نتایج جستجو برای: indol

تعداد نتایج: 1726  

Journal: :organic chemistry research 0
mohsen khezri department of organic chemistry, faculty of chemistry, university of urmia, urmia 57153-165, iran arash afghan urmia university of technology, urmia, iran laya roohi department of organic chemistry, faculty of chemistry, university of urmia, urmia 57153-165, iran mohammad mehdi baradarani department of organic chemistry, faculty of chemistry, university of urmia, urmia 57153-165, iran

vilsmeier-haack reaction of 2,3,3-trimethyl-3h-benzo[g]indole, then aqueous basic work-up, leads to benzo[g]indol-2-ylidene- malondialdehydes. these react with various arylhydrazines and quinolin-2-ylhydrazine to form 3,3-dimethyl-2-(1-aryl-1h-pyrazol-4-yl)- 3h-benzo[g]indoles in good yields.

Journal: :American Journal of Epidemiology 1943

Journal: :Acta Crystallographica Section E Structure Reports Online 2008

Journal: :Journal of Bacteriology 1926

Journal: :Berichte der deutschen chemischen Gesellschaft 1916

Journal: : 2022

Anavatanı Japonya olan Magnolia kobus DC., Magnoliaceae familyasından, kışın yaprağını döken küçük ağaç formunda bir bitkidir. Formu, aromatik yaprakları, bol miktarda açan pembemsi beyaz çiçekleri ve meyve güzelliği ile Peyzaj Mimarlığı bitkilendirme tasarımlarında tercih edilen bitkilerden biridir. Bu çalışmanın amacı, estetik özelikleri etkili bu bitkinin çelikle çoğaltılarak kentsel peyzajd...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2003
Richard A Tschirret-Guth Harold B Wood

The reductive metabolism of a series of 3-(indol-1-yl)-1,2-benzisoxazoles was examined in vitro using rat liver microsomes. 3-(Indol-1-yl)-1,2-benzisoxazole was reduced to the corresponding amidine (resulting from N-O bond cleavage) under anaerobic conditions. The reaction required viable microsomes and NADPH and was inhibited by carbon monoxide, air, and ketoconazole, suggesting the involvemen...

2007
Katsuyuki AOKI Jyun-ichi KOSEKI Shuichi TAKEDA Masaki ABURADA

as an anti-angiogenesis agent by Ladouceur et al. These compounds have a potent inhibitory effect on the growth of tumor cells with angiogenesis activity. We have also carried out a structure–activity relationship (SAR) study of 3-(indol2-yl)quinoxalin-2-ones, which showed a potent inhibitory activity toward the VEGF-induced proliferation of human mesangial cells and the VEGF-induced auto-phosp...

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