| Company Name: |
Sigma-Aldrich |
| Tel: |
021-61415566 800-8193336 |
| Email: |
orderCN@merckgroup.com |
|
| | Benz[g]isoquinoline-5,10-dione Basic information |
| Product Name: | Benz[g]isoquinoline-5,10-dione | | Synonyms: | 2-aza-9,10-anthraquinone;benzo(g)isoquinoline-5,10-dione;2-Azaanthraquinone;3,4-Phthaloylpyridine;5,10-Dihydrobenzo[g]isoquinoline-5,10-dione;β-Anthrapyridinequinone;Bgid;Biquidone | | CAS: | 46492-08-4 | | MF: | C13H7NO2 | | MW: | 209.2 | | EINECS: | | | Product Categories: | | | Mol File: | 46492-08-4.mol | ![Benz[g]isoquinoline-5,10-dione Structure](CAS/GIF/46492-08-4.gif) |
| | Benz[g]isoquinoline-5,10-dione Chemical Properties |
| Melting point | 178-180 °C(lit.) | | Boiling point | 407℃ | | density | 1.373 | | Fp | 202℃ | | pka | 1.10±0.20(Predicted) | | InChI | 1S/C13H7NO2/c15-12-8-3-1-2-4-9(8)13(16)11-7-14-6-5-10(11)12/h1-7H | | InChIKey | ZLLVUAAESHIVAZ-UHFFFAOYSA-N | | SMILES | O=C1c2ccccc2C(=O)c3cnccc13 |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | Benz[g]isoquinoline-5,10-dione Usage And Synthesis |
| Uses | Benz[g]isoquinoline-5,10-dione, an active component isolated from the ethanolic extract of the aerial parts of Mitracarpus scaber, demonstrates notable in vitro inhibitory activity against AIDS-related pathogens, along with significant antibacterial and antifungal properties, as evidenced by the agar well-diffusion assay. | | General Description | Benz[g]isoquinoline-5,10-dione has been isolated as an active component from the ethanolic extract of the aerial parts of Mitracarpus scaber. It exhibits significant in vitro inhibitory activity against the AIDS-related pathogens. The in vitro antibacterial and anti-fungal activity of benz[g]isoquinoline-5,10-dione has been investigated using the agar well-diffusion assay. | | References | [1] Quantitative determination of lysophosphatidic acid by LC/ESI/MS/MS employing a reversed phase HPLC column
[2] Source and role of intestinally derived lysophosphatidic acid in dyslipidemia and atherosclerosis
[3] Lysophosphatidic acid triggers apoptosis in HeLa cells through the upregulation of tumor necrosis factor receptor superfamily member 21
[4] Exogenous lysophospholipids with large head groups perturb clathrin-mediated endocytosis |
| | Benz[g]isoquinoline-5,10-dione Preparation Products And Raw materials |
|