3. 结构
3.1 二维结构
3.2 三维结构
-1
-2
-3
26 26 0 0 0 0 0 0 0999 V2000
3.8563 0.5900 0.0932 O 0 0 0 0 0 0 0 0 0 0 0 0
3.3694 -1.6459 -0.2253 O 0 0 0 0 0 0 0 0 0 0 0 0
-6.0089 0.8404 0.1136 N 0 0 0 0 0 0 0 0 0 0 0 0
-0.8003 -0.4954 -0.0777 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.1918 0.8223 -0.3142 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.7592 -1.4671 0.2082 C 0 0 0 0 0 0 0 0 0 0 0 0
0.6080 -0.8557 -0.1269 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5421 1.1684 -0.2647 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.1095 -1.1212 0.2577 C 0 0 0 0 0 0 0 0 0 0 0 0
-3.5010 0.1967 0.0212 C 0 0 0 0 0 0 0 0 0 0 0 0
5.2579 0.3006 0.0640 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6395 0.0096 -0.0083 C 0 0 0 0 0 0 0 0 0 0 0 0
3.0346 -0.4829 -0.0644 C 0 0 0 0 0 0 0 0 0 0 0 0
6.0312 1.5884 0.2515 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.8841 0.5518 0.0722 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.4831 1.6078 -0.5598 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4730 -2.4990 0.3971 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8148 -1.9157 -0.2592 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.8326 2.1989 -0.4555 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.8453 -1.8897 0.4823 H 0 0 0 0 0 0 0 0 0 0 0 0
5.5030 -0.3994 0.8706 H 0 0 0 0 0 0 0 0 0 0 0 0
5.5176 -0.1504 -0.9003 H 0 0 0 0 0 0 0 0 0 0 0 0
1.5000 1.0728 0.1513 H 0 0 0 0 0 0 0 0 0 0 0 0
7.1089 1.4035 0.2344 H 0 0 0 0 0 0 0 0 0 0 0 0
5.7828 2.3055 -0.5379 H 0 0 0 0 0 0 0 0 0 0 0 0
5.7684 2.0605 1.2039 H 0 0 0 0 0 0 0 0 0 0 0 0
1 11 1 0 0 0 0
1 13 1 0 0 0 0
2 13 2 0 0 0 0
3 15 3 0 0 0 0
4 5 2 0 0 0 0
4 6 1 0 0 0 0
4 7 1 0 0 0 0
5 8 1 0 0 0 0
5 16 1 0 0 0 0
6 9 2 0 0 0 0
6 17 1 0 0 0 0
7 12 2 0 0 0 0
7 18 1 0 0 0 0
8 10 2 0 0 0 0
8 19 1 0 0 0 0
9 10 1 0 0 0 0
9 20 1 0 0 0 0
10 15 1 0 0 0 0
11 14 1 0 0 0 0
11 21 1 0 0 0 0
11 22 1 0 0 0 0
12 13 1 0 0 0 0
12 23 1 0 0 0 0
14 24 1 0 0 0 0
14 25 1 0 0 0 0
14 26 1 0 0 0 0
4. 国际命名与标识
4.1 IUPAC Name
ethyl (E)-3-(4-cyanophenyl)prop-2-enoate
4.2 InChl
InChI=1S/C12H11NO2/c1-2-15-12(14)8-7-10-3-5-11(9-13)6-4-10/h3-8H,2H2,1H3/b8-7+
4.3 InChlKey
NVLBOCIUMFYPGI-BQYQJAHWSA-N
4.4 Canonical SMILES
CCOC(=O)C=CC1=CC=C(C=C1)C#N
4.5 lsomeric SMILES
CCOC(=O)/C=C/C1=CC=C(C=C1)C#N
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
7. 相关靶点
8. 相关疾病