
- 229960004332 ajmaline Drugs 0.000 abstract 1
- 229930013930 alkaloid Natural products 0.000 abstract 1
- 150000003797 alkaloid derivatives Chemical class 0.000 abstract 1
- QDHFHIQKOVNCNC-UHFFFAOYSA-N butane-1-sulfonic acid Chemical class CCCCS(O)(=O)=O QDHFHIQKOVNCNC-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- MHYFEEDKONKGEB-UHFFFAOYSA-N oxathiane 2,2-dioxide Chemical compound O=S1(=O)CCCCO1 MHYFEEDKONKGEB-UHFFFAOYSA-N 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- ZLQMRLSBXKQKMG-UHFFFAOYSA-N rauniticine Natural products COC(=O)C1=CC2CC3N(CCc4c3[nH]c5ccccc45)CC2C(C)O1 ZLQMRLSBXKQKMG-UHFFFAOYSA-N 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
- -1 yofimbine Chemical compound 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D459/00—Heterocyclic compounds containing benz [g] indolo [2, 3-a] quinolizine ring systems, e.g. yohimbine; 16, 18-lactones thereof, e.g. reserpic acid lactone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB628171 | 1971-03-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1331705A true GB1331705A (en) | 1973-09-26 |
Family
ID=9811644
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1331705D Expired GB1331705A (en) | 1971-03-08 | 1972-02-21 | Rauwolfia alkalois derivatives |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE779784A (enrdf_load_stackoverflow) |
FR (1) | FR2128324B1 (enrdf_load_stackoverflow) |
GB (1) | GB1331705A (enrdf_load_stackoverflow) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE636675A (enrdf_load_stackoverflow) * | 1963-08-27 | |||
GB1032269A (en) * | 1963-09-30 | 1966-06-08 | Orgamol Sa | Process for the preparation of water-soluble alkane sulphonic acid salts of isoquinoline bases of the papaverine series |
-
1972
- 1972-02-11 FR FR7204606A patent/FR2128324B1/fr not_active Expired
- 1972-02-21 GB GB1331705D patent/GB1331705A/en not_active Expired
- 1972-02-24 BE BE779784A patent/BE779784A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
FR2128324B1 (enrdf_load_stackoverflow) | 1976-04-16 |
BE779784A (fr) | 1972-06-16 |
FR2128324A1 (enrdf_load_stackoverflow) | 1972-10-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PH11673A (en) | A process for the preparation of pyrano(thiopyrano)(3,4-b)indole derivatives | |
GB1301973A (enrdf_load_stackoverflow) | ||
GB1240420A (en) | 9,10-dihydrolysergic acid derivative | |
GB1268951A (en) | Phenoxy-amines | |
GB1331705A (en) | Rauwolfia alkalois derivatives | |
GB1436080A (en) | Ellipticine derivative and pharmaceutical uses thereof | |
GB1252870A (enrdf_load_stackoverflow) | ||
IE35186L (en) | Amines | |
GB1319841A (en) | Quinine alkaloid derivatives | |
GB1490432A (en) | Derivatives of theo-phylline methods for their preparation and compositions containing them | |
GB1412932A (en) | Pharmaceutically active leurosine derivatives and preparation thereof | |
GB1178012A (en) | A Method for the Production of Pyridine Derivatives | |
GB1410296A (en) | Sulphoglycopeptide salts | |
GB1332635A (en) | Rutin complexes | |
GB1139146A (en) | Benzofuran derivatives and processes for preparing the same | |
GB1267931A (en) | Novel azetidine compounds and process for making such compounds | |
GB1304633A (enrdf_load_stackoverflow) | ||
GB1329130A (en) | Isoindolo 1,2-b benzothiazol-11 -4bh- one 5-oxides | |
GB1173309A (en) | The Manufacture of Benzdiaz[1,4]Epine Derivatives | |
GB1287853A (enrdf_load_stackoverflow) | ||
GB1295209A (enrdf_load_stackoverflow) | ||
GB1451904A (en) | Bromo ergot alkaloid | |
GB1355689A (en) | Piperidylfuranones | |
GB1294825A (enrdf_load_stackoverflow) | ||
GB1298621A (en) | Benzocyclohepta-oxazole and -thiazole compounds |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PLNP | Patent lapsed through nonpayment of renewal fees |