Combined effects of synthetic lipid A analogs and muramyl dipeptide on antitumor activity against Meth A fibrosarcoma in mice.

[1]  T. Shimizu,et al.  Antitumor activity against Meth A fibrosarcoma and biologic activities of synthetic monosaccharide analogs of lipid A in mice. , 1990, Molecular biotherapy.

[2]  T. Shimizu,et al.  Biological activities of chemically synthesized derivatives of lipid A: tetraacetyl-monosaccharides linked to 2,3-acyloxyacylglucosamine-4-phosphate. , 1989, Chemical & pharmaceutical bulletin.

[3]  M. Kiso,et al.  Enhancement of nonspecific resistance to bacterial infections and tumor regressions by treatment with synthetic lipid A-subunit analogs. Critical role of N- and 3-O-linked acyl groups in 4-O-phosphono-D-glucosamine derivatives. , 1989, International journal of immunopharmacology.

[4]  T. Shimizu,et al.  Antitumor activity, mitogenicity, and lethal toxicity of chemically synthesized monosaccharide analogs of lipid A. , 1988, Journal of pharmacobio-dynamics.

[5]  S. Ikeda,et al.  Antitumor and antimicrobial activities of lipid A-subunit analogue GLA-27. , 1988, Journal of clinical & laboratory immunology.

[6]  Y. Yanagihara,et al.  Biological activities of chemically synthesized N‐acetylneuraminic acid‐(α2→6) ‐monosaccharide analogs of lipid A , 1988, FEBS letters.

[7]  T. Shimizu,et al.  Biological activities of chemically synthesized 2-keto-3-deoxyoctonic acid-(alpha 2----6)-D-glucosamine analogs of lipid A , 1987, Infection and immunity.

[8]  Y. Yanagihara,et al.  Biological Activities of Chemically Synthesized Proteus‐Type Lipid A , 1987, Microbiology and immunology.

[9]  T. Shimizu,et al.  Antitumor activity and lethal toxicity of chemically synthesized tetraacetyl-2-keto-3-deoxyoctonic acid-(alpha 2---6)-D-glucosamine analogues of lipid A. , 1987, Chemical & pharmaceutical bulletin.

[10]  T. Shimizu,et al.  Comparison of biological activities of chemically synthesized monosaccharide analogues of reducing and nonreducing sugar moieties of lipid A. , 1986, Chemical & pharmaceutical bulletin.

[11]  T. Shimizu,et al.  Mitogenic activity of chemically synthesized tetraacetyl-2-keto-3-deoxyoctonic acid-(alpha 2----6)-D-glucosamine analogues of lipid A. , 1986, Chemical & pharmaceutical bulletin.

[12]  J. Iida,et al.  Adjuvant and antitumour activities of synthetic lipid A analogues. , 1986, Vaccine.

[13]  T. Shimizu,et al.  Antitumor activity and biological effects of chemically synthesized monosaccharide analogues of lipid A in mice. , 1985, Chemical & pharmaceutical bulletin.

[14]  T. Yasuda,et al.  Structural requirements of lipid A responsible for the functions: a study with chemically synthesized lipid A and its analogues. , 1985, Journal of biochemistry.

[15]  T. Ogawa,et al.  Synthetic lipid A with endotoxic and related biological activities comparable to those of a natural lipid A from an Escherichia coli re-mutant , 1985, Infection and immunity.

[16]  E. Rietschel,et al.  Synthetic and natural Escherichia coli free lipid A express identical endotoxic activities. , 1985, European journal of biochemistry.

[17]  N. Bloksma,et al.  Endotoxin-induced antitumor activity in the mouse is highly potentiated by muramyl dipeptide. , 1984, Cancer letters.

[18]  H. Shin,et al.  Mechanism of macrophage-mediated cytotoxicity: production of a soluble cytotoxic factor. , 1983, Journal of immunology.

[19]  O. Lüderitz,et al.  Über die Extraktion von Bakterien mit Phenol/Wasser , 1952 .