JPS6440496A - Novel macrolide antibiotic substance mycinamicins and production thereof - Google Patents

Novel macrolide antibiotic substance mycinamicins and production thereof

Info

Publication number
JPS6440496A
JPS6440496A JP19554887A JP19554887A JPS6440496A JP S6440496 A JPS6440496 A JP S6440496A JP 19554887 A JP19554887 A JP 19554887A JP 19554887 A JP19554887 A JP 19554887A JP S6440496 A JPS6440496 A JP S6440496A
Authority
JP
Japan
Prior art keywords
reaction
mycinamicins
production
color
macrolide antibiotic
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.)
Pending
Application number
JP19554887A
Other languages
Japanese (ja)
Inventor
Mitsuo Hayashi
Satoshi Takenaka
Kenji Kinoshita
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.)
Toyo Jozo KK
Original Assignee
Toyo Jozo KK
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 Toyo Jozo KK filed Critical Toyo Jozo KK
Priority to JP19554887A priority Critical patent/JPS6440496A/en
Publication of JPS6440496A publication Critical patent/JPS6440496A/en
Pending legal-status Critical Current

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  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Saccharide Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

NEW MATERIAL:The compound of formula (R is H or OH) or its salt. Mycinamicin X has the following physical and chemical properties. Color and appearance, white powder; molecular formula, C42H70N2O15S; elemental analysis (%), C 56.51, H 8.23, N 3.11, S 3.44; molecular weight, 875.08; TLC (silica gel), 0.52; color reaction, positive to decoloration of KMnO4 aqueous solution and negative to ninhydrin reaction, Sakaguchi's reaction and FeCl3 reaction; solubility, soluble in water and alcohol such as methanol, hardly soluble in acetone and insoluble in ethyl acetate, benzene, etc.; acidity or basicity, ampholytic; etc. USE:Antibacterial agent. PREPARATION:The objective compound can be produced by culturing a microbial strain belonging to Micromonospora genus and capable of producing mycinamicins [e.g. Micromonospora griseorubida A11725 (FERM BP-705)].
JP19554887A 1987-08-05 1987-08-05 Novel macrolide antibiotic substance mycinamicins and production thereof Pending JPS6440496A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19554887A JPS6440496A (en) 1987-08-05 1987-08-05 Novel macrolide antibiotic substance mycinamicins and production thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19554887A JPS6440496A (en) 1987-08-05 1987-08-05 Novel macrolide antibiotic substance mycinamicins and production thereof

Publications (1)

Publication Number Publication Date
JPS6440496A true JPS6440496A (en) 1989-02-10

Family

ID=16342930

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19554887A Pending JPS6440496A (en) 1987-08-05 1987-08-05 Novel macrolide antibiotic substance mycinamicins and production thereof

Country Status (1)

Country Link
JP (1) JPS6440496A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001063822A (en) * 1999-08-30 2001-03-13 Watanabe Shoko:Kk Levitation conveying method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001063822A (en) * 1999-08-30 2001-03-13 Watanabe Shoko:Kk Levitation conveying method

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