[go: up one dir, main page]

GB1474879A - Antibiotic 67-121 and process for the preparation thereof - Google Patents

Antibiotic 67-121 and process for the preparation thereof

Info

Publication number
GB1474879A
GB1474879A GB939275A GB939275A GB1474879A GB 1474879 A GB1474879 A GB 1474879A GB 939275 A GB939275 A GB 939275A GB 939275 A GB939275 A GB 939275A GB 1474879 A GB1474879 A GB 1474879A
Authority
GB
United Kingdom
Prior art keywords
antibiotic
maxima
complex
absorption maxima
free form
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
Application number
GB939275A
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.)
MSD International Holdings GmbH
Original Assignee
Scherico Ltd
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.)
Filing date
Publication date
Application filed by Scherico Ltd filed Critical Scherico Ltd
Publication of GB1474879A publication Critical patent/GB1474879A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H17/00Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
    • C07H17/04Heterocyclic radicals containing only oxygen as ring hetero atoms
    • C07H17/08Hetero rings containing eight or more ring members, e.g. erythromycins
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07GCOMPOUNDS OF UNKNOWN CONSTITUTION
    • C07G11/00Antibiotics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

1474879 Antibiotic complex SCHERICO Ltd 6 March 1975 [11 March 1974] 9392/75 Heading C2A The invention is directed to a polyene antibiotic complex designated 67-121 complex, in free form or in the form of a pharmaceutically acceptable derivative. The complex in the free form has the following characteristics; ultraviolet absorption maxima in methanol at 342, 363, 382 and 403 mÁ with corresponding E<SP>1%</SP> 1cm values of 340, 475, 667 and 605, infra-red absorption maxima in mineral oil at 3350, 1725 and 1665 cm<SP>-1</SP> and nuclear magnetic resonance spectra in hexa-deutero-dimethylsulfoxide with maxima at 2À75, 6À56 and 7À64 p.p.m. The complex comprises antibiotic components 67- 121A, 67-121B, 67-121C and 67-121D. The complex or a component antibiotic thereof may be prepared by cultivating a microorganism of the species Actinoplanes coerulus in a nutrient medium under aerobic conditions until substantial antibiotic activity is generated. The preferred microoganism is the strain Actinoplanes coeruleus NRRL 5325. Antibiotic 67-121A, in the free form has the following characteristics, ultra-violet absorption maxima in a 4 : 1 tetrahydrofuran : water mixture of 408, 384 and 363 mÁ with corresponding E<SP>1%</SP> 1cm values of 950, 1100 and 680; infra-red absorption maxima in mineral oil at 3350, 1725 and 1665 cm<SP>-1</SP> and a nuclear magnetic resonance spectrum in hexa-deutero-dimethylsulphoxide with maxima at 2À73, 6À55 and 7À64 p.p.m. Antibiotic 67-121B, in the free form has the following characteristics ultra-violet absorption maxima in a 4 : 1 tetra hydrofuran : water mixture of 408, 383 and 362 mÁ with corresponding E<SP>1%</SP> 1cm values of 620, 750 and 490; infra-red absorption maxima in mineral oil at 3350, 1725 and 1665 cm<SP>-1</SP> and a nuclear magnetic resonance spectrum in hexa-deutro dimethylsulphoxide with maxima at 6À58 and 7À60 p.p.m. Antibiotic 67-121C, in the free form has the following characteristics, ultraviolet absorption maxima in 4 : 1 tetrahydrofuran : water mixture of 408, 383 and 362 mÁ with corresponding E<SP>1%</SP> 1cm value of 800, 910 and 600; infra-red absorption maxima in mineral oil at 3350, 1725 and 1665 cm<SP>-1</SP> and a nuclear magnetic resonance spectrum in hexa-deutero dimethylsulphoxide with maxima at 2À76, 6À57 and 7À65 p.p.m. The polyene antibiotics are further characterized as a heptaene subgroup II antibiotic and having an aromatic moiety of the formula in which for antibiotics 67-121A and C, R is methyl and/or antibiotic 67-121B, R is H. The antibiotics 67-121A and 67-121B are further characterized by a presence of a D- mycosamine sugar unit glycosidically attached to an allylic hydroxy group of the aglycone structure and antibiotic 67-121C is further characterized by the presence of the disaccharide unit [O-#-D-mannopyranosyl(1#4)-D- mycosamine]glycosidically attached to an allylic hydroxy group of the aglycore structure. The complex or components may be in a free form or in the form of a pharmaceutically acceptable derivative. The antibiotic substances may be admixed with a suitable pharmaceutically acceptable carrier. The antibiotic substance may be administered to animals having a fungal infection to elicit an anti-fungal response therefrom.
GB939275A 1974-03-11 1975-03-06 Antibiotic 67-121 and process for the preparation thereof Expired GB1474879A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US45004074A 1974-03-11 1974-03-11

Publications (1)

Publication Number Publication Date
GB1474879A true GB1474879A (en) 1977-05-25

Family

ID=23786522

Family Applications (1)

Application Number Title Priority Date Filing Date
GB939275A Expired GB1474879A (en) 1974-03-11 1975-03-06 Antibiotic 67-121 and process for the preparation thereof

Country Status (9)

Country Link
JP (1) JPS50121496A (en)
BG (1) BG26542A3 (en)
DE (1) DE2509782A1 (en)
FR (1) FR2263782B1 (en)
GB (1) GB1474879A (en)
HU (1) HU175177B (en)
IE (1) IE40821B1 (en)
NL (1) NL7502666A (en)
SE (1) SE7502535L (en)

Also Published As

Publication number Publication date
BG26542A3 (en) 1979-04-12
JPS50121496A (en) 1975-09-23
IE40821L (en) 1975-09-11
DE2509782A1 (en) 1975-09-18
NL7502666A (en) 1975-09-15
SE7502535L (en) 1975-10-03
FR2263782B1 (en) 1978-12-01
FR2263782A1 (en) 1975-10-10
IE40821B1 (en) 1979-08-29
HU175177B (en) 1980-05-28

Similar Documents

Publication Publication Date Title
TAKEUCHI et al. Coriolin, a new basidiomycetes antibiotic
GB1299198A (en) Pyrrolobenzodiazepinone derivatives
DE3323025A1 (en) ANTHRACYCLINE DERIVATIVES, A MICROBIOLOGICAL METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS CYTOSTATICS
EP0048585A1 (en) Antibiotics TM-531 B and TM-531 C
GB1357538A (en) New antibiotic
GB1474879A (en) Antibiotic 67-121 and process for the preparation thereof
Marumo et al. Stemphol from Pleospora herbarum as a self-inhibitor
JPS5515445A (en) Introduction of amino-protecting group by microorganism
DE2921148A1 (en) NEW METABOLITES, THEIR PRODUCTION AND USE
GB1500965A (en) Cyclic ether antibiotics
US4440751A (en) Broad spectrum antibiotic complex produced by a novel micromonospora
Liu et al. BIOSYNTHESIS OF AURODOX (ANTIBIOTIC X-5108) INCORPORATION OF 14 C-LABELLED PRECURSORS INTO AURODOX
US3465079A (en) Antibiotic sl 1846
US3898327A (en) Antibiotic azdimycin
EP0325462A3 (en) Anthelmintic milbemycin derivatives
GB1387080A (en) Antibiotics and the preparation thereof
DE1770441C2 (en) New antibiotics and methods of making them
GB1159970A (en) The Antibiotic Steffisburgensimycin
US3860703A (en) Amides of methobottromycin
JPS57139081A (en) 5-alkylcarbamoyloxy and 5-alkanesulfonyloxy derivative of antibiotic substance b-41 and preparation thereof
JPS57139080A (en) 14,15-epoxy derivative of antibiotic substance b-41 and its preparation
AU613965B2 (en) New anthracycline derivatives, a process for the preparation thereof, and the use thereof as pharmaceuticals
US3767793A (en) Juvenimicin and production thereof
US4248970A (en) Antibiotic complex producing bacterial culture
DD207222A1 (en) PROCESS FOR PREPARING A POLYETHERANT ANTIBIOTICS COMPLEX

Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee