3. 结构
3.1 二维结构
3.2 三维结构
-1
-2
-3
56 59 0 1 0 0 0 0 0999 V2000
-3.3434 -0.4134 -0.6615 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.6477 0.5621 1.3407 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.3616 -2.4561 1.2319 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.5122 -3.2683 -1.4092 O 0 0 0 0 0 0 0 0 0 0 0 0
-4.0782 -1.4140 2.7749 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.6040 -0.8268 -3.2765 O 0 0 0 0 0 0 0 0 0 0 0 0
1.9843 0.1226 0.4207 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.6570 3.1164 0.2783 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.3617 4.2010 -0.7227 O 0 0 0 0 0 0 0 0 0 0 0 0
2.1855 3.8623 -1.1832 O 0 0 0 0 0 0 0 0 0 0 0 0
4.9960 -3.8805 0.0389 O 0 0 0 0 0 0 0 0 0 0 0 0
7.5623 -2.8630 0.3636 O 0 0 0 0 0 0 0 0 0 0 0 0
-5.0368 -2.2682 0.7317 C 0 0 1 0 0 0 0 0 0 0 0 0
-5.1282 -2.0493 -0.7786 C 0 0 1 0 0 0 0 0 0 0 0 0
-4.3957 -1.0672 1.4271 C 0 0 2 0 0 0 0 0 0 0 0 0
-3.7818 -1.5898 -1.3433 C 0 0 1 0 0 0 0 0 0 0 0 0
-3.1059 -0.6416 0.7256 C 0 0 1 0 0 0 0 0 0 0 0 0
-3.8777 -1.2523 -2.8278 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4999 1.1045 0.8411 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4999 2.3926 0.3037 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3214 0.3584 0.8715 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8578 0.9033 0.3630 C 0 0 0 0 0 0 0 0 0 0 0 0
0.8560 2.1900 -0.1731 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3217 2.9404 -0.2053 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1136 2.7403 -0.7013 C 0 0 0 0 0 0 0 0 0 0 0 0
3.1695 0.6349 -0.0845 C 0 0 0 0 0 0 0 0 0 0 0 0
3.2965 1.8599 -0.6190 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3190 -0.2849 0.0326 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9319 3.9369 1.4109 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1203 -1.6668 -0.0193 C 0 0 0 0 0 0 0 0 0 0 0 0
5.6103 0.2228 0.1962 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2059 -2.5356 0.0914 C 0 0 0 0 0 0 0 0 0 0 0 0
6.6959 -0.6458 0.3070 C 0 0 0 0 0 0 0 0 0 0 0 0
6.4937 -2.0250 0.2546 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.4853 -3.1878 0.9631 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.9089 -1.3091 -0.9929 H 0 0 0 0 0 0 0 0 0 0 0 0
-5.1046 -0.2318 1.4733 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.0165 -2.3685 -1.2216 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.3469 -1.4252 0.8494 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.5851 -0.4362 -3.0083 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.1803 -2.1194 -3.4217 H 0 0 0 0 0 0 0 0 0 0 0 0
-6.7452 -3.2160 0.7615 H 0 0 0 0 0 0 0 0 0 0 0 0
-4.8217 -3.9292 -1.2306 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.4501 -2.1562 2.7556 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.3421 -0.0613 -2.7366 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.3039 -0.6380 1.3047 H 0 0 0 0 0 0 0 0 0 0 0 0
4.2213 2.2534 -1.0244 H 0 0 0 0 0 0 0 0 0 0 0 0
0.5128 4.4693 -1.0426 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.8805 4.4525 1.2382 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.1459 4.6868 1.5449 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.0258 3.3265 2.3147 H 0 0 0 0 0 0 0 0 0 0 0 0
3.1254 -2.0856 -0.1542 H 0 0 0 0 0 0 0 0 0 0 0 0
5.8070 1.2895 0.2638 H 0 0 0 0 0 0 0 0 0 0 0 0
7.6935 -0.2352 0.4385 H 0 0 0 0 0 0 0 0 0 0 0 0
5.8551 -4.3280 0.1314 H 0 0 0 0 0 0 0 0 0 0 0 0
8.3709 -2.3331 0.4701 H 0 0 0 0 0 0 0 0 0 0 0 0
1 16 1 0 0 0 0
1 17 1 0 0 0 0
2 17 1 0 0 0 0
2 19 1 0 0 0 0
3 13 1 0 0 0 0
3 42 1 0 0 0 0
4 14 1 0 0 0 0
4 43 1 0 0 0 0
5 15 1 0 0 0 0
5 44 1 0 0 0 0
6 18 1 0 0 0 0
6 45 1 0 0 0 0
7 22 1 0 0 0 0
7 26 1 0 0 0 0
8 20 1 0 0 0 0
8 29 1 0 0 0 0
9 24 1 0 0 0 0
9 48 1 0 0 0 0
10 25 2 0 0 0 0
11 32 1 0 0 0 0
11 55 1 0 0 0 0
12 34 1 0 0 0 0
12 56 1 0 0 0 0
13 14 1 0 0 0 0
13 15 1 0 0 0 0
13 35 1 0 0 0 0
14 16 1 0 0 0 0
14 36 1 0 0 0 0
15 17 1 0 0 0 0
15 37 1 0 0 0 0
16 18 1 0 0 0 0
16 38 1 0 0 0 0
17 39 1 0 0 0 0
18 40 1 0 0 0 0
18 41 1 0 0 0 0
19 20 2 0 0 0 0
19 21 1 0 0 0 0
20 24 1 0 0 0 0
21 22 2 0 0 0 0
21 46 1 0 0 0 0
22 23 1 0 0 0 0
23 24 2 0 0 0 0
23 25 1 0 0 0 0
25 27 1 0 0 0 0
26 27 2 0 0 0 0
26 28 1 0 0 0 0
27 47 1 0 0 0 0
28 30 2 0 0 0 0
28 31 1 0 0 0 0
29 49 1 0 0 0 0
29 50 1 0 0 0 0
29 51 1 0 0 0 0
30 32 1 0 0 0 0
30 52 1 0 0 0 0
31 33 2 0 0 0 0
31 53 1 0 0 0 0
32 34 2 0 0 0 0
33 34 1 0 0 0 0
33 54 1 0 0 0 0
4. 国际命名与标识
4.1 IUPAC Name
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
4.2 InChl
InChI=1S/C22H22O12/c1-31-21-14(33-22-20(30)19(29)17(27)15(7-23)34-22)6-13-16(18(21)28)11(26)5-12(32-13)8-2-3-9(24)10(25)4-8/h2-6,15,17,19-20,22-25,27-30H,7H2,1H3/t15-,17-,19+,20-,22-/m1/s1
4.3 InChlKey
DMXHXBGUNHLMQO-IWLDQSELSA-N
4.4 Canonical SMILES
COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O
4.5 lsomeric SMILES
COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
4.6 SDF文件
5. 波谱数据
5.1 13C核磁共振谱(13C NMR)
5.2 1H核磁共振谱(1H NMR)
5.3 质谱(MS)
5.4 红外光谱(IR)
5.5 紫外/可见光谱(UV/Vis)
6. 相关药材
中文名称 |
英文名称 |
拉丁文名称 |
大麻叶泽兰 |
Hemp-agrimony |
Eupatorium cannabinum |
何首乌 |
Tuber Fleeceflower |
Polygonum multiflorum |
加灰色九里香婆婆纳 |
Thyme Speedwell |
Veronica thymoides ssp. pseudocinerea |
金沸草 |
All - grass of Japanese Inula |
Herba Inulae |
荔枝草 |
Common Sage |
Salvia plebeia |
毛地黄 |
Common Foxglove Equivalent plant: Digitalis lanata |
Digitalis purpurea |
毛花毛地黄 |
Grecian Foxglove |
Digitalis lanata |
迷迭香 |
Rosemary |
Rosmarinus officinalis |
蓬莱草 |
Knotteflower Phyla Herb |
Lippia nodiflora |
向日葵叶 |
Sunflower Leaf |
Helianthus annuus |
7. 相关靶点
8. 相关疾病