CAS: 14401-72-0; 1-(3,5-Dichlorophenyl)Ethanone

相似化合物

259796-12-8 99-02-5 2642-63-9

上下游产品

2-(3,5-dichlorophenyl)-2-propanol 1-(4-amino-3,5-dichlorophenyl)-1-ethanone methyl magnesium iodide 3,5-dichlorobenzonitrile 3,5-Dichlorethylbenzol (+/-)-α-(3,5-dichlorophenyl)ethylamine 3,5-dichlorobenzoic acid 3-(3,5-dichlorophenyl)-1H-pyrazole

4-氨基苯乙酮置于吡啶,盐酸,氯,溶剂黄146,Sodium Nitrite体系中,化学反应生成3',5'-二氯苯乙酮
参考文献:Antimalarials. α-Phenyl-β-Dialkylamino Alcohols1
标题:Antimalarials. α-Phenyl-β-Dialkylamino Alcohols1
摘要:
Doi:10.1021/jo01169A001

专利信息

专利号:US-6005103-A
优先权日:1993-11-19
标题 :Pyrone derivatives as protease inhibitors and antiviral agents
发明人：DOMAGALA JOHN MICHAEL; LUNNEY ELIZABETH; PARA KIMBERLY SUZANNE; PRASAD JOSYULA VENKATA NAGENDR; TAIT BRADLEY DEAN
权利人:WARNER LAMBERT CO
摘要:The present invention relates to novel tri- and tetrasubstituted pyrones and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The pyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized pyrones and of related structures.

专利号:EP-0729465-B1
优先权日:1993-11-19
标 题:Pyrone derivatives as protease inhibitors and antiviral agents
发明人：DOMAGALA JOHN MICHAEL; LUNNEY ELIZABETH; PARA KIMBERLY SUZANNE; PRASAD JOSYULA VENKATA NAGENDR; TAIT BRADLEY DEAN
权利人:PARKE DAVIS & CO
摘要:The present invention relates to novel tri- and tetrasubstituted pyrones and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The pyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized pyrones and of related structures.

专利号:US-2025250218-A1
优先权日:2024-02-07
标题 :Anti-Amyloidogenic Curcumin Analogues
发明人：PRIEFER RONNY; YOUNG MICHELLE; GORDON PATRICK; LANDRY GREG
权利人:MCPHS UNIV
摘要:Extended chalcone compounds with anti-amylogenic activity were prepared and found to lack cytotoxicity and to promote neuroprotection. Testing on an animal model for Alzheimer's Disease revealed improvements in brain function using the high affinity compounds. The compounds inhibited the aggregation of Aβ42 but not its synthesis. The compounds can be used in new therapies for the prevention and treatment of Alzheimer's disease, including in conjunction with antibodies directed at removing amyloid plaques.