Thrazarine, a new antitumor antibiotic. I. Taxonomy, fermentation, isolation and biological properties. 1988

T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
Institute of Microbial Chemistry, Tokyo, Japan.

Thrazarine, O-[(3R)-2-diazo-3-hydroxybutyryl)]-L-serine, is a new antitumor antibiotic produced by Streptomyces coerulescens MH802-fF5. Thrazarine was isolated from culture filtrate by Sephadex LH-20 column chromatography and reversed phase HPLC. Thrazarine induced cytolysis of tumor cell lines co-cultured with nonactivated macrophages. This effect was tumor specific because the nontumorigenic cells were not lysed by macrophages in the presence of thrazarine. Thrazarine inhibited DNA synthesis and growth of tumor cells directly. It showed neither antimicrobial activity nor the inhibition of transamidation reactions in contrast to azaserine. Toxicities of thrazarine were much weaker than those of azaserine.

UI MeSH Term Description Entries
D008264 Macrophages The relatively long-lived phagocytic cell of mammalian tissues that are derived from blood MONOCYTES. Main types are PERITONEAL MACROPHAGES; ALVEOLAR MACROPHAGES; HISTIOCYTES; KUPFFER CELLS of the liver; and OSTEOCLASTS. They may further differentiate within chronic inflammatory lesions to EPITHELIOID CELLS or may fuse to form FOREIGN BODY GIANT CELLS or LANGHANS GIANT CELLS. (from The Dictionary of Cell Biology, Lackie and Dow, 3rd ed.) Bone Marrow-Derived Macrophages,Monocyte-Derived Macrophages,Macrophage,Macrophages, Monocyte-Derived,Bone Marrow Derived Macrophages,Bone Marrow-Derived Macrophage,Macrophage, Bone Marrow-Derived,Macrophage, Monocyte-Derived,Macrophages, Bone Marrow-Derived,Macrophages, Monocyte Derived,Monocyte Derived Macrophages,Monocyte-Derived Macrophage
D005285 Fermentation Anaerobic degradation of GLUCOSE or other organic nutrients to gain energy in the form of ATP. End products vary depending on organisms, substrates, and enzymatic pathways. Common fermentation products include ETHANOL and LACTIC ACID. Fermentations
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006885 Hydroxybutyrates Salts and esters of hydroxybutyric acid. Hydroxybutyric Acid Derivatives,Hydroxybutyric Acids,Acid Derivatives, Hydroxybutyric
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000903 Antibiotics, Antineoplastic Chemical substances, produced by microorganisms, inhibiting or preventing the proliferation of neoplasms. Antineoplastic Antibiotics,Cytotoxic Antibiotics,Antibiotics, Cytotoxic
D001377 Azaserine Antibiotic substance produced by various Streptomyces species. It is an inhibitor of enzymatic activities that involve glutamine and is used as an antineoplastic and immunosuppressive agent. Azeserine,LL-D05139a,O-Diazoacetyl-L-serine,O Diazoacetyl L serine
D012694 Serine A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids. L-Serine,L Serine
D013302 Streptomyces A genus of bacteria that form a nonfragmented aerial mycelium. Many species have been identified with some being pathogenic. This genus is responsible for producing a majority of the ANTI-BACTERIAL AGENTS of practical value.
D014407 Tumor Cells, Cultured Cells grown in vitro from neoplastic tissue. If they can be established as a TUMOR CELL LINE, they can be propagated in cell culture indefinitely. Cultured Tumor Cells,Neoplastic Cells, Cultured,Cultured Neoplastic Cells,Cell, Cultured Neoplastic,Cell, Cultured Tumor,Cells, Cultured Neoplastic,Cells, Cultured Tumor,Cultured Neoplastic Cell,Cultured Tumor Cell,Neoplastic Cell, Cultured,Tumor Cell, Cultured

Related Publications

T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
January 1972, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
August 1991, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
July 1987, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
June 1981, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
November 1989, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
November 1994, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
February 1989, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
November 1993, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
November 2003, The Journal of antibiotics,
T Kameyama, and A Takahashi, and H Matsumoto, and S Kurasawa, and M Hamada, and Y Okami, and M Ishizuka, and T Takeuchi
September 1987, The Journal of antibiotics,
Copied contents to your clipboard!