Photolabile derivatives of indole alkaloid tumor promoter teleocidins: synthesis, biological activities and photoaffinity labeling studies

Tetrahedron ◽  
1993 ◽  
Vol 49 (47) ◽  
pp. 10817-10830 ◽  
Author(s):  
Kazuhiro Irie ◽  
Shigenori Okuno ◽  
Fumito Koizumi ◽  
Koichi Koshimizu ◽  
Hoyoku Nishino ◽  
...  
Keyword(s):  
Biological Activities ◽  
Photoaffinity Labeling ◽  
Indole Alkaloid ◽  
Tumor Promoter ◽  
Derivatives Of

Biological activities and cellular uptake studies of fluorescent derivatives of indole alkaloid tumor promoter teleocidin

1989 ◽  
Vol 43 (3) ◽  
pp. 513-519 ◽  
Author(s):  
Kazuhiro Irie ◽  
Shigenori Okuno ◽  
Koichi Koshimizu ◽  
Harukuni Tokuda ◽  
Hoyoku Nishino ◽  
...  
Keyword(s):  
Cellular Uptake ◽  
Biological Activities ◽  
Indole Alkaloid ◽  
Tumor Promoter ◽  
Uptake Studies ◽  
Derivatives Of ◽  
Fluorescent Derivatives

Synthesis, characterization and biological activities of 1,3,4-oxadiazole derivatives of nalidixic acid and their copper complexes

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Nalidixic Acid ◽  
Copper Complexes ◽  
Biological Activities ◽  
Bidentate Coordination ◽  
Antibacterial And Antifungal Activities ◽  
Elemental Analyses ◽  
Oxadiazole Derivatives ◽  
Antibacterial And Antifungal ◽  
Derivatives Of ◽  
Substituted 1

A series of novel 1, 3, 4-oxadiazole analogues was synthesized from cyclization of hydrazones of substituted 1-ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carbohydrazides were prepared from nalidixic acid. The structures of synthesized oxadiazole derivatives and their copper complexes were elucidated on the basis of FTIR, elemental analyses, 1H-NMR and atomic absorption spectral analysis. It was observed from spectral data that metal ligand ratio was 1:1 in all copper complexes and they were bidentate, coordination was found to be done through oxygen of 4-oxo group and nitrogen of oxadiazole ring. The synthesized compounds were further evaluated with biological activities and compared with parent hydrazones. Copper complexes possess antibacterial and antifungal activities better than the oxadiazoles while they have better antioxidant activity then copper complexes. Parent hydrazones were better in all biological activities than synthesized oxadiazoles.

scholarly journals Synthesis, Antiproliferative Activity and Radical Scavenging Ability of 5-O-Acyl Derivatives of Quercetin

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1608
Author(s):  
Stephen Lo ◽  
Euphemia Leung ◽  
Bruno Fedrizzi ◽  
David Barker
Keyword(s):  
Antiproliferative Activity ◽  
Biological Activities ◽  
Radical Scavenging Activity ◽  
Radical Scavenging ◽  
Breast Cancer Cell Lines ◽  
Scavenging Activity ◽  
Plant Materials ◽  
Wide Range ◽  
Derivatives Of ◽  
Acyl Derivatives

Quercetin is a flavonoid that is found in many plant materials, including commonly eaten fruits and vegetables. The compound is well known for its wide range of biological activities. In this study, 5-O-acyl derivatives of quercetin were synthesised and assessed for their antiproliferative activity against the HCT116 colon cancer and MDA-MB-231 breast cancer cell lines; and their radical scavenging activity against the 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical cation and 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical species. Four derivatives were found to have improved the antiproliferative activity compared to quercetin whilst retaining radical scavenging activity.

scholarly journals Synthetic Derivatives of Natural Alkaloid Harmine

2016 ◽  
Vol 11 (3) ◽  
pp. 199
Author(s):  
N.M. Ismagulova ◽  
Zh.S. Nurmaganbetov ◽  
A.Zh. Turmukhambetov ◽  
T.S. Seitembetov ◽  
S.M. Adekenov
Keyword(s):  
Indole Alkaloid ◽  
Quaternary Ammonium Salts ◽  
Ammonium Salts ◽  
Peganum Harmala ◽  
Underground Part ◽  
X Ray ◽  
Natural Alkaloid ◽  
First Time ◽  
Synthetic Derivatives ◽  
Derivatives Of

The indole alkaloid harmine was extracted from underground part of <em>Peganum harmala L.</em> With the purpose of obtaining the new biological active derivatives on base of alkaloid harmine the chemical modification was carried out. The p-toluolsulfochlorid, p-toluolsulfoacid, hydrochloric, sulfuric, nitric acids, dioxide selenium and phthalic anhydride have been chosen as modifiers. For the first time quaternary ammonium salts, derivatives of N-oxide and N (2)-oxyharminiumphthalate harmine are synthesized. The structure of the synthesized compounds is determined by methods of the spectral analysis and X-ray analysis. Antimicrobic and phagocytosis stimulating activities of isolated alkaloids and their derivatives are investigated.

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