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BE 16627B
Known as:
BE-16627B
, BE16627B
National Institutes of Health
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2006
2006
Apoptotic induction by BE16627B on human malignant glioma cell lines by an anti-matrix metalloproteinase agent
D. Yoshida
,
Kunihiro Watanabe
,
Hiroshi Takahashi
,
Y. Sugisaki
,
A. Teramoto
Brain Tumor Pathology
2006
Corpus ID: 26326355
We have elucidated the pharmacological action of the anti-matrix metalloproteinase inhibitor BE16627B on glioma cells. The study…
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Review
1997
Review
1997
[CDK and MMP inhibitors].
A. Okuyama
,
T. Akiyama
,
M. Nakajima
Gan to kagaku ryoho. Cancer & chemotherapy
1997
Corpus ID: 29237086
CDK inhibitor, Butyrolactone I inhibited CDK1, 2 and 5 in CDKs. In syncronized human lung fibroblast WI38 cells, it inhibited G1…
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1994
1994
Inhibition of Growth of Human Tumor Cells in Nude Mice by a Metalloproteinase Inhibitor
A. Okuyama
,
K. Naito
,
H. Morishima
,
H. Suda
,
S. Nishimura
,
N. Tanaka
International Journal of Cancer
1994
Corpus ID: 38464516
The effects of a new metalloproteinase inhibitor, BE16627B [L-N-(N-hydroxy-2-isobutylsuccinynamoyl)-seryl-L-valine, MW: 375.2…
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1993
1993
Inhibition of metalloproteinase activity of rheumatoid arthritis synovial cells by a new inhibitor [BE16627B;l-N-(N-hydroxy-2-isobutylsuccinamoyl)-seryl-l-valine]
Kyozo Naito
,
Shigeru Nakajima
,
Nobuo Kanbayashi
,
Akira Okuyama
,
M. Goto
Agents and Actions
1993
Corpus ID: 11254020
The effect of a new metalloproteinase (MP) inhibitor [BE16627B;l-N-(N-hydroxy-2-isobutylsuccinamoyl)-seryl-l-valine, MW: 375.2…
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