GB1274518A - Antibiotic 66-40 and methods for its production - Google Patents

Antibiotic 66-40 and methods for its production

Info

Publication number
GB1274518A
GB1274518A GB31887/69A GB3188769A GB1274518A GB 1274518 A GB1274518 A GB 1274518A GB 31887/69 A GB31887/69 A GB 31887/69A GB 3188769 A GB3188769 A GB 3188769A GB 1274518 A GB1274518 A GB 1274518A
Authority
GB
United Kingdom
Prior art keywords
antibiotic
mull
condensation products
aldehydes
ketones
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
GB31887/69A
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.)
Scherico Ltd
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 GB1274518A publication Critical patent/GB1274518A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H15/00Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
    • C07H15/20Carbocyclic rings
    • C07H15/22Cyclohexane rings, substituted by nitrogen atoms
    • C07H15/222Cyclohexane rings substituted by at least two nitrogen atoms
    • C07H15/226Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings
    • C07H15/234Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings attached to non-adjacent ring carbon atoms of the cyclohexane rings, e.g. kanamycins, tobramycin, nebramycin, gentamicin A2
    • C07H15/236Cyclohexane rings substituted by at least two nitrogen atoms with at least two saccharide radicals directly attached to the cyclohexane rings attached to non-adjacent ring carbon atoms of the cyclohexane rings, e.g. kanamycins, tobramycin, nebramycin, gentamicin A2 a saccharide radical being substituted by an alkylamino radical in position 3 and by two substituents different from hydrogen in position 4, e.g. gentamicin complex, sisomicin, verdamycin

Landscapes

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

Abstract

1,274,518. Antibiotic 66-40. SCHERICO Ltd. 24 June, 1969 [27 June, 1968; 16 Dec., 1968], No. 31887/69. Heading C2A. Novel Antibiotic 66-40 having the formula and characterized as being a basic pseudooligosaccharide having the following properties: elemental analysis, C = 49À80, H = 8À20, N = 14À95 and 0=27À05; molecular weight 447À26; empirical formula C 19 H 37 N 5 O 7 .H 2 O; melting point 185-190‹ C.; equivalent weight 92; pKa 8À0; [α]<SP>26‹</SP> D + 188À9‹ (C = 0À3% in H 2 O); U.V. absorption: transparent between 220 and 440 mÁ; I.R. absorption peaks at 2À98, 3À05, 3À16, 3À35- 3À50 (mull), 5À93, 6À25, 6À82 (mull), 7À25 (mull), 8À77, 9À00, 9À47, 9À72-10À07, 10À46, 11À97, 12À75 and 13À45-13À90 Á; and forming hydrates and other solvates, condensation products with aldehydes and ketones and salts with acids, is prepared by aerobically cultivating Micromonospora inyoensis (NRRL 3292). The condensation products, which are probably Schiff bases, are formed by reacting 66-40 with aldehydes and/or ketones such as acetaldehyde, acetone, methyl - ethyl - ketone, crotonaldehyde, furfural, cyclopentylacetaldehyde, vanillin, veratraldehyde, benzophenone, benzaldehyde, acetophenone, salicylaldehyde and pyridoxal. Antibiotic 66-40 has bacteriostatic activity on Gram-positive and Gram-negative bacteria and Rickettsia. Pharmaceutical compositions comprise the antibiotic 66-40 or its acid addition salts or aldehyde or ketone condensation products together with a pharmaceutically acceptable carrier or diluent, and may be in forms for topical, oral or parenteral administration.
GB31887/69A 1968-06-27 1969-06-24 Antibiotic 66-40 and methods for its production Expired GB1274518A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US74074268A 1968-06-27 1968-06-27
US79730468A 1968-12-16 1968-12-16

Publications (1)

Publication Number Publication Date
GB1274518A true GB1274518A (en) 1972-05-17

Family

ID=27113740

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31887/69A Expired GB1274518A (en) 1968-06-27 1969-06-24 Antibiotic 66-40 and methods for its production

Country Status (26)

Country Link
AT (2) AT297929B (en)
BE (1) BE735145A (en)
BG (1) BG15881A3 (en)
BR (1) BR6910078D0 (en)
CA (1) CA931515A (en)
CH (2) CH529743A (en)
CS (1) CS149666B2 (en)
CY (1) CY817A (en)
DE (1) DE1932309C3 (en)
DK (1) DK126510B (en)
ES (1) ES368762A1 (en)
FI (1) FI46177C (en)
FR (1) FR2011732B1 (en)
GB (1) GB1274518A (en)
IE (1) IE33174B1 (en)
IL (1) IL32476A (en)
IT (1) IT1033250B (en)
KE (1) KE2540A (en)
LU (1) LU58942A1 (en)
MY (1) MY7500184A (en)
NL (1) NL155886B (en)
NO (1) NO129960B (en)
OA (1) OA04043A (en)
RO (1) RO57462A (en)
SE (2) SE376425B (en)
YU (1) YU34906B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2452932A1 (en) * 1979-04-04 1980-10-31 Toyo Jozo Kk NOVEL AMINOGLYCOSIDE ANTIBIOTICS AND THEIR PRODUCTION

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5629598A (en) * 1979-08-18 1981-03-24 Toyo Jozo Co Ltd Novel amino sugar antibiotic g-367-2 and its preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2452932A1 (en) * 1979-04-04 1980-10-31 Toyo Jozo Kk NOVEL AMINOGLYCOSIDE ANTIBIOTICS AND THEIR PRODUCTION

Also Published As

Publication number Publication date
FR2011732A1 (en) 1970-03-06
MY7500184A (en) 1975-12-31
DE1932309B2 (en) 1974-06-20
DE1932309A1 (en) 1970-01-29
BE735145A (en) 1969-12-29
BR6910078D0 (en) 1973-02-08
FR2011732B1 (en) 1973-01-12
IE33174L (en) 1969-12-27
DK126510B (en) 1973-07-23
AT299448B (en) 1972-06-26
CA931515A (en) 1973-08-07
RO57462A (en) 1974-12-15
BG15881A3 (en) 1972-04-12
FI46177C (en) 1973-01-10
SE366560B (en) 1974-04-29
CS149666B2 (en) 1973-07-25
FI46177B (en) 1972-10-02
YU34906B (en) 1980-04-30
SE376425B (en) 1975-05-26
DE1932309C3 (en) 1975-02-20
NO129960B (en) 1974-06-17
IT1033250B (en) 1979-07-10
NL155886B (en) 1978-02-15
IE33174B1 (en) 1974-04-03
YU161669A (en) 1979-10-31
CH529833A (en) 1972-10-31
CH529743A (en) 1972-10-31
CY817A (en) 1976-12-01
ES368762A1 (en) 1971-04-01
IL32476A (en) 1972-09-28
LU58942A1 (en) 1969-11-11
KE2540A (en) 1975-07-18
AT297929B (en) 1972-04-10
IL32476A0 (en) 1969-08-27
OA04043A (en) 1979-10-15
NL6909642A (en) 1969-12-30

Similar Documents

Publication Publication Date Title
BE848400A (en) PROCESS FOR SUBSTITUTIVE HALOGENATION OF AROMATIC AND HETEROAROMATIC COMPOUNDS AND PRODUCTS OBTAINED BY THIS PROCESS,
GB1376096A (en) 1-3,4-methylenedioxy-phenyl-4,4-dimethyl-1-pentene derivatives
GB1393521A (en) Berberine derivatives and their use in pharmaceutical compositions
GB1360420A (en) Substituted aminomethyl-dihalophenols
EP0136830A3 (en) Azahomoerythromycin d derivative and intermediates therefor
IE36607L (en) 2 - amino -2&#39;, 6&#39; - propionoxylidide
GB1274518A (en) Antibiotic 66-40 and methods for its production
JPS57203087A (en) Production of antibacterial
Gomez-Lus et al. AAC(3) and AAC(6') Enzymes Produced by R Plasmids Isolated in General Hospital.
IE36781L (en) Antibiotic a477
IE37892B1 (en) Antibiotic a-2315 and process for preparation thereof
GB1418399A (en) Antibiotic derivatives
FR2310336A1 (en) PROCESS FOR THE PRODUCTION OF A 3.5 DISUBSTITUTED 4-HYDROXYBENZALDEHYDE BY FORMYLATION OF A 2.6 DISUBSTITUTED BUTYLPHENOL
GB1462805A (en) Antibiotic and process for the preparation thereof
IE43125L (en) Aminoglycoside derivative
SE8005599L (en) SET TO MAKE AN ANTIBIOTIC
IE40748L (en) Antibiotic 20,798 r.p.
IE38063L (en) Antibiotic g-52
ES8205809A1 (en) 7- alpha -methoxycephalosporin derivatives, and antibacterial drugs onctaining the same
JPS54117478A (en) New antibiotics fortimicin kg1, kg2, and kg3, and their preparation
JPS55151597A (en) New material 2-hydroxysagamicin and its preparation
CA996103A (en) Process for coupling of water-insoluble 2,4-disubstituted phenols with diazotised o-nitroanilines
IE38819L (en) Pivaloyloxymethyl penicillinate
IE34906L (en) Phenylacetonitrile derivatives
JPS5212992A (en) Preparation of antibiotics fa-313

Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PE20 Patent expired after termination of 20 years