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
3.3336 -0.7712 0.3106 O 0 0 0 0 0 0 0 0 0 0 0 0
1.8336 -0.9008 -1.4260 O 0 0 0 0 0 0 0 0 0 0 0 0
-3.3248 -1.8428 0.6564 O 0 5 0 0 0 0 0 0 0 0 0 0
-4.3650 -0.1979 -0.3593 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.0292 0.6607 0.0853 N 0 0 0 0 0 0 0 0 0 0 0 0
-2.0638 1.2281 -0.6007 N 0 0 0 0 0 0 0 0 0 0 0 0
-3.3034 -0.7063 0.1026 N 0 3 0 0 0 0 0 0 0 0 0 0
1.4852 0.7564 0.3406 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1377 2.0392 -0.2165 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7212 0.7307 1.8672 C 0 0 0 0 0 0 0 0 0 0 0 0
2.2037 -0.4090 -0.3653 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.8449 -0.3788 0.4336 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.8052 1.6016 -0.5325 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0954 -0.0056 0.0002 C 0 0 0 0 0 0 0 0 0 0 0 0
4.1166 -1.8044 -0.2961 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7074 2.9370 0.2413 H 0 0 0 0 0 0 0 0 0 0 0 0
3.2176 2.0532 -0.0276 H 0 0 0 0 0 0 0 0 0 0 0 0
2.0005 2.1153 -1.3016 H 0 0 0 0 0 0 0 0 0 0 0 0
1.1286 1.5054 2.3678 H 0 0 0 0 0 0 0 0 0 0 0 0
1.4364 -0.2356 2.2990 H 0 0 0 0 0 0 0 0 0 0 0 0
2.7730 0.9036 2.1225 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.4767 -1.2613 0.9387 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.4179 2.5357 -0.9140 H 0 0 0 0 0 0 0 0 0 0 0 0
4.9825 -1.9944 0.3437 H 0 0 0 0 0 0 0 0 0 0 0 0
4.4709 -1.4825 -1.2800 H 0 0 0 0 0 0 0 0 0 0 0 0
3.5310 -2.7251 -0.3772 H 0 0 0 0 0 0 0 0 0 0 0 0
1 11 1 0 0 0 0
1 15 1 0 0 0 0
2 11 2 0 0 0 0
3 7 1 0 0 0 0
4 7 2 0 0 0 0
5 8 1 0 0 0 0
5 12 1 0 0 0 0
5 13 1 0 0 0 0
6 13 2 0 0 0 0
6 14 1 0 0 0 0
7 14 1 0 0 0 0
8 9 1 0 0 0 0
8 10 1 0 0 0 0
8 11 1 0 0 0 0
9 16 1 0 0 0 0
9 17 1 0 0 0 0
9 18 1 0 0 0 0
10 19 1 0 0 0 0
10 20 1 0 0 0 0
10 21 1 0 0 0 0
12 14 2 0 0 0 0
12 22 1 0 0 0 0
13 23 1 0 0 0 0
15 24 1 0 0 0 0
15 25 1 0 0 0 0
15 26 1 0 0 0 0
M CHG 2 3 -1 7 1
4. 国际命名与标识
4.1 IUPAC Name
methyl 2-methyl-2-(4-nitroimidazol-1-yl)propanoate
4.2 InChl
InChI=1S/C8H11N3O4/c1-8(2,7(12)15-3)10-4-6(9-5-10)11(13)14/h4-5H,1-3H3
4.3 InChlKey
MMZRRMWHKGPBGH-UHFFFAOYSA-N
4.4 Canonical SMILES
CC(C)(C(=O)OC)N1C=C(N=C1)[N+](=O)[O-]
4.5 lsomeric SMILES
-
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