Fig. 12 in Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity
Fig. 12. Inhibitory activity tests of gravitropic bending and elongation for quinoline and quinoxaline analogues 4: (a) 50 μM for 4a-4d, (b) 0.05–50 μM for 4a, (c) 0.05–50 μM for 4b. Data for gravitropic bending (left) and elongation (right) represent the mean ± SD. Asterisk indicates statistically...
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| creator | Shindo, Mitsuru Makigawa, Saki Kodama, Kozue Sugiyama, Hiromi Matsumoto, Kenji Iwata, Takayuki Wasano, Naoya Kano, Arihiro Morita, Miyo Terao Fujii, Yoshiharu |
| description | Fig. 12. Inhibitory activity tests of gravitropic bending and elongation for quinoline and quinoxaline analogues 4: (a) 50 μM for 4a-4d, (b) 0.05–50 μM for 4a, (c) 0.05–50 μM for 4b. Data for gravitropic bending (left) and elongation (right) represent the mean ± SD. Asterisk indicates statistically significant differences between treatments and controls at p |
| doi_str_mv | 10.5281/zenodo.8293337 |
| format | Image |
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Inhibitory activity tests of gravitropic bending and elongation for quinoline and quinoxaline analogues 4: (a) 50 μM for 4a-4d, (b) 0.05–50 μM for 4a, (c) 0.05–50 μM for 4b. Data for gravitropic bending (left) and elongation (right) represent the mean ± SD. 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Inhibitory activity tests of gravitropic bending and elongation for quinoline and quinoxaline analogues 4: (a) 50 μM for 4a-4d, (b) 0.05–50 μM for 4a, (c) 0.05–50 μM for 4b. Data for gravitropic bending (left) and elongation (right) represent the mean ± SD. 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Inhibitory activity tests of gravitropic bending and elongation for quinoline and quinoxaline analogues 4: (a) 50 μM for 4a-4d, (b) 0.05–50 μM for 4a, (c) 0.05–50 μM for 4b. Data for gravitropic bending (left) and elongation (right) represent the mean ± SD. Asterisk indicates statistically significant differences between treatments and controls at p <0.05 (Dunnett's test, n = 7).</abstract><pub>Zenodo</pub><doi>10.5281/zenodo.8293337</doi><oa>free_for_read</oa></addata></record> |
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| title | Fig. 12 in Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity |
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