Antitumor antibiotics MA 144-M.sub.1 and MA 144-M.sub.2
AssigneeZaidan Hojin Biseibutsu Kagaku Kenkyukai
InventorsHamao Umezawa, Tomio Takeuchi, Hiroshi Naganawa, Masaaki, all of Ishizuka, Norio Shibamoto, Toshikazu Oki, Taiji Inui
Life of this patent
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Abstract
New antitumor agents designated MA 144-M.sub.1 and MA 144-M.sub.2, which are anthracycline glycosides and inhibit the growth of gram-positive bacteria, e.g. Staphyococcus aureaus, Bacillus subtilis and Sarcina lutea, and inhibit the growth of animal tumors such as leukemia L 1210, P 388 and sarcoma 180 are produced by fermentation of MA 144-producing strains of streptomyces and by the chemical or enzymatic conversion of aclacinomycin A or cinerubin A.
Claims12
An anthracycline glycoside selected from the group consisting of a compound of the general formula ##STR4## wherein R represents a hydrogen atom or a hydroxyl group, a nontoxic acid addition salt thereof and a complex thereof with deoxyribonucleic acid, said glycoside being substantially free of substances co-produced therewith.
An anthracycline glycoside of the general formula ##STR5## wherein R represents a hydrogen atom or a hydroxyl group, said glycoside being substantially free of substances coproduced therewith.
A compound selected from the group consisting of the anthracycline glycoside, MA 144-M.sub.1, of the formula ##STR6## a nontoxic acid addition salt thereof and a complex thereof with deoxyribonucleic acid, said compound being substantially free of substancs co-produced therewith.
The anthracycline glycoside, MA 144-M.sub.1, of the formula ##STR7## said glycoside being substantially free of substances co-produced therewith.
A compound selected from the group consisting of the anthracycline glycoside, MA 144-M.sub.2, of the formula ##STR8## a nontoxic acid addition salt thereof and a complex therewith with deoxyribonucleic acid, said compound being substantially free of substances co-produced therewith.
The anthracycline glycoside, MA 144-M.sub.2 of the formula ##STR9## said glycoside being substantially free of substances co-produced therewith.
A pharmaceutical composition in a form suitable for parenteral administration to mammals comprising an effective antibacterial amount of an anthracycline glycoside selected from the group consisting of a compound of the general formula ##STR10## wherein R represents a hydrogen atom or a hydroxyl group, a nontoxic acid addition salt thereof and a complex thereof with deoxyribonucleic acid, said glycoside being substantially free of substances co-produced therewith, in combination with an inert pharmaceutically acceptable carrier or diluent suitable for said administration form.
A pharmaceutical composition in a form suitable for parenteral administration to animals comprising an effective tumor inhibiting amount of an anthracycline glycoside selected from the group consisting of a compound of the general formula ##STR11## wherein R represents a hydrogen atom or a hydroxyl group, a nontoxic acid addition salt thereof and a complex thereof with deoxyribonucleic acid, said glycoside being substantially free of substances co-produced therewith, in combination with an inert pharmaceutically acceptable carrier or diluent suitable for said administration form, said tumor being selected from the group consisting of Leukemia L1210, P388 and Sarcoma 180.
Dependencies are inferred from the claim text.