高等学校化学学报 ›› 2017, Vol. 38 ›› Issue (1): 35.doi: 10.7503/cjcu20160654
肖维, 阮祥辉, 李琴, 张菊平, 钟新敏, 谢艳, 王晓斌, 黄民国, 薛伟()
收稿日期:
2016-09-19
出版日期:
2017-01-10
发布日期:
2016-12-15
作者简介:
联系人简介: 薛 伟, 男, 博士, 教授, 主要从事新农药和新医药创制研究. E-mail: 基金资助:
XIAO Wei, RUAN Xianghui, LI Qin, ZHANG Juping, ZHONG Xinmin, XIE Yan, WANG Xiaobin, HUANG Minguo, XUE Wei*()
Received:
2016-09-19
Online:
2017-01-10
Published:
2016-12-15
Contact:
XUE Wei
E-mail:wxue@gzu.edu.cn
Supported by:
摘要:
以杨梅素为先导化合物, 设计合成了12个酰胺类杨梅素衍生物; 利用核磁共振波谱(1H NMR和13C NMR)和高分辨质谱仪(HRMS)对其结构进行了确证. 初步抑菌活性测定结果表明, 该类化合物对水稻白叶枯病菌、 柑橘溃疡病菌和烟草青枯病菌均具有一定的抑制活性, 化合物3a, 3e, 3f, 3h和3k对3种植物病菌表现出较好的抑制活性, 其中200 μg/mL化合物3e对水稻白叶枯病菌和烟草青枯病菌的抑制活性均为100%, 超过对照药叶枯唑(抑菌活性分别为72.85%和75.86%).
中图分类号:
TrendMD:
肖维, 阮祥辉, 李琴, 张菊平, 钟新敏, 谢艳, 王晓斌, 黄民国, 薛伟. 酰胺类杨梅素衍生物的合成及抑菌活性. 高等学校化学学报, 2017, 38(1): 35.
XIAO Wei, RUAN Xianghui, LI Qin, ZHANG Juping, ZHONG Xinmin, XIE Yan, WANG Xiaobin, HUANG Minguo, XUE Wei. Synthesis and Antibacterial Activities of Myricetin Derivatives ontaining Acidamide Moiety†. Chem. J. Chinese Universities, 2017, 38(1): 35.
Compd. | m. p./℃ | Compd. | m. p./℃ | Compd. | m. p./℃ |
---|---|---|---|---|---|
1a | 128—129(130—131[ | 1f | 102—104(106[ | 1j | 85—87(88—90[ |
1b | 98—100(99—100[ | 1g | 47—49(48—49[ | 1k | 89—90(91—92[ |
1c | 90—91(89—90[ | 1h | 118—120(120—122[ | 1l | 77—79(80—82[ |
1d | 95—97(96.5[ | 1i | 170—171(169[ | 2 | 234—235(232—234[ |
1e | 92—93(93.4—94.8[ |
Table 1 Melting points of compounds 1a—1i and 2
Compd. | m. p./℃ | Compd. | m. p./℃ | Compd. | m. p./℃ |
---|---|---|---|---|---|
1a | 128—129(130—131[ | 1f | 102—104(106[ | 1j | 85—87(88—90[ |
1b | 98—100(99—100[ | 1g | 47—49(48—49[ | 1k | 89—90(91—92[ |
1c | 90—91(89—90[ | 1h | 118—120(120—122[ | 1l | 77—79(80—82[ |
1d | 95—97(96.5[ | 1i | 170—171(169[ | 2 | 234—235(232—234[ |
1e | 92—93(93.4—94.8[ |
Compd. | R | Appearance | Yield(%) | m. p./℃ | HRMS(Calcd.)[M+H]+ |
---|---|---|---|---|---|
3a | 4-F-Phenyl | White solid | 43.2 | 196—198 | 540.1664(540.1659) |
3b | 3-Cl-Phenyl | White solid | 46.2 | 167—169 | 556.1369(556.1364) |
3c | Phenyl | White solid | 62.6 | 183—184 | 522.1759(522.1751) |
3d | n-Butyl | White solid | 56.2 | 181—182 | 502.2064(502.2072) |
3e | Benzyl | White solid | 49.3 | 158—160 | 536.1915(536.1904) |
3f | Cyclohexyl | White solid | 56.4 | 150—151 | 528.2228(528.2222) |
3g | 2-OCH3-Phenyl | White solid | 71.8 | 193—195 | 552.1864(552.1855) |
3h | 4-OCH3-Phenyl | White solid | 63.4 | 117—119 | 552.1864(552.1856) |
3i | 4-Cl-Phenyl | White solid | 47.2 | 233—235 | 556.1369(556.1368) |
3j | 2-F-Phenyl | White solid | 64.7 | 122—124 | 540.1664(540.1659) |
3k | 2-CH2CH3-Phenyl | White solid | 30.8 | 199—200 | 550.2072(550.2063) |
3l | Cyclopentyl | White solid | 51.6 | 192—194 | 514.2072(514.2064) |
Table 2 Appearance, yields, melting points and HRMS data for compounds 3a—3l
Compd. | R | Appearance | Yield(%) | m. p./℃ | HRMS(Calcd.)[M+H]+ |
---|---|---|---|---|---|
3a | 4-F-Phenyl | White solid | 43.2 | 196—198 | 540.1664(540.1659) |
3b | 3-Cl-Phenyl | White solid | 46.2 | 167—169 | 556.1369(556.1364) |
3c | Phenyl | White solid | 62.6 | 183—184 | 522.1759(522.1751) |
3d | n-Butyl | White solid | 56.2 | 181—182 | 502.2064(502.2072) |
3e | Benzyl | White solid | 49.3 | 158—160 | 536.1915(536.1904) |
3f | Cyclohexyl | White solid | 56.4 | 150—151 | 528.2228(528.2222) |
3g | 2-OCH3-Phenyl | White solid | 71.8 | 193—195 | 552.1864(552.1855) |
3h | 4-OCH3-Phenyl | White solid | 63.4 | 117—119 | 552.1864(552.1856) |
3i | 4-Cl-Phenyl | White solid | 47.2 | 233—235 | 556.1369(556.1368) |
3j | 2-F-Phenyl | White solid | 64.7 | 122—124 | 540.1664(540.1659) |
3k | 2-CH2CH3-Phenyl | White solid | 30.8 | 199—200 | 550.2072(550.2063) |
3l | Cyclopentyl | White solid | 51.6 | 192—194 | 514.2072(514.2064) |
Compd. | 1H NMR(DMSO-d6, 500 MHz), δ | 13C NMR(DMSO-d6, 125 MHz), δ |
---|---|---|
3a | 10.40(s, 1H), 7.64(s, 2H), 7.43(s, 2H), 7.15(d, J=8.9 Hz, 2H), 6.87(d, J=2.2 Hz, 1H), 6.51(d, J=2.2 Hz, 1H), 4.55(s, 2H), 3.88(s, 3H), 3.83(d, J=4.9 Hz, 9H), 3.70(s, 3H) | 172.94, 167.14, 164.61, 160.90, 159.71, 158.78, 157.80, 153.34, 152.43, 140.18, 140.12, 135.29, 125.67, 121.76, 115.97, 108.74, 106.50, 96.72, 93.76, 71.46, 60.71, 60.30, 56.76, 56.65 |
3b | 10.52(s, 1H), 7.80(s, 1H), 7.51(t, J=9.9 Hz, 1H), 7.41(s, 2H), 7.32(d, J=8.2 Hz, 1H), 7.16—7.10(m, 1H), 6.86(s, 1H), 6.50(s, 1H), 4.57(s, 2H), 3.88(s, 3H), 3.83(s, 9H), 3.70(d, J=0.7 Hz, 3H) | 172.96, 167.70, 164.62, 160.89, 158.77, 153.33, 152.44, 140.36, 140.17, 140.12, 133.59, 131.03, 125.64, 123.92, 119.44, 118.40, 108.71, 106.50, 96.71, 93.75, 71.53, 60.70, 56.74, 56.64, 56.36 |
3c | 10.34(s, 1H), 7.61(d, J=8.1 Hz, 2H), 7.44(s, 2H), 7.29(t, J=7.7 Hz, 2H), 7.05(dd, J=10.7, 4.1 Hz, 1H), 6.87(d, J=1.5 Hz, 1H), 6.50(d, J=1.5 Hz, 1H), 4.55(s, 2H), 3.88(s, 3H), 3.83(d, J=2.9 Hz, 9H), 3.71(d, J=0.7 Hz, 3H) | 172.99, 167.20, 164.61, 160.89, 158.78, 153.34, 152.42, 140.20, 138.88, 129.31, 125.68, 124.21, 119.98, 108.73, 106.49, 96.72, 93.75, 71.56, 60.71, 56.76, 56.65 |
3d | 8.21(t, J=5.6 Hz, 1H), 7.38(s, 2H), 6.83(d, J=2.1 Hz, 1H), 6.48(d, J=2.1 Hz, 1H), 4.32(s, 2H), 3.87(s, 3H), 3.83(d, J=7.5 Hz, 9H), 3.72(s, 3H), 3.07(dd, J=13.1, 6.7 Hz, 2H), 1.39—1.33(m, 2H), 1.22(dd, J=14.9, 7.4 Hz, 2H), 0.83(t, J=7.3 Hz, 3H) | 172.65, 167.99, 164.51, 160.86, 158.74, 153.34, 152.42, 140.13, 139.80, 125.70, 108.79, 106.41, 96.64, 93.72, 70.92, 60.71, 56.70, 56.65, 38.45, 31.70, 20.05, 14.19 |
3e | 8.80(t, J=5.9 Hz, 1H), 7.39(s, 2H), 7.24(tt, J=14.1, 7.2 Hz, 5H), 6.84(s, 1H), 6.49(s, 1H), 4.43(s, 2H), 4.30(d, J=5.9 Hz, 2H), 3.87(s, 3H), 3.82(s, 3H), 3.78(s, 6H), 3.71(d, J=0.8 Hz, 3H) | 172.62, 168.29, 164.52, 160.86, 158.73, 153.33, 152.39, 140.12, 139.74, 139.68, 128.76, 127.81, 127.33, 125.69, 108.79, 106.39, 96.65, 93.72, 70.72, 60.71, 56.70, 56.65, 56.61, 42.30 |
3f | 7.96(d, J=7.9 Hz, 1H), 7.38(d, J=1.4 Hz, 2H), 6.81(s, 1H), 6.47(s, 1H), 4.30(s, 2H), 3.87(d, J=1.3 Hz, 3H), 3.84(d, J=1.3 Hz, 6H), 3.82(s, 3H), 3.72(d, J=1.5 Hz, 3H), 1.64(d, J=8.0 Hz, 4H), 1.51(d, J=11.9 Hz, 1H), 1.25—1.03(m, 6H) | 172.65, 167.07, 164.48, 160.85, 158.72, 153.35, 152.39, 140.10, 139.93, 125.72, 108.79, 106.44, 96.63, 93.68, 70.99, 60.68, 56.68, 56.62, 47.83, 32.73, 25.67, 25.13 |
3g | 9.49(s, 1H), 8.05(d, J=7.8 Hz, 1H), 7.33(d, J=1.4 Hz, 2H), 7.04(dd, J=17.6, 7.8 Hz, 2H), 6.90(t, J=7.5 Hz, 1H), 6.84(s, 1H), 6.50(s, 1H), 4.59(d, J=0.7 Hz, 2H), 3.88(d, J=1.6 Hz, 3H), 3.82(d, J=1.4 Hz, 3H), 3.80(d, J=1.5 Hz, 6H), 3.75(d, J=1.5 Hz, 3H), 3.70(d, J=1.7 Hz, 3H) | 172.65, 166.94, 164.57, 160.88, 158.81, 153.37, 152.70, 149.52, 140.11, 139.94, 127.11, 125.65, 125.06, 121.03, 120.94, 111.64, 108.77, 106.35, 96.69, 93.75, 71.65, 60.70, 56.71, 56.65, 56.55, 56.29 |
3h | 10.21(s, 1H), 7.52(d, J=9.0 Hz, 2H), 7.43(s, 2H), 6.86(dd, J=5.5, 3.3 Hz, 3H), 6.50(d, J=2.0 Hz, 1H), 4.51(s, 2H), 3.88(s, 3H), 3.83(d, J=3.7 Hz, 9H), 3.71(s, 3H), 3.69(s, 3H) | 172.95, 166.65, 164.60, 160.89, 158.78, 156.01, 153.34, 152.43, 140.16, 131.99, 125.68, 121.54, 114.40, 108.73, 106.48, 96.71, 93.75, 71.51, 60.72, 56.75, 56.65, 55.69 |
3i | 10.48(s, 1H), 7.66(s, 1H), 7.65(s, 1H), 7.43(s, 2H), 7.36(d, J=8.8 Hz, 2H), 6.87(d, J=2.2 Hz, 1H), 6.51(d, J=2.2 Hz, 1H), 4.56(s, 2H), 3.88(s, 3H), 3.83(d, J=4.5 Hz, 9H), 3.70(s, 3H) | 172.96, 167.42, 164.63, 160.89, 158.78, 153.33, 152.45, 140.11, 137.87, 132.08, 129.23, 127.79, 125.66, 121.54, 108.71, 106.49, 96.72, 93.76, 71.49, 65.57, 60.71, 56.78, 56.64 |
3j | 8.40(s, 1H), 7.39(s, 2H), 7.23(dd, J=14.0, 6.6 Hz, 2H), 7.14—7.02(m, 2H), 6.85(s, 1H), 6.49(s, 1H), 4.33(s, 2H), 3.88(s, 3H), 3.83(s, 9H), 3.71(d, J=0.9 Hz, 3H) | 172.62, 168.23, 164.53, 162.17, 160.87, 158.74, 153.34, 152.37, 140.13, 139.75, 131.62, 128.83, 124.86, 115.72, 115.54, 108.79, 106.41, 96.66, 93.73, 70.80, 60.71, 56.72, 56.66 |
3k | 9.84(s, 1H), 7.40(d, J=11.4 Hz, 3H), 7.24—7.19(m, 1H), 7.18—7.10(m, 2H), 6.87(d, J=2.2 Hz, 1H), 6.51(d, J=2.1 Hz, 1H), 4.57(s, 2H), 3.88(s, 3H), 3.83(d, J=4.9 Hz, 9H), 3.71(s, 3H), 2.58—2.52(m, 2H), 1.07(t, J=7.5 Hz, 3H) | 173.00, 167.48, 164.63, 160.91, 158.82, 153.39, 152.62, 140.31, 140.18, 137.87, 135.46, 129.10, 126.57, 126.24, 125.70, 108.73, 106.51, 96.73, 93.76, 71.77, 60.71, 56.75, 56.68, 24.15, 14.59 |
Compd. | 1H NMR(DMSO-d6, 500 MHz), δ | 13C NMR(DMSO-d6, 125 MHz), δ |
3l | 8.11(d, J=7.3 Hz, 1H), 7.39(s, 2H), 6.84(d, J=1.6 Hz, 1H), 6.49(d, J=1.7 Hz, 1H), 4.30(s, 2H), 3.99(dd, J=14.0, 6.9 Hz, 1H), 3.87(s, 3H), 3.83(d, J = 10.0 Hz, 9H), 3.72(s, 3H), 1.74(d, J=6.3 Hz, 2H), 1.59(s, 2H), 1.45(d, J=4.3 Hz, 2H), 1.38—1.29(m, 2H) | 172.73, 167.55, 164.52, 160.87, 158.74, 153.35, 152.39, 140.12, 140.02, 125.73, 108.80, 106.46, 96.67, 93.72, 71.10, 60.70, 56.69, 50.51, 32.59, 23.93 |
Table 3 1H NMR data of compounds 3a—3l
Compd. | 1H NMR(DMSO-d6, 500 MHz), δ | 13C NMR(DMSO-d6, 125 MHz), δ |
---|---|---|
3a | 10.40(s, 1H), 7.64(s, 2H), 7.43(s, 2H), 7.15(d, J=8.9 Hz, 2H), 6.87(d, J=2.2 Hz, 1H), 6.51(d, J=2.2 Hz, 1H), 4.55(s, 2H), 3.88(s, 3H), 3.83(d, J=4.9 Hz, 9H), 3.70(s, 3H) | 172.94, 167.14, 164.61, 160.90, 159.71, 158.78, 157.80, 153.34, 152.43, 140.18, 140.12, 135.29, 125.67, 121.76, 115.97, 108.74, 106.50, 96.72, 93.76, 71.46, 60.71, 60.30, 56.76, 56.65 |
3b | 10.52(s, 1H), 7.80(s, 1H), 7.51(t, J=9.9 Hz, 1H), 7.41(s, 2H), 7.32(d, J=8.2 Hz, 1H), 7.16—7.10(m, 1H), 6.86(s, 1H), 6.50(s, 1H), 4.57(s, 2H), 3.88(s, 3H), 3.83(s, 9H), 3.70(d, J=0.7 Hz, 3H) | 172.96, 167.70, 164.62, 160.89, 158.77, 153.33, 152.44, 140.36, 140.17, 140.12, 133.59, 131.03, 125.64, 123.92, 119.44, 118.40, 108.71, 106.50, 96.71, 93.75, 71.53, 60.70, 56.74, 56.64, 56.36 |
3c | 10.34(s, 1H), 7.61(d, J=8.1 Hz, 2H), 7.44(s, 2H), 7.29(t, J=7.7 Hz, 2H), 7.05(dd, J=10.7, 4.1 Hz, 1H), 6.87(d, J=1.5 Hz, 1H), 6.50(d, J=1.5 Hz, 1H), 4.55(s, 2H), 3.88(s, 3H), 3.83(d, J=2.9 Hz, 9H), 3.71(d, J=0.7 Hz, 3H) | 172.99, 167.20, 164.61, 160.89, 158.78, 153.34, 152.42, 140.20, 138.88, 129.31, 125.68, 124.21, 119.98, 108.73, 106.49, 96.72, 93.75, 71.56, 60.71, 56.76, 56.65 |
3d | 8.21(t, J=5.6 Hz, 1H), 7.38(s, 2H), 6.83(d, J=2.1 Hz, 1H), 6.48(d, J=2.1 Hz, 1H), 4.32(s, 2H), 3.87(s, 3H), 3.83(d, J=7.5 Hz, 9H), 3.72(s, 3H), 3.07(dd, J=13.1, 6.7 Hz, 2H), 1.39—1.33(m, 2H), 1.22(dd, J=14.9, 7.4 Hz, 2H), 0.83(t, J=7.3 Hz, 3H) | 172.65, 167.99, 164.51, 160.86, 158.74, 153.34, 152.42, 140.13, 139.80, 125.70, 108.79, 106.41, 96.64, 93.72, 70.92, 60.71, 56.70, 56.65, 38.45, 31.70, 20.05, 14.19 |
3e | 8.80(t, J=5.9 Hz, 1H), 7.39(s, 2H), 7.24(tt, J=14.1, 7.2 Hz, 5H), 6.84(s, 1H), 6.49(s, 1H), 4.43(s, 2H), 4.30(d, J=5.9 Hz, 2H), 3.87(s, 3H), 3.82(s, 3H), 3.78(s, 6H), 3.71(d, J=0.8 Hz, 3H) | 172.62, 168.29, 164.52, 160.86, 158.73, 153.33, 152.39, 140.12, 139.74, 139.68, 128.76, 127.81, 127.33, 125.69, 108.79, 106.39, 96.65, 93.72, 70.72, 60.71, 56.70, 56.65, 56.61, 42.30 |
3f | 7.96(d, J=7.9 Hz, 1H), 7.38(d, J=1.4 Hz, 2H), 6.81(s, 1H), 6.47(s, 1H), 4.30(s, 2H), 3.87(d, J=1.3 Hz, 3H), 3.84(d, J=1.3 Hz, 6H), 3.82(s, 3H), 3.72(d, J=1.5 Hz, 3H), 1.64(d, J=8.0 Hz, 4H), 1.51(d, J=11.9 Hz, 1H), 1.25—1.03(m, 6H) | 172.65, 167.07, 164.48, 160.85, 158.72, 153.35, 152.39, 140.10, 139.93, 125.72, 108.79, 106.44, 96.63, 93.68, 70.99, 60.68, 56.68, 56.62, 47.83, 32.73, 25.67, 25.13 |
3g | 9.49(s, 1H), 8.05(d, J=7.8 Hz, 1H), 7.33(d, J=1.4 Hz, 2H), 7.04(dd, J=17.6, 7.8 Hz, 2H), 6.90(t, J=7.5 Hz, 1H), 6.84(s, 1H), 6.50(s, 1H), 4.59(d, J=0.7 Hz, 2H), 3.88(d, J=1.6 Hz, 3H), 3.82(d, J=1.4 Hz, 3H), 3.80(d, J=1.5 Hz, 6H), 3.75(d, J=1.5 Hz, 3H), 3.70(d, J=1.7 Hz, 3H) | 172.65, 166.94, 164.57, 160.88, 158.81, 153.37, 152.70, 149.52, 140.11, 139.94, 127.11, 125.65, 125.06, 121.03, 120.94, 111.64, 108.77, 106.35, 96.69, 93.75, 71.65, 60.70, 56.71, 56.65, 56.55, 56.29 |
3h | 10.21(s, 1H), 7.52(d, J=9.0 Hz, 2H), 7.43(s, 2H), 6.86(dd, J=5.5, 3.3 Hz, 3H), 6.50(d, J=2.0 Hz, 1H), 4.51(s, 2H), 3.88(s, 3H), 3.83(d, J=3.7 Hz, 9H), 3.71(s, 3H), 3.69(s, 3H) | 172.95, 166.65, 164.60, 160.89, 158.78, 156.01, 153.34, 152.43, 140.16, 131.99, 125.68, 121.54, 114.40, 108.73, 106.48, 96.71, 93.75, 71.51, 60.72, 56.75, 56.65, 55.69 |
3i | 10.48(s, 1H), 7.66(s, 1H), 7.65(s, 1H), 7.43(s, 2H), 7.36(d, J=8.8 Hz, 2H), 6.87(d, J=2.2 Hz, 1H), 6.51(d, J=2.2 Hz, 1H), 4.56(s, 2H), 3.88(s, 3H), 3.83(d, J=4.5 Hz, 9H), 3.70(s, 3H) | 172.96, 167.42, 164.63, 160.89, 158.78, 153.33, 152.45, 140.11, 137.87, 132.08, 129.23, 127.79, 125.66, 121.54, 108.71, 106.49, 96.72, 93.76, 71.49, 65.57, 60.71, 56.78, 56.64 |
3j | 8.40(s, 1H), 7.39(s, 2H), 7.23(dd, J=14.0, 6.6 Hz, 2H), 7.14—7.02(m, 2H), 6.85(s, 1H), 6.49(s, 1H), 4.33(s, 2H), 3.88(s, 3H), 3.83(s, 9H), 3.71(d, J=0.9 Hz, 3H) | 172.62, 168.23, 164.53, 162.17, 160.87, 158.74, 153.34, 152.37, 140.13, 139.75, 131.62, 128.83, 124.86, 115.72, 115.54, 108.79, 106.41, 96.66, 93.73, 70.80, 60.71, 56.72, 56.66 |
3k | 9.84(s, 1H), 7.40(d, J=11.4 Hz, 3H), 7.24—7.19(m, 1H), 7.18—7.10(m, 2H), 6.87(d, J=2.2 Hz, 1H), 6.51(d, J=2.1 Hz, 1H), 4.57(s, 2H), 3.88(s, 3H), 3.83(d, J=4.9 Hz, 9H), 3.71(s, 3H), 2.58—2.52(m, 2H), 1.07(t, J=7.5 Hz, 3H) | 173.00, 167.48, 164.63, 160.91, 158.82, 153.39, 152.62, 140.31, 140.18, 137.87, 135.46, 129.10, 126.57, 126.24, 125.70, 108.73, 106.51, 96.73, 93.76, 71.77, 60.71, 56.75, 56.68, 24.15, 14.59 |
Compd. | 1H NMR(DMSO-d6, 500 MHz), δ | 13C NMR(DMSO-d6, 125 MHz), δ |
3l | 8.11(d, J=7.3 Hz, 1H), 7.39(s, 2H), 6.84(d, J=1.6 Hz, 1H), 6.49(d, J=1.7 Hz, 1H), 4.30(s, 2H), 3.99(dd, J=14.0, 6.9 Hz, 1H), 3.87(s, 3H), 3.83(d, J = 10.0 Hz, 9H), 3.72(s, 3H), 1.74(d, J=6.3 Hz, 2H), 1.59(s, 2H), 1.45(d, J=4.3 Hz, 2H), 1.38—1.29(m, 2H) | 172.73, 167.55, 164.52, 160.87, 158.74, 153.35, 152.39, 140.12, 140.02, 125.73, 108.80, 106.46, 96.67, 93.72, 71.10, 60.70, 56.69, 50.51, 32.59, 23.93 |
Compd. | X. citri | R. solanacearum | X. oryzae | |||
---|---|---|---|---|---|---|
200 μg/mL | 100 μg/mL | 200 μg/mL | 100 μg/mL | 200 μg/mL | 100 μg/mL | |
3a | 71.75±5.68 | 56.82±8.39 | 85.13±8.88 | 60.11±0.61 | 98.67±9.15 | 80.96±9.68 |
3b | 63.20±8.14 | 48.26±1.53 | 58.99±4.72 | 58.42±5.39 | 82.32±5.49 | 65.28±6.32 |
3c | 63.60±8.44 | 54.12±6.34 | 64.91±7.06 | 52.57±5.46 | 49.17±5.51 | 26.63±6.52 |
3d | 62.02±6.07 | 57.23±3.21 | 62.92±2.94 | 59.34±4.32 | 43.32±1.58 | 20.95±0.83 |
3e | 46.93±4.70 | 40.16±2.60 | 100.00±8.64 | 61.98±7.57 | 100.00±6.81 | 83.72±4.67 |
3f | 47.76±2.51 | 46.47±5.87 | 58.32±5.99 | 41.05±9.08 | 92.68±1.27 | 39.98±2.89 |
3g | 57.93±3.47 | 37.23±8.93 | 59.89±9.16 | 41.05±9.08 | 88.96±5.61 | 70.67±9.93 |
3h | 82.18±5.75 | 66.29±6.29 | 55.88±7.28 | 51.94±1.19 | 92.89±6.76 | 62.30±1.14 |
3i | 58.69±9.57 | 53.70±5.09 | 70.71±1.68 | 68.67±4.44 | 73.20±7.33 | 56.17±3.81 |
3j | 69.07±1.76 | 58.04±3.53 | 45.12±3.65 | 31.84±9.82 | 64.21±4.20 | 64.15±3.72 |
3k | 62.27±1.98 | 49.13±3.39 | 56.73±4.15 | 52.33±7.09 | 92.84±9.66 | 49.46±3.12 |
3l | 61.32±8.36 | 60.56±3.25 | 61.56±7.20 | 41.65±5.04 | 78.20±8.29 | 41.91±7.95 |
Bismerthiazolb | 100.70±1.02 | 67.58±1.07 | 75.86±3.50 | 58.21±5.71 | 72.85±1.18 | 54.38±1.56 |
Table 4 Antibacterial activity(%) of the title compoundsa
Compd. | X. citri | R. solanacearum | X. oryzae | |||
---|---|---|---|---|---|---|
200 μg/mL | 100 μg/mL | 200 μg/mL | 100 μg/mL | 200 μg/mL | 100 μg/mL | |
3a | 71.75±5.68 | 56.82±8.39 | 85.13±8.88 | 60.11±0.61 | 98.67±9.15 | 80.96±9.68 |
3b | 63.20±8.14 | 48.26±1.53 | 58.99±4.72 | 58.42±5.39 | 82.32±5.49 | 65.28±6.32 |
3c | 63.60±8.44 | 54.12±6.34 | 64.91±7.06 | 52.57±5.46 | 49.17±5.51 | 26.63±6.52 |
3d | 62.02±6.07 | 57.23±3.21 | 62.92±2.94 | 59.34±4.32 | 43.32±1.58 | 20.95±0.83 |
3e | 46.93±4.70 | 40.16±2.60 | 100.00±8.64 | 61.98±7.57 | 100.00±6.81 | 83.72±4.67 |
3f | 47.76±2.51 | 46.47±5.87 | 58.32±5.99 | 41.05±9.08 | 92.68±1.27 | 39.98±2.89 |
3g | 57.93±3.47 | 37.23±8.93 | 59.89±9.16 | 41.05±9.08 | 88.96±5.61 | 70.67±9.93 |
3h | 82.18±5.75 | 66.29±6.29 | 55.88±7.28 | 51.94±1.19 | 92.89±6.76 | 62.30±1.14 |
3i | 58.69±9.57 | 53.70±5.09 | 70.71±1.68 | 68.67±4.44 | 73.20±7.33 | 56.17±3.81 |
3j | 69.07±1.76 | 58.04±3.53 | 45.12±3.65 | 31.84±9.82 | 64.21±4.20 | 64.15±3.72 |
3k | 62.27±1.98 | 49.13±3.39 | 56.73±4.15 | 52.33±7.09 | 92.84±9.66 | 49.46±3.12 |
3l | 61.32±8.36 | 60.56±3.25 | 61.56±7.20 | 41.65±5.04 | 78.20±8.29 | 41.91±7.95 |
Bismerthiazolb | 100.70±1.02 | 67.58±1.07 | 75.86±3.50 | 58.21±5.71 | 72.85±1.18 | 54.38±1.56 |
[1] | Bors W., Michel C., Stettmaier K., Biofactors,1997, 6(4), 399—402 |
[2] | van Acker S. A., Tromp M. N., Hacnen G. R., Vander V. W. J., Biochem. Biophys Res. Commun., 1995, 214(3), 755—759 |
[3] | Ubeda A., Esteve M. L., Alcaraz M. J., Cheeseman K. H., Slater T. F., Phytother. Res., 1995, 9(6), 416—420 |
[4] | Guo F.B.,Apicultural Science and Technology, 2005, (2), 28—31 |
(郭芳彬. 养蜂科技, 2005, (2), 28—31) | |
[5] | Xu Q., Song Y. J., Li L. Y., Hou Q. Y., World Chin. J. Digestol., 2005, 13(17), 2082—2085 |
(徐庆, 宋芸娟, 李丽亚, 侯巧燕. 世界华人消化杂志, 2005, 13(17), 2082—2085) | |
[6] | Zhou J. R., Mukheriee P., Gugger E. T., Tanaka T., Blackbum G. L., Clinton S. K., Cancer Res., 1998, 58(22), 5231—5238 |
[7] | Zhu J. D., Yang J. J., Foreign. Med. Sci.: Hygenics,1998, 25(5), 257—260 |
(朱俊东, 杨家驹. 国外医学卫生学分册, 1998, 25(5), 257—260) | |
[8] | Zhang Y. F., Yu Q. H., Journal of Shenyang Medical University,1999, 16(2), 122—124, 133 |
(张逸凡, 于庆海. 沈阳医科大学学报, 1999, 16(2), 122—124, 133) | |
[9] | Amoros M., Simoes C. M. O., Girre L., Sauvager F., Cormier M., J. Nat. Prod., 1992, 55(12), 1732—1740 |
[10] | Zhang L. J., Wang M. Q., Lishizhen Med. Mater. Med. Res., 2010, 21, 3221—3222 |
(张莉静, 王明谦. 时珍国医国药, 2010, 21, 3221—3222) | |
[11] | Wu Y.C., Studies on Synthesis and Application of Novel Myricetin Derivatives, Zhejiang University, Hangzhou, 2015 |
(吴月禅. 新型杨梅素衍生物的合成及其应用功能研究, 杭州: 浙江大学, 2015) | |
[12] | Hou X. T., Wang M., Jiang S. R., Niu S. G., Agrochemicals,2006, 45(12), 812—817 |
[13] | Chrispher J., Susan P., Stephen C., Benzazoles: Benzazole Benzothiazole and Benzimidazole Derivatives WO 2000006566,2000-02-10 |
[14] | Richard H. F., Anaheim C., Alkyleneiminoquinazoline-2,4-diones US 3462435,1966-11-15 |
[15] | Xu G. F., Liu Y. H., Yang X. L., Wang D. Q., Yuan D. K., Chem. J. Chinese Universities,2016, 37(3), 486—492 |
(徐高飞, 刘艳红, 杨新玲, 王道全, 袁德凯. 高等学校化学学报, 2016, 37(3), 486—492) | |
[16] | Li L., Li M., Chai B. S., Yang J. C., Song Y. Q., Liu C. L., Chem. J. Chinese Universities,2016, 37(9), 1649—1654 |
(李林, 李淼, 柴宝山, 杨吉春, 宋玉泉, 刘长令. 高等学校化学学报, 2016, 37(9), 1649—1654) | |
[17] | Valiveti A. K., Bhalerao U. M., Acharya J., Karade H. N., Gundapu R., Halve A. K., Kaushik M. P., Chem. Biol. Interact., 2015, 237, 125—132 |
[18] | Xue W., Song B. A., Zhao H. J., Qi X. B., Huang Y. J., Liu X. H., Eur. J. Med. Chem., 2015, 97, 155—163 |
[19] | Harte A. J, Gunnlaugsson T., Tetrahedron Lett., 2006, 47(35), 6321—6324 |
[20] | Wei T. B., Tang J. L., Hong Z., You M., Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem., 2007, 46B(5), 880—883 |
[21] | Lou Z. W., Zhou L., Xiao C. F., Ye Y., Zeng F. B., Huang K. X., Med. Chem. Res., 2008, 16(79), 380—391 |
[22] | Pianka M., Polton D.J.,J. Chem. Soc., 1960, 983—989 |
[23] | Emanuel H. N., Hugo T., Rosa M. P., Hector T. G., Reyna R. M., Roberto C. R., Carlos N. Z., Gabriel N. V., Eur. J. Med. Chem., 2009, 44(7), 2975—2984 |
[24] | Shah V. H., Chauhan N. A., Parikh A. R., J. Indian Chem. Soc., 1987, 64(11), 678—681 |
[25] | Prinz W., Kayle A., Levy P.R., J. Chem. Res.,Synop., 1978, (3), 116 |
[26] | Yang h., Li Z. B., Shin D. S., Wang L. Y., Zhou J. Z., Qiao H. B., Tian X., Ma X. Y., Zuo H.,Synlett., 2010, (3), 483—487 |
[27] | Matulenko M. A., Hakeem A. A., Kolasa T., Nakane M., Terranova M. A., Uchic M. E., Miller L. N., Chang R. J., Donnelly-Roberts D. L., Namovic M. T., Moreland R. B., Brioni J. D., Stewart A. O., Bioorg. Med. Chem., 2004, 12(13), 3471—3483 |
[28] | Svetkin Y.V., Minlibaeva A. N., Khafizova N. A., Zh. Obshch. Khim., 1961, 31, 2023—2025 |
[29] | Xie K. Z., Xie M. F., Lin K. X., Xie K. S., Preparation of Cinnamic Acid Derivatives Useful in the Treatment of Cardiovascular and Cerebrovascular Diseases CN 101928265B,2010-12-29 |
(谢开智, 谢梅芳, 林开喜, 谢开书. 1-(肉桂酰基)-4-烷基酰胺哌嗪化合物及其制备方法, CN 101928265B, 2010-12-29) | |
[30] | Takeshi K., Kurnia F., Phytochemistry,1997, 45(1), 179—181 |
[31] | Xu W. M., Han F. F., He M., Hu D. Y., He J., Yang S., Song B. A., J. Agric. Food Chem., 2011, 60(4), 1036—1041 |
[32] | Wang X., Li P., Li Z. N., Yin J., He M., Xue W., Chen Z. W., Song B. A., J. Agric. Food Chem., 2013, 61(40), 9575—9582 |
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