Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 125

1.

Quantitative Structure-Cytotoxicity Relationship of Chalcones.

Sakagami H, Masuda Y, Tomomura M, Yokose S, Uesawa Y, Ikezoe N, Asahara D, Takao K, Kanamoto T, Terakubo S, Kagaya H, Nakashima H, Sugita Y.

Anticancer Res. 2017 Mar;37(3):1091-1098.

PMID:
28314269
2.

Quantitative Structure-Cytotoxicity Relationship of Newly Synthesized Piperic Acid Esters.

Sakagami H, Uesawa Y, Masuda Y, Tomomura M, Yokose S, Miyashiro T, Murai J, Takao K, Kanamoto T, Terakubo S, Kagaya H, Nakashima H, Sugita Y.

Anticancer Res. 2017 Nov;37(11):6161-6168.

PMID:
29061797
3.

Quantitative Structure-Cytotoxicity Relationship of 2-Azolylchromones.

Sakagami H, Okudaira N, Uesawa Y, Takao K, Kagaya H, Sugita Y.

Anticancer Res. 2018 Feb;38(2):763-770.

PMID:
29374700
4.

Quantitative Structure-Cytotoxicity Relationship of Aurones.

Uesawa Y, Sakagami H, Ikezoe N, Takao K, Kagaya H, Sugita Y.

Anticancer Res. 2017 Nov;37(11):6169-6176.

PMID:
29061798
5.

Quantitative Structure-Cytotoxicity Relationship of Cinnamic Acid Phenetyl Esters.

Uesawa Y, Sakagami H, Okudaira N, Toda K, Takao K, Kagaya H, Sugita Y.

Anticancer Res. 2018 Feb;38(2):817-823.

PMID:
29374707
6.

Quantitative Structure-Cytotoxicity Relationship of 3-(N-Cyclicamino)chromone Derivatives.

Shi H, Nagai J, Sakatsume T, Bandow K, Okudaira N, Uesawa Y, Sakagami H, Tomomura M, Tomomura A, Takao K, Sugita Y.

Anticancer Res. 2018 Aug;38(8):4459-4467. doi: 10.21873/anticanres.12748.

PMID:
30061210
7.

Quantitative Structure-Cytotoxicity Relationship of 2-(N-cyclicamino)chromone Derivatives.

Shi H, Nagai J, Sakatsume T, Bandow K, Okudaira N, Sakagami H, Tomomura M, Tomomura A, Uesawa Y, Takao K, Sugita Y.

Anticancer Res. 2018 Jul;38(7):3897-3906. doi: 10.21873/anticanres.12674.

PMID:
29970510
8.

Quantitative Structure-Cytotoxicity Relationship of Pyrano[4,3-b]chromones.

Nagai J, Shi H, Kubota Y, Bandow K, Okudaira N, Uesawa Y, Sakagami H, Tomomura M, Tomomura A, Takao K, Sugita Y.

Anticancer Res. 2018 Aug;38(8):4449-4457. doi: 10.21873/anticanres.12747.

PMID:
30061209
9.

Quantitative Structure-Cytotoxicity Relationship of Furo[2,3-b]chromones.

Uesawa Y, Sakagami H, Shi H, Hirose M, Takao K, Sugita Y.

Anticancer Res. 2018 Jun;38(6):3283-3290. doi: 10.21873/anticanres.12593.

PMID:
29848675
10.

Quantitative Structure-Cytotoxicity Relationship of 3-Styryl-2H-chromenes.

Uesawa Y, Sakagami H, Ishihara M, Kagaya H, Kanamoto T, Terakubo S, Nakashima H, Yahagi H, Takao K, Sugita Y.

Anticancer Res. 2015 Oct;35(10):5299-307.

PMID:
26408690
11.

Quantitative Structure-Cytotoxicity Relationship of Oleoylamides.

Sakagami H, Uesawa Y, Ishihara M, Kagaya H, Kanamoto T, Terakubo S, Nakashima H, Takao K, Sugita Y.

Anticancer Res. 2015 Oct;35(10):5341-51.

PMID:
26408695
12.

Quantitative structure-cytotoxicity relationship of phenylpropanoid amides.

Shimada C, Uesawa Y, Ishihara M, Kagaya H, Kanamoto T, Terakubo S, Nakashima H, Takao K, Saito T, Sugita Y, Sakagami H.

Anticancer Res. 2014 Jul;34(7):3543-8.

PMID:
24982367
13.

Quantitative structure-cytotoxicity relationship of 3-styrylchromones.

Shimada C, Uesawa Y, Ishii-Nozawa R, Ishihara M, Kagaya H, Kanamoto T, Terakubo S, Nakashima H, Takao K, Sugita Y, Sakagami H.

Anticancer Res. 2014 Oct;34(10):5405-11.

PMID:
25275035
14.

Quantitative Structure-cytotoxicity Relationship of 3-Benzylidenechromanones.

Uesawa Y, Sakagami H, Kagaya H, Yamashita M, Takao K, Sugita Y.

Anticancer Res. 2016 Nov;36(11):5803-5812.

PMID:
27793902
15.

In Vitro Anti-tumor Activity of Azulene Amide Derivatives.

Wada T, Maruyama R, Irie Y, Hashimoto M, Wakabayashi H, Okudaira N, Uesawa Y, Kagaya H, Sakagami H.

In Vivo. 2018 May-Jun;32(3):479-486.

16.

Quantitative Structure-Cytotoxicity Relationship of 2-Arylazolylchromones and 2-Triazolylchromones.

Nagai J, Shi H, Sezaki N, Yoshida N, Bandow K, Uesawa Y, Sakagami H, Tomomura M, Tomomura A, Takao K, Sugita Y.

Anticancer Res. 2019 Dec;39(12):6479-6488. doi: 10.21873/anticanres.13862.

PMID:
31810912
17.

Quantitative Structure-Cytotoxicity Relationship of Azulene Amide Derivatives.

Imanari K, Hashimoto M, Wakabayashi H, Okudaira N, Bandow K, Nagai J, Tomomura M, Tomomura A, Uesawa Y, Sakagami H.

Anticancer Res. 2019 Jul;39(7):3507-3518. doi: 10.21873/anticanres.13497.

PMID:
31262875
18.

Synthesis and Cytotoxic Activities of Difluoro-Dimethoxy Chalcones.

Yamali C, Gul HI, Ozgun DO, Sakagam H, Umemura N, Kazaz C, Gul M.

Anticancer Agents Med Chem. 2017;17(10):1426-1433. doi: 10.2174/1871520617666170327123909.

PMID:
28356013
19.

Quantitative Structure-Cytotoxicity Relationship of 2-Styrylchromones.

Uesawa Y, Nagai J, Shi H, Sakagami H, Bandow K, Tomomura A, Tomomura M, Endo S, Takao K, Sugita Y.

Anticancer Res. 2019 Dec;39(12):6489-6498. doi: 10.21873/anticanres.13863.

PMID:
31810913
20.

Enhancement of Cytotoxicity of Three Apoptosis-inducing Agents Against Human Oral Squamous Cell Carcinoma Cell Line by Benzoxazinotropone.

Tomikoshi Y, Nomura M, Okudaira N, Sakagami H, Wakabayashi H.

In Vivo. 2016 09-10;30(5):645-50.

PMID:
27566085

Supplemental Content

Support Center