GB1105237A

GB1105237A – Conessine derivatives
– Google Patents

GB1105237A – Conessine derivatives
– Google Patents
Conessine derivatives

Info

Publication number
GB1105237A

GB1105237A
GB32946/66A
GB3294666A
GB1105237A
GB 1105237 A
GB1105237 A
GB 1105237A
GB 32946/66 A
GB32946/66 A
GB 32946/66A
GB 3294666 A
GB3294666 A
GB 3294666A
GB 1105237 A
GB1105237 A
GB 1105237A
Authority
GB
United Kingdom
Prior art keywords
conessine
hydroxy
prepared
dimethylaminoconanine
dimethylamino
Prior art date
1965-07-30
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

Application number
GB32946/66A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

DSM Delft BV

Original Assignee
Koninklijke Nederlandsche Gist en Spiritusfabriek BV
Priority date (The priority date 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 date listed.)
1965-07-30
Filing date
1966-07-22
Publication date
1968-03-06

1966-07-22
Application filed by Koninklijke Nederlandsche Gist en Spiritusfabriek BV
filed
Critical
Koninklijke Nederlandsche Gist en Spiritusfabriek BV

1968-03-06
Publication of GB1105237A
publication
Critical
patent/GB1105237A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

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

C12P33/00—Preparation of steroids

C—CHEMISTRY; METALLURGY

C07—ORGANIC CHEMISTRY

C07J—STEROIDS

C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring

C07J71/0036—Nitrogen-containing hetero ring

C07J71/0042—Nitrogen only

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S435/00—Chemistry: molecular biology and microbiology

Y10S435/8215—Microorganisms

Y10S435/911—Microorganisms using fungi

Abstract

The novel steroids 9a -hydroxyconessine and 12a -hydroxyconnesine are prepared by microbiological hydroxylation of conessine with enzymes of Botryodiplodia theobromae Pat. They may be converted to acid-addition salts and quaternary ammonium compounds, and they may be separated via the hemi-succinate of the 12a -ol which is formed at pH 9.5, unlike the 9a -ol which does not form such a salt. The 12a -ol may be oxidized to the 12-ketoconessine and acetylated to the 12a -acetoxy-conessine. The 9a -ol may be dehydrated to D 9(11)-conessine, which is also prepared by dehydration of 11a -hydroxy-conessine. The 9a -ol may be hydrogenated to 9a – hydroxy – 3b – dimethylaminoconanine which is also prepared by hydrogenating 11a – hydroxy – conessine to 11a – hydroxy – 3b -dimethylaminoconanine, dehydrating this to 3b – dimethylamino – D 9(11) – conenine, oxidizing this to 3b -dimethylamino-9a ,11a -epoxy-conanine 3-N-oxide and reducing this. Quaternary ammonium derivatives of the steroids of the invention, which are stated to be useful as muscular relaxing agents, may be made up into pharmaceutical compositions with suitable carriers. Suitable quaternizing agents are the esters of aliphatic and araliphatic alcohols with strong acids.

GB32946/66A
1965-07-30
1966-07-22
Conessine derivatives

Expired

GB1105237A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

NL6509936A

NL6509936A
(en)

1965-07-30
1965-07-30

Publications (1)

Publication Number
Publication Date

GB1105237A
true

GB1105237A
(en)

1968-03-06

Family
ID=19793779
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB32946/66A
Expired

GB1105237A
(en)

1965-07-30
1966-07-22
Conessine derivatives

Country Status (7)

Country
Link

US
(2)

US3466279A
(en)

BE
(1)

BE684672A
(en)

CH
(1)

CH492693A
(en)

DE
(1)

DE1568920A1
(en)

FR
(1)

FR1499235A
(en)

GB
(1)

GB1105237A
(en)

NL
(1)

NL6509936A
(en)

Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US5364453A
(en)

*

1992-09-22
1994-11-15
Geobiotics, Inc.
Method for recovering gold and other precious metals from carbonaceous ores

Families Citing this family (5)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US4301246A
(en)

*

1979-04-12
1981-11-17
Hoffmann-La Roche Inc.
Process for chenodeoxycholic acid production

US20100040568A1
(en)

*

2008-04-30
2010-02-18
Skinmedica, Inc.
Steroidal compounds as melanogenesis modifiers and uses thereof

JP5808797B2
(en)

2010-05-20
2015-11-10
ユニバーシティ オブ アイオワ リサーチ ファウンデーション

Methods for inhibiting muscle atrophy

US11090313B2
(en)

2010-05-20
2021-08-17
University Of Iowa Research Foundation
Methods for inhibiting muscle atrophy

JP6001060B2
(en)

2011-06-06
2016-10-05
ユニバーシティ オブ アイオワ リサーチ ファウンデーション

Methods for inhibiting muscle atrophy

Family Cites Families (5)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US2814629A
(en)

*

1956-07-30
1957-11-26
Olin Mathieson
12-oxygenated-4, 9(11)-pregnadiene-3, 20-dione

US2914543A
(en)

*

1957-03-01
1959-11-24
Olin Mathieson
Synthesis of steroids

US3067196A
(en)

*

1959-06-18
1962-12-04
Roussel Uclaf
Process for the preparation of steroids substituted in the 12-position and products resulting therefrom

US3047470A
(en)

*

1959-11-30
1962-07-31
American Cyanamid Co
Microbiological 11alpha-hydroxylation of 16alpha, 17alpha-epoxy pregnenes

NL126232C
(en)

*

1964-03-03
1969-04-15

1965

1965-07-30
NL
NL6509936A
patent/NL6509936A/xx
unknown

1966

1966-07-21
DE
DE19661568920
patent/DE1568920A1/en
active
Pending

1966-07-22
GB
GB32946/66A
patent/GB1105237A/en
not_active
Expired

1966-07-27
BE
BE684672D
patent/BE684672A/xx
unknown

1966-07-29
US
US568896A
patent/US3466279A/en
not_active
Expired – Lifetime

1966-07-29
FR
FR71536A
patent/FR1499235A/en
not_active
Expired

1966-07-29
CH
CH1100166A
patent/CH492693A/en
unknown

1969

1969-04-17
US
US817161A
patent/US3539449A/en
not_active
Expired – Lifetime

Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

US5364453A
(en)

*

1992-09-22
1994-11-15
Geobiotics, Inc.
Method for recovering gold and other precious metals from carbonaceous ores

Also Published As

Publication number
Publication date

DE1568920A1
(en)

1971-03-25

NL6509936A
(en)

1967-01-31

CH492693A
(en)

1970-06-30

US3539449A
(en)

1970-11-10

BE684672A
(en)

1967-01-27

FR1499235A
(en)

1967-10-27

US3466279A
(en)

1969-09-09

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