Y. Hanasaki

发表

Discovery of anti-influenza A virus activity of a corynanthe-type indole alkaloid, hirsutine, in vitro and the structure-activity relationship of natural and synthetic analogs

H. Inoue, H. Takayama, T. Yokota, 1997 .

Inhibition of cholesterol biosynthesis by squalene epoxidase inhibitor avoids apoptotic cell death in L6 myoblasts.

S. Matzno, Y. Hanasaki, N. Nakamura, 1997, Journal of lipid research.

THERMAL BEHAVIOR OF BICYCLO[2.2.2]OCTADIENE-INSTALLED PRECURSORS FOR 2H-ANTHRA[2,3-c]PYRROLES AND ANTHRA [2,3-c] THIOPHENE

Hiroki Uoyama, H. Yamada, T. Okujima, 2010 .

Anti-HIV-1 activity of thiadiazole derivatives: structure-activity relationship, reverse transcriptase inhibition, and lipophilicity.

M. Matsushima, M. Baba, H. Takayama, 1996, Antiviral research.

Potent and specific inhibition of human immunodeficiency virus type 1 replication by 4-(2,6-dichlorophenyl)-1,2,5-thiadiazol-3-Y1 N,N-dialkylcarbamate derivatives

H. Takayama, K. Konno, M. Fujiwara, 1995, Antimicrobial agents and chemotherapy.

RD6-2198, a novel betain-type fluoroalkylated oligomer, inhibits the replications of human immunodeficiency virus type 1 and other enveloped viruses.

M. Baba, H. Sawada, M. Okamoto, 1998, Antiviral research.

Inhibitory effect of hirsutine on influenza virus replication in vitro

H. Takayama, T. Yokota, K. Konno, 1997 .

Thiadiazole derivatives: highly potent and specific HIV-1 reverse transcriptase inhibitors.

H. Takayama, K. Konno, S Sakai, 1995, Journal of medicinal chemistry.

Upregulation of HIV-1 replication in chronically infected cells by ingenol derivatives

M. Baba, M. Okamoto, T. Yokota, 1998, Archives of Virology.

Thiadiazole derivatives as highly potent inhibitor of human immunodeficiency virus type 1 (HIV-1)

M. Baba, H. Takayama, T. Yokota, 1995 .

Characterization of Human Immunodeficiency Virus Type 1 Strains Resistant to the Non-Nucleoside Reverse Transcriptase Inhibitor RD4–2217

H. Mitsuya, M. Baba, E. Kodama, 1999, Antiviral chemistry & chemotherapy.

Thiadiazole Derivatives: Highly Potent and Selective Inhibitors of Human Immunodeficiency Virus Type 1 (HIV‐1) Replications In Vitro

M. Baba, H. Takayama, T. Yokota, 1997, Microbiology and immunology.

Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity

M. Baba, H. Takayama, T. Yokota, 1996 .

Utilization of Wieland Furoxan Synthesis for Preparation of 4-Aryl-1,2, 5-oxadiazole-3-yl Carbamate Derivatives Having Potent Anti-HIV Activity.

M. Baba, H. Takayama, T. Yokota, 1996 .