GB883329A - Process for the production of alkaloid derivatives of lyserqic acid - Google Patents
Process for the production of alkaloid derivatives of lyserqic acidInfo
- Publication number
- GB883329A GB883329A GB23303/60A GB2330360A GB883329A GB 883329 A GB883329 A GB 883329A GB 23303/60 A GB23303/60 A GB 23303/60A GB 2330360 A GB2330360 A GB 2330360A GB 883329 A GB883329 A GB 883329A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- lysergic
- embryos
- isolysergic
- alkaloid derivatives
- 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
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/18—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
- C12P17/182—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system
- C12P17/183—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system containing an indolo[4,3-F,G]quinoleine nucleus, e.g. compound containing the lysergic acid nucleus as well as the dimeric ergot nucleus
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Lysergic acid amide and isolysergic acid amide are prepared by fermenting under aerobic conditions an aqueous nutrient medium containing a source of carbon, nitrogen and mineral salt with a new strain of Claviceps paspali Stevens and Hall. The process is preferably conducted between 22 DEG C. and 30 DEG C. and at a pH between 4.2 and 6, the alkaloid derivatives being isolated by filtration, rendering the filtrate alkaline, extracting with a water-immiscible organic solvent or by absorbtion on a solid absorbant material. Subsequent hydrolysis with alkali yields lysergic acid or isolysergic acid. The new virulented strain of Claviceps paspali is obtained by inoculating embryos of Rosen 4n rye, cultivating in vitro and isolating the sub-species from sclerotia on the embryos. Detailed examples illustrate the preparation of the alkaloids and their hydrolysis to lysergic and isolysergic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT883329X | 1959-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB883329A true GB883329A (en) | 1961-11-29 |
Family
ID=11331122
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23303/60A Expired GB883329A (en) | 1959-07-07 | 1960-07-04 | Process for the production of alkaloid derivatives of lyserqic acid |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB883329A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1219173B (en) * | 1962-08-30 | 1966-06-16 | Sandoz Ag | Process for the production of lysergic acid derivatives |
-
1960
- 1960-07-04 GB GB23303/60A patent/GB883329A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1219173B (en) * | 1962-08-30 | 1966-06-16 | Sandoz Ag | Process for the production of lysergic acid derivatives |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1083662A (en) | A novel antibiotic, methods for its production and therapeutic compositions containing it | |
GB1385274A (en) | Process for the preparation of zeaxanthin | |
GB1121308A (en) | Cephalosporins | |
GB883329A (en) | Process for the production of alkaloid derivatives of lyserqic acid | |
GB1111010A (en) | Process for the production of the antibiotic pleuromutilin | |
GB1331959A (en) | Process for producing 6-aminopenicillanic acid | |
GB891173A (en) | Method for the production of 6-amino-penicillanic acid | |
ES340130A1 (en) | Penicillins | |
GB999794A (en) | Improvements in or relating to the production of an antibiotic containing a cyclopentanophenanthrene nucleus and salts thereof | |
GB925282A (en) | Fermentation process for the production of demethyltetracycline | |
GB975880A (en) | Lysergic acid | |
JPS5682100A (en) | Production of beta-lactam antibiotic | |
GB1065380A (en) | Process for the production of uridylic acid by fermentation | |
GB1041246A (en) | Process for the production of lysergic acid derivatives | |
JPS5272886A (en) | Preparation of cephalosporin compound | |
US3567584A (en) | Process for the preparation of ergocornine and ergosine | |
GB1115550A (en) | Process for the preparation of 5-aminovaleric acid | |
ES260746A2 (en) | Procedure for the production of alkaloid derivatives of lystric acid (Machine-translation by Google Translate, not legally binding) | |
GB1277356A (en) | Process for the production of l-histidine | |
GB897618A (en) | Process for the enzymatic acylation of 6-amino-penicillanic acids | |
GB1452457A (en) | Microbiological production of biologically active 8,8-bi-1h- naphthol-2,3-c-pyrans | |
GB795570A (en) | Thiostrepton, its salts and method of manufacture | |
GB883330A (en) | Lysergic acid-alkaloids | |
GB870396A (en) | Improvements in or relating to substances produced by penicillin-producing moulds | |
ES389257A3 (en) | Procedure for the obtaining of penicilline derivatives. (Machine-translation by Google Translate, not legally binding) |