HRID1733197

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：O=S([O-])CNc1ccc(S(=O)(=O)c2ccc(NCS(=O)[O-])cc2)cc1.[Na+].[Na+]

HCID8954

Adesulfone sodium

C14H14N2Na2O6S3

结构：CN[C@@H]1[C@H](O[C@H]2[C@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](N=C(N)N)[C@@H](O)[C@@H]3N=C(N)N)O[C@@H](C)[C@]2(O)C=O)O[C@@H](CO)[C@H](O)[C@H]1O.O=S(=O)(O)O

HCID16051958

未命名化合物

结构：O=C1O[C@H]([C@@H](O)CO)C([O-])=C1O.[Na+]

HCID23667548

Sodium L-ascorbate

C6H7NaO6

PRODUCTS

生成物

结构：O=S(O)CNc1ccc(S(=O)(=O)c2ccc(NCS(=O)O)cc2)cc1

HCID5351

Sulfoxone

C14H16N2O6S3

PROCEDURE

实验过程

Similarly, repeating the above procedure but replacing the sulfoxone sodium and sodium ascorbate with 50 mg/ml streptomycin sulfate, synthetic lipid vesicles are obtained encapsulating such material, for use as an antibacterial preparation for applications to plants.

WORKUP

后处理

customare obtained
customfor use as an antibacterial preparation for applications to plants

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-be9d9e42ddae4b5aad68502328374e5d
来源数据集: uspto-grants-1980_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04241046
来源说明: uspto-grants-1980_12

反应 SMILES

[CH:1]1[C:6]([NH:7][CH2:8][S:9]([O-:11])=[O:10])=[CH:5][CH:4]=[C:3]([S:12]([C:15]2[CH:16]=[CH:17][C:18]([NH:21][CH2:22][S:23]([O-:25])=[O:24])=[CH:19][CH:20]=2)(=[O:14])=[O:13])[CH:2]=1.[Na+].[Na+].O=C1O[C@H]([C@H](CO)O)C([O-])=C1O.[Na+].C[C@@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](N=C(N)N)[C@@H](O)[C@@H]2N=C(N)N)[C@H](O[C@@H]2O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]2NC)[C@@]1(O)C=O.OS(O)(=O)=O>>[CH:19]1[C:18]([NH:21][CH2:22][S:23]([OH:25])=[O:24])=[CH:17][CH:16]=[C:15]([S:12]([C:3]2[CH:2]=[CH:1][C:6]([NH:7][CH2:8][S:9]([OH:11])=[O:10])=[CH:5][CH:4]=2)(=[O:14])=[O:13])[CH:20]=1