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| | 2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione Basic information |
| Product Name: | 2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione | | Synonyms: | 2-Bromoaldisine;2-bromo-1,5,6,7-tetrahydropyrrolo[2,3-c]azepine-4,8-dione;2-bromo-1H,4H,5H,6H,7H,8H-pyrrolo[2,3-c]azepine-4,8-dione;2-BROMO-6,7-DIHYDRO-1H,5H-PYRR;Pyrrolo[2,3-c]azepine-4,8(1H,5H)-dione, 2-bromo-6,7-dihydro-;2-Bromo-6,7-dihydropyrrolo[2,3-c]azepine-4,8(1H,5H)-dione;2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione | | CAS: | 96562-96-8 | | MF: | C8H7BrN2O2 | | MW: | 243.06 | | EINECS: | | | Product Categories: | pharmacetical | | Mol File: | 96562-96-8.mol | ![2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione Structure](CAS/GIF/96562-96-8.gif) |
| | 2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione Chemical Properties |
| form | White to off-white powder. | | color | White to off-white |
| | 2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione Usage And Synthesis |
| Uses | 2-Bromoaldisine is a pyrrole alkaloid that can be isolated from the Red Sea: marine sponge Stylissa carter. 2-Bromoaldisine inhibits HIV-1 vector infection. 2-Bromoaldisine inhibits Raf/MEK/MAPK pathway[1]. | | References | [1] Izumida M, et al. The Spirocyclic Imine from a Marine Benthic Dinoflagellate, Portimine, Is a Potent Anti-Human Immunodeficiency Virus Type 1 Therapeutic Lead Compound. Mar Drugs. 2019 Aug 24;17(9):495. DOI:10.3390/md17090495 |
| | 2-Bromo-6,7-dihydro-1H,5H-pyrrolo[2,3-c]azepine-4,8-dione Preparation Products And Raw materials |
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