Chem. J. Chinese Universities ›› 2026, Vol. 47 ›› Issue (3): 20250320.doi: 10.7503/cjcu20250320
• Organic Chemistry • Previous Articles Next Articles
FENG Junjun1,3, QI Mingli1, MAO Weilong1, WANG Jingxuan1, CHEN Li1,2(
)
Received:2025-10-31
Online:2026-03-10
Published:2025-12-03
Contact:
CHEN Li
E-mail:chenliyss@nankai.edu.cn
Supported by:CLC Number:
TrendMD:
FENG Junjun, QI Mingli, MAO Weilong, WANG Jingxuan, CHEN Li. Synthesis, Characterization and Antiproliferative Activity of Regioselectively Reduced and Aminated Derivatives of Gambogic Acid[J]. Chem. J. Chinese Universities, 2026, 47(3): 20250320.
| Compd. | Appearance | Yield a (%) | m. p./°C | m/z[M+Na]+ |
|---|---|---|---|---|
| 1 | Orange crystal | 66 | 97—99 | 665.3091(665.3089) |
| 2 | Orange amorphous solid | 14 | — | 665.3091(665.3084) |
| 3 | Orange amorphous solid | 4 | — | 667.3247(667.3236) |
| 4a | Orange amorphous solid | 8 | — | 641.3454(641.3454) |
| 4b | Orange amorphous solid | 8 | — | 641.3454(641.3449) |
| 5 | Orange amorphous solid | 83 | — | 639.3298(639.3296) |
| 6 | Orange amorphous solid | 57 | — | 639.3298(639.3296) |
| 7 | Orange amorphous solid | 98 | — | 637.3142(637.3136) |
| 8 | Orange amorphous solid | 47 | — | 637.3142(637.3141) |
| 9b | Orange amorphous solid | 4 | — | 644.3951(644.3949) |
| iso⁃9b | Orange amorphous solid | 22 | — | 644.3951(644.3951) |
| 10b | Orange amorphous solid | 43 | — | 686.4058(686.4056) |
| iso⁃10b | Orange amorphous solid | 11 | — | 686.4056(686.4053) |
| 11b | Orange amorphous solid | 37 | — | 699.4374(699.4374) |
Table 1 Appearance, yields, melting points(m. p.) and HRMS data of compounds 1—10
| Compd. | Appearance | Yield a (%) | m. p./°C | m/z[M+Na]+ |
|---|---|---|---|---|
| 1 | Orange crystal | 66 | 97—99 | 665.3091(665.3089) |
| 2 | Orange amorphous solid | 14 | — | 665.3091(665.3084) |
| 3 | Orange amorphous solid | 4 | — | 667.3247(667.3236) |
| 4a | Orange amorphous solid | 8 | — | 641.3454(641.3454) |
| 4b | Orange amorphous solid | 8 | — | 641.3454(641.3449) |
| 5 | Orange amorphous solid | 83 | — | 639.3298(639.3296) |
| 6 | Orange amorphous solid | 57 | — | 639.3298(639.3296) |
| 7 | Orange amorphous solid | 98 | — | 637.3142(637.3136) |
| 8 | Orange amorphous solid | 47 | — | 637.3142(637.3141) |
| 9b | Orange amorphous solid | 4 | — | 644.3951(644.3949) |
| iso⁃9b | Orange amorphous solid | 22 | — | 644.3951(644.3951) |
| 10b | Orange amorphous solid | 43 | — | 686.4058(686.4056) |
| iso⁃10b | Orange amorphous solid | 11 | — | 686.4056(686.4053) |
| 11b | Orange amorphous solid | 37 | — | 699.4374(699.4374) |
| Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
|---|---|---|
| 1 | 12.85(s, 1H), 7.54(d, J=6.9 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.93(td, J=7.4, 1.3 Hz, 1H), 5.44(d, J=10.2 Hz, 1H), 5.10—5.00(m, 2H), 3.48(dd, J=6.8, 4.6 Hz, 1H), 3.43(s, 3H), 3.31(dd, J=14.6, 8.0 Hz, 1H), 3.15(dd, J=14.6, 5.3 Hz, 1H), 3.07—2.92(m, 2H), 2.52(d, J=9.3 Hz, 1H), 2.31(dd, J=13.4, 4.7 Hz, 1H), 2.03(dd, J=16.2, 7.3 Hz, 2H), 1.83—1.76(m, 1H), 1.74(s, 3H), 1.69(s, 3H), 1.67(d, J=1.2 Hz, 3H), 1.65(s, 3H), 1.65(s, 3H), 1.62—1.58(m, 1H), 1.55(s, 3H), 1.44(s, 3H), 1.38(dd, J=13.4, 9.6 Hz, 1H) , 1.29(s, 3H) | 203.5, 179.0, 167.3, 161.3, 157.6, 136.1, 135.0, 133.6, 131.9, 131.5, 127.8, 124.5, 123.8, 122.2, 115.9, 107.5, 102.5, 100.5, 90.9, 83.9, 83.7, 81.3, 51.1, 49.1, 46.8, 42.1, 29.9, 29.1, 28.8, 28.0, 25.8, 25.7, 25.1, 22.7, 21.6, 20.9, 18.1, 17.6 |
| 2 | 12.79(s, 1H), 7.52(d, J=6.9 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 6.37(t, J=7.4 Hz, 1H), 5.45(d, J=10.1 Hz, 1H), 5.13(t, J=6.1 Hz, 1H), 5.06(t, J=6.7 Hz, 1H), 3.65(s, 3H), 3.53—3.48(m, 1H), 3.25(d, J=6.5 Hz, 2H), 2.62(d, J=7.6 Hz, 2H), 2.52(d, J=9.4 Hz, 1H), 2.34(dd, J=13.5, 4.4 Hz, 1H), 2.10—1.97(m, 2H), 1.79(dd, J=14.3, 8.2 Hz, 1H), 1.74(s, 3H), 1.71(s, 3H), 1.65(s, 6H), 1.63—1.58(m, 1H), 1.55(s, 3H), 1.42(s, 3H), 1.39—1.32(m, 4H), 1.29(s, 3H) | 202.9, 179.0, 167.6, 161.2, 157.6, 157.4, 135.2, 134.3, 133.4, 131.9, 131.7, 129.4, 124.8, 123.8, 122.2, 115.9, 107.8, 102.8, 100.4, 90.7, 83.7, 83.7, 81.3, 51.7, 49.1, 46.9, 41.9, 30.0, 29.0, 28.9, 27.5, 25.7, 25.7, 25.4, 22.7, 21.6, 18.1, 17.6, 11.8 |
| 3 | 13.02(s, 1H), 7.65(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.96(t, J=6.8 Hz, 1H), 5.43(d, J=10.1 Hz, 1H), 5.12—5.00(m, 2H), 3.54(s, 3H), 3.33(dd, J=14.8, 7.8 Hz, 1H), 3.29—3.26(m, 1H), 3.23(dd, J=15.4, 4.4 Hz, 1H), 3.04(d, J=5.6 Hz, 1H), 2.93—2.88(m, 1H), 2.84(dd, J=16.4, 6.4 Hz, 1H), 2.61(dd, J=15.7, 7.8 Hz, 1H), 2.33(dd, J=14.2, 4.1 Hz, 1H), 2.17(d, J=10.0 Hz, 1H), 2.04(dd, J=15.9, 7.8 Hz, 2H), 1.84—1.76(m, 7H), 1.74(s, 3H), 1.65(s, 3H), 1.63(s, 3H), 1.62—1.58(m, 1H), 1.55(s, 3H), 1.54(s, 3H), 1.43(s, 3H), 1.40—1.36(m, 1H) | 180.0, 167.8, 161.0, 158.2, 157.6, 142.4, 136.0, 131.8, 131.3, 131.0, 129.1, 124.4, 123.8, 122.6, 116.0, 107.4, 102.4, 100.2, 92.7, 84.5, 84.1, 81.1, 71.1, 51.1, 49.0, 42.0, 36.9, 34.3, 30.2, 28.4, 27.8, 25.7, 24.8, 22.7, 21.9, 20.9, 18.1, 17.6 |
| Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
| 4a | 12.14(s, 1H), 6.63(d, J=10.1 Hz, 1H), 5.42(d, J=10.1 Hz, 1H), 5.31—5.22(m, 1H), 5.17(t, J=6.6 Hz, 1H), 5.06(t, J=7.0 Hz, 1H), 4.08(d, J=11.7 Hz, 1H), 3.64—3.60(m, 2H), 3.34(dd, J=11.7, 7.2 Hz, 1H), 3.28(d, J=6.7 Hz, 2H), 2.64(br, 2H) 2.43(d, J=9.6 Hz, 1H), 2.36(dd, J=13.6, 10.0 Hz, 1H), 2.29(d, J=14.4 Hz, 1H), 2.13(dd, J=13.5, 7.0 Hz, 1H), 2.05(dd, J=15.7, 7.8 Hz, 2H), 1.97(dd, J=12.5, 4.5 Hz, 1H), 1.90(d, J=10.2 Hz, 1H), 1.84—1.73(m, 12H), 1.69(s, 3H), 1.65(s, 3H), 1.63—1.58(m, 1H), 1.56(s, 3H), 1.46(s, 3H), 1.42(s, 3H) | 196.2, 160.5, 158.2, 155.6, 140.4, 131.9, 131.8, 124.7, 123.8, 121.8, 120.2, 115.9, 107.4, 102.2, 101.8, 90.0, 86.5, 82.5, 81.0, 76.5, 61.1, 51.3, 41.9, 40.1, 34.1, 30.3, 29.8, 27.4, 27.0, 26.3, 25.9, 25.7, 25.6, 22.8, 22.7, 21.8, 18.2, 17.6 |
| 4b | 12.02(s, 1H), 6.66(d, J=10.1 Hz, 1H), 5.54(t, J=7.8 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.14(t, J=7.3 Hz, 1H), 5.09(t, J=6.7 Hz, 1H), 4.31(d, J=11.7 Hz, 1H), 3.90(d, J=11.7 Hz, 1H), 3.76(s, 1H), 3.34—3.21(m, 2H), 3.05—2.92(m, 2H), 2.76(br, 2H), 2.54(d, J=13.6 Hz, 1H), 2.39—2.27(m, 2H), 2.16—2.02(m, 3H), 1.88(s, 3H), 1.77(s, 5H), 1.70—1.54(m, 11H), 1.49(dd, J=14.6, 9.9 Hz, 1H), 1.39(s, 3H), 1.38(s, 3H), 1.36(s, 3H) | 196.3, 160.6, 155.9, 155.7, 140.5, 131.8, 131.2, 124.9, 123.8, 122.6, 120.7, 116.0, 108.3, 102.5, 102.2, 89.4, 85.5, 83.0, 80.8, 75.8, 61.3, 43.6, 41.8, 39.9, 31.6, 29.7, 29.5, 27.1, 26.4, 25.7, 25.7, 25.3, 24.4, 22.8, 22.7, 21.7, 18.1, 17.6 |
| 5 | 13.00(s, 1H), 7.66(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.20(t, J=7.9 Hz, 1H), 5.12—5.02(m, 2H), 4.15(d, J=11.9 Hz, 1H), 3.72(d, J=11.5 Hz, 1H), 3.42—3.27(m, 3H), 2.97—2.89(m, 1H), 2.77(d, J=4.1 Hz, 1H), 2.62(dd, J=14.0, 9.0 Hz, 1H), 2.43—2.30(m, 2H), 2.20(d, J=10.0 Hz, 1H), 2.10—1.99(m, 2H), 1.90—1.70(m, 11H), 1.65(s, 3H), 1.64(s, 3H), 1.63—1.58(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.43(s, 3H), 1.30(dd, J=14.0, 10.4 Hz, 1H) | 180.0, 161.3, 158.3, 157.6, 142.4, 140.2, 131.9, 131.8, 131.0, 124.6, 123.8, 122.3, 120.2, 115.9, 107.5, 102.5, 100.3, 92.4, 84.5, 84.3, 81.2, 70.8, 61.2, 49.1, 42.1, 36.7, 32.2, 30.2, 28.4, 27.8, 25.7, 25.7, 24.9, 22.7, 22.5, 21.9, 18.2, 17.6 |
| 6 | 12.99(s, 1H), 7.62(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H),5.24(t, J=6.8 Hz, 1H), 5.11(t, J=6.7 Hz, 1H), 5.06(t, J=7.1 Hz, 1H), 3.83(m, 2H), 3.32(d, J=7.7 Hz, 3H), 2.95—2.86(m, 1H), 2.42(dd, J=14.6, 5.8 Hz, 1H), 2.34(dd, J=14.1, 4.1 Hz, 1H), 2.21—2.12(m, 2H), 2.05(dd, J=15.6, 7.8 Hz, 2H), 1.82—1.77(m, 4H), 1.75(s, 3H), 1.65(s, 6H), 1.63— 1.57(m, 1H), 1.56(s, 3H), 1.53(s, 3H), 1.42(s, 3H), 1.40(s, 3H), 1.30—1.23(m, 1H) | 180.3, 161.1, 158.4, 157.5, 142.0, 138.3, 131.9, 131.5, 131.3, 124.6, 123.8, 122.5, 118.3, 116.0, 107.6, 102.4, 100.3, 92.6, 84.9, 83.9, 81.1, 70.4, 68.4, 49.1, 42.0, 36.9, 32.2, 30.3, 28.5, 27.6, 25.7, 25.7, 25.0, 22.7, 21.9, 18.2, 17.6, 13.7 |
| 7 | 12.96(s, 1H), 9.89(s, 1H), 7.68(d, J=7.2 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 6.41(t, J=7.8 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.10—5.02(m, 2H), 3.41—3.28(m, 2H), 3.24(dd, J=14.7, 5.1 Hz, 1H), 3.02(d, J=5.8 Hz, 1H), 3.01—2.92(m, 2H), 2.48(dd, J=14.6, 8.4 Hz, 1H), 2.35(dd, J=14.2, 4.0 Hz, 1H), 2.21(d, J=10.0 Hz, 1H), 2.05(dd, J=15.6, 7.8 Hz, 2H), 1.83—1.77(m, 4H), 1.76(s, 3H), 1.69(s, 3H), 1.65(s, 6H), 1.62—1.57(m, 1H), 1.56(s, 3H), 1.53(s, 3H), 1.44(s, 3H), 1.31(dd, J=14.0, 10.5 Hz, 1H) | 190.4, 179.7, 161.3, 157.9, 157.6, 142.5, 140.8, 138.5, 131.9, 131.8, 130.8, 124.7, 123.8, 122.3, 115.8, 107.4, 102.7, 100.1, 92.5, 84.4, 84.1, 81.3, 70.8, 49.1, 42.0, 36.9, 31.2, 30.1, 28.5, 27.7, 25.7, 25.7, 24.9, 22.7, 21.9, 18.2, 17.6, 16.7 |
| 8 | 12.99(s, 1H), 9.34(s, 1H), 7.69(d, J=7.1 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 6.50(t, J=7.1 Hz, 1H), 5.45(d, J=10.1 Hz, 1H), 5.10—5.01(m, 2H), 3.32(dd, J=14.4, 7.6 Hz, 1H), 3.24(dd, J=14.1, 5.2 Hz, 2H), 3.05(d, J=5.8 Hz, 1H), 2.98—2.91(m, 1H), 2.76(dd, J=15.4, 7.3 Hz, 1H), 2.35(dd, J=14.3, 3.8 Hz, 1H), 2.26(dd, J=15.6, 7.2 Hz, 1H), 2.21(d, J=10.1 Hz, 1H), 2.04(dd, J=15.4, 7.4 Hz, 2H), 1.81(s, 3H), 1.79—1.75(m, 1H), 1.74(s, 3H), 1.65(s, 3H), 1.66—1.62(m, 1H), 1.62(s, 3H), 1.55(s, 9H), 1.42(s, 3H), 1.35—1.25(m, 1H) | 194.8, 179.7, 161.3, 157.9, 157.7, 147.2, 142.7, 141.2, 131.9, 131.8, 130.8, 124.8, 123.8, 122.3, 115.9, 107.5, 102.7, 100.2, 92.6, 84.5, 84.2, 81.3, 71.5, 49.0, 42.0, 37.0, 34.0, 30.2, 28.6, 27.7, 25.7, 25.7, 24.9, 22.7, 21.9, 18.2, 17.7, 9.3 |
| 9 | 13.04(s, 1H), 7.63(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.17(t, J=6.6 Hz, 1H), 5.10(t, J=6.4 Hz, 1H), 5.07(t, J=7.2 Hz, 1H), 3.33(d, J=6.4 Hz, 2H), 3.29(s, 1H), 2.94—2.89(m, 1H), 2.66(d, J=12.3 Hz, 1H), 2.53(d, J=12.4 Hz, 1H), 2.47(dd, J=14.4, 6.5 Hz, 1H), 2.34(dd, J=14.0, 4.0 Hz, 1H), 2.19—2.14(m, 2H), 2.10—2.02(m, 8H), 1.83—1.77(m, 4H), 1.76(s, 3H), 1.65(s, 6H), 1.63(s, 3H), 1.62—1.59(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.42(s, 3H), 1.34—1.28(m, 1H) | 180.1, 161.0, 158.4, 157.6, 142.0, 136.2, 131.9, 131.4, 131.2, 124.5, 123.8, 122.6, 121.8, 116.0, 107.4, 102.4, 100.3, 100.0, 92.6, 84.7, 83.7, 81.1, 70.5, 59.7, 49.2, 45.2, 42.0, 36.9, 32.2, 30.3, 28.5, 27.7, 25.8, 25.6, 25.0, 23.0, 22.7, 22.0, 18.2, 17.6 |
| Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
| iso⁃9 | 13.04(s, 1H), 7.61(d, J=7.1 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 5.43(d, J=10.1 Hz, 1H), 5.15—5.03(m, 3H), 3.32(d, J=6.1 Hz, 2H), 3.25(s, 1H), 3.01(br, 1H), 2.90—2.86(m, 1H), 2.62(q, J=12.2 Hz, 2H), 2.46(dd, J=14.4, 6.4 Hz, 1H), 2.33(dd, J=14.0, 3.7 Hz, 1H), 2.21—1.99(m, 10H), 1.83—1.70(m, 7H), 1.69—1.59(m, 7H), 1.55(s, 3H), 1.51(s, 3H), 1.47(s, 3H), 1.42(s, 3H), 1.35—1.25(m, 1H) | 179.1, 160.0, 157.4, 156.6, 140.9, 135.8, 130.8, 130.4, 130.2, 123.5, 122.8, 121.6, 119.6, 115.0, 106.5, 101.4, 99.3, 91.5, 83.9, 82.6, 80.0, 69.3, 67.9, 48.2, 44.1, 41.0, 35.9, 31.4, 29.3, 28.7, 27.5, 26.6, 24.7, 24.6, 24.1, 21.7, 20.9, 17.2, 16.6, 14.0 |
| 10 | 13.03(s, 1H), 7.63(d, J=6.9 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.43(d, J=10.1 Hz, 1H), 5.20(t, J=6.9 Hz, 1H), 5.14—5.03(m, 2H), 3.65—3.53(m, 4H), 3.33(d, J=5.6 Hz, 2H), 3.30(s, 1H), 3.09(br, 1H), 2.95—2.88(m, 1H), 2.69(d, J=12.4 Hz, 1H), 2.56(d, J=12.4 Hz, 1H), 2.45(dd, J=14.1, 5.9 Hz, 1H), 2.38—2.30(m, 1H), 2.27—2.13(m, 6H), 2.11—2.01(m, 2H), 1.80—1.73(m, 1H), 1.78(s, 3H), 1.76(s, 3H), 1.65(s, 6H), 1.62(s, 3H), 1.62—1.56(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.42(s, 3H), 1.37—1.28 (m, 1H) | 180.1, 161.0, 158.4, 157.6, 141.9, 135.4, 131.8, 131.4, 131.3, 124.5, 123.8, 122.5, 122.0, 116.0, 107.4, 102.4, 100.3, 92.6, 84.7, 83.8, 81.1, 70.5, 67.0, 58.9, 53.4, 49.2, 42.0, 36.9, 32.3, 30.3, 28.5, 27.7, 25.8, 25.6, 25.0, 23.3, 22.7, 22.0, 18.2, 17.6 |
| iso⁃10 | 13.04(s, 1H), 7.61(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.17—5.08(m, 2H), 5.06(t, J=7.8 Hz, 1H), 3.68—3.58(m, 4H), 3.32(d, J=6.3 Hz, 2H), 3.25(s, 1H), 3.01(d, J=4.8 Hz, 1H), 2.94—2.87(m, 1H), 2.68(s, 2H), 2.44(dd, J=14.5, 6.2 Hz, 1H), 2.33(dd, J=14.1, 3.8 Hz, 1H), 2.26—2.17(m, 4H), 2.14(dd, J=13.4, 8.5 Hz, 2H), 2.09—2.02(m, 2H), 1.82—1.76(m, 4H), 1.75(s, 3H), 1.65(s, 3H), 1.64(s, 3H), 1.62—1.59(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.45(s, 3H), 1.42(s, 3H), 1.31—1.25(m, 1H) | 180.0, 161.0, 158.4, 157.5, 141.9, 135.6, 131.8, 131.4, 131.2, 124.5, 123.8, 122.6, 120.9, 116.0, 107.5, 102.4, 100.3, 92.5, 84.9, 83.7, 81.1, 70.3, 67.6, 67.0, 53.4, 49.2, 42.0, 36.9, 32.4, 30.3, 28.5, 27.6, 25.7, 25.7, 25.1, 22.7, 21.9, 18.2, 17.6, 15.1 |
| 11 | 13.02(s, 1H), 7.60(d, J=7.1 Hz, 1H), 6.65(d, J=10.1 Hz, 1H), 5.40(d, J=10.1 Hz, 1H), 5.14(t, J=6.9 Hz, 1H), 5.11—4.97(m, 2H), 3.38—3.02(m, 4H), 2.87(s, 1H), 2.67(d, J=12.5 Hz, 1H), 2.55(d, J=12.7 Hz, 1H), 2.45—2.10(m, 15H), 2.07—1.97(m, 2H), 1.80—1.78(m, 1H), 1.75(s, 3H), 1.72(s, 3H), 1.62(s, 6H), 1.61—1.58(m, 1H), 1.57(s, 3H), 1.53(s, 3H), 1.49(s, 3H), 1.40(s, 3H), 1.38—1.31(m, 1H) | 180.2, 161.1, 158.5, 157.7, 142.1, 136.0, 132.0, 131.5, 131.4, 124.5, 124.0, 122.7, 121.9, 116.2, 107.6, 102.5, 100.4, 92.8, 84.9, 83.9, 81.2, 70.6, 58.7, 55.2, 53.0, 49.3, 46.1, 42.2, 37.1, 32.4, 30.5, 28.7, 27.9, 25.9, 25.8, 25.2, 23.6, 22.8, 22.1, 18.4, 17.8 |
Table 2 1H NMR and 13C NMR data of compounds 1—10
| Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
|---|---|---|
| 1 | 12.85(s, 1H), 7.54(d, J=6.9 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.93(td, J=7.4, 1.3 Hz, 1H), 5.44(d, J=10.2 Hz, 1H), 5.10—5.00(m, 2H), 3.48(dd, J=6.8, 4.6 Hz, 1H), 3.43(s, 3H), 3.31(dd, J=14.6, 8.0 Hz, 1H), 3.15(dd, J=14.6, 5.3 Hz, 1H), 3.07—2.92(m, 2H), 2.52(d, J=9.3 Hz, 1H), 2.31(dd, J=13.4, 4.7 Hz, 1H), 2.03(dd, J=16.2, 7.3 Hz, 2H), 1.83—1.76(m, 1H), 1.74(s, 3H), 1.69(s, 3H), 1.67(d, J=1.2 Hz, 3H), 1.65(s, 3H), 1.65(s, 3H), 1.62—1.58(m, 1H), 1.55(s, 3H), 1.44(s, 3H), 1.38(dd, J=13.4, 9.6 Hz, 1H) , 1.29(s, 3H) | 203.5, 179.0, 167.3, 161.3, 157.6, 136.1, 135.0, 133.6, 131.9, 131.5, 127.8, 124.5, 123.8, 122.2, 115.9, 107.5, 102.5, 100.5, 90.9, 83.9, 83.7, 81.3, 51.1, 49.1, 46.8, 42.1, 29.9, 29.1, 28.8, 28.0, 25.8, 25.7, 25.1, 22.7, 21.6, 20.9, 18.1, 17.6 |
| 2 | 12.79(s, 1H), 7.52(d, J=6.9 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 6.37(t, J=7.4 Hz, 1H), 5.45(d, J=10.1 Hz, 1H), 5.13(t, J=6.1 Hz, 1H), 5.06(t, J=6.7 Hz, 1H), 3.65(s, 3H), 3.53—3.48(m, 1H), 3.25(d, J=6.5 Hz, 2H), 2.62(d, J=7.6 Hz, 2H), 2.52(d, J=9.4 Hz, 1H), 2.34(dd, J=13.5, 4.4 Hz, 1H), 2.10—1.97(m, 2H), 1.79(dd, J=14.3, 8.2 Hz, 1H), 1.74(s, 3H), 1.71(s, 3H), 1.65(s, 6H), 1.63—1.58(m, 1H), 1.55(s, 3H), 1.42(s, 3H), 1.39—1.32(m, 4H), 1.29(s, 3H) | 202.9, 179.0, 167.6, 161.2, 157.6, 157.4, 135.2, 134.3, 133.4, 131.9, 131.7, 129.4, 124.8, 123.8, 122.2, 115.9, 107.8, 102.8, 100.4, 90.7, 83.7, 83.7, 81.3, 51.7, 49.1, 46.9, 41.9, 30.0, 29.0, 28.9, 27.5, 25.7, 25.7, 25.4, 22.7, 21.6, 18.1, 17.6, 11.8 |
| 3 | 13.02(s, 1H), 7.65(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.96(t, J=6.8 Hz, 1H), 5.43(d, J=10.1 Hz, 1H), 5.12—5.00(m, 2H), 3.54(s, 3H), 3.33(dd, J=14.8, 7.8 Hz, 1H), 3.29—3.26(m, 1H), 3.23(dd, J=15.4, 4.4 Hz, 1H), 3.04(d, J=5.6 Hz, 1H), 2.93—2.88(m, 1H), 2.84(dd, J=16.4, 6.4 Hz, 1H), 2.61(dd, J=15.7, 7.8 Hz, 1H), 2.33(dd, J=14.2, 4.1 Hz, 1H), 2.17(d, J=10.0 Hz, 1H), 2.04(dd, J=15.9, 7.8 Hz, 2H), 1.84—1.76(m, 7H), 1.74(s, 3H), 1.65(s, 3H), 1.63(s, 3H), 1.62—1.58(m, 1H), 1.55(s, 3H), 1.54(s, 3H), 1.43(s, 3H), 1.40—1.36(m, 1H) | 180.0, 167.8, 161.0, 158.2, 157.6, 142.4, 136.0, 131.8, 131.3, 131.0, 129.1, 124.4, 123.8, 122.6, 116.0, 107.4, 102.4, 100.2, 92.7, 84.5, 84.1, 81.1, 71.1, 51.1, 49.0, 42.0, 36.9, 34.3, 30.2, 28.4, 27.8, 25.7, 24.8, 22.7, 21.9, 20.9, 18.1, 17.6 |
| Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
| 4a | 12.14(s, 1H), 6.63(d, J=10.1 Hz, 1H), 5.42(d, J=10.1 Hz, 1H), 5.31—5.22(m, 1H), 5.17(t, J=6.6 Hz, 1H), 5.06(t, J=7.0 Hz, 1H), 4.08(d, J=11.7 Hz, 1H), 3.64—3.60(m, 2H), 3.34(dd, J=11.7, 7.2 Hz, 1H), 3.28(d, J=6.7 Hz, 2H), 2.64(br, 2H) 2.43(d, J=9.6 Hz, 1H), 2.36(dd, J=13.6, 10.0 Hz, 1H), 2.29(d, J=14.4 Hz, 1H), 2.13(dd, J=13.5, 7.0 Hz, 1H), 2.05(dd, J=15.7, 7.8 Hz, 2H), 1.97(dd, J=12.5, 4.5 Hz, 1H), 1.90(d, J=10.2 Hz, 1H), 1.84—1.73(m, 12H), 1.69(s, 3H), 1.65(s, 3H), 1.63—1.58(m, 1H), 1.56(s, 3H), 1.46(s, 3H), 1.42(s, 3H) | 196.2, 160.5, 158.2, 155.6, 140.4, 131.9, 131.8, 124.7, 123.8, 121.8, 120.2, 115.9, 107.4, 102.2, 101.8, 90.0, 86.5, 82.5, 81.0, 76.5, 61.1, 51.3, 41.9, 40.1, 34.1, 30.3, 29.8, 27.4, 27.0, 26.3, 25.9, 25.7, 25.6, 22.8, 22.7, 21.8, 18.2, 17.6 |
| 4b | 12.02(s, 1H), 6.66(d, J=10.1 Hz, 1H), 5.54(t, J=7.8 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.14(t, J=7.3 Hz, 1H), 5.09(t, J=6.7 Hz, 1H), 4.31(d, J=11.7 Hz, 1H), 3.90(d, J=11.7 Hz, 1H), 3.76(s, 1H), 3.34—3.21(m, 2H), 3.05—2.92(m, 2H), 2.76(br, 2H), 2.54(d, J=13.6 Hz, 1H), 2.39—2.27(m, 2H), 2.16—2.02(m, 3H), 1.88(s, 3H), 1.77(s, 5H), 1.70—1.54(m, 11H), 1.49(dd, J=14.6, 9.9 Hz, 1H), 1.39(s, 3H), 1.38(s, 3H), 1.36(s, 3H) | 196.3, 160.6, 155.9, 155.7, 140.5, 131.8, 131.2, 124.9, 123.8, 122.6, 120.7, 116.0, 108.3, 102.5, 102.2, 89.4, 85.5, 83.0, 80.8, 75.8, 61.3, 43.6, 41.8, 39.9, 31.6, 29.7, 29.5, 27.1, 26.4, 25.7, 25.7, 25.3, 24.4, 22.8, 22.7, 21.7, 18.1, 17.6 |
| 5 | 13.00(s, 1H), 7.66(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.20(t, J=7.9 Hz, 1H), 5.12—5.02(m, 2H), 4.15(d, J=11.9 Hz, 1H), 3.72(d, J=11.5 Hz, 1H), 3.42—3.27(m, 3H), 2.97—2.89(m, 1H), 2.77(d, J=4.1 Hz, 1H), 2.62(dd, J=14.0, 9.0 Hz, 1H), 2.43—2.30(m, 2H), 2.20(d, J=10.0 Hz, 1H), 2.10—1.99(m, 2H), 1.90—1.70(m, 11H), 1.65(s, 3H), 1.64(s, 3H), 1.63—1.58(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.43(s, 3H), 1.30(dd, J=14.0, 10.4 Hz, 1H) | 180.0, 161.3, 158.3, 157.6, 142.4, 140.2, 131.9, 131.8, 131.0, 124.6, 123.8, 122.3, 120.2, 115.9, 107.5, 102.5, 100.3, 92.4, 84.5, 84.3, 81.2, 70.8, 61.2, 49.1, 42.1, 36.7, 32.2, 30.2, 28.4, 27.8, 25.7, 25.7, 24.9, 22.7, 22.5, 21.9, 18.2, 17.6 |
| 6 | 12.99(s, 1H), 7.62(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H),5.24(t, J=6.8 Hz, 1H), 5.11(t, J=6.7 Hz, 1H), 5.06(t, J=7.1 Hz, 1H), 3.83(m, 2H), 3.32(d, J=7.7 Hz, 3H), 2.95—2.86(m, 1H), 2.42(dd, J=14.6, 5.8 Hz, 1H), 2.34(dd, J=14.1, 4.1 Hz, 1H), 2.21—2.12(m, 2H), 2.05(dd, J=15.6, 7.8 Hz, 2H), 1.82—1.77(m, 4H), 1.75(s, 3H), 1.65(s, 6H), 1.63— 1.57(m, 1H), 1.56(s, 3H), 1.53(s, 3H), 1.42(s, 3H), 1.40(s, 3H), 1.30—1.23(m, 1H) | 180.3, 161.1, 158.4, 157.5, 142.0, 138.3, 131.9, 131.5, 131.3, 124.6, 123.8, 122.5, 118.3, 116.0, 107.6, 102.4, 100.3, 92.6, 84.9, 83.9, 81.1, 70.4, 68.4, 49.1, 42.0, 36.9, 32.2, 30.3, 28.5, 27.6, 25.7, 25.7, 25.0, 22.7, 21.9, 18.2, 17.6, 13.7 |
| 7 | 12.96(s, 1H), 9.89(s, 1H), 7.68(d, J=7.2 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 6.41(t, J=7.8 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.10—5.02(m, 2H), 3.41—3.28(m, 2H), 3.24(dd, J=14.7, 5.1 Hz, 1H), 3.02(d, J=5.8 Hz, 1H), 3.01—2.92(m, 2H), 2.48(dd, J=14.6, 8.4 Hz, 1H), 2.35(dd, J=14.2, 4.0 Hz, 1H), 2.21(d, J=10.0 Hz, 1H), 2.05(dd, J=15.6, 7.8 Hz, 2H), 1.83—1.77(m, 4H), 1.76(s, 3H), 1.69(s, 3H), 1.65(s, 6H), 1.62—1.57(m, 1H), 1.56(s, 3H), 1.53(s, 3H), 1.44(s, 3H), 1.31(dd, J=14.0, 10.5 Hz, 1H) | 190.4, 179.7, 161.3, 157.9, 157.6, 142.5, 140.8, 138.5, 131.9, 131.8, 130.8, 124.7, 123.8, 122.3, 115.8, 107.4, 102.7, 100.1, 92.5, 84.4, 84.1, 81.3, 70.8, 49.1, 42.0, 36.9, 31.2, 30.1, 28.5, 27.7, 25.7, 25.7, 24.9, 22.7, 21.9, 18.2, 17.6, 16.7 |
| 8 | 12.99(s, 1H), 9.34(s, 1H), 7.69(d, J=7.1 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 6.50(t, J=7.1 Hz, 1H), 5.45(d, J=10.1 Hz, 1H), 5.10—5.01(m, 2H), 3.32(dd, J=14.4, 7.6 Hz, 1H), 3.24(dd, J=14.1, 5.2 Hz, 2H), 3.05(d, J=5.8 Hz, 1H), 2.98—2.91(m, 1H), 2.76(dd, J=15.4, 7.3 Hz, 1H), 2.35(dd, J=14.3, 3.8 Hz, 1H), 2.26(dd, J=15.6, 7.2 Hz, 1H), 2.21(d, J=10.1 Hz, 1H), 2.04(dd, J=15.4, 7.4 Hz, 2H), 1.81(s, 3H), 1.79—1.75(m, 1H), 1.74(s, 3H), 1.65(s, 3H), 1.66—1.62(m, 1H), 1.62(s, 3H), 1.55(s, 9H), 1.42(s, 3H), 1.35—1.25(m, 1H) | 194.8, 179.7, 161.3, 157.9, 157.7, 147.2, 142.7, 141.2, 131.9, 131.8, 130.8, 124.8, 123.8, 122.3, 115.9, 107.5, 102.7, 100.2, 92.6, 84.5, 84.2, 81.3, 71.5, 49.0, 42.0, 37.0, 34.0, 30.2, 28.6, 27.7, 25.7, 25.7, 24.9, 22.7, 21.9, 18.2, 17.7, 9.3 |
| 9 | 13.04(s, 1H), 7.63(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.17(t, J=6.6 Hz, 1H), 5.10(t, J=6.4 Hz, 1H), 5.07(t, J=7.2 Hz, 1H), 3.33(d, J=6.4 Hz, 2H), 3.29(s, 1H), 2.94—2.89(m, 1H), 2.66(d, J=12.3 Hz, 1H), 2.53(d, J=12.4 Hz, 1H), 2.47(dd, J=14.4, 6.5 Hz, 1H), 2.34(dd, J=14.0, 4.0 Hz, 1H), 2.19—2.14(m, 2H), 2.10—2.02(m, 8H), 1.83—1.77(m, 4H), 1.76(s, 3H), 1.65(s, 6H), 1.63(s, 3H), 1.62—1.59(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.42(s, 3H), 1.34—1.28(m, 1H) | 180.1, 161.0, 158.4, 157.6, 142.0, 136.2, 131.9, 131.4, 131.2, 124.5, 123.8, 122.6, 121.8, 116.0, 107.4, 102.4, 100.3, 100.0, 92.6, 84.7, 83.7, 81.1, 70.5, 59.7, 49.2, 45.2, 42.0, 36.9, 32.2, 30.3, 28.5, 27.7, 25.8, 25.6, 25.0, 23.0, 22.7, 22.0, 18.2, 17.6 |
| Compd. | 1H NMR(400 MHz, CDCl3), δ | 13C NMR(101 MHz, CDCl3), δ |
| iso⁃9 | 13.04(s, 1H), 7.61(d, J=7.1 Hz, 1H), 6.67(d, J=10.1 Hz, 1H), 5.43(d, J=10.1 Hz, 1H), 5.15—5.03(m, 3H), 3.32(d, J=6.1 Hz, 2H), 3.25(s, 1H), 3.01(br, 1H), 2.90—2.86(m, 1H), 2.62(q, J=12.2 Hz, 2H), 2.46(dd, J=14.4, 6.4 Hz, 1H), 2.33(dd, J=14.0, 3.7 Hz, 1H), 2.21—1.99(m, 10H), 1.83—1.70(m, 7H), 1.69—1.59(m, 7H), 1.55(s, 3H), 1.51(s, 3H), 1.47(s, 3H), 1.42(s, 3H), 1.35—1.25(m, 1H) | 179.1, 160.0, 157.4, 156.6, 140.9, 135.8, 130.8, 130.4, 130.2, 123.5, 122.8, 121.6, 119.6, 115.0, 106.5, 101.4, 99.3, 91.5, 83.9, 82.6, 80.0, 69.3, 67.9, 48.2, 44.1, 41.0, 35.9, 31.4, 29.3, 28.7, 27.5, 26.6, 24.7, 24.6, 24.1, 21.7, 20.9, 17.2, 16.6, 14.0 |
| 10 | 13.03(s, 1H), 7.63(d, J=6.9 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.43(d, J=10.1 Hz, 1H), 5.20(t, J=6.9 Hz, 1H), 5.14—5.03(m, 2H), 3.65—3.53(m, 4H), 3.33(d, J=5.6 Hz, 2H), 3.30(s, 1H), 3.09(br, 1H), 2.95—2.88(m, 1H), 2.69(d, J=12.4 Hz, 1H), 2.56(d, J=12.4 Hz, 1H), 2.45(dd, J=14.1, 5.9 Hz, 1H), 2.38—2.30(m, 1H), 2.27—2.13(m, 6H), 2.11—2.01(m, 2H), 1.80—1.73(m, 1H), 1.78(s, 3H), 1.76(s, 3H), 1.65(s, 6H), 1.62(s, 3H), 1.62—1.56(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.42(s, 3H), 1.37—1.28 (m, 1H) | 180.1, 161.0, 158.4, 157.6, 141.9, 135.4, 131.8, 131.4, 131.3, 124.5, 123.8, 122.5, 122.0, 116.0, 107.4, 102.4, 100.3, 92.6, 84.7, 83.8, 81.1, 70.5, 67.0, 58.9, 53.4, 49.2, 42.0, 36.9, 32.3, 30.3, 28.5, 27.7, 25.8, 25.6, 25.0, 23.3, 22.7, 22.0, 18.2, 17.6 |
| iso⁃10 | 13.04(s, 1H), 7.61(d, J=7.2 Hz, 1H), 6.68(d, J=10.1 Hz, 1H), 5.44(d, J=10.1 Hz, 1H), 5.17—5.08(m, 2H), 5.06(t, J=7.8 Hz, 1H), 3.68—3.58(m, 4H), 3.32(d, J=6.3 Hz, 2H), 3.25(s, 1H), 3.01(d, J=4.8 Hz, 1H), 2.94—2.87(m, 1H), 2.68(s, 2H), 2.44(dd, J=14.5, 6.2 Hz, 1H), 2.33(dd, J=14.1, 3.8 Hz, 1H), 2.26—2.17(m, 4H), 2.14(dd, J=13.4, 8.5 Hz, 2H), 2.09—2.02(m, 2H), 1.82—1.76(m, 4H), 1.75(s, 3H), 1.65(s, 3H), 1.64(s, 3H), 1.62—1.59(m, 1H), 1.56(s, 3H), 1.52(s, 3H), 1.45(s, 3H), 1.42(s, 3H), 1.31—1.25(m, 1H) | 180.0, 161.0, 158.4, 157.5, 141.9, 135.6, 131.8, 131.4, 131.2, 124.5, 123.8, 122.6, 120.9, 116.0, 107.5, 102.4, 100.3, 92.5, 84.9, 83.7, 81.1, 70.3, 67.6, 67.0, 53.4, 49.2, 42.0, 36.9, 32.4, 30.3, 28.5, 27.6, 25.7, 25.7, 25.1, 22.7, 21.9, 18.2, 17.6, 15.1 |
| 11 | 13.02(s, 1H), 7.60(d, J=7.1 Hz, 1H), 6.65(d, J=10.1 Hz, 1H), 5.40(d, J=10.1 Hz, 1H), 5.14(t, J=6.9 Hz, 1H), 5.11—4.97(m, 2H), 3.38—3.02(m, 4H), 2.87(s, 1H), 2.67(d, J=12.5 Hz, 1H), 2.55(d, J=12.7 Hz, 1H), 2.45—2.10(m, 15H), 2.07—1.97(m, 2H), 1.80—1.78(m, 1H), 1.75(s, 3H), 1.72(s, 3H), 1.62(s, 6H), 1.61—1.58(m, 1H), 1.57(s, 3H), 1.53(s, 3H), 1.49(s, 3H), 1.40(s, 3H), 1.38—1.31(m, 1H) | 180.2, 161.1, 158.5, 157.7, 142.1, 136.0, 132.0, 131.5, 131.4, 124.5, 124.0, 122.7, 121.9, 116.2, 107.6, 102.5, 100.4, 92.8, 84.9, 83.9, 81.2, 70.6, 58.7, 55.2, 53.0, 49.3, 46.1, 42.2, 37.1, 32.4, 30.5, 28.7, 27.9, 25.9, 25.8, 25.2, 23.6, 22.8, 22.1, 18.4, 17.8 |
| Compd. | HL⁃60 | BEL⁃7402 | A⁃549 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 10-4 mol/L | 10-5 mol/L | 10-6 mol/L | 10-7 mol/L | 10-4 mol/L | 10-5 mol/L | 10-6 mol/L | 10-4 mol/L | 10-5 mol/L | 10-6 mol/L | |||
| 2 | 57.5 | 79.7 | 84.5 | 9.2 | 55.0 | 57.6 | 0 | 87.0 | 94.5 | 88.2 | ||
| 5 | 77.4 | 80.6 | 79.8 | 29.4 | 82.1 | 73.3 | 10.5 | 95.0 | 96.9 | 86.1 | ||
| 6 | 69.6 | 81.6 | 84.9 | 17.9 | 79.0 | 59.1 | 0 | 92.6 | 96.8 | 86.7 | ||
| 7 | 77.9 | 74.6 | 65.3 | 25.2 | 77.1 | 26.0 | 15.2 | 96.3 | 96.4 | 51.4 | ||
| 8 | 76.3 | 75.0 | 81.7 | 20.9 | 80.0 | 64.2 | 11.3 | 96.3 | 97.0 | 87.8 | ||
| 9 | 59.7 | 75.5 | 84.9 | 21.1 | 87.7 | 86.6 | 10.3 | 91.6 | 97.6 | 3.7 | ||
| 10 | 61.4 | 82.7 | 82.6 | 27.1 | 75.9 | 50.0 | 28.2 | 93.0 | 96.4 | 67.8 | ||
| 11 | 45.1 | 81.0 | 86.7 | 27.5 | 85.1 | 93.1 | 20.9 | 88.0 | 97.1 | 4.2 | ||
| GA | 80.7 | 84.6 | 85.5 | 57.0 | 90.8 | 94.2 | 12.5 | 95.4 | 96.4 | 79.8 | ||
Table 3 In vitro inhibition(%) of cancer cell proliferation by GA derivatives*
| Compd. | HL⁃60 | BEL⁃7402 | A⁃549 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 10-4 mol/L | 10-5 mol/L | 10-6 mol/L | 10-7 mol/L | 10-4 mol/L | 10-5 mol/L | 10-6 mol/L | 10-4 mol/L | 10-5 mol/L | 10-6 mol/L | |||
| 2 | 57.5 | 79.7 | 84.5 | 9.2 | 55.0 | 57.6 | 0 | 87.0 | 94.5 | 88.2 | ||
| 5 | 77.4 | 80.6 | 79.8 | 29.4 | 82.1 | 73.3 | 10.5 | 95.0 | 96.9 | 86.1 | ||
| 6 | 69.6 | 81.6 | 84.9 | 17.9 | 79.0 | 59.1 | 0 | 92.6 | 96.8 | 86.7 | ||
| 7 | 77.9 | 74.6 | 65.3 | 25.2 | 77.1 | 26.0 | 15.2 | 96.3 | 96.4 | 51.4 | ||
| 8 | 76.3 | 75.0 | 81.7 | 20.9 | 80.0 | 64.2 | 11.3 | 96.3 | 97.0 | 87.8 | ||
| 9 | 59.7 | 75.5 | 84.9 | 21.1 | 87.7 | 86.6 | 10.3 | 91.6 | 97.6 | 3.7 | ||
| 10 | 61.4 | 82.7 | 82.6 | 27.1 | 75.9 | 50.0 | 28.2 | 93.0 | 96.4 | 67.8 | ||
| 11 | 45.1 | 81.0 | 86.7 | 27.5 | 85.1 | 93.1 | 20.9 | 88.0 | 97.1 | 4.2 | ||
| GA | 80.7 | 84.6 | 85.5 | 57.0 | 90.8 | 94.2 | 12.5 | 95.4 | 96.4 | 79.8 | ||
| Compd. | A⁃549 | HELF⁃6 | Compd. | A⁃549 | HELF⁃6 |
|---|---|---|---|---|---|
| 2 | 6.3±1.6 | 28.3±3.1 | 9 | 9.4±3.2 | 47±3.4 |
| 3 | 3.1±0.0 | 33.0±7.7 | 10 | 3.9±0.0 | 77.0±22.6 |
| 5 | 1.8±0.0 | 4.9±0.0 | 11 | 6.1±0.0 | 68.0±11.8 |
| 6 | 6.5±1.6 | 11.4±0.0 | iso⁃9 | 8.6±3.2 | 134.2±8.8 |
| 7 | 2.4±0.0 | 3.2±1.6 | iso⁃10 | 1.2±0.0 | 22.6±2.6 |
| 8 | 2.1±0.0 | 4.9±1.6 | GA | 1.1±0.0 | 4.8±1.6 |
Table 4 In vitro IC50(μmol∙L-1) by GA derivatives
| Compd. | A⁃549 | HELF⁃6 | Compd. | A⁃549 | HELF⁃6 |
|---|---|---|---|---|---|
| 2 | 6.3±1.6 | 28.3±3.1 | 9 | 9.4±3.2 | 47±3.4 |
| 3 | 3.1±0.0 | 33.0±7.7 | 10 | 3.9±0.0 | 77.0±22.6 |
| 5 | 1.8±0.0 | 4.9±0.0 | 11 | 6.1±0.0 | 68.0±11.8 |
| 6 | 6.5±1.6 | 11.4±0.0 | iso⁃9 | 8.6±3.2 | 134.2±8.8 |
| 7 | 2.4±0.0 | 3.2±1.6 | iso⁃10 | 1.2±0.0 | 22.6±2.6 |
| 8 | 2.1±0.0 | 4.9±1.6 | GA | 1.1±0.0 | 4.8±1.6 |
| [1] | Zhang N., Deng C. X., Lin H. L., Gao Y. G., Chem. J. Chinese Universities, 2024, 45(12), 20240363 |
| 张楠, 邓昌选, 林汉琳, 高阳光. 高等学校化学学报, 2024, 45(12), 20240363 | |
| [2] | Chen Y. M., She H. X., Wang Q., Yang J. Q., Chem. J. Chinese Universities, 2025, 46(9), 20250147 |
| 陈阳密, 佘慧娴, 汪晴, 杨家强. 高等学校化学学报, 2025, 46(9), 20250147 | |
| [3] | Yang Y., Yang L., You Q. D., Nie F. F., Gu H. Y., Zhao L., Wang X. T., Guo Q. L., Cancer Lett., 2007, 256(2), 259—266 |
| [4] | Duan D. Z., Zhang B. X., Yao J., Liu Y. P., Sun J. Y., Ge C. P., Peng S. J., Fang J. G., Free Radical Bio. Med., 2014, 69, 15—25 |
| [5] | Hatami E., Nagesh P. K. B., Jaggi M., Chauhan S. C., Yallapu M. M., Eur. J. Pharmacol., 2020, 888, 173486 |
| [6] | Lee P. N. H., Ho W. S., Oncol. Rep., 2013, 29(5), 1744—1750 |
| [7] | Jang J. H., Kim J. Y., Sung E. G., Kim E. A., Lee T. J., Int. J. Oncol., 2016, 48(1), 376—384 |
| [8] | Kuemmerle J., Jiang S. C., Tseng B., Kasibhatla S., Drewe J., Cai S. X., Bioorg. Med. Chem., 2008, 16(8), 4233—4241 |
| [9] | Sun H. P., Chen F. H., Wang X. J., Liu Z. L., Yang Q., Zhang X. J., Zhu J., Qiang L., Guo Q. L., You Q. D., Eur. J Med. Chem., 2012, 51, 110—123 |
| [10] | Li X., Zhang X. J., Wang X. J., Li N. G., Lin C. J., Gao Y., Yu Z. Q., Guo Q. L., You Q. D., Chin. J. Chem., 2012, 30(1), 35—42 |
| [11] | Weakley T. J. R., Cai S. X., Zhang H. Z., Keana J. F. W., J. Chem. Crystallogr., 2002, 31(11—12), 501—505 |
| [12] | Chen T., Zhang R. H., He S. C., Xu Q. Y., Ma L., Wang G. C., Qiu N., Peng F., Chen J. Y., Qiu J. X., Peng A. H., Chen L. J., Molecules., 2012, 17(6), 6249—6268 |
| [13] | Yang J., Li C. L., Ding L., Guo Q. L., You Q. D., Jin S. H., J. Nat. Prod., 2012, 75(6), 1108—1116 |
| [14] | Zhang H. Z., Kasibhatla S., Wang Y., Herich J., Guastella J., Tseng B., Drewe J., Cai S. X., Bioorg. Med. Chem., 2004, 12(2), 309—317 |
| [15] | Liu Y. L., Chen Y. C., Lin L. F., Li H., Int. J. Nanomed., 2020, 15, 10385—10399 |
| [16] | Li M., Su F. L., Zhu M. T., Zhang H., Wei Y. X., Zhao Y., Li J. M., Lv S. W., Molecules, 2022, 27(9), 2937 |
| [17] | Wang J. X., Zhao L., Hu Y., Guo Q. L., Zhang L., Wang X. J., Li N. G., You Q. D., Eur. J. Med. Chem., 2009, 44(6), 2611—2620 |
| [18] | Zhang X. J., Li X., Yang Y. R., Sun H. P., Gao Y., Zhang L., Wang J. X., Guo Q. L., You Q. D., Chem. Biodivers., 2012, 9(10), 2295—2308 |
| [19] | Xu W., Wang H. L., Dong L. H., Zhang P., Mu Y., Cui X. Y., Zhou J. P., Huo M. R., Yin T. J., Int. J. Nanomed., 2019, 14, 4649—4666 |
| [20] | Wang X. J., Lu N., Yang Q., Dai Q. S.,Tao L., Guo X. K., Guo Q. L., You Q. D., Bioorg. Med. Chem. Lett., 2010, 20(8), 2438—2442 |
| [21] | Wang J. X., Yang Y., Ma J. H., Zhang L., Guo Q. L., You Q. D., Chem. J. Chinese Universities, 2010, 31(6), 1172—1178 |
| 王进欣, 杨燕, 马俊海, 张磊, 郭青龙, 尤启冬. 高等学校化学学报, 2010, 31(6), 1172—1178 | |
| [22] | He L. Q., Ling Y., Fu L., Yin D. K., Wang X. S., Zhang Y. H., Bioorg. Med. Chem. Lett., 2012, 22(1), 289—292 |
| [23] | Ling H. P., Li H., Chen M. J., Lai B. L., Zhou H. M., Gao H., Zhang J. Y., Huang Y., Tao Y. W., Anticancer Agents Med. Chem., 2021, 21(9), 1110—1119 |
| [24] | Seo M. J., Lee D. M., Kim I. Y., Lee D., Choi M. K., Lee J. Y., Park S. S., Jeong S. Y., Choi E. K., Choi K. S., Cell. Death Dis., 2019, 10, 187 |
| [25] | Zhao Y., Qiao L., Zhao G. F., Chen L., Chem. J. Chinese Universities, 2021, 42(9), 2789—2797 |
| 赵莹, 乔玲, 赵国锋, 陈莉. 高等学校化学学报, 2021, 42(9), 2789—2797 | |
| [26] | Lee S. B., Fractionated Products Obtained from Gamboge Resin, and Medical Uses of the Same,EP2395007, 2011⁃12⁃14 |
| [27] | Ren Y. L., Yuan C. H., Chai H. B., Ding Y. Q., Li X. C., Ferreira D., Kinghorn A. D., J. Nat. Prod., 2011, 74(3), 460—463 |
| [1] | LIU Hong,ZOU Guojun,SUN Xinyuan,OUYANG Jianming. Differences of Growth and Cytotoxicity of Calcium Oxalate Crystals Formed on HK-2 Cells Under Different Oxalic Acid/Calcium Ratios [J]. Chem. J. Chinese Universities, 2020, 41(6): 1231. |
| [2] | LUO Zewei, WANG Yimin, LIU Kunping, WEI Fujing, LI Yu, DUAN Yixiang. Preparation of a Functionalized Graphene and Its Role as Delivery Carrier for Anti-cancer Drug† [J]. Chem. J. Chinese Universities, 2016, 37(10): 1900. |
| [3] | ZHANG Jianghua, LÜ Ying, JIA Hongliang, SONG Yinyin, SUN Xiaoxia, CHAI Dunxiao, WANG Lanying. Synthesis, Crystal Structure and Spectral Properties of Six Indole Dimethine Cyanines as Well as Their Biological Application† [J]. Chem. J. Chinese Universities, 2015, 36(10): 1924. |
| [4] | ZHENG Yongbiao, PANG Haiyue, WANG Jifeng, CHEN Danxia, SHI Guowei, HUANG Jianzhong. Novel Diketopiperazine and Ten-membered Macrolides from the Entomogenous Fungus Paecilomyces tenuipes† [J]. Chem. J. Chinese Universities, 2014, 35(8): 1665. |
| [5] | ZENG Li, Hu Jun, WEI Junchao. Controlled Release of Multiple Hydrophilic and Hydrophobic Drugs and in vitro Cytotoxicity of Electrospun Poly(lactic-co-glycolic acid)/ZnO Nanofibers Encapsulated with Dual Drugs† [J]. Chem. J. Chinese Universities, 2014, 35(8): 1788. |
| [6] | WANG Hai, ZHANG Chao, ZHANG Linhua, LIU Lanxia, ZHENG Yi, ZHU Dunwan. Synthesis of Nanoparticles of Star-shaped Mannitol-core PLA-TPGS Copolymer for Delivery of Paclitaxel and Activity of Anti-prostate Cancer† [J]. Chem. J. Chinese Universities, 2014, 35(10): 2239. |
| [7] | XU Yu-Dong, ZHANG Zheng-Yong, KONG Ji-Lie, LI Guo-Dong, XIONG Huan-Ming. Photoluminescent ZnO Quantum Dots Coated by Polymethacrylamide and Their Application in Cell Imaging [J]. Chem. J. Chinese Universities, 2013, 34(7): 1565. |
| [8] | LI Xiao-Dong, YANG Shu-Min, XU Hong, MA Yu-Guang. Evaluation of the Cytotoxicity About Photic Organic Nanoparticles [J]. Chem. J. Chinese Universities, 2012, 33(01): 210. |
| [9] | YANG Bao-Chun, JIANG Yao-Dong, QIN Xue-Juan, CHEN Zhi-Liang, REN Fei. Loaded and in vitro Drug Release of Anticancer Drugs in Porous Metal-Organic Frameworks [J]. Chem. J. Chinese Universities, 2012, 33(01): 26. |
| [10] | GUO Ling-Xiang, GAO Qiu-Duan. Synthesis and Performance of PAMAM-Lys Dendrimer [J]. Chem. J. Chinese Universities, 2012, 33(01): 176. |
| [11] | LI Fei-Fan, TIAN Hua-Fu, CHEN Lei, XIA Jia-Liang, CHEN Xue-Si*, JING Xia-Bin. Synthesis and Characterization of the Hexachlorotriphosphaxene Cross-linked Oligo(ethyleneimine) as Gene Carrier [J]. Chem. J. Chinese Universities, 2010, 31(9): 1896. |
| [12] | WANG Jin-Xin, YANG Yan, MA Jun-Hai, ZHANG Lei, GUO Qing-Long, YOU Qi-Dong. Synthesis of Gambogic Acid Oxidative Analogues and Their Dimension Quantity Structure-activity Relationship Analysis [J]. Chem. J. Chinese Universities, 2010, 31(6): 1172. |
| [13] | YIN Yue-Fan, LI Yan-Mei, ZI Yan-Nan, Zhou Yi-Ping, BI Yun-Mei*. Synthesis, Characterization, in Vitro Degradation and Cytotoxicity of Poly{[2-(2-oxy-1-pyrrolidiny) ethoxy]1.0(methoxyethoxyethoxy)1.0] phosphazene} [J]. Chem. J. Chinese Universities, 2009, 30(6): 1245. |
| [14] | CHEN Su-Yun, SUN Guo-Ming, JIANG Lei, LI Nan, LI Pei-Yong*, ZHU Xin-Yuan*. Biocompatibility and Biodistribution of a Novel Cationic Polymer——Hyperbranched Poly(sulfone-amine) as an Intracellular Delivery System [J]. Chem. J. Chinese Universities, 2009, 30(4): 825. |
| [15] | JIANG Cheng, CHEN Su-Ting, YOU Qi-Dong*, LI Zhi-Yu, TANG Wei-Juan. Synthesis and Bioactivities of Novel Indolocarbazole Derivatives [J]. Chem. J. Chinese Universities, 2009, 30(10): 1972. |
| Viewed | ||||||
|
Full text |
|
|||||
|
Abstract |
|
|||||