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Dive into the research topics where Mitsunobu Hara is active.

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Featured researches published by Mitsunobu Hara.


Bioorganic & Medicinal Chemistry Letters | 2001

Synthesis of tetrocarcin derivatives with specific inhibitory activity towards Bcl-2 functions

Masami Kaneko; Takayuki Nakashima; Yuko Uosaki; Mitsunobu Hara; Shun-ichi Ikeda; Yutaka Kanda

Tetrocarcin A was recently identified as an inhibitor of the anti-apoptotic function of Bcl-2. We synthesized novel tetrocarcin derivatives in order to increase their selective inhibitory activity against Bcl-2. It was found that 21-acetoxy-9-glycosyloxy derivatives had potent Bcl-2 inhibitory activity without significant antimicrobial activity.


Biochemical and Biophysical Research Communications | 1984

High pressure NMR studies of hemoproteins. The effect of pressure on the quaternary structure of hemoglobin

Isao Morishima; Mitsunobu Hara

Proton NMR spectra for nitrosyl-, aquomet - and deoxy des-Arg (alpha 141)-hemoglobin in H2O were studied at high pressures up to 1400 atm with attention to the exchangeable proton resonances due to the intra- and intersubunit hydrogen bonds. For aquomethemoglobin , the T state marker signal at 6.4 ppm is insensitive to pressure while the R state marker signal at 6.0 ppm exhibits progressive upfield shift upon pressurization . For nitrosylhemoglobin, the T state signals at 9.6 and 6.5 ppm decrease their intensities upon pressurization while the R state marker signal at 6. 0 ppm remains unchanged. Pressure-induced spectral changes for some of exchangeable resonances are also encountered for deoxy des-Arg (alpha 141)-hemoglobin while the R and T quaternary structural indicators at 6.0 and 9.4 ppm are insensitive to pressure. These pressure-induced spectral changes for these hemoglobin derivatives are significantly distinguished from those associated with the R-T transition induced by addition of IHP or by variation of pH. It is therefore concluded that pressure induces subtle quaternary structural changes in these hemoglobin derivatives without causing the R-T transition.


Journal of the American Chemical Society | 1996

Thiol-Mediated DNA Alkylation by the Novel Antitumor Antibiotic Leinamycin

Akira Asai; Mitsunobu Hara; Shingo Kakita; Yutaka Kanda; Mayumi Yoshida; Hiromitsu Saito; Yutaka Saitoh


Biochemistry | 1990

DNA strand scission by the novel antitumor antibiotic leinamycin

Mitsunobu Hara; Yutaka Saitoh; Hirofumi Nakano


Journal of Medicinal Chemistry | 2003

Discovery and Structure−Activity Relationships of Novel Piperidine Inhibitors of Farnesyltransferase

Shinji Nara; Rieko Tanaka; Jun Eishima; Mitsunobu Hara; Yuichi Takahashi; Shizuo Otaki; Robert J. Foglesong; Philip F. Hughes; Shelley Turkington; Yutaka Kanda


Biochemistry | 1983

High-pressure nuclear magnetic resonance studies of hemoproteins. Pressure-induced structural changes in the heme environments of ferric low-spin metmyoglobin complexes.

Isao Morishima; Mitsunobu Hara


Biochemistry | 1990

Covalent modification and single-strand scission of DNA by a new antitumor antibiotic Kapurimycin A3

Mitsunobu Hara; Mayumi Yoshida; Hirofumi Nakano


Journal of the American Chemical Society | 1982

High-pressure NMR studies of hemoproteins. Pressure-induced structural changes in the heme environments of cyanometmyoglobin

Isao Morishima; Mitsunobu Hara


Bioorganic & Medicinal Chemistry | 2007

Design and synthesis of piperidine farnesyltransferase inhibitors with reduced glucuronidation potential.

Rieko Tanaka; Almudena Rubio; Nancy K. Harn; Douglas Linn Gernert; Timothy Alan Grese; Jun Eishima; Mitsunobu Hara; Nobuyuki Yoda; Rui Ohashi; Takashi Kuwabara; Shiro Soga; Shiro Akinaga; Shinji Nara; Yutaka Kanda


Archive | 2000

2-piperidone compounds for the treatment of cancer

Yutaka Kanda; Rieko Tanaka; Mitsunobu Hara; Jun Eishima; Shiro Akinaga; Tadashi Ashizawa

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Yutaka Kanda

University of Texas MD Anderson Cancer Center

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